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Copy file name to clipboardExpand all lines: shared/utils.py
+2-2Lines changed: 2 additions & 2 deletions
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@@ -281,7 +281,7 @@ def get_header(reference_file_path=None, cmd_fn=None, sample_name="SAMPLE", vers
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##FORMAT=<ID=AD,Number=R,Type=Integer,Description="Allelic depths for the ref and alt alleles in the order listed">
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##FORMAT=<ID=MIN_DP,Number=1,Type=Integer,Description="Minimum DP observed within the GVCF block">
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##FORMAT=<ID=PL,Number=G,Type=Integer,Description="Normalized, Phred-scaled likelihoods for genotypes as defined in the VCF specification">
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##FORMAT=<ID=AF,Number=G,Type=Float,Description="Observed allele frequency in reads, for each ALT allele, in the same order as listed, or the REF allele for a RefCall">\n""".format(
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##FORMAT=<ID=AF,Number=A,Type=Float,Description="Observed allele frequency in reads, for each ALT allele, in the same order as listed, or the REF allele for a RefCall">\n""".format(
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version))
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else:
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header=dedent("""\
@@ -298,7 +298,7 @@ def get_header(reference_file_path=None, cmd_fn=None, sample_name="SAMPLE", vers
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##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Approximate read depth (reads 1. with MQ below 5 or an user-specified threshold, or 2. selected by 'samtools view -F 2316', are filtered)">
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##FORMAT=<ID=AD,Number=R,Type=Integer,Description="Allelic depths for the ref and alt alleles in the order listed">
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##FORMAT=<ID=PL,Number=G,Type=Integer,Description="Normalized, Phred-scaled likelihoods for genotypes as defined in the VCF specification">
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##FORMAT=<ID=AF,Number=G,Type=Float,Description="Observed allele frequency in reads, for each ALT allele, in the same order as listed, or the REF allele for a RefCall">\n""".format(
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+
##FORMAT=<ID=AF,Number=A,Type=Float,Description="Observed allele frequency in reads, for each ALT allele, in the same order as listed, or the REF allele for a RefCall">\n""".format(
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