b=load_list(
args.individual_list_exclude))
indiv_list = sorted(indiv_list)
df_pheno = rearrange_rows(df_pheno, indiv_list)
df_pheno = transpose_df(df_pheno, col='indiv')
if df_covar is not None:
df_covar = rearrange_rows(df_covar, indiv_list)
df_covar.set_index('indiv', inplace=True)
logging.info('There are {} individauls being included.'.format(
df_pheno.shape[1]))
logging.info('Loading genotypes.')
pr = genotypeio.PlinkReader(args.geno_bed_prefix,
select_samples=df_pheno.columns,
dtype=np.int8)
variant_df = pr.bim.set_index('snp')[['chrom', 'pos']]
genotype_df = pd.DataFrame(pr.load_genotypes(),
index=pr.bim['snp'],
columns=pr.fam['iid'])
if args.map_trans_params is None:
map_args = {}
else:
map_args = read_yaml(args.map_trans_params)
logging.info('Arguments used for tensorqtl: ' + dict_to_str(map_args))
logging.info('Start mapping.')
pairs_df = trans.map_trans(genotype_df,
df_pheno,
def main():
parser = argparse.ArgumentParser(
description='tensorQTL: GPU-based QTL mapper')
parser.add_argument('genotype_path', help='Genotypes in PLINK format')
parser.add_argument('phenotype_bed', help='Phenotypes in BED format')
parser.add_argument('prefix', help='Prefix for output file names')
parser.add_argument(
'--mode',
default='cis',
choices=['cis', 'cis_nominal', 'cis_independent', 'trans'],
help='Mapping mode. Default: cis')
parser.add_argument(
'--covariates',
default=None,
help='Covariates file, tab-delimited, covariates x samples')
parser.add_argument('--permutations',
type=int,
default=10000,
help='Number of permutations. Default: 10000')
parser.add_argument('--interaction',
default=None,
type=str,
help='Interaction term')
parser.add_argument(
'--cis_output',
default=None,
type=str,
help=
"Output from 'cis' mode with q-values. Required for independent cis-QTL mapping."
)
parser.add_argument(
'--phenotype_groups',
default=None,
type=str,
help=
'Phenotype groups. Header-less TSV with two columns: phenotype_id, group_id'
)
parser.add_argument('--window',
default=1000000,
type=np.int32,
help='Cis-window size, in bases. Default: 1000000.')
parser.add_argument(
'--pval_threshold',
default=None,
type=np.float64,
help=
'Output only significant phenotype-variant pairs with a p-value below threshold. Default: 1e-5 for trans-QTL'
)
parser.add_argument(
'--maf_threshold',
default=None,
type=np.float64,
help=
'Include only genotypes with minor allele frequency >= maf_threshold. Default: 0'
)
parser.add_argument(
'--maf_threshold_interaction',
default=0.05,
type=np.float64,
help=
'MAF threshold for interactions, applied to lower and upper half of samples'
)
parser.add_argument('--return_dense',
action='store_true',
help='Return dense output for trans-QTL.')
parser.add_argument('--return_r2',
action='store_true',
help='Return r2 (only for sparse trans-QTL output)')
parser.add_argument(
'--best_only',
action='store_true',
help=
'Only write lead association for each phenotype (interaction mode only)'
)
parser.add_argument(
'--output_text',
action='store_true',
help=
'Write output in txt.gz format instead of parquet (trans-QTL mode only)'
)
parser.add_argument(
'--batch_size',
type=int,
default=20000,
help='Batch size. Reduce this if encountering OOM errors.')
parser.add_argument(
'--load_split',
action='store_true',
help='Load genotypes into memory separately for each chromosome.')
parser.add_argument('--fdr',
default=0.05,
type=np.float64,
help='FDR for cis-QTLs')
parser.add_argument('--qvalue_lambda',
default=None,
type=np.float64,
help='lambda parameter for pi0est in qvalue.')
parser.add_argument('--seed',
default=None,
type=int,
help='Seed for permutations.')
parser.add_argument('-o',
'--output_dir',
default='.',
help='Output directory')
args = parser.parse_args()
# check inputs
if args.mode == 'cis_independent' and (
args.cis_output is None or not os.path.exists(args.cis_output)):
raise ValueError("Output from 'cis' mode must be provided.")
