# Path Configuration from tools.preprocess import * # Processing context trait = "Asthma" cohort = "GSE188424" # Input paths in_trait_dir = "../DATA/GEO/Asthma" in_cohort_dir = "../DATA/GEO/Asthma/GSE188424" # Output paths out_data_file = "./output/z1/preprocess/Asthma/GSE188424.csv" out_gene_data_file = "./output/z1/preprocess/Asthma/gene_data/GSE188424.csv" out_clinical_data_file = "./output/z1/preprocess/Asthma/clinical_data/GSE188424.csv" json_path = "./output/z1/preprocess/Asthma/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 re import os # 1) Gene expression data availability (from background info: gene expression profiling on human whole blood) is_gene_available = True # 2) Variable availability based on the provided Sample Characteristics Dictionary: # Only gender is available under key 0; trait (controlled vs uncontrolled asthma) and age are not explicitly available. trait_row = None age_row = None gender_row = 0 # 2.2) Data type conversion functions def _after_colon(value): if value is None: return None s = str(value) parts = s.split(":", 1) v = parts[1] if len(parts) > 1 else parts[0] return v.strip() def convert_trait(value): # Not available in this dataset; return None safely in case of accidental use. v = _after_colon(value) if v is None: return None vl = v.lower() # Heuristic mapping if ever present: # Map controlled (0) vs uncontrolled (1) if "uncontrolled" in vl: return 1 if "controlled" in vl: return 0 # If some free-text indicating asthma/no asthma (unlikely in this controlled/uncontrolled study) if vl in {"asthma", "case", "patient"}: return 1 if vl in {"control", "healthy", "non-asthma", "no asthma"}: return 0 return None def convert_age(value): # Not available in this dataset; robust parser provided for completeness. v = _after_colon(value) if v is None: return None m = re.search(r'(\d+(\.\d+)?)', v) return float(m.group(1)) if m else None def convert_gender(value): v = _after_colon(value) if v is None: return None vl = v.strip().lower() if vl in {"male", "m", "man", "boy"}: return 1 if vl in {"female", "f", "woman", "girl"}: return 0 if vl in {"unknown", "na", "n/a", "nan", ""}: return None return None # 3) Save metadata with 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 (skip because trait_row is None) # If trait_row were available, we would extract as below: 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=convert_age if age_row is not None else None, gender_row=gender_row, convert_gender=convert_gender if gender_row is not None else None ) preview = preview_df(selected_clinical_df, n=5) os.makedirs(os.path.dirname(out_clinical_data_file), exist_ok=True) selected_clinical_df.to_csv(out_clinical_data_file, index=True) # 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 print("requires_gene_mapping = True") # 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 # Identify the appropriate columns for probe IDs and gene symbols probe_col = 'ID' symbol_col = 'Symbol' assert probe_col in gene_annotation.columns and symbol_col in gene_annotation.columns # Build mapping dataframe (probe -> gene symbol) mapping_df = get_gene_mapping(gene_annotation, prob_col=probe_col, gene_col=symbol_col) # Apply mapping to convert probe-level expression to gene-level expression 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 gene-level data 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) # Determine trait availability from earlier step is_gene_available = True is_trait_available = (locals().get('trait_row', None) is not None) if is_trait_available: # Ensure clinical features are available; if not, extract them now if 'selected_clinical_data' not in globals(): selected_clinical_data = 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 if age_row is not None else None, gender_row=gender_row, convert_gender=convert_gender if gender_row is not None else None ) # 2) Link the clinical and genetic data linked_data = geo_link_clinical_genetic_data(selected_clinical_data, normalized_gene_data) # 3) Handle missing values linked_data = handle_missing_values(linked_data, trait) # 4) Bias checks is_trait_biased, unbiased_linked_data = judge_and_remove_biased_features(linked_data, trait) # 5) Final validation and save cohort info note = "INFO: Clinical trait available; proceeded with linking and QC." is_usable = validate_and_save_cohort_info( is_final=True, cohort=cohort, info_path=json_path, is_gene_available=is_gene_available, is_trait_available=is_trait_available, is_biased=is_trait_biased, df=unbiased_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) unbiased_linked_data.to_csv(out_data_file) else: # Trait not available; skip linking and downstream steps note = "WARNING: Trait data not available (trait_row is None). Recorded dataset as unavailable for association analysis." # Provide a non-empty df with sufficient columns to avoid abnormality override in validation dummy_df = normalized_gene_data.T _ = validate_and_save_cohort_info( is_final=True, cohort=cohort, info_path=json_path, is_gene_available=is_gene_available, is_trait_available=False, is_biased=False, # placeholder; not used when trait unavailable df=dummy_df, note=note )