def gatk_rnaseq_calling(data):
"""Use GATK to perform gVCF variant calling on RNA-seq data
"""
from bcbio.bam import callable
data = utils.deepish_copy(data)
tools_on = dd.get_tools_on(data)
if not tools_on:
tools_on = []
tools_on.append("gvcf")
data = dd.set_tools_on(data, tools_on)
data = dd.set_jointcaller(data, ["%s-joint" % v for v in dd.get_variantcaller(data)])
out_dir = utils.safe_makedir(os.path.join(dd.get_work_dir(data),
"variation", "rnaseq", "gatk-haplotype"))
data = _setup_variant_regions(data, out_dir)
out_file = os.path.join(out_dir, "%s-gatk-haplotype.vcf.gz" % dd.get_sample_name(data))
if not utils.file_exists(out_file):
region_files = []
regions = []
for cur_region in callable.get_split_regions(dd.get_variant_regions(data), data):
str_region = "_".join([str(x) for x in cur_region])
region_file = os.path.join(utils.safe_makedir(os.path.join(dd.get_work_dir(data),
"variation", "rnaseq", "gatk-haplotype",
"regions")),
"%s-%s-gatk-haplotype.vcf.gz" % (dd.get_sample_name(data), str_region))
region_file = gatk.haplotype_caller([dd.get_split_bam(data)], [data], dd.get_ref_file(data), {},
region=cur_region, out_file=region_file)
region_files.append(region_file)
regions.append(cur_region)
out_file = vcfutils.concat_variant_files(region_files, out_file, regions,
dd.get_ref_file(data), data["config"])
return dd.set_vrn_file(data, out_file)
def gatk_rnaseq_calling(data):
"""Use GATK to perform gVCF variant calling on RNA-seq data
"""
from bcbio.bam import callable
data = utils.deepish_copy(data)
tools_on = dd.get_tools_on(data)
if not tools_on:
tools_on = []
tools_on.append("gvcf")
data = dd.set_tools_on(data, tools_on)
data = dd.set_jointcaller(data, ["%s-joint" % v for v in dd.get_variantcaller(data)])
out_dir = utils.safe_makedir(os.path.join(dd.get_work_dir(data),
"variation", "rnaseq", "gatk-haplotype"))
data = _setup_variant_regions(data, out_dir)
out_file = os.path.join(out_dir, "%s-gatk-haplotype.vcf.gz" % dd.get_sample_name(data))
if not utils.file_exists(out_file):
region_files = []
regions = []
for cur_region in callable.get_split_regions(dd.get_variant_regions(data), data):
str_region = "_".join([str(x) for x in cur_region])
region_file = os.path.join(utils.safe_makedir(os.path.join(dd.get_work_dir(data),
"variation", "rnaseq", "gatk-haplotype",
"regions")),
"%s-%s-gatk-haplotype.vcf.gz" % (dd.get_sample_name(data), str_region))
region_file = gatk.haplotype_caller([dd.get_split_bam(data)], [data], dd.get_ref_file(data), {},
region=cur_region, out_file=region_file)
region_files.append(region_file)
regions.append(cur_region)
out_file = vcfutils.concat_variant_files(region_files, out_file, regions,
dd.get_ref_file(data), data["config"])
return dd.set_vrn_file(data, out_file)
def gatk_rnaseq_calling(data):
"""Use GATK to perform gVCF variant calling on RNA-seq data
"""
data = utils.deepish_copy(data)
tools_on = dd.get_tools_on(data)
if not tools_on:
tools_on = []
tools_on.append("gvcf")
data = dd.set_tools_on(data, tools_on)
data = dd.set_jointcaller(data, ["%s-joint" % v for v in dd.get_variantcaller(data)])
out_file = os.path.join(utils.safe_makedir(os.path.join("variation", "rnaseq", "gatk-haplotype")),
"%s-gatk-haplotype.vcf.gz" % dd.get_sample_name(data))
out_file = gatk.haplotype_caller([dd.get_split_bam(data)], [data], dd.get_ref_file(data), {},
out_file=out_file)
return dd.set_vrn_file(data, out_file)
