# Path Configuration from tools.preprocess import * # Processing context trait = "Endometrioid_Cancer" cohort = "GSE68600" # Input paths in_trait_dir = "../DATA/GEO/Endometrioid_Cancer" in_cohort_dir = "../DATA/GEO/Endometrioid_Cancer/GSE68600" # Output paths out_data_file = "./output/z2/preprocess/Endometrioid_Cancer/GSE68600.csv" out_gene_data_file = "./output/z2/preprocess/Endometrioid_Cancer/gene_data/GSE68600.csv" out_clinical_data_file = "./output/z2/preprocess/Endometrioid_Cancer/clinical_data/GSE68600.csv" json_path = "./output/z2/preprocess/Endometrioid_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 # 1. Gene Expression Data Availability is_gene_available = True # This is an Affymetrix gene expression microarray dataset # 2. Variable Availability and Data Type Conversion # 2.1 Data Availability trait_row = 4 # histology information is in key 4 age_row = None # No age information available gender_row = None # All samples are female (constant), not useful # 2.2 Data Type Conversion Functions def convert_trait(value): """Convert histology to binary (0/1) for endometrioid cancer presence""" if ':' in value: histology = value.split(':')[1].strip().lower() # Check if endometrioid is mentioned in the histology if 'endometrioid' in histology: return 1 else: return 0 return None def convert_age(value): """Convert age - not applicable since age data is not available""" return None def convert_gender(value): """Convert gender - not applicable since all samples are female""" return None # 3. Save Metadata is_trait_available = trait_row is not None is_usable = 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 if trait_row is not None: selected_clinical_data = geo_select_clinical_features( clinical_data, trait, trait_row, convert_trait, age_row, convert_age, gender_row, convert_gender ) print("Preview of selected clinical data:") print(preview_df(selected_clinical_data)) # Save clinical data os.makedirs(os.path.dirname(out_clinical_data_file), exist_ok=True) selected_clinical_data.to_csv(out_clinical_data_file) print(f"Clinical data saved to {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 # Examine the gene identifiers shown in the previous step output # The identifiers follow patterns like 'A28102_at', 'AB000114_at', 'AB000381_s_at' # These are Affymetrix microarray probe set identifiers, not human gene symbols # Human gene symbols would be names like 'BRCA1', 'TP53', 'EGFR', etc. # The '_at' and '_s_at' suffixes are characteristic of Affymetrix probe nomenclature 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 # 1. Based on the analysis, 'ID' column contains probe identifiers matching gene expression data, # and 'Gene Symbol' column contains the human gene symbols we need prob_col = 'ID' gene_col = 'Gene Symbol' # 2. Extract gene mapping dataframe with probe ID to gene symbol mapping gene_mapping = get_gene_mapping(gene_annotation, prob_col, gene_col) # 3. Apply gene mapping to convert probe-level measurements to gene expression data gene_data = apply_gene_mapping(gene_data, gene_mapping) print(f"Gene expression data shape after mapping: {gene_data.shape}") print(f"First 10 gene symbols: {list(gene_data.index[:10])}") # Step 7: Data Normalization and Linking # 1. Normalize the obtained gene data with the 'normalize_gene_symbols_in_index' function from the library. normalized_gene_data = normalize_gene_symbols_in_index(gene_data) normalized_gene_data.to_csv(out_gene_data_file) # 2. Link the clinical and genetic data with the 'geo_link_clinical_genetic_data' function from the library. linked_data = geo_link_clinical_genetic_data(selected_clinical_data, normalized_gene_data) # 3. Handle missing values in the linked data linked_data = handle_missing_values(linked_data, trait) # 4. Determine whether the trait and some demographic features are severely biased, and remove biased features. is_trait_biased, unbiased_linked_data = judge_and_remove_biased_features(linked_data, trait) # 5. Conduct quality check and save the cohort information. is_usable = validate_and_save_cohort_info(True, cohort, json_path, True, True, is_trait_biased, unbiased_linked_data) # 6. If the linked data is usable, save it as a CSV file to 'out_data_file'. if is_usable: unbiased_linked_data.to_csv(out_data_file)