# Path Configuration from tools.preprocess import * # Processing context trait = "Bladder_Cancer" cohort = "GSE201395" # Input paths in_trait_dir = "../DATA/GEO/Bladder_Cancer" in_cohort_dir = "../DATA/GEO/Bladder_Cancer/GSE201395" # Output paths out_data_file = "./output/z1/preprocess/Bladder_Cancer/GSE201395.csv" out_gene_data_file = "./output/z1/preprocess/Bladder_Cancer/gene_data/GSE201395.csv" out_clinical_data_file = "./output/z1/preprocess/Bladder_Cancer/clinical_data/GSE201395.csv" json_path = "./output/z1/preprocess/Bladder_Cancer/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 # Step 1: Determine gene expression availability based on background info # Affymetrix HTA 2.0 is a gene expression microarray platform. is_gene_available = True # Step 2: Determine availability of trait, age, and gender # The dataset consists of urothelial carcinoma cell lines only; no human subject-level trait variability. # Sample characteristics only include cell line names; no age or gender data. trait_row = None age_row = None gender_row = None # Step 2.2: Define conversion functions def _after_colon(value): if value is None: return None s = str(value) return s.split(":", 1)[-1].strip() if ":" in s else s.strip() def convert_trait(value): """ Map to binary bladder cancer status if inferable: - 1: cancer/urothelial carcinoma/tumor - 0: normal/control/non-tumor/benign - None: unknown """ v = _after_colon(value) if not v: return None vl = v.lower() non_tumor_tokens = ["normal", "control", "healthy", "non-tumor", "benign", "adjacent normal", "no cancer"] tumor_tokens = ["cancer", "carcinoma", "tumor", "malignant", "urothelial", "bladder"] if any(t in vl for t in non_tumor_tokens): return 0 if any(t in vl for t in tumor_tokens): return 1 return None def convert_age(value): v = _after_colon(value) if not v: return None vl = v.lower() if vl in {"na", "n/a", "unknown", "none", "missing"}: return None # Extract first number as age import re m = re.search(r"(\d+(\.\d+)?)", vl) if m: try: return float(m.group(1)) except Exception: return None return None def convert_gender(value): v = _after_colon(value) if not v: return None vl = v.lower() if vl in {"female", "f", "woman", "women"}: return 0 if vl in {"male", "m", "man", "men"}: return 1 return None # Step 3: Initial filtering and save metadata 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 ) # Step 4: Clinical feature extraction (skip because trait_row is None) # If trait_row were available, we would extract and save clinical features like this: # 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 = preview_df(selected_clinical_df) # selected_clinical_df.to_csv(out_clinical_data_file, index=True)