# Path Configuration from tools.preprocess import * # Processing context trait = "Ankylosing_Spondylitis" cohort = "GSE73754" # Input paths in_trait_dir = "../DATA/GEO/Ankylosing_Spondylitis" in_cohort_dir = "../DATA/GEO/Ankylosing_Spondylitis/GSE73754" # Output paths out_data_file = "./output/preprocess/3/Ankylosing_Spondylitis/GSE73754.csv" out_gene_data_file = "./output/preprocess/3/Ankylosing_Spondylitis/gene_data/GSE73754.csv" out_clinical_data_file = "./output/preprocess/3/Ankylosing_Spondylitis/clinical_data/GSE73754.csv" json_path = "./output/preprocess/3/Ankylosing_Spondylitis/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 check is_gene_available = True # Based on series title and background, this is gene expression data # 2.1 Data availability check trait_row = 3 # 'disease' field contains trait info age_row = 1 # 'age (yr)' field contains age info gender_row = 0 # 'Sex' field contains gender info # 2.2 Data type conversion functions def convert_trait(value: str) -> int: """Convert trait value to binary: 1 for AS, 0 for healthy control""" if not value or 'disease:' not in value: return None value = value.split('disease:')[1].strip().lower() if 'ankylosing spondylitis' in value: return 1 elif 'healthy control' in value: return 0 return None def convert_age(value: str) -> float: """Convert age value to continuous numeric""" if not value or 'age (yr):' not in value: return None try: return float(value.split('age (yr):')[1].strip()) except: return None def convert_gender(value: str) -> int: """Convert gender to binary: 1 for male, 0 for female""" if not value or 'Sex:' not in value: return None value = value.split('Sex:')[1].strip().lower() if 'male' in value: return 1 elif 'female' in value: return 0 return None # 3. Save 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. Extract clinical features if trait data available 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 extracted features preview = preview_df(clinical_features) print("Preview of clinical features:", preview) # Save clinical data clinical_features.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) # The identifiers starting with "ILMN_" indicate these are Illumina probe IDs # They need to be mapped to standard human gene symbols for analysis 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)) # Get gene mapping from probe IDs to gene symbols mapping_data = get_gene_mapping(gene_annotation, prob_col='ID', gene_col='Symbol') # Convert probe measurements to gene expression data gene_data = apply_gene_mapping(gene_data, mapping_data) # Normalize gene symbols to ensure consistency gene_data = normalize_gene_symbols_in_index(gene_data) # Save gene expression data gene_data.to_csv(out_gene_data_file) # 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)}" )