File size: 6,262 Bytes
a0b62f5 |
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 100 101 102 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 119 120 121 122 123 124 125 126 127 128 129 130 131 132 133 134 135 136 137 138 139 140 141 142 143 144 145 146 147 148 149 150 151 152 153 154 155 156 157 158 159 160 161 162 163 164 165 166 167 168 169 170 171 172 173 174 175 176 177 178 179 180 181 182 183 184 185 186 187 188 189 190 191 192 |
# Path Configuration
from tools.preprocess import *
# Processing context
trait = "Aniridia"
cohort = "GSE137996"
# Input paths
in_trait_dir = "../DATA/GEO/Aniridia"
in_cohort_dir = "../DATA/GEO/Aniridia/GSE137996"
# Output paths
out_data_file = "./output/preprocess/3/Aniridia/GSE137996.csv"
out_gene_data_file = "./output/preprocess/3/Aniridia/gene_data/GSE137996.csv"
out_clinical_data_file = "./output/preprocess/3/Aniridia/clinical_data/GSE137996.csv"
json_path = "./output/preprocess/3/Aniridia/cohort_info.json"
# Get file paths
soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir)
# Extract background info and clinical data
background_info, clinical_data = get_background_and_clinical_data(matrix_file)
# Get unique values per clinical feature
sample_characteristics = get_unique_values_by_row(clinical_data)
# Print background info
print("Dataset Background Information:")
print(f"{background_info}\n")
# Print sample characteristics
print("Sample Characteristics:")
for feature, values in sample_characteristics.items():
print(f"Feature: {feature}")
print(f"Values: {values}\n")
# 1. Gene Expression Data Availability
is_gene_available = True # Series summary mentions mRNA analysis with microarrays
# 2.1 Data Availability
trait_row = 2 # Disease status in Feature 2
age_row = 0 # Age data in Feature 0
gender_row = 1 # Gender data in Feature 1
# 2.2 Data Type Conversion Functions
def convert_trait(x):
# Binary: 0 for control, 1 for disease
if not isinstance(x, str):
return None
value = x.split(": ")[-1].lower()
if "aak" in value:
return 1
elif "control" in value:
return 0
return None
def convert_age(x):
# Continuous
if not isinstance(x, str):
return None
try:
return float(x.split(": ")[-1])
except:
return None
def convert_gender(x):
# Binary: 0 for female, 1 for male
if not isinstance(x, str):
return None
value = x.split(": ")[-1].lower()
if value in ['f', 'w']: # 'w' likely means woman
return 0
elif value == 'm':
return 1
return None
# 3. Save Initial Metadata
validate_and_save_cohort_info(
is_final=False,
cohort=cohort,
info_path=json_path,
is_gene_available=is_gene_available,
is_trait_available=trait_row is not None
)
# 4. Clinical Feature Extraction
if trait_row is not None:
selected_clinical_df = geo_select_clinical_features(
clinical_df=clinical_data,
trait=trait,
trait_row=trait_row,
convert_trait=convert_trait,
age_row=age_row,
convert_age=convert_age,
gender_row=gender_row,
convert_gender=convert_gender
)
# Preview the selected features
print("Preview of selected clinical features:")
print(preview_df(selected_clinical_df))
# Save clinical data
os.makedirs(os.path.dirname(out_clinical_data_file), exist_ok=True)
selected_clinical_df.to_csv(out_clinical_data_file)
# Extract gene expression data from matrix file
gene_data = get_genetic_data(matrix_file)
# Print first 20 row IDs and shape of data to help debug
print("Shape of gene expression data:", gene_data.shape)
print("\nFirst few rows of data:")
print(gene_data.head())
print("\nFirst 20 gene/probe identifiers:")
print(gene_data.index[:20])
# Inspect a snippet of raw file to verify identifier format
import gzip
with gzip.open(matrix_file, 'rt', encoding='utf-8') as f:
lines = []
for i, line in enumerate(f):
if "!series_matrix_table_begin" in line:
# Get the next 5 lines after the marker
for _ in range(5):
lines.append(next(f).strip())
break
print("\nFirst few lines after matrix marker in raw file:")
for line in lines:
print(line)
# Based on the provided data, the gene identifiers are Agilent probe IDs (A_19_P format)
# These are not standard human gene symbols and need to be mapped
requires_gene_mapping = True
# Extract gene annotation from SOFT file
gene_annotation = get_gene_annotation(soft_file)
# Preview annotation dataframe structure
print("Gene Annotation Preview:")
print("Column names:", gene_annotation.columns.tolist())
print("\nFirst few rows as dictionary:")
print(preview_df(gene_annotation))
# 1. Looking at the gene identifiers in gene expression data (e.g., A_19_P00315452)
# and in gene annotation data, 'ID' column has the same format
# 'GENE_SYMBOL' column contains the gene symbols we want to map to
# 2. Get mapping between probe IDs and gene symbols
probe_to_gene_map = get_gene_mapping(gene_annotation, prob_col='ID', gene_col='GENE_SYMBOL')
# 3. Apply mapping to convert probe-level data to gene-level data
gene_data = apply_gene_mapping(gene_data, probe_to_gene_map)
# 1. Normalize gene symbols
gene_data = normalize_gene_symbols_in_index(gene_data)
# Save normalized gene data
gene_data.to_csv(out_gene_data_file)
# 2. Link clinical and genetic data
try:
clinical_data = pd.read_csv(out_clinical_data_file, index_col=0)
linked_data = geo_link_clinical_genetic_data(clinical_data, gene_data)
# 3. Handle missing values
linked_data = handle_missing_values(linked_data, trait)
# 4. Determine if features are biased
is_trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait)
# 5. Validate and save cohort info
is_usable = validate_and_save_cohort_info(
is_final=True,
cohort=cohort,
info_path=json_path,
is_gene_available=True,
is_trait_available=True,
is_biased=is_trait_biased,
df=linked_data,
note="Gene expression data successfully mapped and linked with clinical features"
)
# 6. Save linked data only if usable AND trait is not biased
if is_usable and not is_trait_biased:
linked_data.to_csv(out_data_file)
except Exception as e:
print(f"Error in data linking and processing: {str(e)}")
is_usable = validate_and_save_cohort_info(
is_final=True,
cohort=cohort,
info_path=json_path,
is_gene_available=True,
is_trait_available=True,
is_biased=True,
df=pd.DataFrame(),
note=f"Data processing failed: {str(e)}"
) |