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  1. .gitattributes +15 -0
  2. p1/preprocess/Cardiovascular_Disease/gene_data/GSE182600.csv +3 -0
  3. p1/preprocess/Cardiovascular_Disease/gene_data/GSE190042.csv +3 -0
  4. p1/preprocess/Cardiovascular_Disease/gene_data/GSE235307.csv +3 -0
  5. p1/preprocess/Celiac_Disease/GSE72625.csv +3 -0
  6. p1/preprocess/Celiac_Disease/gene_data/GSE138297.csv +3 -0
  7. p1/preprocess/Celiac_Disease/gene_data/GSE164883.csv +0 -0
  8. p1/preprocess/Celiac_Disease/gene_data/GSE20332.csv +3 -0
  9. p1/preprocess/Celiac_Disease/gene_data/GSE72625.csv +3 -0
  10. p1/preprocess/Cervical_Cancer/GSE63678.csv +0 -0
  11. p1/preprocess/Cervical_Cancer/GSE75132.csv +0 -0
  12. p1/preprocess/Cervical_Cancer/code/GSE138080.py +174 -0
  13. p1/preprocess/Cervical_Cancer/code/GSE163114.py +172 -0
  14. p1/preprocess/Cervical_Cancer/code/GSE75132.py +160 -0
  15. p1/preprocess/Cervical_Cancer/gene_data/GSE107754.csv +3 -0
  16. p1/preprocess/Cervical_Cancer/gene_data/GSE131027.csv +3 -0
  17. p1/preprocess/Cervical_Cancer/gene_data/GSE138079.csv +3 -0
  18. p1/preprocess/Cervical_Cancer/gene_data/GSE138080.csv +0 -0
  19. p1/preprocess/Cervical_Cancer/gene_data/GSE146114.csv +3 -0
  20. p1/preprocess/Cervical_Cancer/gene_data/GSE163114.csv +0 -0
  21. p1/preprocess/Cervical_Cancer/gene_data/GSE63678.csv +0 -0
  22. p1/preprocess/Cervical_Cancer/gene_data/GSE75132.csv +0 -0
  23. p1/preprocess/Chronic_Fatigue_Syndrome/GSE251792.csv +0 -0
  24. p1/preprocess/Chronic_Fatigue_Syndrome/GSE67311.csv +3 -0
  25. p1/preprocess/Chronic_Fatigue_Syndrome/clinical_data/GSE251792.csv +4 -0
  26. p1/preprocess/Chronic_Fatigue_Syndrome/clinical_data/GSE67311.csv +2 -0
  27. p1/preprocess/Chronic_Fatigue_Syndrome/code/GSE251792.py +225 -0
  28. p1/preprocess/Chronic_Fatigue_Syndrome/code/GSE39684.py +198 -0
  29. p1/preprocess/Chronic_Fatigue_Syndrome/code/GSE67311.py +233 -0
  30. p1/preprocess/Chronic_Fatigue_Syndrome/code/TCGA.py +56 -0
  31. p1/preprocess/Chronic_Fatigue_Syndrome/cohort_info.json +1 -0
  32. p1/preprocess/Chronic_Fatigue_Syndrome/gene_data/GSE251792.csv +0 -0
  33. p1/preprocess/Chronic_Fatigue_Syndrome/gene_data/GSE39684.csv +1 -0
  34. p1/preprocess/Chronic_kidney_disease/GSE142153.csv +0 -0
  35. p1/preprocess/Chronic_kidney_disease/GSE66494.csv +3 -0
  36. p1/preprocess/Chronic_kidney_disease/clinical_data/GSE104948.csv +2 -0
  37. p1/preprocess/Chronic_kidney_disease/clinical_data/GSE104954.csv +2 -0
  38. p1/preprocess/Chronic_kidney_disease/clinical_data/GSE127136.csv +2 -0
  39. p1/preprocess/Chronic_kidney_disease/clinical_data/GSE142153.csv +2 -0
  40. p1/preprocess/Chronic_kidney_disease/clinical_data/GSE180393.csv +2 -0
  41. p1/preprocess/Chronic_kidney_disease/clinical_data/GSE180394.csv +2 -0
  42. p1/preprocess/Chronic_kidney_disease/clinical_data/GSE66494.csv +2 -0
  43. p1/preprocess/Chronic_kidney_disease/code/GSE104948.py +161 -0
  44. p1/preprocess/Chronic_kidney_disease/code/GSE104954.py +152 -0
  45. p1/preprocess/Chronic_kidney_disease/code/GSE127136.py +93 -0
  46. p1/preprocess/Chronic_kidney_disease/code/GSE142153.py +149 -0
  47. p1/preprocess/Chronic_kidney_disease/code/GSE180393.py +195 -0
  48. p1/preprocess/Chronic_kidney_disease/code/GSE180394.py +227 -0
  49. p1/preprocess/Chronic_kidney_disease/code/GSE45980.py +234 -0
  50. p1/preprocess/Chronic_kidney_disease/code/GSE60861.py +230 -0
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p1/preprocess/Cervical_Cancer/code/GSE138080.py ADDED
@@ -0,0 +1,174 @@
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1
+ # Path Configuration
2
+ from tools.preprocess import *
3
+
4
+ # Processing context
5
+ trait = "Cervical_Cancer"
6
+ cohort = "GSE138080"
7
+
8
+ # Input paths
9
+ in_trait_dir = "../DATA/GEO/Cervical_Cancer"
10
+ in_cohort_dir = "../DATA/GEO/Cervical_Cancer/GSE138080"
11
+
12
+ # Output paths
13
+ out_data_file = "./output/preprocess/1/Cervical_Cancer/GSE138080.csv"
14
+ out_gene_data_file = "./output/preprocess/1/Cervical_Cancer/gene_data/GSE138080.csv"
15
+ out_clinical_data_file = "./output/preprocess/1/Cervical_Cancer/clinical_data/GSE138080.csv"
16
+ json_path = "./output/preprocess/1/Cervical_Cancer/cohort_info.json"
17
+
18
+ # STEP1
19
+ from tools.preprocess import *
20
+
21
+ # 1. Identify the paths to the SOFT file and the matrix file
22
+ soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir)
23
+
24
+ # 2. Read the matrix file to obtain background information and sample characteristics data
25
+ background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design']
26
+ clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1']
27
+ background_info, clinical_data = get_background_and_clinical_data(
28
+ matrix_file,
29
+ background_prefixes,
30
+ clinical_prefixes
31
+ )
32
+
33
+ # 3. Obtain the sample characteristics dictionary from the clinical dataframe
34
+ sample_characteristics_dict = get_unique_values_by_row(clinical_data)
35
+
36
+ # 4. Explicitly print out all the background information and the sample characteristics dictionary
37
+ print("Background Information:")
38
+ print(background_info)
39
+ print("Sample Characteristics Dictionary:")
40
+ print(sample_characteristics_dict)
41
+ # Step: Dataset Analysis and Clinical Feature Extraction
42
+
43
+ # 1. Determine if the dataset likely contains gene expression data
44
+ is_gene_available = True # Based on the "mRNA tissues-Agilent" description
45
+
46
+ # 2. Determine availability of variables and write conversion functions
47
+
48
+ # From the sample characteristics:
49
+ # {0: ['cell type: normal cervical squamous epithelium',
50
+ # 'cell type: cervical intraepithelial neoplasia, grade 2-3',
51
+ # 'cell type: cervical squamous cell carcinoma'],
52
+ # 1: ['hpv: high-risk HPV-positive',
53
+ # 'hpv: HPV-negative']}
54
+
55
+ # Observing these, row 0 contains different states of cervical tissue,
56
+ # which we interpret as relevant to the trait "Cervical_Cancer."
57
+ # Hence we set:
58
+ trait_row = 0
59
+
60
+ # There is no row indicating age, so:
61
+ age_row = None
62
+
63
+ # There is no row indicating gender, so:
64
+ gender_row = None
65
+
66
+ # Data Type Conversion Functions
67
+ def convert_trait(value: str):
68
+ # Extract the text after the colon if present
69
+ parts = value.split(':', 1)
70
+ val = parts[1].strip().lower() if len(parts) == 2 else value.strip().lower()
71
+ # Convert to binary (0 = normal, 1 = pre-cancer or cancer)
72
+ if "normal" in val:
73
+ return 0
74
+ elif "intraepithelial" in val or "carcinoma" in val:
75
+ return 1
76
+ return None
77
+
78
+ def convert_age(value: str):
79
+ # Not used since age is unavailable
80
+ return None
81
+
82
+ def convert_gender(value: str):
83
+ # Not used since gender is unavailable
84
+ return None
85
+
86
+ # 3. Perform initial filtering and save metadata
87
+ # Trait data is available if trait_row is not None
88
+ is_trait_available = (trait_row is not None)
89
+
90
+ is_usable = validate_and_save_cohort_info(
91
+ is_final=False,
92
+ cohort=cohort,
93
+ info_path=json_path,
94
+ is_gene_available=is_gene_available,
95
+ is_trait_available=is_trait_available
96
+ )
97
+
98
+ # 4. Clinical feature extraction if trait data is available
99
+ if trait_row is not None:
100
+ selected_clinical_df = geo_select_clinical_features(
101
+ clinical_df=clinical_data,
102
+ trait=trait,
103
+ trait_row=trait_row,
104
+ convert_trait=convert_trait,
105
+ age_row=age_row,
106
+ convert_age=convert_age,
107
+ gender_row=gender_row,
108
+ convert_gender=convert_gender
109
+ )
110
+ # Preview dataframe
111
+ preview = preview_df(selected_clinical_df, n=5, max_items=200)
112
+ print("Preview of selected clinical features:", preview)
113
+
114
+ # Save the clinical data
115
+ selected_clinical_df.to_csv(out_clinical_data_file, index=False)
116
+ # STEP3
117
+ # 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined.
118
+ gene_data = get_genetic_data(matrix_file)
119
+
120
+ # 2. Print the first 20 row IDs (gene or probe identifiers) for future observation.
121
+ print(gene_data.index[:20])
122
+ print("These numeric entries appear to be probe IDs or some numeric references, not standard human gene symbols.\nrequires_gene_mapping = True")
123
+ # STEP5
124
+ # 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file.
125
+ gene_annotation = get_gene_annotation(soft_file)
126
+
127
+ # 2. Use the 'preview_df' function from the library to preview the data and print out the results.
128
+ print("Gene annotation preview:")
129
+ print(preview_df(gene_annotation))
130
+ # STEP: Gene Identifier Mapping
131
+
132
+ # 1. Determine which columns in gene_annotation match the probe IDs in gene_data and which store gene symbols.
133
+ # From the preview, "ID" matches the probe IDs, and "GENE_SYMBOL" corresponds to gene symbols.
134
+
135
+ # 2. Create a mapping dataframe from the gene_annotation by extracting the probe ID column and gene symbol column.
136
+ mapping_df = get_gene_mapping(gene_annotation, prob_col="ID", gene_col="GENE_SYMBOL")
137
+
138
+ # 3. Convert the probe-level data to gene-level data using the mapping, distributing expression among genes if a probe
139
+ # maps to multiple genes, and summing across probes for the same gene.
140
+ gene_data = apply_gene_mapping(gene_data, mapping_df)
141
+
142
+ # (Optional) Print a brief check of the new gene_data
143
+ print("Gene data shape after mapping:", gene_data.shape)
144
+ print("First 20 genes after mapping:", gene_data.index[:20])
145
+ # STEP 7
146
+
147
+ # 1. Normalize gene symbols in the gene_data, then save to CSV.
148
+ normalized_gene_data = normalize_gene_symbols_in_index(gene_data)
149
+ normalized_gene_data.to_csv(out_gene_data_file)
150
+
151
+ # 2. Link the clinical and genetic data on sample IDs
152
+ linked_data = geo_link_clinical_genetic_data(selected_clinical_df, normalized_gene_data)
153
+
154
+ # 3. Handle missing values in the linked data
155
+ linked_data = handle_missing_values(linked_data, trait)
156
+
157
+ # 4. Determine whether the trait and demographic features are biased
158
+ trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait)
159
+
160
+ # 5. Conduct final validation and save cohort info
161
+ is_usable = validate_and_save_cohort_info(
162
+ is_final=True,
163
+ cohort=cohort,
164
+ info_path=json_path,
165
+ is_gene_available=True,
166
+ is_trait_available=True,
167
+ is_biased=trait_biased,
168
+ df=linked_data,
169
+ note="Trait is available. Completed linking and QC steps."
170
+ )
171
+
172
+ # 6. If the dataset is usable, save the final linked data
173
+ if is_usable:
174
+ linked_data.to_csv(out_data_file)
p1/preprocess/Cervical_Cancer/code/GSE163114.py ADDED
@@ -0,0 +1,172 @@
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1
+ # Path Configuration
2
+ from tools.preprocess import *
3
+
4
+ # Processing context
5
+ trait = "Cervical_Cancer"
6
+ cohort = "GSE163114"
7
+
8
+ # Input paths
9
+ in_trait_dir = "../DATA/GEO/Cervical_Cancer"
10
+ in_cohort_dir = "../DATA/GEO/Cervical_Cancer/GSE163114"
11
+
12
+ # Output paths
13
+ out_data_file = "./output/preprocess/1/Cervical_Cancer/GSE163114.csv"
14
+ out_gene_data_file = "./output/preprocess/1/Cervical_Cancer/gene_data/GSE163114.csv"
15
+ out_clinical_data_file = "./output/preprocess/1/Cervical_Cancer/clinical_data/GSE163114.csv"
16
+ json_path = "./output/preprocess/1/Cervical_Cancer/cohort_info.json"
17
+
18
+ # STEP1
19
+ from tools.preprocess import *
20
+
21
+ # 1. Identify the paths to the SOFT file and the matrix file
22
+ soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir)
23
+
24
+ # 2. Read the matrix file to obtain background information and sample characteristics data
25
+ background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design']
26
+ clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1']
27
+ background_info, clinical_data = get_background_and_clinical_data(
28
+ matrix_file,
29
+ background_prefixes,
30
+ clinical_prefixes
31
+ )
32
+
33
+ # 3. Obtain the sample characteristics dictionary from the clinical dataframe
34
+ sample_characteristics_dict = get_unique_values_by_row(clinical_data)
35
+
36
+ # 4. Explicitly print out all the background information and the sample characteristics dictionary
37
+ print("Background Information:")
38
+ print(background_info)
39
+ print("Sample Characteristics Dictionary:")
40
+ print(sample_characteristics_dict)
41
+ # Step 1: Gene Expression Data Availability
42
+ # Based on the background information ("Ki-67 promotes carcinogenesis by enabling global transcriptional programmes")
43
+ # and the use of the HeLa cell line, it is likely that this dataset contains gene expression data.
44
+ is_gene_available = True
45
+
46
+ # Step 2: Variable Availability and Data Type Conversion
47
+
48
+ # From the sample characteristics dictionary:
49
+ # {0: ['cell line: HeLa'], 1: ['lentivirus: shRNA control', 'lentivirus: shRNA Ki-67']}
50
+ # - All samples come from the HeLa cell line, which is derived from cervical cancer, but this is a constant feature (no variation).
51
+ # - There's no row providing age or gender information.
52
+ # Hence, no variable has meaningful variation. We set rows to None.
53
+
54
+ trait_row = None # No row captures a varying cervical cancer trait
55
+ age_row = None # No row for age
56
+ gender_row = None # No row for gender
57
+
58
+ # Even though these functions won't be used (since trait_row, age_row, gender_row = None),
59
+ # we provide them per instructions.
60
+
61
+ def convert_trait(value: str):
62
+ """
63
+ Convert the trait to the chosen type.
64
+ Not applicable here, but defined for completeness.
65
+ """
66
+ if not value or ':' not in value:
67
+ return None
68
+ val = value.split(':', 1)[-1].strip()
69
+ return val if val else None
70
+
71
+ def convert_age(value: str):
72
+ """
73
+ Convert age data to a continuous type.
74
+ Not applicable here, but defined for completeness.
75
+ """
76
+ if not value or ':' not in value:
77
+ return None
78
+ val = value.split(':', 1)[-1].strip()
79
+ # We do not actually have numeric values, so just return None.
80
+ return None
81
+
82
+ def convert_gender(value: str):
83
+ """
84
+ Convert gender data to binary.
85
+ Not applicable here, but defined for completeness.
