# Path Configuration from tools.preprocess import * # Processing context trait = "Parkinsons_Disease" cohort = "GSE202665" # Input paths in_trait_dir = "../DATA/GEO/Parkinsons_Disease" in_cohort_dir = "../DATA/GEO/Parkinsons_Disease/GSE202665" # Output paths out_data_file = "./output/preprocess/3/Parkinsons_Disease/GSE202665.csv" out_gene_data_file = "./output/preprocess/3/Parkinsons_Disease/gene_data/GSE202665.csv" out_clinical_data_file = "./output/preprocess/3/Parkinsons_Disease/clinical_data/GSE202665.csv" json_path = "./output/preprocess/3/Parkinsons_Disease/cohort_info.json" # Get file paths soft_file_path, matrix_file_path = geo_get_relevant_filepaths(in_cohort_dir) # Get background info and clinical data background_info, clinical_data = get_background_and_clinical_data(matrix_file_path) print("Background Information:") print(background_info) print("\nSample Characteristics:") # Get dictionary of unique values per row unique_values_dict = get_unique_values_by_row(clinical_data) for row, values in unique_values_dict.items(): print(f"\n{row}:") print(values) # 1. Gene Expression Data Availability - yes, mRNA array data is available is_gene_available = True # 2.1 Data Availability trait_row = 0 # Disease state in row 0 age_row = 3 # Age in row 3 gender_row = 2 # Gender in row 2 # 2.2 Data Type Conversion Functions def convert_trait(value): if value is None: return None value = value.lower().split(': ')[-1] if "parkinson" in value: return 1 elif "healthy control" in value: return 0 return None def convert_age(value): if value is None: return None try: return float(value.split(': ')[-1]) except: return None def convert_gender(value): if value is None: return None value = value.lower().split(': ')[-1] if value == 'male': return 1 elif value == 'female': return 0 return None # 3. Save Metadata (Initial Filtering) is_trait_available = trait_row is not None 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 if trait_row is not None: clinical_features = 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 processed clinical data preview = preview_df(clinical_features) print("Preview of clinical features:") print(preview) # Save clinical features clinical_features.to_csv(out_clinical_data_file) # Get gene expression data from matrix file genetic_data = get_genetic_data(matrix_file_path) # Examine data structure print("Data structure and head:") print(genetic_data.head()) print("\nShape:", genetic_data.shape) print("\nFirst 20 row IDs (gene/probe identifiers):") print(list(genetic_data.index)[:20]) # Get a few column names to verify sample IDs print("\nFirst 5 column names:") print(list(genetic_data.columns)[:5]) # The gene expression data appears to use probe IDs (simple numeric identifiers) rather than gene symbols # For example, IDs like '1', '2', '3', etc. are numeric probe IDs that need to be mapped to human gene symbols requires_gene_mapping = True # Extract gene annotation data gene_annotation = get_gene_annotation(soft_file_path) # Display column names and preview data print("Column names:") print(gene_annotation.columns) print("\nPreview of gene annotation data:") print(preview_df(gene_annotation)) # 1. Identify columns for mapping - 'ID' matches the probe IDs in expression data, 'GENE_SYMBOL' contains gene symbols prob_col = 'ID' gene_col = 'GENE_SYMBOL' # 2. Get mapping between probe IDs and gene symbols mapping_df = get_gene_mapping(gene_annotation, prob_col, gene_col) # 3. Apply mapping to convert probe-level data to gene expression data gene_data = apply_gene_mapping(genetic_data, mapping_df) # Preview the converted gene data print("\nShape of gene expression data after mapping:", gene_data.shape) print("\nFirst few rows of gene expression data:") print(gene_data.head()) # Preview some gene symbols print("\nFirst 20 gene symbols:") print(list(gene_data.index)[:20]) # Reload clinical data that was processed earlier selected_clinical_df = pd.read_csv(out_clinical_data_file, index_col=0) # 1. Normalize gene symbols genetic_data = normalize_gene_symbols_in_index(gene_data) genetic_data.to_csv(out_gene_data_file) # 2. Link clinical and genetic data linked_data = geo_link_clinical_genetic_data(selected_clinical_df, genetic_data) # 3. Handle missing values systematically linked_data = handle_missing_values(linked_data, trait) # 4. Check for bias in trait and demographic features trait_biased, linked_data = judge_and_remove_biased_features(linked_data, trait) # 5. Final validation and information saving note = "Contains gene expression data with metabolic rate (inferred from multicentric occurrence-free survival days) measurements" 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=trait_biased, df=linked_data, note=note ) # 6. Save linked data only if usable if is_usable: os.makedirs(os.path.dirname(out_data_file), exist_ok=True) linked_data.to_csv(out_data_file)