# Path Configuration from tools.preprocess import * # Processing context trait = "Allergies" cohort = "GSE185658" # Input paths in_trait_dir = "../DATA/GEO/Allergies" in_cohort_dir = "../DATA/GEO/Allergies/GSE185658" # Output paths out_data_file = "./output/z1/preprocess/Allergies/GSE185658.csv" out_gene_data_file = "./output/z1/preprocess/Allergies/gene_data/GSE185658.csv" out_clinical_data_file = "./output/z1/preprocess/Allergies/clinical_data/GSE185658.csv" json_path = "./output/z1/preprocess/Allergies/cohort_info.json" # Step 1: Initial Data Loading 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) # Step 2: Dataset Analysis and Clinical Feature Extraction import os import re import pandas as pd # 1. Gene Expression Data Availability is_gene_available = True # Affymetrix microarrays -> gene expression data present # 2. Variable Availability and Data Type Conversion # From the sample characteristics: # 0: time: DAY14/DAY4 # 1: group: AsthmaHDM / Healthy / AsthmaHDMNeg # 2: donor: unique IDs # Operationalize 'Allergies' as HDM sensitization using the 'group' field. trait_row = 1 age_row = None gender_row = None def _after_colon(value: str) -> str: if value is None or (isinstance(value, float) and pd.isna(value)): return "" s = str(value) return s.split(":", 1)[1].strip() if ":" in s else s.strip() def convert_trait(x): """ Map 'group' to Allergies (binary): - AsthmaHDM -> 1 (allergic / HDM-sensitized) - Healthy, AsthmaHDMNeg -> 0 (non-allergic for HDM) Unknowns -> None """ val = _after_colon(x).lower() if val in {"asthmahdm"}: return 1 if val in {"healthy", "asthmahdmneg"}: return 0 # Heuristics if "hdm" in val and "neg" in val: return 0 if "healthy" in val: return 0 if "hdm" in val and ("pos" in val or "+" in val): return 1 return None def convert_age(x): """ Extract continuous age from strings like 'age: 45', 'age: 45 years' """ val = _after_colon(x) m = re.search(r"[-+]?\d*\.?\d+", val) if m: try: return float(m.group()) except Exception: return None return None def convert_gender(x): """ Map gender to binary: female->0, male->1 """ val = _after_colon(x).strip().lower() if val in {"female", "f", "woman", "women"}: return 0 if val in {"male", "m", "man", "men"}: return 1 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 (only if trait is available) 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=None, gender_row=gender_row, convert_gender=None ) preview = preview_df(selected_clinical_df, n=5) print(preview) # Save clinical features out_dir = os.path.dirname(out_clinical_data_file) os.makedirs(out_dir, exist_ok=True) selected_clinical_df.to_csv(out_clinical_data_file) # Step 3: Gene Data Extraction # 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]) # Step 4: Gene Identifier Review # Based on the observed numeric probe-like IDs (e.g., '7892501'), mapping to human gene symbols is required. requires_gene_mapping = True print(f"requires_gene_mapping = {requires_gene_mapping}") # Step 5: Gene Annotation # 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 6: Gene Identifier Mapping # Decide columns for mapping: probe IDs are in 'ID'; gene symbols can be parsed from 'gene_assignment' probe_col = 'ID' gene_symbol_col = 'gene_assignment' # Build mapping dataframe mapping_df = get_gene_mapping(gene_annotation, prob_col=probe_col, gene_col=gene_symbol_col) # Apply mapping to convert probe-level data to gene-level data gene_data = apply_gene_mapping(expression_df=gene_data, mapping_df=mapping_df) # Step 7: Data Normalization and Linking import os # 1. Normalize gene symbols and save normalized_gene_data = normalize_gene_symbols_in_index(gene_data) os.makedirs(os.path.dirname(out_gene_data_file), exist_ok=True) normalized_gene_data.to_csv(out_gene_data_file) # 2. Link clinical and genetic data linked_data = geo_link_clinical_genetic_data(selected_clinical_df, normalized_gene_data) # 3. Handle missing values linked_data = handle_missing_values(linked_data, trait) # 4. Determine bias and remove biased demographics is_trait_biased, unbiased_linked_data = judge_and_remove_biased_features(linked_data, trait) # 5. Final validation and save cohort info note = "INFO: Trait operationalized as HDM sensitization from 'group' field: AsthmaHDM=1; Healthy/AsthmaHDMNeg=0." 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=unbiased_linked_data, note=note ) # 6. Save linked data if usable if is_usable: os.makedirs(os.path.dirname(out_data_file), exist_ok=True) unbiased_linked_data.to_csv(out_data_file)