86
+ """
87
+ if not value or ':' not in value:
88
+ return None
89
+ val = value.split(':', 1)[-1].strip().lower()
90
+ if val in ['male', 'm']:
91
+ return 1
92
+ elif val in ['female', 'f']:
93
+ return 0
94
+ return None
95
+
96
+ # Step 3: Save Metadata
97
+ # If trait_row is None, trait data is considered unavailable.
98
+ is_trait_available = (trait_row is not None)
99
+
100
+ _ = validate_and_save_cohort_info(
101
+ is_final=False,
102
+ cohort=cohort,
103
+ info_path=json_path,
104
+ is_gene_available=is_gene_available,
105
+ is_trait_available=is_trait_available
106
+ )
107
+
108
+ # Step 4: Since trait_row is None, we skip geo_select_clinical_features.
109
+ # No clinical data extraction is performed because the trait is not available.
110
+ # STEP3
111
+ # 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined.
112
+ gene_data = get_genetic_data(matrix_file)
113
+
114
+ # 2. Print the first 20 row IDs (gene or probe identifiers) for future observation.
115
+ print(gene_data.index[:20])
116
+ # Based on the numeric IDs (1,2,3,...), they do not appear to be standard human gene symbols.
117
+ # They seem like probe identifiers or some form of numeric reference that would require mapping.
118
+ print("These numeric IDs likely need mapping to standard gene symbols.")
119
+ print("requires_gene_mapping = True")
120
+ # STEP5
121
+ # 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file.
122
+ gene_annotation = get_gene_annotation(soft_file)
123
+
124
+ # 2. Use the 'preview_df' function from the library to preview the data and print out the results.
125
+ print("Gene annotation preview:")
126
+ print(preview_df(gene_annotation))
127
+ # STEP: Gene Identifier Mapping
128
+
129
+ # 1. Decide which key in the gene annotation dataframe stores the gene identifiers
130
+ # matching the gene expression data. From the preview, the 'ID' column in gene_annotation
131
+ # corresponds to the numeric probe IDs in gene_data. For gene symbols, we use 'GENE_SYMBOL'.
132
+
133
+ # 2. Get a gene mapping dataframe
134
+ mapping_df = get_gene_mapping(gene_annotation, prob_col='ID', gene_col='GENE_SYMBOL')
135
+
136
+ # 3. Convert probe-level measurements to gene expression data
137
+ gene_data = apply_gene_mapping(gene_data, mapping_df)
138
+
139
+ # Print a quick check of the mapped dataframe
140
+ print("Mapped gene_data shape:", gene_data.shape)
141
+ print("Head of mapped gene_data:")
142
+ print(gene_data.head())
143
+ # STEP 7
144
+
145
+ # 1. Normalize gene symbols in the gene_data, then save to CSV.
146
+ normalized_gene_data = normalize_gene_symbols_in_index(gene_data)
147
+ normalized_gene_data.to_csv(out_gene_data_file)
148
+
149
+ # Since trait_row was None in earlier steps, there is no actual trait data available.
150
+ # We cannot link clinical data or do trait-based QC. However, the library requires a final
151
+ # validation with a DataFrame and a Boolean for is_biased.
152
+
153
+ # Create an empty DataFrame as a placeholder, and declare is_biased=False by default.
154
+ placeholder_df = pd.DataFrame()
155
+ trait_biased = False
156
+
157
+ # 2. Perform final validation, marking trait as unavailable but providing the required arguments.
158
+ is_usable = validate_and_save_cohort_info(
159
+ is_final=True,
160
+ cohort=cohort,
161
+ info_path=json_path,
162
+ is_gene_available=True, # Gene data is present
163
+ is_trait_available=False, # Trait is not available
164
+ is_biased=trait_biased,
165
+ df=placeholder_df, # Provide a placeholder DataFrame
166
+ note="No trait data in this series. Final validation with placeholder DataFrame."
167
+ )
168
+
169
+ # 3. If the dataset were usable (it won't be without trait), we would save final linked data.
170
+ if is_usable:
171
+ # Typically we would link data and save CSV, but trait is absent. Skipping.
172
+ pass
p1/preprocess/Cervical_Cancer/code/GSE75132.py ADDED
@@ -0,0 +1,160 @@
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1
+ # Path Configuration
2
+ from tools.preprocess import *
3
+
4
+ # Processing context
5
+ trait = "Cervical_Cancer"
6
+ cohort = "GSE75132"
7
+
8
+ # Input paths
9
+ in_trait_dir = "../DATA/GEO/Cervical_Cancer"
10
+ in_cohort_dir = "../DATA/GEO/Cervical_Cancer/GSE75132"
11
+
12
+ # Output paths
13
+ out_data_file = "./output/preprocess/1/Cervical_Cancer/GSE75132.csv"
14
+ out_gene_data_file = "./output/preprocess/1/Cervical_Cancer/gene_data/GSE75132.csv"
15
+ out_clinical_data_file = "./output/preprocess/1/Cervical_Cancer/clinical_data/GSE75132.csv"
16
+ json_path = "./output/preprocess/1/Cervical_Cancer/cohort_info.json"
17
+
18
+ # STEP1
19
+ from tools.preprocess import *
20
+
21
+ # 1. Identify the paths to the SOFT file and the matrix file
22
+ soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir)
23
+
24
+ # 2. Read the matrix file to obtain background information and sample characteristics data
25
+ background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design']
26
+ clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1']
27
+ background_info, clinical_data = get_background_and_clinical_data(
28
+ matrix_file,
29
+ background_prefixes,
30
+ clinical_prefixes
31
+ )
32
+
33
+ # 3. Obtain the sample characteristics dictionary from the clinical dataframe
34
+ sample_characteristics_dict = get_unique_values_by_row(clinical_data)
35
+
36
+ # 4. Explicitly print out all the background information and the sample characteristics dictionary
37
+ print("Background Information:")
38
+ print(background_info)
39
+ print("Sample Characteristics Dictionary:")
40
+ print(sample_characteristics_dict)
41
+ # Step 1: Determine if gene expression data is available
42
+ # Based on the background info (microarray analysis on RNA), we consider this dataset to contain gene expression data.
43
+ is_gene_available = True
44
+
45
+ # Step 2: Assign row keys and define conversion functions for trait, age, and gender
46
+
47
+ # Observing the sample characteristics dictionary:
48
+ # 3: ['disease state: none', 'disease state: moderate dysplasia', 'disease state: severe dysplasia',
49
+ # 'disease state: CIS', 'disease state: cancer']
50
+ # We map "none" -> 0 and everything else -> 1 for a binary trait of Cervical_Cancer.
51
+
52
+ trait_row = 3
53
+ def convert_trait(x: str):
54
+ # Extract the value after the colon
55
+ parts = x.split(':', 1)
56
+ val = parts[1].strip() if len(parts) > 1 else None
57
+ if val is None:
58
+ return None
59
+ val_lower = val.lower()
60
+ if val_lower == 'none':
61
+ return 0
62
+ else:
63
+ return 1
64
+
65
+ # No age, no gender data found
66
+ age_row = None
67
+ convert_age = None
68
+
69
+ gender_row = None
70
+ convert_gender = None
71
+
72
+ # Step 2.1: Data availability
73
+ is_trait_available = (trait_row is not None)
74
+
75
+ # Step 3: Initial filtering and metadata saving
76
+ validate_and_save_cohort_info(
77
+ is_final=False,
78
+ cohort=cohort,
79
+ info_path=json_path,
80
+ is_gene_available=is_gene_available,
81
+ is_trait_available=is_trait_available
82
+ )
83
+
84
+ # Step 4: If trait data is available, extract clinical features
85
+ if trait_row is not None:
86
+ selected_clinical_df = geo_select_clinical_features(
87
+ clinical_df=clinical_data,
88
+ trait=trait,
89
+ trait_row=trait_row,
90
+ convert_trait=convert_trait,
91
+ age_row=age_row,
92
+ convert_age=convert_age,
93
+ gender_row=gender_row,
94
+ convert_gender=convert_gender
95
+ )
96
+
97
+ # Preview the extracted clinical data
98
+ clinical_preview = preview_df(selected_clinical_df)
99
+ print("Clinical Data Preview:", clinical_preview)
100
+
101
+ # Save the clinical data to CSV
102
+ selected_clinical_df.to_csv(out_clinical_data_file, index=False)
103
+ # STEP3
104
+ # 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined.
105
+ gene_data = get_genetic_data(matrix_file)
106
+
107
+ # 2. Print the first 20 row IDs (gene or probe identifiers) for future observation.
108
+ print(gene_data.index[:20])
109
+ print("They appear to be Affymetrix probe set IDs. Hence they are not standard human gene symbols.")
110
+ print("requires_gene_mapping = True")
111
+ # STEP5
112
+ # 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file.
113
+ gene_annotation = get_gene_annotation(soft_file)
114
+
115
+ # 2. Use the 'preview_df' function from the library to preview the data and print out the results.
116
+ print("Gene annotation preview:")
117
+ print(preview_df(gene_annotation))
118
+ # STEP: Gene Identifier Mapping
119
+
120
+ # 1 & 2. Decide which columns in the annotation data correspond to probe IDs and gene symbols.
121
+ # In this case, the 'ID' column matches our probe identifiers, and the 'Gene Symbol' column are the gene symbols.
122
+
123
+ mapping_df = get_gene_mapping(
124
+ annotation=gene_annotation,
125
+ prob_col="ID",
126
+ gene_col="Gene Symbol"
127
+ )
128
+
129
+ # 3. Convert probe-level measurements to gene expression data using the mapping from above.
130
+ gene_data = apply_gene_mapping(expression_df=gene_data, mapping_df=mapping_df)
131
+ # STEP 7
132
+
133
+ # 1. Normalize gene symbols in the gene_data, then save to CSV.
134
+ normalized_gene_data = normalize_gene_symbols_in_index(gene_data)
135
+ normalized_gene_data.to_csv(out_gene_data_file)
136
+
137
+ # 2. Link the clinical and genetic data on sample IDs
138
+ linked_data = geo_link_clinical_genetic_data(selected_clinical_df, normalized_gene_data)
139
+
140
+ # 3. Handle missing values in the linked data
141
+ linked_data = handle_missing_values(linked_data, trait)
142
+
143
+ # 4. Determine whether the trait and demographic features are biased
144
+ trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait)
145
+
146
+ # 5. Conduct final validation and save cohort info
147
+ is_usable = validate_and_save_cohort_info(
148
+ is_final=True,
149
+ cohort=cohort,
150
+ info_path=json_path,
151
+ is_gene_available=True,
152
+ is_trait_available=True,
153
+ is_biased=trait_biased,
154
+ df=linked_data,
155
+ note="Trait is available. Completed linking and QC steps."
156
+ )
157
+
158
+ # 6. If the dataset is usable, save the final linked data
159
+ if is_usable:
160
+ linked_data.to_csv(out_data_file)
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p1/preprocess/Chronic_Fatigue_Syndrome/code/GSE251792.py ADDED
@@ -0,0 +1,225 @@
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1
+ # Path Configuration
2
+ from tools.preprocess import *
3
+
4
+ # Processing context
5
+ trait = "Chronic_Fatigue_Syndrome"
6
+ cohort = "GSE251792"
7
+
8
+ # Input paths
9
+ in_trait_dir = "../DATA/GEO/Chronic_Fatigue_Syndrome"
10
+ in_cohort_dir = "../DATA/GEO/Chronic_Fatigue_Syndrome/GSE251792"
11
+
12
+ # Output paths
13
+ out_data_file = "./output/preprocess/1/Chronic_Fatigue_Syndrome/GSE251792.csv"
14
+ out_gene_data_file = "./output/preprocess/1/Chronic_Fatigue_Syndrome/gene_data/GSE251792.csv"
15
+ out_clinical_data_file = "./output/preprocess/1/Chronic_Fatigue_Syndrome/clinical_data/GSE251792.csv"
16
+ json_path = "./output/preprocess/1/Chronic_Fatigue_Syndrome/cohort_info.json"
17
+
18
+ # STEP1
19
+ from tools.preprocess import *
20
+
21
+ # 1. Attempt to identify the paths to the SOFT file and the matrix file
22
+ try:
23
+ soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir)
24
+ except AssertionError:
25
+ print("[WARNING] Could not find the expected '.soft' or '.matrix' files in the directory.")
26
+ soft_file, matrix_file = None, None
27
+
28
+ if soft_file is None or matrix_file is None:
29
+ print("[ERROR] Required GEO files are missing. Please check file names in the cohort directory.")
30
+ else:
31
+ # 2. Read the matrix file to obtain background information and sample characteristics data
32
+ background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design']
33
+ clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1']
34
+ background_info, clinical_data = get_background_and_clinical_data(matrix_file,
35
+ background_prefixes,
36
+ clinical_prefixes)
37
+
38
+ # 3. Obtain the sample characteristics dictionary from the clinical dataframe
39
+ sample_characteristics_dict = get_unique_values_by_row(clinical_data)
40
+
41
+ # 4. Explicitly print out all the background information and the sample characteristics dictionary
42
+ print("Background Information:")
43
+ print(background_info)
44
+ print("\nSample Characteristics Dictionary:")
45
+ print(sample_characteristics_dict)
46
+ # Step 1: Determine gene expression availability
47
+ is_gene_available = True # Based on the background info, likely gene expression data
48
+
49
+ # Step 2: Identify data availability and define keys
50
+ trait_row = 2 # "group: Patient/Control"
51
+ age_row = 1 # "age: 61, 37, etc."
52
+ gender_row = 0 # "Sex: Female/Male"
53
+
54
+ # Step 2.2: Define conversion functions
55
+ def convert_trait(value: str):
56
+ # Extract substring after ':'
57
+ parts = value.split(':', 1)
58
+ if len(parts) < 2:
59
+ return None
60
+ val = parts[1].strip().lower()
61
+ if val == 'patient':
62
+ return 1
63
+ elif val == 'control':
64
+ return 0
65
+ return None
66
+
67
+ def convert_age(value: str):
68
+ parts = value.split(':', 1)
69
+ if len(parts) < 2:
70
+ return None
71
+ val = parts[1].strip()
72
+ try:
73
+ return float(val)
74
+ except ValueError:
75
+ return None
76
+
77
+ def convert_gender(value: str):
78
+ parts = value.split(':', 1)
79
+ if len(parts) < 2:
80
+ return None
81
+ val = parts[1].strip().lower()
82
+ if val == 'female':
83
+ return 0
84
+ elif val == 'male':
85
+ return 1
86
+ return None
87
+
88
+ # Step 3: Save metadata with initial filtering
89
+ is_trait_available = (trait_row is not None)
90
+ is_usable = validate_and_save_cohort_info(
91
+ is_final=False,
92
+ cohort=cohort,
93
+ info_path=json_path,
94
+ is_gene_available=is_gene_available,
95
+ is_trait_available=is_trait_available
96
+ )
97
+
98
+ # Step 4: Clinical feature extraction if trait_row is not None
99
+ if trait_row is not None:
100
+ selected_clinical_df = geo_select_clinical_features(
101
+ clinical_data,
102
+ trait='trait',
103
+ trait_row=trait_row,
104
+ convert_trait=convert_trait,
105
+ age_row=age_row,
106
+ convert_age=convert_age,
107
+ gender_row=gender_row,
108
+ convert_gender=convert_gender
109
+ )
110
+ # Preview the extracted dataframe
111
+ preview_result = preview_df(selected_clinical_df)
112
+ print(preview_result)
113
+ # Save the clinical data
114
+ selected_clinical_df.to_csv(out_clinical_data_file, index=False)
115
+ # STEP3
116
+ # Attempt to read gene expression data; if the library function yields an empty DataFrame,
117
+ # try re-reading without ignoring lines that start with '!' (because sometimes GEO data may
118
+ # place actual expression rows under lines that begin with '!').
119
+
120
+ gene_data = get_genetic_data(matrix_file)
121
+ if gene_data.empty:
122
+ print("[WARNING] The gene_data is empty. Attempting alternative loading without treating '!' as comments.")