logger = SimpleLogger(
os.path.join(args.output_dir,
args.prefix + '.tensorQTL.{}.log'.format(args.mode)))
logger.write('[{}] Running TensorQTL: {}-QTL mapping'.format(
datetime.now().strftime("%b %d %H:%M:%S"),
args.mode.split('_')[0]))
if torch.cuda.is_available():
logger.write(' * using GPU ({})'.format(
torch.cuda.get_device_name(torch.cuda.current_device())))
else:
logger.write(' * WARNING: using CPU!')
device = torch.device("cuda" if torch.cuda.is_available() else "cpu")
if args.seed is not None:
logger.write(' * using seed {}'.format(args.seed))
# load inputs
logger.write(' * reading phenotypes ({})'.format(args.phenotype_bed))
phenotype_df, phenotype_pos_df = read_phenotype_bed(args.phenotype_bed)
tss_dict = phenotype_pos_df.T.to_dict()
if args.covariates is not None:
logger.write(' * reading covariates ({})'.format(args.covariates))
covariates_df = pd.read_csv(args.covariates, sep='\t', index_col=0).T
assert np.all(phenotype_df.columns == covariates_df.index)
if args.interaction is not None:
logger.write(' * reading interaction term ({})'.format(
args.interaction))
interaction_s = pd.read_csv(args.interaction,
sep='\t',
index_col=0,
header=None,
squeeze=True)
assert covariates_df.index.isin(interaction_s.index).all()
interaction_s = interaction_s.loc[covariates_df.index].astype(
np.float32)
else:
interaction_s = None
if args.maf_threshold is None:
if args.mode == 'trans':
maf_threshold = 0.05
else:
maf_threshold = 0
else:
maf_threshold = args.maf_threshold
if args.phenotype_groups is not None:
group_s = pd.read_csv(args.phenotype_groups,
sep='\t',
index_col=0,
header=None,
squeeze=True)
# verify sort order
group_dict = group_s.to_dict()
previous_group = ''
parsed_groups = 0
for i in phenotype_df.index:
if group_dict[i] != previous_group:
parsed_groups += 1
previous_group = group_dict[i]
if not parsed_groups == len(group_s.unique()):
raise ValueError(
'Groups defined in input do not match phenotype file (check sort order).'
)
else:
group_s = None
# load genotypes
pr = genotypeio.PlinkReader(args.genotype_path,
select_samples=phenotype_df.columns,
dtype=np.int8)
variant_df = pr.bim.set_index('snp')[['chrom', 'pos']]
if args.mode != 'cis_nominal' or not args.load_split: # load all genotypes into memory
genotype_df = pd.DataFrame(pr.load_genotypes(),
index=pr.bim['snp'],
columns=pr.fam['iid'])
if args.mode.startswith('cis'):
if args.mode == 'cis':
res_df = cis.map_cis(genotype_df,
variant_df,
phenotype_df,
phenotype_pos_df,
covariates_df,
group_s=group_s,
nperm=args.permutations,
window=args.window,
logger=logger,
seed=args.seed,
verbose=True)
logger.write(' * writing output')
out_file = os.path.join(args.output_dir,
args.prefix + '.cis_qtl.txt.gz')
res_df.to_csv(
out_file, sep='\t',
float_format='%.6g') # to output table without qvalue
if has_rpy2:
calculate_qvalues(res_df,
fdr=args.fdr,
qvalue_lambda=args.qvalue_lambda,
logger=logger)
# out_file = os.path.join(args.output_dir, args.prefix+'.cis_qtl.txt.gz')
res_df.to_csv(out_file, sep='\t', float_format='%.6g')
elif args.mode == 'cis_nominal':
if not args.load_split:
cis.map_nominal(
genotype_df,
variant_df,
phenotype_df,
phenotype_pos_df,
args.prefix,
covariates_df=covariates_df,
interaction_s=interaction_s,
maf_threshold_interaction=args.maf_threshold_interaction,
group_s=None,
window=args.window,
run_eigenmt=True,
output_dir=args.output_dir,
write_top=True,
write_stats=not args.best_only,
logger=logger,
verbose=True)
else: # load genotypes for each chromosome separately
top_df = []
for chrom in pr.chrs:
g, pos_s = pr.get_region(chrom)
genotype_df = pd.DataFrame(
g, index=pos_s.index,
columns=pr.fam['iid'])[phenotype_df.columns]
variant_df = pr.bim.set_index('snp')[['chrom', 'pos']]
chr_df = cis.map_nominal(
genotype_df,
variant_df[variant_df['chrom'] == chrom],
phenotype_df[phenotype_pos_df['chr'] == chrom],
phenotype_pos_df[phenotype_pos_df['chr'] == chrom],
args.prefix,
covariates_df=covariates_df,
interaction_s=interaction_s,
maf_threshold_interaction=args.
