# Path Configuration from tools.preprocess import * # Processing context trait = "Colon_and_Rectal_Cancer" cohort = "GSE46517" # Input paths in_trait_dir = "../DATA/GEO/Colon_and_Rectal_Cancer" in_cohort_dir = "../DATA/GEO/Colon_and_Rectal_Cancer/GSE46517" # Output paths out_data_file = "./output/preprocess/1/Colon_and_Rectal_Cancer/GSE46517.csv" out_gene_data_file = "./output/preprocess/1/Colon_and_Rectal_Cancer/gene_data/GSE46517.csv" out_clinical_data_file = "./output/preprocess/1/Colon_and_Rectal_Cancer/clinical_data/GSE46517.csv" json_path = "./output/preprocess/1/Colon_and_Rectal_Cancer/cohort_info.json" # STEP1 from tools.preprocess import * # 1. Identify the paths to the SOFT file and the matrix file soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) # 2. Read the matrix file to obtain background information and sample characteristics data background_prefixes = ['!Series_title', '!Series_summary', '!Series_overall_design'] clinical_prefixes = ['!Sample_geo_accession', '!Sample_characteristics_ch1'] background_info, clinical_data = get_background_and_clinical_data(matrix_file, background_prefixes, clinical_prefixes) # 3. Obtain the sample characteristics dictionary from the clinical dataframe sample_characteristics_dict = get_unique_values_by_row(clinical_data) # 4. Explicitly print out all the background information and the sample characteristics dictionary print("Background Information:") print(background_info) print("Sample Characteristics Dictionary:") print(sample_characteristics_dict) # 1. Gene Expression Data Availability # Based on the background info: "RNA was extracted and run on the ... microarray chip" # This indicates standard gene expression data is very likely available. is_gene_available = True # 2. Variable Availability and Data Type Conversion # 2.1 Data Availability # We look for the trait "Colon_and_Rectal_Cancer" in the sample characteristics. # No rows show consistent data indicating colon/rectal cancer as the primary trait. # Therefore, we consider that trait data is NOT available. trait_row = None # For age: row 7 contains multiple entries of "age at time of resection: ...", # indicating distinct numeric values. Thus, age data is available at row 7. age_row = 7 # For gender: row 8 has both "gender: male" and "gender: female", hence it # carries at least two distinct values. So let's use row 8 for gender. gender_row = 8 # 2.2 Data Type Conversion def convert_trait(raw_value: str) -> int: """ Since trait data is not available (trait_row=None), this function is not expected to be called. However, we define a stub to maintain consistency. """ return None def convert_age(raw_value: str) -> float: """ Convert age string (e.g. 'age at time of resection: 72y 4m') to a numeric value in years (float). If parsing fails, return None. """ try: # The value after the colon might look like '72y 4m' # We'll extract that part and parse the years. value_part = raw_value.split(':', 1)[-1].strip() # '72y 4m' # Split on space => ['72y', '4m'] or just one piece if months missing parts = value_part.split() # The first part is something like '72y' year_str = parts[0].lower().replace('y', '') year_val = float(year_str) return year_val except Exception: return None def convert_gender(raw_value: str) -> int: """ Convert gender string (e.g. 'gender: male' or 'gender: female') to a binary (female=0, male=1). If parsing fails, return None. """ try: value_part = raw_value.split(':', 1)[-1].strip().lower() # 'male' or 'female' if value_part == 'female': return 0 elif value_part == 'male': return 1 else: return None except Exception: return None # 3. Save Metadata # Perform initial filtering. Trait is not available, so is_trait_available=False. # This dataset will fail initial filtering due to missing trait, but we still log metadata. is_trait_available = (trait_row is not None) is_usable = validate_and_save_cohort_info( is_final=False, cohort=cohort, info_path=json_path, is_gene_available=is_gene_available, is_trait_available=is_trait_available ) # 4. Clinical Feature Extraction # We only do this if trait_row is not None. Here, trait_row = None, so we skip extraction. # End of this step. # STEP3 # 1. Use the get_genetic_data function from the library to get the gene_data from the matrix_file previously defined. gene_data = get_genetic_data(matrix_file) # 2. Print the first 20 row IDs (gene or probe identifiers) for future observation. print(gene_data.index[:20]) # The gene identifiers resemble Affymetrix probe set IDs, which are not official gene symbols. # Therefore, these identifiers will need to be mapped to gene symbols. print("\nrequires_gene_mapping = True") # STEP5 # 1. Use the 'get_gene_annotation' function from the library to get gene annotation data from the SOFT file. gene_annotation = get_gene_annotation(soft_file) # 2. Use the 'preview_df' function from the library to preview the data and print out the results. print("Gene annotation preview:") print(preview_df(gene_annotation)) # STEP: Gene Identifier Mapping # 1. From the annotation preview, we see 'ID' corresponds to the probe ids in gene_data.index, # and 'Gene Symbol' holds the corresponding gene symbols. mapping_df = get_gene_mapping(gene_annotation, prob_col="ID", gene_col="Gene Symbol") # 2. Convert probe-level measurements to gene-level expression by applying the mapping. gene_data = apply_gene_mapping(gene_data, mapping_df) # Print a brief summary to confirm successful mapping print("Gene-level expression data dimensions:", gene_data.shape) # STEP7 # 1. Normalize the obtained gene data with the 'normalize_gene_symbols_in_index' function from the library. normalized_gene_data = normalize_gene_symbols_in_index(gene_data) normalized_gene_data.to_csv(out_gene_data_file) # According to previous steps, we found that trait data is not available (trait_row was None), # so is_trait_available is False. is_trait_available = False if not is_trait_available: # 5. Conduct final validation to record metadata. Since we have no trait data, the dataset won't be usable. # We must provide 'df' and 'is_biased' to the function; passing an empty DataFrame and is_biased=True # ensures it is marked as not usable. is_usable = validate_and_save_cohort_info( is_final=True, cohort=cohort, info_path=json_path, is_gene_available=True, # We do have gene data is_trait_available=False, # Trait is not available is_biased=True, # This will mark it as not usable df=pd.DataFrame(), # Placeholder DataFrame note="Trait data not available; dataset is not usable." ) # Since trait is unavailable, we must skip linking or saving any final linked data. else: # If trait data were available, we would proceed with linking and further steps. # But since it is not, this branch is never entered. pass