# Path Configuration from tools.preprocess import * # Processing context trait = "Stroke" cohort = "GSE48424" # Input paths in_trait_dir = "../DATA/GEO/Stroke" in_cohort_dir = "../DATA/GEO/Stroke/GSE48424" # Output paths out_data_file = "./output/preprocess/3/Stroke/GSE48424.csv" out_gene_data_file = "./output/preprocess/3/Stroke/gene_data/GSE48424.csv" out_clinical_data_file = "./output/preprocess/3/Stroke/clinical_data/GSE48424.csv" json_path = "./output/preprocess/3/Stroke/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 # Yes, this dataset contains gene expression data based on the dataset description is_gene_available = True # 2.1 Data Availability # Trait (Stroke/PE) is available in feature 1 "disease status" trait_row = 1 # Age is available in feature 3 age_row = 3 # Gender is not available - all subjects are female (pregnant women) based on study description gender_row = None # 2.2 Data Type Conversion Functions def convert_trait(value: str) -> int: # Extract value after colon and strip whitespace if ":" not in value: return None value = value.split(":")[1].strip().lower() # Convert to binary where preeclampsia = 1, healthy = 0 if value == "preeclampsia": return 1 elif value == "healthy": return 0 return None def convert_age(value: str) -> float: # Extract age value after colon if ":" not in value: return None value = value.split(":")[1].strip() try: return float(value) except: return None def convert_gender(value: str) -> None: # No gender conversion needed since not available 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. Extract Clinical Features if trait_row is not None: # Extract clinical features 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 data preview = preview_df(selected_clinical_df) print("Preview of clinical data:") print(preview) # Save to CSV selected_clinical_df.to_csv(out_clinical_data_file) # Get file paths soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) # 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 gene IDs are Agilent probe IDs (A_23_P format) # These need to be mapped to gene symbols requires_gene_mapping = True # Get file paths soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) # 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 file paths soft_file, matrix_file = geo_get_relevant_filepaths(in_cohort_dir) # Load gene expression data gene_data = get_genetic_data(matrix_file) # Extract gene mapping from annotation data # ID column contains probe IDs (A_23_P format) matching gene expression data # GENE_SYMBOL column contains human gene symbols mapping_data = get_gene_mapping(gene_annotation, prob_col='ID', gene_col='GENE_SYMBOL') # Apply gene mapping to convert probe measurements to gene expression gene_data = apply_gene_mapping(gene_data, mapping_data) # Save mapped gene data gene_data.to_csv(out_gene_data_file) # 1. Normalize gene symbols gene_data = normalize_gene_symbols_in_index(gene_data) gene_data.to_csv(out_gene_data_file) # 2. Load clinical data and link with genetic data 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. Evaluate bias is_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_biased, df=linked_data, note="Study examining transcriptome profiles from peripheral blood of older adults, including some with stroke history." ) # 6. Save linked data if usable if is_usable: linked_data.to_csv(out_data_file)