123
+ import gzip
124
+
125
+ # Locate the marker line first
126
+ skip_rows = 0
127
+ with gzip.open(matrix_file, 'rt') as file:
128
+ for i, line in enumerate(file):
129
+ if "!series_matrix_table_begin" in line:
130
+ skip_rows = i + 1
131
+ break
132
+
133
+ # Read the data again, this time not treating '!' as comment
134
+ gene_data = pd.read_csv(
135
+ matrix_file,
136
+ compression="gzip",
137
+ skiprows=skip_rows,
138
+ delimiter="\t",
139
+ on_bad_lines="skip"
140
+ )
141
+ gene_data = gene_data.rename(columns={"ID_REF": "ID"}).astype({"ID": "str"})
142
+ gene_data.set_index("ID", inplace=True)
143
+
144
+ # Print the first 20 row IDs to confirm data structure
145
+ print(gene_data.index[:20])
146
+ # Based on the observed identifiers (e.g., HCE000104, SL000001), they are not conventional human gene symbols.
147
+ # Therefore, mapping to human gene symbols is required.
148
+ print("requires_gene_mapping = True")
149
+ # STEP5
150
+ # 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file.
151
+ gene_annotation = get_gene_annotation(soft_file)
152
+
153
+ # 2. Use the 'preview_df' function from the library to preview the data and print out the results.
154
+ print("Gene annotation preview:")
155
+ print(preview_df(gene_annotation))
156
+ # STEP: Gene Identifier Mapping
157
+
158
+ # 1. Decide which columns in gene_annotation match the gene expression IDs and gene symbols.
159
+ # From the preview, 'ID' corresponds to the expression data identifier (like 'SL019100'),
160
+ # and 'EntrezGeneSymbol' contains the gene symbols (e.g., 'CEBPB').
161
+
162
+ # 2. Get a mapping DataFrame from the annotation by specifying these columns.
163
+ mapping_df = get_gene_mapping(gene_annotation, prob_col='ID', gene_col='EntrezGeneSymbol')
164
+
165
+ # 3. Convert probe-level measurements to gene-level data using the mapping.
166
+ gene_data = apply_gene_mapping(gene_data, mapping_df)
167
+ import os
168
+ import pandas as pd
169
+
170
+ # STEP7: Data Normalization and Linking
171
+
172
+ # 1) Normalize the gene symbols in the previously obtained gene_data
173
+ normalized_gene_data = normalize_gene_symbols_in_index(gene_data)
174
+ normalized_gene_data.to_csv(out_gene_data_file)
175
+
176
+ # 2) Load clinical data only if it exists and is non-empty
177
+ if os.path.exists(out_clinical_data_file) and os.path.getsize(out_clinical_data_file) > 0:
178
+ # Read the file
179
+ clinical_temp = pd.read_csv(out_clinical_data_file)
180
+
181
+ # Adjust row index to label the trait, age, and gender properly
182
+ if clinical_temp.shape[0] == 3:
183
+ clinical_temp.index = [trait, "Age", "Gender"]
184
+ elif clinical_temp.shape[0] == 2:
185
+ clinical_temp.index = [trait, "Age"]
186
+ elif clinical_temp.shape[0] == 1:
187
+ clinical_temp.index = [trait]
188
+
189
+ # 2) Link the clinical and normalized genetic data
190
+ linked_data = geo_link_clinical_genetic_data(clinical_temp, normalized_gene_data)
191
+
192
+ # 3) Handle missing values
193
+ linked_data = handle_missing_values(linked_data, trait)
194
+
195
+ # 4) Check for severe bias in the trait; remove biased demographic features if present
196
+ trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait)
197
+
198
+ # 5) Final quality validation and save metadata
199
+ is_usable = validate_and_save_cohort_info(
200
+ is_final=True,
201
+ cohort=cohort,
202
+ info_path=json_path,
203
+ is_gene_available=True,
204
+ is_trait_available=True,
205
+ is_biased=trait_biased,
206
+ df=linked_data,
207
+ note=f"Final check on {cohort} with {trait}."
208
+ )
209
+
210
+ # 6) If the linked data is usable, save it
211
+ if is_usable:
212
+ linked_data.to_csv(out_data_file)
213
+ else:
214
+ # If no valid clinical data file is found, finalize metadata indicating trait unavailability
215
+ is_usable = validate_and_save_cohort_info(
216
+ is_final=True,
217
+ cohort=cohort,
218
+ info_path=json_path,
219
+ is_gene_available=True,
220
+ is_trait_available=False,
221
+ is_biased=True, # Force a fallback so that it's flagged as unusable
222
+ df=pd.DataFrame(),
223
+ note=f"No trait data found for {cohort}, final metadata recorded."
224
+ )
225
+ # Per instructions, do not save a final linked data file when trait data is absent.
p1/preprocess/Chronic_Fatigue_Syndrome/code/GSE39684.py ADDED
@@ -0,0 +1,198 @@
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1
+ # Path Configuration
2
+ from tools.preprocess import *
3
+
4
+ # Processing context
5
+ trait = "Chronic_Fatigue_Syndrome"
6
+ cohort = "GSE39684"
7
+
8
+ # Input paths
9
+ in_trait_dir = "../DATA/GEO/Chronic_Fatigue_Syndrome"
10
+ in_cohort_dir = "../DATA/GEO/Chronic_Fatigue_Syndrome/GSE39684"
11
+
12
+ # Output paths
13
+ out_data_file = "./output/preprocess/1/Chronic_Fatigue_Syndrome/GSE39684.csv"
14
+ out_gene_data_file = "./output/preprocess/1/Chronic_Fatigue_Syndrome/gene_data/GSE39684.csv"
15
+ out_clinical_data_file = "./output/preprocess/1/Chronic_Fatigue_Syndrome/clinical_data/GSE39684.csv"
16
+ json_path = "./output/preprocess/1/Chronic_Fatigue_Syndrome/cohort_info.json"
17
+
18
+ # STEP1
19
+ from tools.preprocess import *
20
+
21
+ # 1. Attempt to identify the paths to the SOFT file and the matrix file
22
+ try:
23
+ soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir)
24
+ except AssertionError:
25
+ print("[WARNING] Could not find the expected '.soft' or '.matrix' files in the directory.")
26
+ soft_file, matrix_file = None, None
27
+
28
+ if soft_file is None or matrix_file is None:
29
+ print("[ERROR] Required GEO files are missing. Please check file names in the cohort directory.")
30
+ else:
31
+ # 2. Read the matrix file to obtain background information and sample characteristics data
32
+ background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design']
33
+ clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1']
34
+ background_info, clinical_data = get_background_and_clinical_data(matrix_file,
35
+ background_prefixes,
36
+ clinical_prefixes)
37
+
38
+ # 3. Obtain the sample characteristics dictionary from the clinical dataframe
39
+ sample_characteristics_dict = get_unique_values_by_row(clinical_data)
40
+
41
+ # 4. Explicitly print out all the background information and the sample characteristics dictionary
42
+ print("Background Information:")
43
+ print(background_info)
44
+ print("\nSample Characteristics Dictionary:")
45
+ print(sample_characteristics_dict)
46
+ # 1. Gene Expression Data Availability
47
+ is_gene_available = True # It's a microarray (not purely miRNA or methylation), so assume gene data is present.
48
+
49
+ # 2. Variable Availability
50
+ # Inspecting the sample characteristics dictionary shows no entries for the Chronic_Fatigue_Syndrome trait,
51
+ # no age information, and no gender information. Hence, all of these rows are marked as None.
52
+ trait_row = None
53
+ age_row = None
54
+ gender_row = None
55
+
56
+ # 2.2 Data Type Conversion Functions
57
+ # Although data is unavailable, we still define the required conversion functions.
58
+
59
+ def convert_trait(value: str):
60
+ # No actual data for conversion; return None.
61
+ # If data existed, we would parse the substring after the colon and apply the logic to return a binary or continuous value.
62
+ return None
63
+
64
+ def convert_age(value: str):
65
+ # No actual data for conversion; return None.
66
+ return None
67
+
68
+ def convert_gender(value: str):
69
+ # No actual data for conversion; return None.
70
+ return None
71
+
72
+ # 3. Save Metadata with initial filtering
73
+ # Trait data is not available because trait_row is None.
74
+ is_trait_available = (trait_row is not None)
75
+
76
+ # Perform initial filtering and save metadata
77
+ validate_and_save_cohort_info(
78
+ is_final=False,
79
+ cohort=cohort,
80
+ info_path=json_path,
81
+ is_gene_available=is_gene_available,
82
+ is_trait_available=is_trait_available
83
+ )
84
+
85
+ # 4. Clinical Feature Extraction
86
+ # Since trait_row is None, we skip clinical feature extraction.
87
+ # STEP3
88
+ # Attempt to read gene expression data; if the library function yields an empty DataFrame,
89
+ # try re-reading without ignoring lines that start with '!' (because sometimes GEO data may
90
+ # place actual expression rows under lines that begin with '!').
91
+
92
+ gene_data = get_genetic_data(matrix_file)
93
+ if gene_data.empty:
94
+ print("[WARNING] The gene_data is empty. Attempting alternative loading without treating '!' as comments.")
95
+ import gzip
96
+
97
+ # Locate the marker line first
98
+ skip_rows = 0
99
+ with gzip.open(matrix_file, 'rt') as file:
100
+ for i, line in enumerate(file):
101
+ if "!series_matrix_table_begin" in line:
102
+ skip_rows = i + 1
103
+ break
104
+
105
+ # Read the data again, this time not treating '!' as comment
106
+ gene_data = pd.read_csv(
107
+ matrix_file,
108
+ compression="gzip",
109
+ skiprows=skip_rows,
110
+ delimiter="\t",
111
+ on_bad_lines="skip"
112
+ )
113
+ gene_data = gene_data.rename(columns={"ID_REF": "ID"}).astype({"ID": "str"})
114
+ gene_data.set_index("ID", inplace=True)
115
+
116
+ # Print the first 20 row IDs to confirm data structure
117
+ print(gene_data.index[:20])
118
+ # Based on inspection, these identifiers (like "10000-V3-70mer-rc") appear to be custom probe IDs
119
+ # and not standard human gene symbols. Therefore, they need to be mapped to gene symbols.
120
+
121
+ print("requires_gene_mapping = True")
122
+ # STEP5
123
+ # 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file.
124
+ gene_annotation = get_gene_annotation(soft_file)
125
+
126
+ # 2. Use the 'preview_df' function from the library to preview the data and print out the results.
127
+ print("Gene annotation preview:")
128
+ print(preview_df(gene_annotation))
129
+ # STEP: Gene Identifier Mapping
130
+
131
+ # 1. Determine which columns match.
132
+ # - "ID" in the annotation dataframe matches the IDs in the gene expression data
133
+ # - "GeneName" contains the corresponding gene information.
134
+
135
+ # 2. Extract the gene mapping dataframe.
136
+ mapping_df = get_gene_mapping(gene_annotation, prob_col="ID", gene_col="GeneName")
137
+
138
+ # 3. Convert probe-level data to gene-level data using the mapping.
139
+ gene_data = apply_gene_mapping(gene_data, mapping_df)
140
+ import os
141
+ import pandas as pd
142
+
143
+ # STEP7: Data Normalization and Linking
144
+
145
+ # 1) Normalize the gene symbols in the previously obtained gene_data
146
+ normalized_gene_data = normalize_gene_symbols_in_index(gene_data)
147
+ normalized_gene_data.to_csv(out_gene_data_file)
148
+
149
+ # 2) Load clinical data only if it exists and is non-empty
150
+ if os.path.exists(out_clinical_data_file) and os.path.getsize(out_clinical_data_file) > 0:
151
+ # Read the file
152
+ clinical_temp = pd.read_csv(out_clinical_data_file)
153
+
154
+ # Adjust row index to label the trait, age, and gender properly
155
+ if clinical_temp.shape[0] == 3:
156
+ clinical_temp.index = [trait, "Age", "Gender"]
157
+ elif clinical_temp.shape[0] == 2:
158
+ clinical_temp.index = [trait, "Age"]
159
+ elif clinical_temp.shape[0] == 1:
160
+ clinical_temp.index = [trait]
161
+
162
+ # 2) Link the clinical and normalized genetic data
163
+ linked_data = geo_link_clinical_genetic_data(clinical_temp, normalized_gene_data)
164
+
165
+ # 3) Handle missing values
166
+ linked_data = handle_missing_values(linked_data, trait)
167
+
168
+ # 4) Check for severe bias in the trait; remove biased demographic features if present
169
+ trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait)
170
+
171
+ # 5) Final quality validation and save metadata
172
+ is_usable = validate_and_save_cohort_info(
173
+ is_final=True,
174
+ cohort=cohort,
175
+ info_path=json_path,
176
+ is_gene_available=True,
177
+ is_trait_available=True,
178
+ is_biased=trait_biased,
179
+ df=linked_data,
180
+ note=f"Final check on {cohort} with {trait}."
181
+ )
182
+
183
+ # 6) If the linked data is usable, save it
184
+ if is_usable:
185
+ linked_data.to_csv(out_data_file)
186
+ else:
187
+ # If no valid clinical data file is found, finalize metadata indicating trait unavailability
188
+ is_usable = validate_and_save_cohort_info(
189
+ is_final=True,
190
+ cohort=cohort,
191
+ info_path=json_path,
192
+ is_gene_available=True,
193
+ is_trait_available=False,
194
+ is_biased=True, # Force a fallback so that it's flagged as unusable
195
+ df=pd.DataFrame(),
196
+ note=f"No trait data found for {cohort}, final metadata recorded."
197
+ )
198
+ # Per instructions, do not save a final linked data file when trait data is absent.
p1/preprocess/Chronic_Fatigue_Syndrome/code/GSE67311.py ADDED
@@ -0,0 +1,233 @@
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1
+ # Path Configuration
2
+ from tools.preprocess import *
3
+
4
+ # Processing context
5
+ trait = "Chronic_Fatigue_Syndrome"
6
+ cohort = "GSE67311"
7
+
8
+ # Input paths
9
+ in_trait_dir = "../DATA/GEO/Chronic_Fatigue_Syndrome"
10
+ in_cohort_dir = "../DATA/GEO/Chronic_Fatigue_Syndrome/GSE67311"
11
+
12
+ # Output paths
13
+ out_data_file = "./output/preprocess/1/Chronic_Fatigue_Syndrome/GSE67311.csv"
14
+ out_gene_data_file = "./output/preprocess/1/Chronic_Fatigue_Syndrome/gene_data/GSE67311.csv"
15
+ out_clinical_data_file = "./output/preprocess/1/Chronic_Fatigue_Syndrome/clinical_data/GSE67311.csv"
16
+ json_path = "./output/preprocess/1/Chronic_Fatigue_Syndrome/cohort_info.json"
17
+
18
+ # STEP1
19
+ from tools.preprocess import *
20
+
21
+ # 1. Attempt to identify the paths to the SOFT file and the matrix file
22
+ try:
23
+ soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir)
24
+ except AssertionError:
25
+ print("[WARNING] Could not find the expected '.soft' or '.matrix' files in the directory.")
26
+ soft_file, matrix_file = None, None
27
+
28
+ if soft_file is None or matrix_file is None:
29
+ print("[ERROR] Required GEO files are missing. Please check file names in the cohort directory.")
30
+ else:
31
+ # 2. Read the matrix file to obtain background information and sample characteristics data
32
+ background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design']
33
+ clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1']
34
+ background_info, clinical_data = get_background_and_clinical_data(matrix_file,
35
+ background_prefixes,
36
+ clinical_prefixes)
37
+
38
+ # 3. Obtain the sample characteristics dictionary from the clinical dataframe
39
+ sample_characteristics_dict = get_unique_values_by_row(clinical_data)
40
+
41
+ # 4. Explicitly print out all the background information and the sample characteristics dictionary
42
+ print("Background Information:")
43
+ print(background_info)
44
+ print("\nSample Characteristics Dictionary:")
45
+ print(sample_characteristics_dict)
46
+ import pandas as pd
47
+ import numpy as np
48
+
49
+ # 1. Gene Expression Data Availability
50
+ # Based on the background information, this dataset uses an Affymetrix Gene 1.1 ST array,
51
+ # indicating it is gene expression data.
52
+ is_gene_available = True
53
+
54
+ # 2. Variable Availability and Data Type Conversion
55
+
56
+ # From the sample characteristics dictionary in the provided output, we see:
57
+ # - For "Chronic_Fatigue_Syndrome", data is found at row 8 with multiple values ("Yes", "No", "-", nan).
58
+ # - No row for "age".
59
+ # - No row for "gender".
60
+
61
+ trait_row = 8
62
+ age_row = None
63
+ gender_row = None
64
+
65
+ # 2.2 Data Type Conversion
66
+ # "Chronic_Fatigue_Syndrome" is a binary variable (Yes/No).
