Mercurial > repos > bgruening > ml_visualization_ex
diff model_prediction.py @ 0:f96efab83b65 draft
"planemo upload for repository https://github.com/bgruening/galaxytools/tree/master/tools/sklearn commit ba6a47bdf76bbf4cb276206ac1a8cbf61332fd16"
author | bgruening |
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date | Fri, 13 Sep 2019 12:23:39 -0400 |
parents | |
children | 6b94d76a1397 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/model_prediction.py Fri Sep 13 12:23:39 2019 -0400 @@ -0,0 +1,262 @@ +import argparse +import json +import numpy as np +import pandas as pd +import tabix +import warnings + +from scipy.io import mmread +from sklearn.pipeline import Pipeline + +from galaxy_ml.externals.selene_sdk.sequences import Genome +from galaxy_ml.utils import (load_model, read_columns, + get_module, try_get_attr) + + +N_JOBS = int(__import__('os').environ.get('GALAXY_SLOTS', 1)) + + +def main(inputs, infile_estimator, outfile_predict, + infile_weights=None, infile1=None, + fasta_path=None, ref_seq=None, + vcf_path=None): + """ + Parameter + --------- + inputs : str + File path to galaxy tool parameter + + infile_estimator : strgit + File path to trained estimator input + + outfile_predict : str + File path to save the prediction results, tabular + + infile_weights : str + File path to weights input + + infile1 : str + File path to dataset containing features + + fasta_path : str + File path to dataset containing fasta file + + ref_seq : str + File path to dataset containing the reference genome sequence. + + vcf_path : str + File path to dataset containing variants info. + """ + warnings.filterwarnings('ignore') + + with open(inputs, 'r') as param_handler: + params = json.load(param_handler) + + # load model + with open(infile_estimator, 'rb') as est_handler: + estimator = load_model(est_handler) + + main_est = estimator + if isinstance(estimator, Pipeline): + main_est = estimator.steps[-1][-1] + if hasattr(main_est, 'config') and hasattr(main_est, 'load_weights'): + if not infile_weights or infile_weights == 'None': + raise ValueError("The selected model skeleton asks for weights, " + "but dataset for weights wan not selected!") + main_est.load_weights(infile_weights) + + # handle data input + input_type = params['input_options']['selected_input'] + # tabular input + if input_type == 'tabular': + header = 'infer' if params['input_options']['header1'] else None + column_option = (params['input_options'] + ['column_selector_options_1'] + ['selected_column_selector_option']) + if column_option in ['by_index_number', 'all_but_by_index_number', + 'by_header_name', 'all_but_by_header_name']: + c = params['input_options']['column_selector_options_1']['col1'] + else: + c = None + + df = pd.read_csv(infile1, sep='\t', header=header, parse_dates=True) + + X = read_columns(df, c=c, c_option=column_option).astype(float) + + if params['method'] == 'predict': + preds = estimator.predict(X) + else: + preds = estimator.predict_proba(X) + + # sparse input + elif input_type == 'sparse': + X = mmread(open(infile1, 'r')) + if params['method'] == 'predict': + preds = estimator.predict(X) + else: + preds = estimator.predict_proba(X) + + # fasta input + elif input_type == 'seq_fasta': + if not hasattr(estimator, 'data_batch_generator'): + raise ValueError( + "To do prediction on sequences in fasta input, " + "the estimator must be a `KerasGBatchClassifier`" + "equipped with data_batch_generator!") + pyfaidx = get_module('pyfaidx') + sequences = pyfaidx.Fasta(fasta_path) + n_seqs = len(sequences.keys()) + X = np.arange(n_seqs)[:, np.newaxis] + seq_length = estimator.data_batch_generator.seq_length + batch_size = getattr(estimator, 'batch_size', 32) + steps = (n_seqs + batch_size - 1) // batch_size + + seq_type = params['input_options']['seq_type'] + klass = try_get_attr( + 'galaxy_ml.preprocessors', seq_type) + + pred_data_generator = klass( + fasta_path, seq_length=seq_length) + + if params['method'] == 'predict': + preds = estimator.predict( + X, data_generator=pred_data_generator, steps=steps) + else: + preds = estimator.predict_proba( + X, data_generator=pred_data_generator, steps=steps) + + # vcf input + elif input_type == 'variant_effect': + klass = try_get_attr('galaxy_ml.preprocessors', + 'GenomicVariantBatchGenerator') + + options = params['input_options'] + options.pop('selected_input') + if options['blacklist_regions'] == 'none': + options['blacklist_regions'] = None + + pred_data_generator = klass( + ref_genome_path=ref_seq, vcf_path=vcf_path, **options) + + pred_data_generator.fit() + + variants = pred_data_generator.variants + # TODO : remove the following block after galaxy-ml v0.7.13 + blacklist_tabix = getattr(pred_data_generator.reference_genome_, + '_blacklist_tabix', None) + clean_variants = [] + if blacklist_tabix: + start_radius = pred_data_generator.start_radius_ + end_radius = pred_data_generator.end_radius_ + + for chrom, pos, name, ref, alt, strand in variants: + center = pos + len(ref) // 2 + start = center - start_radius + end = center + end_radius + + if isinstance(pred_data_generator.reference_genome_, Genome): + if "chr" not in chrom: + chrom = "chr" + chrom + if "MT" in chrom: + chrom = chrom[:-1] + try: + rows = blacklist_tabix.query(chrom, start, end) + found = 0 + for row in rows: + found = 1 + break + if found: + continue + except tabix.TabixError: + pass + + clean_variants.append((chrom, pos, name, ref, alt, strand)) + else: + clean_variants = variants + + setattr(pred_data_generator, 'variants', clean_variants) + + variants = np.array(clean_variants) + # predict 1600 sample at once then write to file + gen_flow = pred_data_generator.flow(batch_size=1600) + + file_writer = open(outfile_predict, 'w') + header_row = '\t'.join(['chrom', 'pos', 'name', 'ref', + 'alt', 'strand']) + file_writer.write(header_row) + header_done = False + + steps_done = 0 + + # TODO: multiple threading + try: + while steps_done < len(gen_flow): + index_array = next(gen_flow.index_generator) + batch_X = gen_flow._get_batches_of_transformed_samples( + index_array) + + if params['method'] == 'predict': + batch_preds = estimator.predict( + batch_X, + # The presence of `pred_data_generator` below is to + # override model carrying data_generator if there + # is any. + data_generator=pred_data_generator) + else: + batch_preds = estimator.predict_proba( + batch_X, + # The presence of `pred_data_generator` below is to + # override model carrying data_generator if there + # is any. + data_generator=pred_data_generator) + + if batch_preds.ndim == 1: + batch_preds = batch_preds[:, np.newaxis] + + batch_meta = variants[index_array] + batch_out = np.column_stack([batch_meta, batch_preds]) + + if not header_done: + heads = np.arange(batch_preds.shape[-1]).astype(str) + heads_str = '\t'.join(heads) + file_writer.write("\t%s\n" % heads_str) + header_done = True + + for row in batch_out: + row_str = '\t'.join(row) + file_writer.write("%s\n" % row_str) + + steps_done += 1 + + finally: + file_writer.close() + # TODO: make api `pred_data_generator.close()` + pred_data_generator.close() + return 0 + # end input + + # output + if len(preds.shape) == 1: + rval = pd.DataFrame(preds, columns=['Predicted']) + else: + rval = pd.DataFrame(preds) + + rval.to_csv(outfile_predict, sep='\t', header=True, index=False) + + +if __name__ == '__main__': + aparser = argparse.ArgumentParser() + aparser.add_argument("-i", "--inputs", dest="inputs", required=True) + aparser.add_argument("-e", "--infile_estimator", dest="infile_estimator") + aparser.add_argument("-w", "--infile_weights", dest="infile_weights") + aparser.add_argument("-X", "--infile1", dest="infile1") + aparser.add_argument("-O", "--outfile_predict", dest="outfile_predict") + aparser.add_argument("-f", "--fasta_path", dest="fasta_path") + aparser.add_argument("-r", "--ref_seq", dest="ref_seq") + aparser.add_argument("-v", "--vcf_path", dest="vcf_path") + args = aparser.parse_args() + + main(args.inputs, args.infile_estimator, args.outfile_predict, + infile_weights=args.infile_weights, infile1=args.infile1, + fasta_path=args.fasta_path, ref_seq=args.ref_seq, + vcf_path=args.vcf_path)