maf_threshold_interaction,
group_s=None,
window=args.window,
run_eigenmt=True,
output_dir=args.output_dir,
write_top=True,
write_stats=not args.best_only,
logger=logger,
verbose=True)
top_df.append(chr_df)
if interaction_s is not None:
top_df = pd.concat(top_df)
top_df.to_csv(os.path.join(
args.output_dir,
'{}.cis_qtl_top_assoc.txt.gz'.format(args.prefix)),
sep='\t',
float_format='%.6g')
elif args.mode == 'cis_independent':
summary_df = pd.read_csv(args.cis_output, sep='\t', index_col=0)
summary_df.rename(columns={
'minor_allele_samples': 'ma_samples',
'minor_allele_count': 'ma_count'
},
inplace=True)
res_df = cis.map_independent(genotype_df,
variant_df,
summary_df,
phenotype_df,
phenotype_pos_df,
covariates_df,
group_s=group_s,
fdr=args.fdr,
nperm=args.permutations,
window=args.window,
logger=logger,
seed=args.seed,
verbose=True)
logger.write(' * writing output')
out_file = os.path.join(
args.output_dir, args.prefix + '.cis_independent_qtl.txt.gz')
res_df.to_csv(out_file, sep='\t', index=False, float_format='%.6g')
elif args.mode == 'trans':
return_sparse = not args.return_dense
pval_threshold = args.pval_threshold
if pval_threshold is None and return_sparse:
pval_threshold = 1e-5
logger.write(
' * p-value threshold: {:.2g}'.format(pval_threshold))
pairs_df = trans.map_trans(genotype_df,
phenotype_df,
covariates_df,
interaction_s=interaction_s,
return_sparse=return_sparse,
pval_threshold=pval_threshold,
maf_threshold=maf_threshold,
batch_size=args.batch_size,
return_r2=args.return_r2,
logger=logger)
logger.write(' * filtering out cis-QTLs (within +/-5Mb)')
pairs_df = trans.filter_cis(pairs_df,
tss_dict,
variant_df,
window=5000000)
logger.write(' * writing output')
if not args.output_text:
pairs_df.to_parquet(
os.path.join(args.output_dir,
args.prefix + '.trans_qtl_pairs.parquet'))
else:
out_file = os.path.join(args.output_dir,
args.prefix + '.trans_qtl_pairs.txt.gz')
pairs_df.to_csv(out_file,
sep='\t',
index=False,
float_format='%.6g')
logger.write('[{}] Finished mapping'.format(
datetime.now().strftime("%b %d %H:%M:%S")))
# load phenotypes and covariates
logger.write(' * reading phenotypes ({})'.format(args.input))
phenotype_df, phenotype_pos_df = read_phenotype_bed(args.input)
# covariates_df = pd.read_csv(covariates_file, sep='\t', index_col=0).T
if args.cov is not None:
logger.write(' * reading covariates ({})'.format(args.cov))
covariates_df = pd.read_csv(args.cov, sep='\t', index_col=0).T
assert np.all(phenotype_df.columns == covariates_df.index)
if args.cond_exp is not None:
express_df, express_pos_df = read_phenotype_bed(args.cond_exp)
assert np.all(phenotype_df.columns == express_df.columns)
pr = genotypeio.PlinkReader(plink_prefix_path, exclude_chrs=excluded_chr_list)
genotype_df = pr.load_genotypes()
variant_df = pr.bim.set_index('snp')[['chrom', 'pos']]
if mode == 'cis':
# cis-QTL: empirical p-values for phenotypes
if args.cond_exp: # gene expression as condition
if excluded_chr_list:
cis_df = cis_exon.map_cis(
genotype_df,
variant_df,
phenotype_df.loc[phenotype_pos_df['chr'] == chr_id],
phenotype_pos_df.loc[phenotype_pos_df['chr'] == chr_id],
covariates_df=covariates_df,
seed=args.seed,
express_df=express_df,