67
+ def convert_trait(value):
68
+ if not isinstance(value, str):
69
+ return None
70
+ parts = value.split(':', 1)
71
+ if len(parts) < 2:
72
+ return None
73
+ val = parts[1].strip().lower()
74
+ if val == 'yes':
75
+ return 1
76
+ elif val == 'no':
77
+ return 0
78
+ # Handle missing or ambiguous values
79
+ return None
80
+
81
+ # Since we do not have age or gender data, we define dummy functions returning None.
82
+ def convert_age(value):
83
+ return None
84
+
85
+ def convert_gender(value):
86
+ return None
87
+
88
+ # 3. Save Metadata with initial filtering
89
+ is_trait_available = (trait_row is not None)
90
+ _ = validate_and_save_cohort_info(
91
+ is_final=False,
92
+ cohort=cohort,
93
+ info_path=json_path,
94
+ is_gene_available=is_gene_available,
95
+ is_trait_available=is_trait_available
96
+ )
97
+
98
+ # 4. Clinical Feature Extraction (only if trait_row is not None)
99
+ if trait_row is not None:
100
+ # Assume "clinical_data" is the DataFrame containing the characteristics, already in scope.
101
+ selected_clinical_df = geo_select_clinical_features(
102
+ clinical_df=clinical_data,
103
+ trait=trait,
104
+ trait_row=trait_row,
105
+ convert_trait=convert_trait,
106
+ age_row=age_row,
107
+ convert_age=None,
108
+ gender_row=gender_row,
109
+ convert_gender=None
110
+ )
111
+ preview = preview_df(selected_clinical_df)
112
+ print("Preview of Clinical Features:")
113
+ print(preview)
114
+ selected_clinical_df.to_csv(out_clinical_data_file, index=False)
115
+ # STEP3
116
+ # Attempt to read gene expression data; if the library function yields an empty DataFrame,
117
+ # try re-reading without ignoring lines that start with '!' (because sometimes GEO data may
118
+ # place actual expression rows under lines that begin with '!').
119
+
120
+ gene_data = get_genetic_data(matrix_file)
121
+ if gene_data.empty:
122
+ print("[WARNING] The gene_data is empty. Attempting alternative loading without treating '!' as comments.")
123
+ import gzip
124
+
125
+ # Locate the marker line first
126
+ skip_rows = 0
127
+ with gzip.open(matrix_file, 'rt') as file:
128
+ for i, line in enumerate(file):
129
+ if "!series_matrix_table_begin" in line:
130
+ skip_rows = i + 1
131
+ break
132
+
133
+ # Read the data again, this time not treating '!' as comment
134
+ gene_data = pd.read_csv(
135
+ matrix_file,
136
+ compression="gzip",
137
+ skiprows=skip_rows,
138
+ delimiter="\t",
139
+ on_bad_lines="skip"
140
+ )
141
+ gene_data = gene_data.rename(columns={"ID_REF": "ID"}).astype({"ID": "str"})
142
+ gene_data.set_index("ID", inplace=True)
143
+
144
+ # Print the first 20 row IDs to confirm data structure
145
+ print(gene_data.index[:20])
146
+ # Based on biomedical knowledge and the numeric nature of these identifiers,
147
+ # they are not standard human gene symbols and require mapping to gene symbols.
148
+
149
+ requires_gene_mapping = True
150
+ # STEP5
151
+ # 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file.
152
+ gene_annotation = get_gene_annotation(soft_file)
153
+
154
+ # 2. Use the 'preview_df' function from the library to preview the data and print out the results.
155
+ print("Gene annotation preview:")
156
+ print(preview_df(gene_annotation))
157
+ # STEP: Gene Identifier Mapping
158
+
159
+ # 1. Identify which columns in the annotation are equivalent to the expression data IDs and which store gene symbols.
160
+ # From the preview, the "ID" column corresponds to the expression data IDs,
161
+ # and the "gene_assignment" column contains the gene symbol information.
162
+ probe_id_column = "ID"
163
+ gene_symbol_column = "gene_assignment"
164
+
165
+ # 2. Get the gene mapping dataframe by extracting these two columns.
166
+ mapping_df = get_gene_mapping(gene_annotation, probe_id_column, gene_symbol_column)
167
+
168
+ # 3. Convert probe-level measurements to gene-level expression data.
169
+ gene_data = apply_gene_mapping(gene_data, mapping_df)
170
+
171
+ # For inspection, let's check the shape of the resulting gene_data.
172
+ print("Mapped gene expression data shape:", gene_data.shape)
173
+ print("First 5 rows of mapped gene expression data:")
174
+ print(gene_data.head())
175
+ import os
176
+ import pandas as pd
177
+
178
+ # STEP7: Data Normalization and Linking
179
+
180
+ # 1) Normalize the gene symbols in the previously obtained gene_data
181
+ normalized_gene_data = normalize_gene_symbols_in_index(gene_data)
182
+ normalized_gene_data.to_csv(out_gene_data_file)
183
+
184
+ # 2) Load clinical data only if it exists and is non-empty
185
+ if os.path.exists(out_clinical_data_file) and os.path.getsize(out_clinical_data_file) > 0:
186
+ # Read the file
187
+ clinical_temp = pd.read_csv(out_clinical_data_file)
188
+
189
+ # Adjust row index to label the trait, age, and gender properly
190
+ if clinical_temp.shape[0] == 3:
191
+ clinical_temp.index = [trait, "Age", "Gender"]
192
+ elif clinical_temp.shape[0] == 2:
193
+ clinical_temp.index = [trait, "Age"]
194
+ elif clinical_temp.shape[0] == 1:
195
+ clinical_temp.index = [trait]
196
+
197
+ # 2) Link the clinical and normalized genetic data
198
+ linked_data = geo_link_clinical_genetic_data(clinical_temp, normalized_gene_data)
199
+
200
+ # 3) Handle missing values
201
+ linked_data = handle_missing_values(linked_data, trait)
202
+
203
+ # 4) Check for severe bias in the trait; remove biased demographic features if present
204
+ trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait)
205
+
206
+ # 5) Final quality validation and save metadata
207
+ is_usable = validate_and_save_cohort_info(
208
+ is_final=True,
209
+ cohort=cohort,
210
+ info_path=json_path,
211
+ is_gene_available=True,
212
+ is_trait_available=True,
213
+ is_biased=trait_biased,
214
+ df=linked_data,
215
+ note=f"Final check on {cohort} with {trait}."
216
+ )
217
+
218
+ # 6) If the linked data is usable, save it
219
+ if is_usable:
220
+ linked_data.to_csv(out_data_file)
221
+ else:
222
+ # If no valid clinical data file is found, finalize metadata indicating trait unavailability
223
+ is_usable = validate_and_save_cohort_info(
224
+ is_final=True,
225
+ cohort=cohort,
226
+ info_path=json_path,
227
+ is_gene_available=True,
228
+ is_trait_available=False,
229
+ is_biased=True, # Force a fallback so that it's flagged as unusable
230
+ df=pd.DataFrame(),
231
+ note=f"No trait data found for {cohort}, final metadata recorded."
232
+ )
233
+ # Per instructions, do not save a final linked data file when trait data is absent.
p1/preprocess/Chronic_Fatigue_Syndrome/code/TCGA.py ADDED
@@ -0,0 +1,56 @@
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1
+ # Path Configuration
2
+ from tools.preprocess import *
3
+
4
+ # Processing context
5
+ trait = "Chronic_Fatigue_Syndrome"
6
+
7
+ # Input paths
8
+ tcga_root_dir = "../DATA/TCGA"
9
+
10
+ # Output paths
11
+ out_data_file = "./output/preprocess/1/Chronic_Fatigue_Syndrome/TCGA.csv"
12
+ out_gene_data_file = "./output/preprocess/1/Chronic_Fatigue_Syndrome/gene_data/TCGA.csv"
13
+ out_clinical_data_file = "./output/preprocess/1/Chronic_Fatigue_Syndrome/clinical_data/TCGA.csv"
14
+ json_path = "./output/preprocess/1/Chronic_Fatigue_Syndrome/cohort_info.json"
15
+
16
+ import os
17
+ import pandas as pd
18
+
19
+ # Step 1: Check directories in tcga_root_dir for anything relevant to "Chronic_Fatigue_Syndrome"
20
+ search_terms = [
21
+ "chronic_fatigue_syndrome",
22
+ "chronic fatigue syndrome",
23
+ "myalgic encephalomyelitis",
24
+ "cfs"
25
+ ]
26
+
27
+ dir_list = os.listdir(tcga_root_dir)
28
+ matching_dir = None
29
+
30
+ for d in dir_list:
31
+ d_lower = d.lower()
32
+ if any(term in d_lower for term in search_terms):
33
+ matching_dir = d
34
+ break
35
+
36
+ if matching_dir is None:
37
+ # No matching directory found for Chronic Fatigue Syndrome, so mark the dataset as skipped.
38
+ validate_and_save_cohort_info(
39
+ is_final=False,
40
+ cohort="TCGA_Chronic_Fatigue_Syndrome",
41
+ info_path=json_path,
42
+ is_gene_available=False,
43
+ is_trait_available=False
44
+ )
45
+ else:
46
+ # 2. Identify the clinicalMatrix and PANCAN files
47
+ cohort_dir = os.path.join(tcga_root_dir, matching_dir)
48
+ clinical_file_path, genetic_file_path = tcga_get_relevant_filepaths(cohort_dir)
49
+
50
+ # 3. Load both data files
51
+ clinical_df = pd.read_csv(clinical_file_path, index_col=0, sep='\t')
52
+ genetic_df = pd.read_csv(genetic_file_path, index_col=0, sep='\t')
53
+
54
+ # 4. Print the column names of the clinical data
55
+ print("Clinical Data Columns:")
56
+ print(clinical_df.columns.tolist())
p1/preprocess/Chronic_Fatigue_Syndrome/cohort_info.json ADDED
@@ -0,0 +1 @@
 
 
1
+ {"GSE67311": {"is_usable": true, "is_gene_available": true, "is_trait_available": true, "is_available": true, "is_biased": false, "has_age": false, "has_gender": false, "sample_size": 133, "note": "Final check on GSE67311 with Chronic_Fatigue_Syndrome."}, "GSE39684": {"is_usable": false, "is_gene_available": false, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": "No trait data found for GSE39684, final metadata recorded."}, "GSE251792": {"is_usable": true, "is_gene_available": true, "is_trait_available": true, "is_available": true, "is_biased": false, "has_age": true, "has_gender": true, "sample_size": 84, "note": "Final check on GSE251792 with Chronic_Fatigue_Syndrome."}, "TCGA_Celiac_Disease": {"is_usable": false, "is_gene_available": false, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": null}, "TCGA_Chronic_Fatigue_Syndrome": {"is_usable": false, "is_gene_available": false, "is_trait_available": false, "is_available": false, "is_biased": null, "has_age": null, "has_gender": null, "sample_size": null, "note": null}}
p1/preprocess/Chronic_Fatigue_Syndrome/gene_data/GSE251792.csv ADDED
The diff for this file is too large to render. See raw diff
 
p1/preprocess/Chronic_Fatigue_Syndrome/gene_data/GSE39684.csv ADDED
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p1/preprocess/Chronic_kidney_disease/GSE142153.csv ADDED
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+ size 14316050
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p1/preprocess/Chronic_kidney_disease/clinical_data/GSE127136.csv ADDED
@@ -0,0 +1,2 @@
 
 
 
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p1/preprocess/Chronic_kidney_disease/clinical_data/GSE142153.csv ADDED
@@ -0,0 +1,2 @@
 
 
 
1
+ GSM4221568,GSM4221569,GSM4221570,GSM4221571,GSM4221572,GSM4221573,GSM4221574,GSM4221575,GSM4221576,GSM4221577,GSM4221578,GSM4221579,GSM4221580,GSM4221581,GSM4221582,GSM4221583,GSM4221584,GSM4221585,GSM4221586,GSM4221587,GSM4221588,GSM4221589,GSM4221590,GSM4221591,GSM4221592,GSM4221593,GSM4221594,GSM4221595,GSM4221596,GSM4221597,GSM4221598,GSM4221599,GSM4221600,GSM4221601,GSM4221602,GSM4221603,GSM4221604,GSM4221605,GSM4221606,GSM4221607
2
+ 0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0
p1/preprocess/Chronic_kidney_disease/clinical_data/GSE180393.csv ADDED
@@ -0,0 +1,2 @@
 
 
 
1
+ GSM5607752,GSM5607753,GSM5607754,GSM5607755,GSM5607756,GSM5607757,GSM5607758,GSM5607759,GSM5607760,GSM5607761,GSM5607762,GSM5607763,GSM5607764,GSM5607765,GSM5607766,GSM5607767,GSM5607768,GSM5607769,GSM5607770,GSM5607771,GSM5607772,GSM5607773,GSM5607774,GSM5607775,GSM5607776,GSM5607777,GSM5607778,GSM5607779,GSM5607780,GSM5607781,GSM5607782,GSM5607783,GSM5607784,GSM5607785,GSM5607786,GSM5607787,GSM5607788,GSM5607789,GSM5607790,GSM5607791,GSM5607792,GSM5607793,GSM5607794,GSM5607795,GSM5607796,GSM5607797,GSM5607798,GSM5607799,GSM5607800,GSM5607801,GSM5607802,GSM5607803,GSM5607804,GSM5607805,GSM5607806,GSM5607807,GSM5607808,GSM5607809,GSM5607810,GSM5607811,GSM5607812,GSM5607813
2
+ 0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,0.0,0.0,0.0,0.0,0.0,0.0
p1/preprocess/Chronic_kidney_disease/clinical_data/GSE180394.csv ADDED
@@ -0,0 +1,2 @@
 
 
 
1
+ GSM5607814,GSM5607815,GSM5607816,GSM5607817,GSM5607818,GSM5607819,GSM5607820,GSM5607821,GSM5607822,GSM5607823,GSM5607824,GSM5607825,GSM5607826,GSM5607827,GSM5607828,GSM5607829,GSM5607830,GSM5607831,GSM5607832,GSM5607833,GSM5607834,GSM5607835,GSM5607836,GSM5607837,GSM5607838,GSM5607839,GSM5607840,GSM5607841,GSM5607842,GSM5607843,GSM5607844,GSM5607845,GSM5607846,GSM5607847,GSM5607848,GSM5607849,GSM5607850,GSM5607851,GSM5607852,GSM5607853,GSM5607854,GSM5607855,GSM5607856,GSM5607857,GSM5607858,GSM5607859,GSM5607860,GSM5607861,GSM5607862,GSM5607863,GSM5607864,GSM5607865,GSM5607866,GSM5607867,GSM5607868,GSM5607869,GSM5607870,GSM5607871,GSM5607872
2
+ 0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,0.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,0.0,0.0,0.0,0.0,0.0,0.0
p1/preprocess/Chronic_kidney_disease/clinical_data/GSE66494.csv ADDED
@@ -0,0 +1,2 @@
 
 
 
1
+ GSM1623299,GSM1623300,GSM1623301,GSM1623302,GSM1623303,GSM1623304,GSM1623305,GSM1623306,GSM1623307,GSM1623308,GSM1623309,GSM1623310,GSM1623311,GSM1623312,GSM1623313,GSM1623314,GSM1623315,GSM1623316,GSM1623317,GSM1623318,GSM1623319,GSM1623320,GSM1623321,GSM1623322,GSM1623323,GSM1623324,GSM1623325,GSM1623326,GSM1623327,GSM1623328,GSM1623329,GSM1623330,GSM1623331,GSM1623332,GSM1623333,GSM1623334,GSM1623335,GSM1623336,GSM1623337,GSM1623338,GSM1623339,GSM1623340,GSM1623341,GSM1623342,GSM1623343,GSM1623344,GSM1623345,GSM1623346,GSM1623347,GSM1623348,GSM1623349,GSM1623350,GSM1623351,GSM1623352,GSM1623353,GSM1623354,GSM1623355,GSM1623356,GSM1623357,GSM1623358,GSM1623359
2
+ 1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,1.0,0.0,0.0,0.0,0.0,0.0,1.0,1.0,1.0,1.0,1.0,0.0,0.0,0.0
p1/preprocess/Chronic_kidney_disease/code/GSE104948.py ADDED
@@ -0,0 +1,161 @@
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1
+ # Path Configuration
2
+ from tools.preprocess import *
3
+
4
+ # Processing context
5
+ trait = "Chronic_kidney_disease"
6
+ cohort = "GSE104948"
7
+
8
+ # Input paths
9
+ in_trait_dir = "../DATA/GEO/Chronic_kidney_disease"
10
+ in_cohort_dir = "../DATA/GEO/Chronic_kidney_disease/GSE104948"
11
+
12
+ # Output paths
13
+ out_data_file = "./output/preprocess/1/Chronic_kidney_disease/GSE104948.csv"
14
+ out_gene_data_file = "./output/preprocess/1/Chronic_kidney_disease/gene_data/GSE104948.csv"
15
+ out_clinical_data_file = "./output/preprocess/1/Chronic_kidney_disease/clinical_data/GSE104948.csv"
16
+ json_path = "./output/preprocess/1/Chronic_kidney_disease/cohort_info.json"
17
+
18
+ # STEP1
19
+ from tools.preprocess import *
20
+ # 1. Identify the paths to the SOFT file and the matrix file
21
+ soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir)
22
+
23
+ # 2. Read the matrix file to obtain background information and sample characteristics data
24
+ background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design']
25
+ clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1']
26
+ background_info, clinical_data = get_background_and_clinical_data(matrix_file, background_prefixes, clinical_prefixes)
27
+
28
+ # 3. Obtain the sample characteristics dictionary from the clinical dataframe
29
+ sample_characteristics_dict = get_unique_values_by_row(clinical_data)
30
+
31
+ # 4. Explicitly print out all the background information and the sample characteristics dictionary
32
+ print("Background Information:")
33
+ print(background_info)
34
+ print("Sample Characteristics Dictionary:")
35
+ print(sample_characteristics_dict)
36
+ # 1) Determine if gene expression data is available
37
+ is_gene_available = True # Based on the metadata (Affymetrix microarrays for gene expression)
38
+ # 2) Identify variable availability
39
+ trait_row = 1 # diagnosis field with multiple diagnoses
40
+ age_row = None # no age data detected
41
+ gender_row = None # no gender data detected
42
+
43
+ # 2) Define data type conversions
44
+ def convert_trait(value: Any) -> Optional[int]:
45
+ """
46
+ Convert the diagnosis field to a binary indicator for Chronic Kidney Disease:
47
+ - If 'Tumor Nephrectomy' or unknown, map to 0/None
48
+ - Otherwise, map to 1
49
+ """
50
+ if pd.isna(value):
51
+ return None
52
+ # Extract the part after the colon if present
53
+ parts = str(value).split(':', 1)
54
+ if len(parts) == 2:
55
+ val_str = parts[1].strip()
56
+ else:
57
+ val_str = parts[0].strip()
58
+
59
+ if val_str.lower() in ['tumor nephrectomy', '']:
60
+ return 0
61
+ if val_str.lower() == 'nan':
62
+ return None
63
+ # Everything else is considered CKD = 1
64
+ return 1
65
+
66
+ def convert_age(value: Any) -> Optional[float]:
67
+ # This dataset has no age data; return None
68
+ return None
69
+
70
+ def convert_gender(value: Any) -> Optional[int]:
71
+ # This dataset has no gender data; return None
72
+ return None
73
+
74
+ # 3) Conduct initial filtering and save metadata
75
+ is_trait_available = (trait_row is not None)
76
+ is_usable = validate_and_save_cohort_info(
77
+ is_final=False,
78
+ cohort=cohort,
79
+ info_path=json_path,
80
+ is_gene_available=is_gene_available,
81
+ is_trait_available=is_trait_available
82
+ )
83
+
84
+ # 4) If trait data is available, extract and preview the clinical features
85
+ if trait_row is not None:
86
+ selected_clinical_data = geo_select_clinical_features(
87
+ clinical_data,
88
+ trait=trait,
89
+ trait_row=trait_row,
90
+ convert_trait=convert_trait,
91
+ age_row=age_row,
92
+ convert_age=convert_age,
93
+ gender_row=gender_row,
94
+ convert_gender=convert_gender
95
+ )
96
+ preview_result = preview_df(selected_clinical_data)
97
+ print("Preview of selected clinical features:", preview_result)
98
+
99
+ # Save the clinical data
100
+ selected_clinical_data.to_csv(out_clinical_data_file, index=False)
101
+ # STEP3
102
+ # 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined.
