Downloading: s3://natera-rnd-pltf-dev-nextflow-scratch-01/work/d7/365f648ddc8f5bfbc5da115e39fbd6/.command.sh
  Downloading: s3://natera-rnd-pltf-dev-nextflow-scratch-01/work/d7/365f648ddc8f5bfbc5da115e39fbd6/.command.run
  Downloading: s3://natera-rnd-pltf-dev-nextflow-scratch-01/work/59/a2b97bf9f52ed19f9b248fa5c00ddc/HCC1395_tumor_vs_HCC1395_BL.strelka.somatic_snvs.vcf.gz
  Downloading: s3://natera-platform-sandbox/pipeline-resources/ngi-igenomes/igenomes/Homo_sapiens/GATK/GRCh38/Annotation/intervals/regression_intervals/xgen-exome-hyb-panel-v2-targets-hg38_AND_altera_v3_targets_postQC_hg38_chr21.bed
==> STAGING COMPLETE (4 inputs)


VCFtools - 0.1.16
(C) Adam Auton and Anthony Marcketta 2009

Parameters as interpreted:
	--gzvcf HCC1395_tumor_vs_HCC1395_BL.strelka.somatic_snvs.vcf.gz
	--FILTER-summary
	--out HCC1395_tumor_vs_HCC1395_BL.strelka.somatic_snvs

Using zlib version: 1.2.11
Warning: Expected at least 2 parts in FORMAT entry: ID=AU,Number=2,Type=Integer,Description="Number of 'A' alleles used in tiers 1,2">
Warning: Expected at least 2 parts in FORMAT entry: ID=CU,Number=2,Type=Integer,Description="Number of 'C' alleles used in tiers 1,2">
Warning: Expected at least 2 parts in FORMAT entry: ID=GU,Number=2,Type=Integer,Description="Number of 'G' alleles used in tiers 1,2">
Warning: Expected at least 2 parts in FORMAT entry: ID=TU,Number=2,Type=Integer,Description="Number of 'T' alleles used in tiers 1,2">
Warning: Expected at least 2 parts in INFO entry: ID=NT,Number=1,Type=String,Description="Genotype of the normal in all data tiers, as used to classify somatic variants. One of {ref,het,hom,conflict}.">
Warning: Expected at least 2 parts in INFO entry: ID=NT,Number=1,Type=String,Description="Genotype of the normal in all data tiers, as used to classify somatic variants. One of {ref,het,hom,conflict}.">
Warning: Expected at least 2 parts in INFO entry: ID=NT,Number=1,Type=String,Description="Genotype of the normal in all data tiers, as used to classify somatic variants. One of {ref,het,hom,conflict}.">
Warning: Expected at least 2 parts in INFO entry: ID=NT,Number=1,Type=String,Description="Genotype of the normal in all data tiers, as used to classify somatic variants. One of {ref,het,hom,conflict}.">
Warning: Expected at least 2 parts in INFO entry: ID=QSS,Number=1,Type=Integer,Description="Quality score for any somatic snv, ie. for the ALT allele to be present at a significantly different frequency in the tumor and normal">
After filtering, kept 2 out of 2 Individuals
Outputting Filter Summary (for bi-allelic loci only)
After filtering, kept 300 out of a possible 300 Sites
Run Time = 0.00 seconds
ls: *.vcf: No such file or directory
ls: *.bcf: No such file or directory
ls: *.frq: No such file or directory
ls: *.frq.count: No such file or directory
ls: *.idepth: No such file or directory
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ls: *.geno.ld: No such file or directory
ls: *.geno.chisq: No such file or directory
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ls: *.interchrom.hap.ld: No such file or directory
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ls: *.TsTv: No such file or directory
ls: *.TsTv.summary: No such file or directory
ls: *.TsTv.count: No such file or directory
ls: *.TsTv.qual: No such file or directory
ls: *.sites.pi: No such file or directory
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ls: *.het: No such file or directory
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ls: *.impute.hap: No such file or directory
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ls: *.impute.hap.indv: No such file or directory
ls: *.ldhat.sites: No such file or directory
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ls: *.BEAGLE.GL: No such file or directory
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ls: *.ped: No such file or directory
ls: *.map: No such file or directory
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ls: *.diff.sites_in_files: No such file or directory
ls: *.diff.indv_in_files: No such file or directory
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ls: *.diff.discordance.matrix: No such file or directory
ls: *.diff.switch: No such file or directory