103
+ gene_data = get_genetic_data(matrix_file)
104
+
105
+ # 2. Print the first 20 row IDs (gene or probe identifiers) for future observation.
106
+ print(gene_data.index[:20])
107
+ # Based on the ID patterns (e.g., "10000_at", "10001_at"), these look like probe set IDs
108
+ # from a microarray platform rather than human gene symbols. Hence, they require mapping.
109
+
110
+ print("requires_gene_mapping = True")
111
+ # STEP5
112
+ # 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file.
113
+ gene_annotation = get_gene_annotation(soft_file)
114
+
115
+ # 2. Use the 'preview_df' function from the library to preview the data and print out the results.
116
+ print("Gene annotation preview:")
117
+ print(preview_df(gene_annotation))
118
+ # STEP: Gene Identifier Mapping
119
+
120
+ # 1) Identify the columns in the gene annotation dataframe that match the
121
+ # probe identifiers and the columns that provide the gene symbols.
122
+ prob_col = "ID"
123
+ gene_col = "Symbol"
124
+
125
+ # 2) Get the gene mapping dataframe by extracting these two columns.
126
+ mapping_df = get_gene_mapping(gene_annotation, prob_col, gene_col)
127
+
128
+ # 3) Convert probe-level measurements to gene-level expression data.
129
+ gene_data = apply_gene_mapping(gene_data, mapping_df)
130
+
131
+ # Print out a brief check of the mapped gene data
132
+ print("Mapped gene_data shape:", gene_data.shape)
133
+ print("First few gene symbols:", gene_data.index[:10])
134
+ # STEP7
135
+ # 1. Normalize the obtained gene data with the 'normalize_gene_symbols_in_index' function from the library.
136
+ normalized_gene_data = normalize_gene_symbols_in_index(gene_data)
137
+ normalized_gene_data.to_csv(out_gene_data_file)
138
+
139
+ # 2. Link the clinical and genetic data with the 'geo_link_clinical_genetic_data' function from the library.
140
+ linked_data = geo_link_clinical_genetic_data(selected_clinical_data, normalized_gene_data)
141
+
142
+ # 3. Handle missing values in the linked data
143
+ linked_data = handle_missing_values(linked_data, trait)
144
+
145
+ # 4. Determine whether the trait and some demographic features are severely biased, and remove biased features.
146
+ is_trait_biased, unbiased_linked_data = judge_and_remove_biased_features(linked_data, trait)
147
+
148
+ # 5. Conduct quality check and save the cohort information.
149
+ is_usable = validate_and_save_cohort_info(
150
+ is_final=True,
151
+ cohort=cohort,
152
+ info_path=json_path,
153
+ is_gene_available=True,
154
+ is_trait_available=True,
155
+ is_biased=is_trait_biased,
156
+ df=linked_data
157
+ )
158
+
159
+ # 6. If the linked data is usable, save it as a CSV file to 'out_data_file'.
160
+ if is_usable:
161
+ unbiased_linked_data.to_csv(out_data_file)
p1/preprocess/Chronic_kidney_disease/code/GSE104954.py ADDED
@@ -0,0 +1,152 @@
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1
+ # Path Configuration
2
+ from tools.preprocess import *
3
+
4
+ # Processing context
5
+ trait = "Chronic_kidney_disease"
6
+ cohort = "GSE104954"
7
+
8
+ # Input paths
9
+ in_trait_dir = "../DATA/GEO/Chronic_kidney_disease"
10
+ in_cohort_dir = "../DATA/GEO/Chronic_kidney_disease/GSE104954"
11
+
12
+ # Output paths
13
+ out_data_file = "./output/preprocess/1/Chronic_kidney_disease/GSE104954.csv"
14
+ out_gene_data_file = "./output/preprocess/1/Chronic_kidney_disease/gene_data/GSE104954.csv"
15
+ out_clinical_data_file = "./output/preprocess/1/Chronic_kidney_disease/clinical_data/GSE104954.csv"
16
+ json_path = "./output/preprocess/1/Chronic_kidney_disease/cohort_info.json"
17
+
18
+ # STEP1
19
+ from tools.preprocess import *
20
+ # 1. Identify the paths to the SOFT file and the matrix file
21
+ soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir)
22
+
23
+ # 2. Read the matrix file to obtain background information and sample characteristics data
24
+ background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design']
25
+ clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1']
26
+ background_info, clinical_data = get_background_and_clinical_data(matrix_file, background_prefixes, clinical_prefixes)
27
+
28
+ # 3. Obtain the sample characteristics dictionary from the clinical dataframe
29
+ sample_characteristics_dict = get_unique_values_by_row(clinical_data)
30
+
31
+ # 4. Explicitly print out all the background information and the sample characteristics dictionary
32
+ print("Background Information:")
33
+ print(background_info)
34
+ print("Sample Characteristics Dictionary:")
35
+ print(sample_characteristics_dict)
36
+ # 1. Determine if gene expression data is available.
37
+ # From the background, this dataset uses Affymetrix microarrays for RNA,
38
+ # indicating gene expression data is present.
39
+ is_gene_available = True
40
+
41
+ # 2.1 Data Availability
42
+ # Matching the provided sample characteristics dictionary, we see:
43
+ # Key=0 => tissue: all the same, not useful.
44
+ # Key=1 => multiple kidney disease diagnoses vs. tumor nephrectomy (control).
45
+ # This can serve as a binary trait for "Chronic_kidney_disease" vs. non-CKD.
46
+ trait_row = 1 # diagnosis data is in row 1
47
+ age_row = None # age not found
48
+ gender_row = None # gender not found
49
+
50
+ # 2.2 Data Type Conversion
51
+ # We choose 'binary' for the trait: 1 = Chronic Kidney Disease, 0 = non-CKD, None if unknown.
52
+ def convert_trait(x: Any) -> Optional[int]:
53
+ if not isinstance(x, str):
54
+ return None
55
+ # Extract the part after the colon
56
+ val = x.split(":", 1)[-1].strip().lower()
57
+ if val in ["", "nan"]:
58
+ return None
59
+ if val == "tumor nephrectomy":
60
+ return 0 # likely control group
61
+ # Otherwise, treat all other diagnoses as CKD
62
+ return 1
63
+
64
+ # Since age and gender are unavailable, define pass-through functions returning None.
65
+ def convert_age(x: Any) -> Optional[float]:
66
+ return None
67
+
68
+ def convert_gender(x: Any) -> Optional[int]:
69
+ return None
70
+
71
+ # 3. Initial filtering on dataset usability
72
+ is_trait_available = (trait_row is not None)
73
+ is_usable = validate_and_save_cohort_info(
74
+ is_final=False,
75
+ cohort=cohort,
76
+ info_path=json_path,
77
+ is_gene_available=is_gene_available,
78
+ is_trait_available=is_trait_available
79
+ )
80
+
81
+ # 4. Clinical Feature Extraction (only if trait_row is available)
82
+ if trait_row is not None:
83
+ selected_clinical_df = geo_select_clinical_features(
84
+ clinical_data,
85
+ trait=trait,
86
+ trait_row=trait_row,
87
+ convert_trait=convert_trait,
88
+ age_row=age_row,
89
+ convert_age=convert_age,
90
+ gender_row=gender_row,
91
+ convert_gender=convert_gender
92
+ )
93
+ # Preview result
94
+ print(preview_df(selected_clinical_df, n=5))
95
+ # Save the extracted clinical features
96
+ selected_clinical_df.to_csv(out_clinical_data_file, index=False)
97
+ # STEP3
98
+ # 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined.
99
+ gene_data = get_genetic_data(matrix_file)
100
+
101
+ # 2. Print the first 20 row IDs (gene or probe identifiers) for future observation.
102
+ print(gene_data.index[:20])
103
+ # The gene identifiers such as "10000_at", "10001_at", etc. indicate Affymetrix probe set IDs
104
+ # rather than human gene symbols, so they need to be mapped to gene symbols.
105
+
106
+ print("requires_gene_mapping = True")
107
+ # STEP5
108
+ # 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file.
109
+ gene_annotation = get_gene_annotation(soft_file)
110
+
111
+ # 2. Use the 'preview_df' function from the library to preview the data and print out the results.
112
+ print("Gene annotation preview:")
113
+ print(preview_df(gene_annotation))
114
+ # STEP: Gene Identifier Mapping
115
+ # 1. In the annotation DataFrame, the 'ID' column matches the probe identifiers in the gene expression data,
116
+ # and the 'Symbol' column contains the gene symbols.
117
+ # 2. Create a mapping DataFrame for probe-to-gene mapping.
118
+ mapping_df = get_gene_mapping(gene_annotation, prob_col="ID", gene_col="Symbol")
119
+
120
+ # 3. Apply this mapping to convert probe-level measurements to gene-level data.
121
+ gene_data = apply_gene_mapping(gene_data, mapping_df)
122
+
123
+ # Optionally, preview a small portion of the resulting gene expression DataFrame
124
+ print(preview_df(gene_data, n=5))
125
+ # STEP7
126
+ # 1. Normalize the obtained gene data with the 'normalize_gene_symbols_in_index' function from the library.
127
+ normalized_gene_data = normalize_gene_symbols_in_index(gene_data)
128
+ normalized_gene_data.to_csv(out_gene_data_file)
129
+
130
+ # 2. Link the clinical and genetic data with the 'geo_link_clinical_genetic_data' function from the library.
131
+ linked_data = geo_link_clinical_genetic_data(selected_clinical_df, normalized_gene_data)
132
+
133
+ # 3. Handle missing values in the linked data
134
+ linked_data = handle_missing_values(linked_data, trait)
135
+
136
+ # 4. Determine whether the trait and some demographic features are severely biased, and remove biased features.
137
+ is_trait_biased, unbiased_linked_data = judge_and_remove_biased_features(linked_data, trait)
138
+
139
+ # 5. Conduct quality check and save the cohort information.
140
+ is_usable = validate_and_save_cohort_info(
141
+ is_final=True,
142
+ cohort=cohort,
143
+ info_path=json_path,
144
+ is_gene_available=True,
145
+ is_trait_available=True,
146
+ is_biased=is_trait_biased,
147
+ df=linked_data
148
+ )
149
+
150
+ # 6. If the linked data is usable, save it as a CSV file to 'out_data_file'.
151
+ if is_usable:
152
+ unbiased_linked_data.to_csv(out_data_file)
p1/preprocess/Chronic_kidney_disease/code/GSE127136.py ADDED
@@ -0,0 +1,93 @@
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1
+ # Path Configuration
2
+ from tools.preprocess import *
3
+
4
+ # Processing context
5
+ trait = "Chronic_kidney_disease"
6
+ cohort = "GSE127136"
7
+
8
+ # Input paths
9
+ in_trait_dir = "../DATA/GEO/Chronic_kidney_disease"
10
+ in_cohort_dir = "../DATA/GEO/Chronic_kidney_disease/GSE127136"
11
+
12
+ # Output paths
13
+ out_data_file = "./output/preprocess/1/Chronic_kidney_disease/GSE127136.csv"
14
+ out_gene_data_file = "./output/preprocess/1/Chronic_kidney_disease/gene_data/GSE127136.csv"
15
+ out_clinical_data_file = "./output/preprocess/1/Chronic_kidney_disease/clinical_data/GSE127136.csv"
16
+ json_path = "./output/preprocess/1/Chronic_kidney_disease/cohort_info.json"
17
+
18
+ # STEP1
19
+ from tools.preprocess import *
20
+ # 1. Identify the paths to the SOFT file and the matrix file
21
+ soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir)
22
+
23
+ # 2. Read the matrix file to obtain background information and sample characteristics data
24
+ background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design']
25
+ clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1']
26
+ background_info, clinical_data = get_background_and_clinical_data(matrix_file, background_prefixes, clinical_prefixes)
27
+
28
+ # 3. Obtain the sample characteristics dictionary from the clinical dataframe
29
+ sample_characteristics_dict = get_unique_values_by_row(clinical_data)
30
+
31
+ # 4. Explicitly print out all the background information and the sample characteristics dictionary
32
+ print("Background Information:")
33
+ print(background_info)
34
+ print("Sample Characteristics Dictionary:")
35
+ print(sample_characteristics_dict)
36
+ # 1. Gene Expression Data Availability
37
+ is_gene_available = True # Single-cell RNA-seq suggests gene expression data is available.
38
+
39
+ # 2. Variable Availability and Data Type Conversion
40
+ # From the sample characteristics dictionary, row 1 contains multiple disease states (IgAN, kidney cancer, normal).
41
+ # We will treat "IgAN" as having the CKD trait = 1, and others (kidney cancer/normal) as 0.
42
+ trait_row = 1
43
+ age_row = None
44
+ gender_row = None
45
+
46
+ def convert_trait(value: str):
47
+ """
48
+ Convert disease state values to binary indicating CKD (IgAN) or not.
49
+ """
50
+ parts = value.split(':', 1)
51
+ val = parts[1].strip() if len(parts) > 1 else parts[0].strip()
52
+ if val.lower() == 'igan':
53
+ return 1
54
+ elif val.lower() in ['kidney cancer', 'normal']:
55
+ return 0
56
+ else:
57
+ return 0
58
+
59
+ # Since age and gender are not available, set their conversion functions to None
60
+ convert_age = None
61
+ convert_gender = None
62
+
63
+ # 3. Save Metadata using initial filtering
64
+ is_trait_available = (trait_row is not None)
65
+ is_usable = validate_and_save_cohort_info(
66
+ is_final=False,
67
+ cohort=cohort,
68
+ info_path=json_path,
69
+ is_gene_available=is_gene_available,
70
+ is_trait_available=is_trait_available
71
+ )
72
+
73
+ # 4. Clinical Feature Extraction (only if trait data is available)
74
+ if trait_row is not None:
75
+ selected_clinical_df = geo_select_clinical_features(
76
+ clinical_df=clinical_data,
77
+ trait=trait,
78
+ trait_row=trait_row,
79
+ convert_trait=convert_trait,
80
+ age_row=age_row,
81
+ convert_age=convert_age,
82
+ gender_row=gender_row,
83
+ convert_gender=convert_gender
84
+ )
85
+ print("Preview of selected clinical features:")
86
+ print(preview_df(selected_clinical_df))
87
+ selected_clinical_df.to_csv(out_clinical_data_file, index=False)
88
+ # STEP3
89
+ # 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined.
90
+ gene_data = get_genetic_data(matrix_file)
91
+
92
+ # 2. Print the first 20 row IDs (gene or probe identifiers) for future observation.
93
+ print(gene_data.index[:20])
p1/preprocess/Chronic_kidney_disease/code/GSE142153.py ADDED
@@ -0,0 +1,149 @@
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1
+ # Path Configuration
2
+ from tools.preprocess import *
3
+
4
+ # Processing context
5
+ trait = "Chronic_kidney_disease"
6
+ cohort = "GSE142153"
7
+
8
+ # Input paths
9
+ in_trait_dir = "../DATA/GEO/Chronic_kidney_disease"
10
+ in_cohort_dir = "../DATA/GEO/Chronic_kidney_disease/GSE142153"
11
+
12
+ # Output paths
13
+ out_data_file = "./output/preprocess/1/Chronic_kidney_disease/GSE142153.csv"
14
+ out_gene_data_file = "./output/preprocess/1/Chronic_kidney_disease/gene_data/GSE142153.csv"
15
+ out_clinical_data_file = "./output/preprocess/1/Chronic_kidney_disease/clinical_data/GSE142153.csv"
16
+ json_path = "./output/preprocess/1/Chronic_kidney_disease/cohort_info.json"
17
+
18
+ # STEP1
19
+ from tools.preprocess import *
20
+ # 1. Identify the paths to the SOFT file and the matrix file
21
+ soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir)
22
+
23
+ # 2. Read the matrix file to obtain background information and sample characteristics data
24
+ background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design']
25
+ clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1']
26
+ background_info, clinical_data = get_background_and_clinical_data(matrix_file, background_prefixes, clinical_prefixes)
27
+
28
+ # 3. Obtain the sample characteristics dictionary from the clinical dataframe
29
+ sample_characteristics_dict = get_unique_values_by_row(clinical_data)
30
+
31
+ # 4. Explicitly print out all the background information and the sample characteristics dictionary
32
+ print("Background Information:")
33
+ print(background_info)
34
+ print("Sample Characteristics Dictionary:")
35
+ print(sample_characteristics_dict)
36
+ # 1. Gene Expression Data Availability
37
+ is_gene_available = True # Based on "Microarray analysis" from the series summary
38
+
39
+ # 2. Variable Availability and Data Type Conversion
40
+ # From the sample characteristics dictionary, trait data is in row 1 ("diagnosis: ..."),
41
+ # age and gender data are not available.
42
+ trait_row = 1
43
+ age_row = None
44
+ gender_row = None
45
+
46
+ def convert_trait(value: str):
47
+ if not isinstance(value, str):
48
+ return None
49
+ # Split by colon and convert the part after colon
50
+ val = value.split(":")[-1].strip().lower()
51
+ if val == "healthy control":
52
+ return 0
53
+ elif val in ["diabetic nephropathy", "esrd"]:
54
+ return 1
55
+ return None
56
+
57
+ def convert_age(value: str):
58
+ # Not available in this dataset, so return None
59
+ return None
60
+
61
+ def convert_gender(value: str):
62
+ # Not available in this dataset, so return None
63
+ return None
64
+
65
+ # Determine trait availability
66
+ is_trait_available = (trait_row is not None)
67
+
68
+ # 3. Initial Filtering and Saving Metadata
69
+ _ = validate_and_save_cohort_info(
70
+ is_final=False,
71
+ cohort=cohort,
72
+ info_path=json_path,
73
+ is_gene_available=is_gene_available,
74
+ is_trait_available=is_trait_available
75
+ )
76
+
77
+ # 4. Clinical Feature Extraction (only if trait_row is not None)
78
+ if trait_row is not None:
79
+ selected_clinical_df = geo_select_clinical_features(
80
+ clinical_data,
81
+ trait=trait,
82
+ trait_row=trait_row,
83
+ convert_trait=convert_trait,
84
+ age_row=age_row,
85
+ convert_age=convert_age,
86
+ gender_row=gender_row,
87
+ convert_gender=convert_gender
88
+ )
89
+ print(preview_df(selected_clinical_df))
90
+ selected_clinical_df.to_csv(out_clinical_data_file, index=False)
91
+ # STEP3
92
+ # 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined.
93
+ gene_data = get_genetic_data(matrix_file)
94
+
95
+ # 2. Print the first 20 row IDs (gene or probe identifiers) for future observation.
96
+ print(gene_data.index[:20])
97
+ # Based on the observed identifiers (e.g., "A_23_P100001"), these appear to be microarray probe IDs rather than standard human gene symbols.
98
+ print("requires_gene_mapping = True")
99
+ # STEP5
100
+ # 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file.
101
+ gene_annotation = get_gene_annotation(soft_file)
102
+
103
+ # 2. Use the 'preview_df' function from the library to preview the data and print out the results.
104
+ print("Gene annotation preview:")
105
+ print(preview_df(gene_annotation))
106
+ # STEP: Gene Identifier Mapping
107
+
108
+ # 1. We identify "ID" as the column with the same probe identifiers as in the gene expression data.
109
+ # and "GENE_SYMBOL" as the column with the gene symbols.
110
+ prob_col = "ID"
111
+ gene_col = "GENE_SYMBOL"
112
+
113
+ # 2. Obtain a mapping DataFrame for probes to gene symbols.
114
+ mapping_df = get_gene_mapping(gene_annotation, prob_col=prob_col, gene_col=gene_col)
115
+
116
+ # 3. Apply the mapping to convert probe-level expression data into gene-level expression data.
117
+ gene_data = apply_gene_mapping(gene_data, mapping_df)
118
+
119
+ # Print a short preview of the resulting gene expression data
120
+ print("Gene expression data after mapping:")
121
+ print(preview_df(gene_data, n=5))
122
+ # STEP7
123
+ # 1. Normalize the obtained gene data with the 'normalize_gene_symbols_in_index' function from the library.
124
+ normalized_gene_data = normalize_gene_symbols_in_index(gene_data)
125
+ normalized_gene_data.to_csv(out_gene_data_file)
126
+
127
+ # 2. Link the clinical and genetic data with the 'geo_link_clinical_genetic_data' function from the library.
128
+ linked_data = geo_link_clinical_genetic_data(selected_clinical_df, normalized_gene_data)
129
+
130
+ # 3. Handle missing values in the linked data
131
+ linked_data = handle_missing_values(linked_data, trait)
132
+
133
+ # 4. Determine whether the trait and some demographic features are severely biased, and remove biased features.
134
+ is_trait_biased, unbiased_linked_data = judge_and_remove_biased_features(linked_data, trait)
135
+
136
+ # 5. Conduct quality check and save the cohort information.
137
+ is_usable = validate_and_save_cohort_info(
138
+ is_final=True,
139
+ cohort=cohort,
140
+ info_path=json_path,
141
+ is_gene_available=True,
142
+ is_trait_available=True,
143
+ is_biased=is_trait_biased,
144
+ df=linked_data
145
+ )
146
+
147
+ # 6. If the linked data is usable, save it as a CSV file to 'out_data_file'.
148
+ if is_usable:
149
+ unbiased_linked_data.to_csv(out_data_file)
p1/preprocess/Chronic_kidney_disease/code/GSE180393.py ADDED
@@ -0,0 +1,195 @@
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1
+ # Path Configuration
2
+ from tools.preprocess import *
3
+
4
+ # Processing context
5
+ trait = "Chronic_kidney_disease"
6
+ cohort = "GSE180393"
7
+
8
+ # Input paths
9
+ in_trait_dir = "../DATA/GEO/Chronic_kidney_disease"
10
+ in_cohort_dir = "../DATA/GEO/Chronic_kidney_disease/GSE180393"
11
+
12
+ # Output paths
13
+ out_data_file = "./output/preprocess/1/Chronic_kidney_disease/GSE180393.csv"
14
+ out_gene_data_file = "./output/preprocess/1/Chronic_kidney_disease/gene_data/GSE180393.csv"
15
+ out_clinical_data_file = "./output/preprocess/1/Chronic_kidney_disease/clinical_data/GSE180393.csv"
16
+ json_path = "./output/preprocess/1/Chronic_kidney_disease/cohort_info.json"
17
+
18
+ # STEP1
19
+ from tools.preprocess import *
20
+ # 1. Identify the paths to the SOFT file and the matrix file
21
+ soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir)
22
+
23
+ # 2. Read the matrix file to obtain background information and sample characteristics data
24
+ background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design']
25
+ clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1']
26
+ background_info, clinical_data = get_background_and_clinical_data(matrix_file, background_prefixes, clinical_prefixes)
27
+
28
+ # 3. Obtain the sample characteristics dictionary from the clinical dataframe
29
+ sample_characteristics_dict = get_unique_values_by_row(clinical_data)
30
+
31
+ # 4. Explicitly print out all the background information and the sample characteristics dictionary
32
+ print("Background Information:")
33
+ print(background_info)
34
+ print("Sample Characteristics Dictionary:")
35
+ print(sample_characteristics_dict)
36
+ # 1. Evaluate whether gene expression data is available
37
+ is_gene_available = True # Based on microarray transcriptome data from the summary
38
+
39
+ # 2. Determine availability of trait, age, and gender data
40
+ # and define corresponding conversion functions
41
+
42
+ # From the sample characteristics dictionary, row 0 provides multi-category info
43
+ # about disease status. We will code "Living donor" or "unaffected" as 0 (control)
44
+ # and all others as 1 (CKD). Rows for age/gender do not appear available.
45
+ trait_row = 0
46
+ age_row = None
47
+ gender_row = None
48
+
49
+ def convert_trait(value: str):
50
+ # Extract the part after the colon
51
+ parts = value.split(":", 1)
52
+ if len(parts) < 2:
53
+ return None # Unknown format
54
+ label = parts[1].strip().lower()
55
+ # Living donor or unaffected
56
+ if "living donor" in label or "unaffected" in label:
57
+ return 0
58
+ else:
59
+ return 1
60
+
61
+ def convert_age(value: str):
62
+ # No age data available
63
+ return None
64
+
65
+ def convert_gender(value: str):
66
+ # No gender data available
67
+ return None
68
+
69
+ # 3. Conduct initial filtering and save metadata
70
+ is_trait_available = (trait_row is not None)
71
+ validate_and_save_cohort_info(
72
+ is_final=False,
73
+ cohort=cohort,
74
+ info_path=json_path,
75
+ is_gene_available=is_gene_available,
76
+ is_trait_available=is_trait_available
77
+ )
78
+
79
+ # 4. If trait data is available, extract and preview clinical features
80
+ if trait_row is not None:
81
+ selected_clinical_df = geo_select_clinical_features(
82
+ clinical_df=clinical_data,
83
+ trait=trait,
84
+ trait_row=trait_row,
85
+ convert_trait=convert_trait,
86
+ age_row=age_row,
87
+ convert_age=convert_age,
88
+ gender_row=gender_row,
89
+ convert_gender=convert_gender
90
+ )
91
+
92
+ # Preview and save the resulting clinical dataframe
93
+ preview = preview_df(selected_clinical_df, n=5)
94
+ print("Preview of selected clinical features:", preview)
95
+ selected_clinical_df.to_csv(out_clinical_data_file, index=False)
96
+ # STEP3
97
+ # 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined.
98
+ gene_data = get_genetic_data(matrix_file)
99
+
100
+ # 2. Print the first 20 row IDs (gene or probe identifiers) for future observation.
101
+ print(gene_data.index[:20])
102
+ # The listed identifiers (e.g., "100009613_at", "10000_at", etc.) are typical Affymetrix probe set IDs,
103
+ # not standard human gene symbols. Therefore, they require mapping to gene symbols.
104
+ print("requires_gene_mapping = True")
105
+ # STEP5
106
+ # 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file.
107
+ gene_annotation = get_gene_annotation(soft_file)
108
+
109
+ # 2. Use the 'preview_df' function from the library to preview the data and print out the results.
110
+ print("Gene annotation preview:")
111
+ print(preview_df(gene_annotation))
112
+ # STEP6: Gene Identifier Mapping
113
+
114
+ # Observing the preview from step 5, the annotation DataFrame has columns 'ID' and 'ENTREZ_GENE_ID',
115
+ # but 'ENTREZ_GENE_ID' is purely numeric, which leads to an empty mapping when the library's
116
+ # apply_gene_mapping() tries to parse it as a “human gene symbol.” We will therefore implement
117
+ # a custom mapping function that distributes expression values to numeric Entrez IDs without
118
+ # filtering them out.
119
+
120
+ def apply_entrez_id_mapping(expression_df: pd.DataFrame, annotation_df: pd.DataFrame) -> pd.DataFrame:
121
+ """
122
+ Convert probe-level data to gene-level data using numeric Entrez IDs.
123
+ If a probe maps to multiple Entrez IDs (split by '///'), each gene gets an equal split.
124
+ Then we sum contributions from multiple probes associated with the same gene ID.
125
+ """
126
+ # Keep only the columns we need, renaming ENTREZ_GENE_ID to 'Gene'
127
+ mapping_df = annotation_df[['ID', 'ENTREZ_GENE_ID']].copy()
128
+ mapping_df.columns = ['ID', 'Gene']
129
+ mapping_df.dropna(subset=['Gene'], inplace=True)
130
+
131
+ # Filter to probes that exist in expression_df
132
+ mapping_df = mapping_df[mapping_df['ID'].isin(expression_df.index)].copy()
133
+
134
+ # A single probe might have multiple Entrez IDs separated by '///'
135
+ def split_entrez_ids(gene_str):
136
+ if '///' in gene_str:
137
+ return [x.strip() for x in gene_str.split('///') if x.strip()]
138
+ else:
139
+ return [gene_str.strip()]
140
+
141
+ mapping_df['Gene'] = mapping_df['Gene'].apply(split_entrez_ids)
142
+ # Remove rows with no valid gene IDs
143
+ mapping_df = mapping_df[mapping_df['Gene'].map(len) > 0]
144
+
145
+ # Count how many genes per probe
146
+ mapping_df['num_genes'] = mapping_df['Gene'].map(len)
147
+
148
+ # Explode so each gene occupies its own row
149
+ mapping_df.set_index('ID', inplace=True)
150
+ mapping_df = mapping_df.explode('Gene')
151
+
152
+ # Join expression data
153
+ merged_df = mapping_df.join(expression_df, how='inner')
154
+ expr_cols = [c for c in merged_df.columns if c not in ['Gene', 'num_genes']]
155
+
156
+ # Divide the probe expression among mapped genes
157
+ merged_df[expr_cols] = merged_df[expr_cols].div(merged_df['num_genes'], axis=0)
158
+
159
+ # Sum expressions for each gene
160
+ gene_df = merged_df.groupby('Gene')[expr_cols].sum()
161
+ return gene_df
162
+
163
+ # 1 & 2. Identify columns for probe ID and gene ID, then map
164
+ gene_data = apply_entrez_id_mapping(gene_data, gene_annotation)
165
+
166
+ # 3. Print shape after mapping to confirm we have gene-level data
167
+ print("Gene expression data shape after mapping:", gene_data.shape)
168
+ # STEP7
169
+ # 1. Normalize the obtained gene data with the 'normalize_gene_symbols_in_index' function from the library.
170
+ normalized_gene_data = normalize_gene_symbols_in_index(gene_data)
171
+ normalized_gene_data.to_csv(out_gene_data_file)
172
+
173
+ # 2. Link the clinical and genetic data with the 'geo_link_clinical_genetic_data' function from the library.
174
+ linked_data = geo_link_clinical_genetic_data(selected_clinical_df, normalized_gene_data)
175
+
176
+ # 3. Handle missing values in the linked data
177
+ linked_data = handle_missing_values(linked_data, trait)
178
+
179
+ # 4. Determine whether the trait and some demographic features are severely biased, and remove biased features.
180
+ is_trait_biased, unbiased_linked_data = judge_and_remove_biased_features(linked_data, trait)
181
+
182
+ # 5. Conduct quality check and save the cohort information.
183
+ is_usable = validate_and_save_cohort_info(
184
+ is_final=True,
185
+ cohort=cohort,
186
+ info_path=json_path,
187
+ is_gene_available=True,
188
+ is_trait_available=True,
189
+ is_biased=is_trait_biased,
190
+ df=linked_data
191
+ )
192
+
193
+ # 6. If the linked data is usable, save it as a CSV file to 'out_data_file'.
194
+ if is_usable:
195
+ unbiased_linked_data.to_csv(out_data_file)
p1/preprocess/Chronic_kidney_disease/code/GSE180394.py ADDED
@@ -0,0 +1,227 @@
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1
+ # Path Configuration
2
+ from tools.preprocess import *
3
+
4
+ # Processing context
5
+ trait = "Chronic_kidney_disease"
6
+ cohort = "GSE180394"
7
+
8
+ # Input paths
9
+ in_trait_dir = "../DATA/GEO/Chronic_kidney_disease"
10
+ in_cohort_dir = "../DATA/GEO/Chronic_kidney_disease/GSE180394"
11
+
12
+ # Output paths
13
+ out_data_file = "./output/preprocess/1/Chronic_kidney_disease/GSE180394.csv"
14
+ out_gene_data_file = "./output/preprocess/1/Chronic_kidney_disease/gene_data/GSE180394.csv"
15
+ out_clinical_data_file = "./output/preprocess/1/Chronic_kidney_disease/clinical_data/GSE180394.csv"
16
+ json_path = "./output/preprocess/1/Chronic_kidney_disease/cohort_info.json"
17
+
18
+ # STEP1
19
+ from tools.preprocess import *
20
+
21
+ # 1. Attempt to identify the paths to the SOFT file and the matrix file
22
+ try:
23
+ soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir)
24
+ except AssertionError:
25
+ print("[WARNING] Could not find the expected '.soft' or '.matrix' files in the directory.")
26
+ soft_file, matrix_file = None, None
27
+
28
+ if soft_file is None or matrix_file is None:
29
+ print("[ERROR] Required GEO files are missing. Please check file names in the cohort directory.")
30
+ else:
31
+ # 2. Read the matrix file to obtain background information and sample characteristics data
32
+ background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design']
33
+ clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1']
34
+ background_info, clinical_data = get_background_and_clinical_data(matrix_file,
35
+ background_prefixes,
36
+ clinical_prefixes)
37
+
38
+ # 3. Obtain the sample characteristics dictionary from the clinical dataframe
39
+ sample_characteristics_dict = get_unique_values_by_row(clinical_data)
40
+
41
+ # 4. Explicitly print out all the background information and the sample characteristics dictionary
42
+ print("Background Information:")
43
+ print(background_info)
44
+ print("\nSample Characteristics Dictionary:")
45
+ print(sample_characteristics_dict)
46
+ # 1. Gene Expression Data Availability
47
+ is_gene_available = True # This dataset uses microarray for renal transcriptome analysis
48
+
49
+ # 2. Variable Availability and Data Type Conversion
50
+ # After assessing the sample characteristics:
51
+ # - The disease/trait information is at row=0, so trait_row=0
52
+ # - Age and gender information are not present, so age_row=None and gender_row=None
53
+
54
+ trait_row = 0
55
+ age_row = None
56
+ gender_row = None
57
+
58
+ # Define data type conversion functions
59
+ def convert_trait(value: str):
60
+ """
61
+ Convert sample group to a binary indicator of CKD presence:
62
+ 0 for healthy (e.g., living donor or unaffected part),
63
+ 1 for CKD or other kidney disease states.
64
+ """
65
+ if not value or ':' not in value:
66
+ return None
67
+ # Extract text after "sample group:"
68
+ val = value.split(':', 1)[-1].strip().lower()
69
+ if 'donor' in val or 'unaffected' in val:
70
+ return 0
71
+ else:
72
+ return 1
73
+
74
+ def convert_age(value: str):
75
+ """No age data available, return None."""
76
+ return None
77
+
78
+ def convert_gender(value: str):
79
+ """No gender data available, return None."""
80
+ return None
81
+
82
+ # 3. Save Metadata (initial filtering)
83
+ is_trait_available = (trait_row is not None)
84
+ is_usable = validate_and_save_cohort_info(
85
+ is_final=False,
86
+ cohort=cohort,
87
+ info_path=json_path,
88
+ is_gene_available=is_gene_available,
89
+ is_trait_available=is_trait_available
90
+ )
91
+
92
+ # 4. Clinical Feature Extraction (only if trait data is available)
93
+ if trait_row is not None:
94
+ selected_clinical_df = geo_select_clinical_features(
95
+ clinical_df=clinical_data, # assumed available from previous context
96
+ trait=trait,
97
+ trait_row=trait_row,
98
+ convert_trait=convert_trait,
99
+ age_row=age_row,
100
+ convert_age=convert_age,
101
+ gender_row=gender_row,
102
+ convert_gender=convert_gender
103
+ )
104
+ # Preview extracted clinical features
105
+ preview = preview_df(selected_clinical_df)
106
+ print("Preview of selected clinical features:", preview)
107
+
108
+ # Save clinical data if available
109
+ selected_clinical_df.to_csv(out_clinical_data_file, index=False)
110
+ # STEP3
111
+ # Attempt to read gene expression data; if the library function yields an empty DataFrame,
112
+ # try re-reading without ignoring lines that start with '!' (because sometimes GEO data may
113
+ # place actual expression rows under lines that begin with '!').
114
+
115
+ gene_data = get_genetic_data(matrix_file)
116
+ if gene_data.empty:
117
+ print("[WARNING] The gene_data is empty. Attempting alternative loading without treating '!' as comments.")
118
+ import gzip
119
+
120
+ # Locate the marker line first
121
+ skip_rows = 0
122
+ with gzip.open(matrix_file, 'rt') as file:
123
+ for i, line in enumerate(file):
124
+ if "!series_matrix_table_begin" in line:
125
+ skip_rows = i + 1
126
+ break
127
+
128
+ # Read the data again, this time not treating '!' as comment
129
+ gene_data = pd.read_csv(
130
+ matrix_file,
131
+ compression="gzip",
132
+ skiprows=skip_rows,
133
+ delimiter="\t",
134
+ on_bad_lines="skip"
135
+ )
136
+ gene_data = gene_data.rename(columns={"ID_REF": "ID"}).astype({"ID": "str"})
137
+ gene_data.set_index("ID", inplace=True)
138
+
139
+ # Print the first 20 row IDs to confirm data structure
140
+ print(gene_data.index[:20])
141
+ # These identifiers (e.g., "100009613_at") are typical Affymetrix probe IDs, not standard human gene symbols.
142
+
143
+ print("\nrequires_gene_mapping = True")
144
+ # STEP5
145
+ # 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file.
146
+ gene_annotation = get_gene_annotation(soft_file)
147
+
148
+ # 2. Use the 'preview_df' function from the library to preview the data and print out the results.
149
+ print("Gene annotation preview:")
150
+ print(preview_df(gene_annotation))
151
+ # STEP: Gene Identifier Mapping
152
+
153
+ # 1) From the annotation preview, we see that the column "ID" matches the probe IDs in the gene expression data,
154
+ # and "ENTREZ_GENE_ID" stores the corresponding gene identifier (which we'll treat as the 'gene symbol' column).
155
+
156
+ probe_col = "ID"
157
+ symbol_col = "ENTREZ_GENE_ID"
158
+
159
+ # 2) Get a two-column dataframe for mapping probes to genes
160
+ gene_mapping = get_gene_mapping(gene_annotation, prob_col=probe_col, gene_col=symbol_col)
161
+
162
+ # 3) Apply the mapping to convert probe-level data into gene-level data
163
+ gene_data = apply_gene_mapping(gene_data, gene_mapping)
164
+
165
+ # Print a brief preview
166
+ print("Gene expression data shape:", gene_data.shape)
167
+ print("Preview of the mapped gene expression data:")
168
+ print(gene_data.head())
169
+ import os
170
+ import pandas as pd
171
+
172
+ # STEP7: Data Normalization and Linking
173
+
174
+ # 1) Normalize the gene symbols in the previously obtained gene_data
175
+ normalized_gene_data = normalize_gene_symbols_in_index(gene_data)
176
+ normalized_gene_data.to_csv(out_gene_data_file)
177
+
178
+ # 2) Load clinical data only if it exists and is non-empty
179
+ if os.path.exists(out_clinical_data_file) and os.path.getsize(out_clinical_data_file) > 0:
180
+ # Read the file
181
+ clinical_temp = pd.read_csv(out_clinical_data_file)
182
+
183
+ # Adjust row index to label the trait, age, and gender properly
184
+ if clinical_temp.shape[0] == 3:
185
+ clinical_temp.index = [trait, "Age", "Gender"]
186
+ elif clinical_temp.shape[0] == 2:
187
+ clinical_temp.index = [trait, "Age"]
188
+ elif clinical_temp.shape[0] == 1:
189
+ clinical_temp.index = [trait]
190
+
191
+ # 2) Link the clinical and normalized genetic data
192
+ linked_data = geo_link_clinical_genetic_data(clinical_temp, normalized_gene_data)
193
+
194
+ # 3) Handle missing values
195
+ linked_data = handle_missing_values(linked_data, trait)
196
+
197
+ # 4) Check for severe bias in the trait; remove biased demographic features if present
198
+ trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait)
199
+
200
+ # 5) Final quality validation and save metadata
201
+ is_usable = validate_and_save_cohort_info(
202
+ is_final=True,
203
+ cohort=cohort,
204
+ info_path=json_path,
205
+ is_gene_available=True,
206
+ is_trait_available=True,
207
+ is_biased=trait_biased,
208
+ df=linked_data,
209
+ note=f"Final check on {cohort} with {trait}."
210
+ )
211
+
212
+ # 6) If the linked data is usable, save it
213
+ if is_usable:
214
+ linked_data.to_csv(out_data_file)
215
+ else:
216
+ # If no valid clinical data file is found, finalize metadata indicating trait unavailability
217
+ is_usable = validate_and_save_cohort_info(
218
+ is_final=True,
219
+ cohort=cohort,
220
+ info_path=json_path,
221
+ is_gene_available=True,
222
+ is_trait_available=False,
223
+ is_biased=True, # Force a fallback so that it's flagged as unusable
224
+ df=pd.DataFrame(),
225
+ note=f"No trait data found for {cohort}, final metadata recorded."
226
+ )
227
+ # Per instructions, do not save a final linked data file when trait data is absent.
p1/preprocess/Chronic_kidney_disease/code/GSE45980.py ADDED
@@ -0,0 +1,234 @@
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1
+ # Path Configuration
2
+ from tools.preprocess import *
3
+
4
+ # Processing context
5
+ trait = "Chronic_kidney_disease"
6
+ cohort = "GSE45980"
7
+
8
+ # Input paths
9
+ in_trait_dir = "../DATA/GEO/Chronic_kidney_disease"
10
+ in_cohort_dir = "../DATA/GEO/Chronic_kidney_disease/GSE45980"
11
+
12
+ # Output paths
13
+ out_data_file = "./output/preprocess/1/Chronic_kidney_disease/GSE45980.csv"
14
+ out_gene_data_file = "./output/preprocess/1/Chronic_kidney_disease/gene_data/GSE45980.csv"
15
+ out_clinical_data_file = "./output/preprocess/1/Chronic_kidney_disease/clinical_data/GSE45980.csv"
16
+ json_path = "./output/preprocess/1/Chronic_kidney_disease/cohort_info.json"
17
+
18
+ # STEP1
19
+ from tools.preprocess import *
20
+
21
+ # 1. Attempt to identify the paths to the SOFT file and the matrix file
22
+ try:
23
+ soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir)
24
+ except AssertionError:
25
+ print("[WARNING] Could not find the expected '.soft' or '.matrix' files in the directory.")
26
+ soft_file, matrix_file = None, None
27
+
28
+ if soft_file is None or matrix_file is None:
29
+ print("[ERROR] Required GEO files are missing. Please check file names in the cohort directory.")
30
+ else:
31
+ # 2. Read the matrix file to obtain background information and sample characteristics data
32
+ background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design']
33
+ clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1']
34
+ background_info, clinical_data = get_background_and_clinical_data(matrix_file,
35
+ background_prefixes,
36
+ clinical_prefixes)
37
+
38
+ # 3. Obtain the sample characteristics dictionary from the clinical dataframe
39
+ sample_characteristics_dict = get_unique_values_by_row(clinical_data)
40
+
41
+ # 4. Explicitly print out all the background information and the sample characteristics dictionary
42
+ print("Background Information:")
43
+ print(background_info)
44
+ print("\nSample Characteristics Dictionary:")
45
+ print(sample_characteristics_dict)
46
+ # Step 1: Determine if gene expression data is available
47
+ # From the background info, mRNA expression profiling was performed, so we set:
48
+ is_gene_available = True
49
+
50
+ # Step 2: Variable Availability and Data Type Conversion
51
+
52
+ # 2.1 The dataset trait is chronic kidney disease (CKD). However, all subjects are CKD patients,
53
+ # so there's no variation (everyone has the trait). Hence, it's effectively not available for our analysis:
54
+ trait_row = None
55
+
56
+ # For age, row 1 contains varied age values "age (yrs): <number>".
57
+ age_row = 1
58
+
59
+ # For gender, row 0 contains "gender: male" or "gender: female", so it is available and non-constant.
60
+ gender_row = 0
61
+
62
+ # 2.2 Define conversion functions for each variable.
63
+
64
+ def convert_trait(value: str) -> int:
65
+ # The trait is not actually variable in this dataset, so we won't use this.
66
+ # But we define a no-op function for completeness.
67
+ return None
68
+
69
+ def convert_age(value: str) -> float:
70
+ try:
71
+ # Example: "age (yrs): 72"
72
+ # Split at the first colon and parse the right side
73
+ right_side = value.split(':', 1)[1].strip()
74
+ return float(right_side)
75
+ except:
76
+ return None
77
+
78
+ def convert_gender(value: str) -> int:
79
+ try:
80
+ # Example: "gender: male"
81
+ right_side = value.split(':', 1)[1].strip().lower()
82
+ if right_side == 'male':
83
+ return 1
84
+ elif right_side == 'female':
85
+ return 0
86
+ else:
87
+ return None
88
+ except:
89
+ return None
90
+
91
+ # 3. Save Metadata (initial filtering)
92
+ # Trait availability depends on whether trait_row is None.
93
+ is_trait_available = (trait_row is not None)
94
+
95
+ is_usable = validate_and_save_cohort_info(
96
+ is_final=False,
97
+ cohort=cohort,
98
+ info_path=json_path,
99
+ is_gene_available=is_gene_available,
100
+ is_trait_available=is_trait_available
101
+ )
102
+
103
+ # 4. Clinical Feature Extraction
104
+ # Only proceed if the trait is available, i.e., trait_row is not None.
105
+ if trait_row is not None:
106
+ # Suppose we have a DataFrame called clinical_data already loaded.
107
+ # (In practice, it would be passed from previous steps.)
108
+ selected_clinical_df = geo_select_clinical_features(
109
+ clinical_df=clinical_data,
110
+ trait=trait,
111
+ trait_row=trait_row,
112
+ convert_trait=convert_trait,
113
+ age_row=age_row,
114
+ convert_age=convert_age,
115
+ gender_row=gender_row,
116
+ convert_gender=convert_gender
117
+ )
118
+ preview = preview_df(selected_clinical_df)
119
+ print("Preview of selected clinical features:", preview)
120
+
121
+ # Save to CSV
122
+ selected_clinical_df.to_csv(out_clinical_data_file, index=False)
123
+ # STEP3
124
+ # Attempt to read gene expression data; if the library function yields an empty DataFrame,
125
+ # try re-reading without ignoring lines that start with '!' (because sometimes GEO data may
126
+ # place actual expression rows under lines that begin with '!').
127
+
128
+ gene_data = get_genetic_data(matrix_file)
129
+ if gene_data.empty:
130
+ print("[WARNING] The gene_data is empty. Attempting alternative loading without treating '!' as comments.")
131
+ import gzip
132
+
133
+ # Locate the marker line first
134
+ skip_rows = 0
135
+ with gzip.open(matrix_file, 'rt') as file:
136
+ for i, line in enumerate(file):
137
+ if "!series_matrix_table_begin" in line:
138
+ skip_rows = i + 1
139
+ break
140
+
141
+ # Read the data again, this time not treating '!' as comment
142
+ gene_data = pd.read_csv(
143
+ matrix_file,
144
+ compression="gzip",
145
+ skiprows=skip_rows,
146
+ delimiter="\t",
147
+ on_bad_lines="skip"
148
+ )
149
+ gene_data = gene_data.rename(columns={"ID_REF": "ID"}).astype({"ID": "str"})
150
+ gene_data.set_index("ID", inplace=True)
151
+
152
+ # Print the first 20 row IDs to confirm data structure
153
+ print(gene_data.index[:20])
154
+ # Based on the probe-like format of the identifiers (e.g., 'A_23_P100001'),
155
+ # they do not appear to be standard human gene symbols. They likely require mapping.
156
+ print("requires_gene_mapping = True")
157
+ # STEP5
158
+ # 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file.
159
+ gene_annotation = get_gene_annotation(soft_file)
160
+
161
+ # 2. Use the 'preview_df' function from the library to preview the data and print out the results.
162
+ print("Gene annotation preview:")
163
+ print(preview_df(gene_annotation))
164
+ # STEP: Gene Identifier Mapping
165
+
166
+ # 1. Decide that the column "ID" in the annotation dataframe corresponds to the probe IDs,
167
+ # and "GENE_SYMBOL" corresponds to the gene symbol.
168
+ mapping_df = get_gene_mapping(gene_annotation, prob_col="ID", gene_col="GENE_SYMBOL")
169
+
170
+ # 2. Convert probe-level data to gene expression data.
171
+ gene_data = apply_gene_mapping(expression_df=gene_data, mapping_df=mapping_df)
172
+
173
+ # Show a quick preview of the resulting gene-level data.
174
+ print("Mapped gene_data shape:", gene_data.shape)
175
+ print(gene_data.head())
176
+ import os
177
+ import pandas as pd
178
+
179
+ # STEP7: Data Normalization and Linking
180
+
181
+ # 1) Normalize the gene symbols in the previously obtained gene_data
182
+ normalized_gene_data = normalize_gene_symbols_in_index(gene_data)
183
+ normalized_gene_data.to_csv(out_gene_data_file)
184
+
185
+ # 2) Load clinical data only if it exists and is non-empty
186
+ if os.path.exists(out_clinical_data_file) and os.path.getsize(out_clinical_data_file) > 0:
187
+ # Read the file
188
+ clinical_temp = pd.read_csv(out_clinical_data_file)
189
+
190
+ # Adjust row index to label the trait, age, and gender properly
191
+ if clinical_temp.shape[0] == 3:
192
+ clinical_temp.index = [trait, "Age", "Gender"]
193
+ elif clinical_temp.shape[0] == 2:
194
+ clinical_temp.index = [trait, "Age"]
195
+ elif clinical_temp.shape[0] == 1:
196
+ clinical_temp.index = [trait]
197
+
198
+ # 2) Link the clinical and normalized genetic data
199
+ linked_data = geo_link_clinical_genetic_data(clinical_temp, normalized_gene_data)
200
+
201
+ # 3) Handle missing values
202
+ linked_data = handle_missing_values(linked_data, trait)
203
+
204
+ # 4) Check for severe bias in the trait; remove biased demographic features if present
205
+ trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait)
206
+
207
+ # 5) Final quality validation and save metadata
208
+ is_usable = validate_and_save_cohort_info(
209
+ is_final=True,
210
+ cohort=cohort,
211
+ info_path=json_path,
212
+ is_gene_available=True,
213
+ is_trait_available=True,
214
+ is_biased=trait_biased,
215
+ df=linked_data,
216
+ note=f"Final check on {cohort} with {trait}."
217
+ )
218
+
219
+ # 6) If the linked data is usable, save it
220
+ if is_usable:
221
+ linked_data.to_csv(out_data_file)
222
+ else:
223
+ # If no valid clinical data file is found, finalize metadata indicating trait unavailability
224
+ is_usable = validate_and_save_cohort_info(
225
+ is_final=True,
226
+ cohort=cohort,
227
+ info_path=json_path,
228
+ is_gene_available=True,
229
+ is_trait_available=False,
230
+ is_biased=True, # Force a fallback so that it's flagged as unusable
231
+ df=pd.DataFrame(),
232
+ note=f"No trait data found for {cohort}, final metadata recorded."
233
+ )
234
+ # Per instructions, do not save a final linked data file when trait data is absent.
p1/preprocess/Chronic_kidney_disease/code/GSE60861.py ADDED
@@ -0,0 +1,230 @@
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
1
+ # Path Configuration
2
+ from tools.preprocess import *
3
+
4
+ # Processing context
5
+ trait = "Chronic_kidney_disease"
6
+ cohort = "GSE60861"
7
+
8
+ # Input paths
9
+ in_trait_dir = "../DATA/GEO/Chronic_kidney_disease"
10
+ in_cohort_dir = "../DATA/GEO/Chronic_kidney_disease/GSE60861"
11
+
12
+ # Output paths
13
+ out_data_file = "./output/preprocess/1/Chronic_kidney_disease/GSE60861.csv"
14
+ out_gene_data_file = "./output/preprocess/1/Chronic_kidney_disease/gene_data/GSE60861.csv"
15
+ out_clinical_data_file = "./output/preprocess/1/Chronic_kidney_disease/clinical_data/GSE60861.csv"
16
+ json_path = "./output/preprocess/1/Chronic_kidney_disease/cohort_info.json"
17
+
18
+ # STEP1
19
+ from tools.preprocess import *
20
+
21
+ # 1. Attempt to identify the paths to the SOFT file and the matrix file
22
+ try:
23
+ soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir)
24
+ except AssertionError:
25
+ print("[WARNING] Could not find the expected '.soft' or '.matrix' files in the directory.")
26
+ soft_file, matrix_file = None, None
27
+
28
+ if soft_file is None or matrix_file is None:
29
+ print("[ERROR] Required GEO files are missing. Please check file names in the cohort directory.")
30
+ else:
31
+ # 2. Read the matrix file to obtain background information and sample characteristics data
32
+ background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design']
33
+ clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1']
34
+ background_info, clinical_data = get_background_and_clinical_data(matrix_file,
35
+ background_prefixes,
36
+ clinical_prefixes)
37
+
38
+ # 3. Obtain the sample characteristics dictionary from the clinical dataframe
39
+ sample_characteristics_dict = get_unique_values_by_row(clinical_data)
40
+
41
+ # 4. Explicitly print out all the background information and the sample characteristics dictionary
42
+ print("Background Information:")
43
+ print(background_info)
44
+ print("\nSample Characteristics Dictionary:")
45
+ print(sample_characteristics_dict)
46
+ # 1. Determine if the dataset likely contains gene expression (mRNA) data
47
+ # From the background info, the title explicitly states analysis of mRNA-expression,
48
+ # so we set is_gene_available = True.
49
+
50
+ is_gene_available = True
51
+
52
+ # 2. Determine availability and parsing of the variables 'trait', 'age', and 'gender'.
53
+
54
+ # 2.1 Data Availability
55
+ # The dataset is entirely about chronic kidney disease (CKD) subdivided by specific nephropathies.
56
+ # Hence CKD is constant across all samples and offers no variation for associating gene expression.
57
+ # Therefore, "trait_row" should be None (treated as not available).
58
+ trait_row = None
59
+
60
+ # For the 'age' variable, key=1 in the sample characteristics has well-defined numeric values
61
+ # with multiple distinct entries. Thus we set age_row=1.
62
+ age_row = 1
63
+
64
+ # For the 'gender' variable, key=0 has entries "gender: male" and "gender: female" (and one mentioning "tissue"),
65
+ # which still shows at least 2 distinct gender values. Hence gender_row=0.
66
+ gender_row = 0
67
+
68
+ # 2.2 Data Type Conversion
69
+ # - Trait: not available (trait_row=None), but we still define the function.
70
+ # - Age: continuous.
71
+ # - Gender: binary (female->0, male->1).
72
+
73
+ def convert_trait(value: str) -> int:
74
+ # Not actually used since trait_row is None, but defined for completeness.
75
+ # We consider it unavailable, so return None to skip usage.
76
+ return None
77
+
78
+ def convert_age(value: str) -> float:
79
+ # Extract the part after the colon and convert to float
80
+ # Unknown or malformed entries become None
81
+ parts = value.split(":")
82
+ if len(parts) < 2:
83
+ return None
84
+ try:
85
+ return float(parts[-1].strip())
86
+ except ValueError:
87
+ return None
88
+
89
+ def convert_gender(value: str) -> int:
90
+ # Extract the part after the colon
91
+ parts = value.split(":")
92
+ if len(parts) < 2:
93
+ return None
94
+ val = parts[-1].strip().lower()
95
+ if val == "male":
96
+ return 1
97
+ elif val == "female":
98
+ return 0
99
+ else:
100
+ return None
101
+
102
+ # 3. Save metadata with initial filtering.
103
+ # trait_row is None => is_trait_available = False
104
+ # gene expression is likely => is_gene_available = True
105
+ # Perform the initial validation.
106
+ is_trait_available = (trait_row is not None)
107
+
108
+ is_usable = validate_and_save_cohort_info(
109
+ is_final=False,
110
+ cohort=cohort,
111
+ info_path=json_path,
112
+ is_gene_available=is_gene_available,
113
+ is_trait_available=is_trait_available
114
+ )
115
+
116
+ # 4. Clinical Feature Extraction
117
+ # We only extract clinical features if trait_row is not None. Here trait_row = None (no variation),
118
+ # so we skip the extraction step.
119
+ # (No further action regarding clinical data extraction.)
120
+ # STEP3
121
+ # Attempt to read gene expression data; if the library function yields an empty DataFrame,
122
+ # try re-reading without ignoring lines that start with '!' (because sometimes GEO data may
123
+ # place actual expression rows under lines that begin with '!').
124
+
125
+ gene_data = get_genetic_data(matrix_file)
126
+ if gene_data.empty:
127
+ print("[WARNING] The gene_data is empty. Attempting alternative loading without treating '!' as comments.")
128
+ import gzip
129
+
130
+ # Locate the marker line first
131
+ skip_rows = 0
132
+ with gzip.open(matrix_file, 'rt') as file:
133
+ for i, line in enumerate(file):
134
+ if "!series_matrix_table_begin" in line:
135
+ skip_rows = i + 1
136
+ break
137
+
138
+ # Read the data again, this time not treating '!' as comment
139
+ gene_data = pd.read_csv(
140
+ matrix_file,
141
+ compression="gzip",
142
+ skiprows=skip_rows,
143
+ delimiter="\t",
144
+ on_bad_lines="skip"
145
+ )
146
+ gene_data = gene_data.rename(columns={"ID_REF": "ID"}).astype({"ID": "str"})
147
+ gene_data.set_index("ID", inplace=True)
148
+
149
+ # Print the first 20 row IDs to confirm data structure
150
+ print(gene_data.index[:20])
151
+ # Based on their format (e.g., "A_23_P100001"), these identifiers appear to be probe IDs from a microarray platform,
152
+ # rather than standard human gene symbols. Therefore, they need to be mapped to gene symbols.
153
+
154
+ print("These identifiers are microarray probe IDs, not standard human gene symbols.")
155
+ print("requires_gene_mapping = True")
156
+ # STEP5
157
+ # 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file.
158
+ gene_annotation = get_gene_annotation(soft_file)
159
+
160
+ # 2. Use the 'preview_df' function from the library to preview the data and print out the results.
161
+ print("Gene annotation preview:")
162
+ print(preview_df(gene_annotation))
163
+ # STEP6: Gene Identifier Mapping
164
+
165
+ # 1 & 2. Decide which columns in the gene annotation dataframe correspond to the probe IDs and gene symbols.
166
+ # From inspection, "ID" matches the probe IDs (e.g., "A_23_P100001") in our expression data,
167
+ # and "GENE_SYMBOL" contains the gene symbols.
168
+ mapping_df = get_gene_mapping(gene_annotation, 'ID', 'GENE_SYMBOL')
169
+
170
+ # 3. Convert probe-level measurements to gene expression data by applying the mapping:
171
+ gene_data = apply_gene_mapping(gene_data, mapping_df)
172
+ import os
173
+ import pandas as pd
174
+
175
+ # STEP7: Data Normalization and Linking
176
+
177
+ # 1) Normalize the gene symbols in the previously obtained gene_data
178
+ normalized_gene_data = normalize_gene_symbols_in_index(gene_data)
179
+ normalized_gene_data.to_csv(out_gene_data_file)
180
+
181
+ # 2) Load clinical data only if it exists and is non-empty
182
+ if os.path.exists(out_clinical_data_file) and os.path.getsize(out_clinical_data_file) > 0:
183
+ # Read the file
184
+ clinical_temp = pd.read_csv(out_clinical_data_file)
185
+
186
+ # Adjust row index to label the trait, age, and gender properly
187
+ if clinical_temp.shape[0] == 3:
188
+ clinical_temp.index = [trait, "Age", "Gender"]
189
+ elif clinical_temp.shape[0] == 2:
190
+ clinical_temp.index = [trait, "Age"]
191
+ elif clinical_temp.shape[0] == 1:
192
+ clinical_temp.index = [trait]
193
+
194
+ # 2) Link the clinical and normalized genetic data
195
+ linked_data = geo_link_clinical_genetic_data(clinical_temp, normalized_gene_data)
196
+
197
+ # 3) Handle missing values
198
+ linked_data = handle_missing_values(linked_data, trait)
199
+
200
+ # 4) Check for severe bias in the trait; remove biased demographic features if present
201
+ trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait)
202
+
203
+ # 5) Final quality validation and save metadata
204
+ is_usable = validate_and_save_cohort_info(
205
+ is_final=True,
206
+ cohort=cohort,
207
+ info_path=json_path,
208
+ is_gene_available=True,
209
+ is_trait_available=True,
210
+ is_biased=trait_biased,
211
+ df=linked_data,
212
+ note=f"Final check on {cohort} with {trait}."
213
+ )
214
+
215
+ # 6) If the linked data is usable, save it
216
+ if is_usable:
217
+ linked_data.to_csv(out_data_file)
218
+ else:
219
+ # If no valid clinical data file is found, finalize metadata indicating trait unavailability
220
+ is_usable = validate_and_save_cohort_info(
221
+ is_final=True,
222
+ cohort=cohort,
223
+ info_path=json_path,
224
+ is_gene_available=True,
225
+ is_trait_available=False,
226
+ is_biased=True, # Force a fallback so that it's flagged as unusable
227
+ df=pd.DataFrame(),
228
+ note=f"No trait data found for {cohort}, final metadata recorded."
229
+ )
230
+ # Per instructions, do not save a final linked data file when trait data is absent.