Showing: vcfreset
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Change sample names in vcf
vcf sample name written 17 months ago by leeandroid90 • updated 2 days ago by Phoenix Mu0
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Beagle imputation results quality control
vcf imputation beagle written 3.7 years ago by eyb180 • updated 3 days ago by Kevin Blighe39k
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all non-ALT position in a VCF are non-variants?
vcf altered alt variant written 3 days ago by cocchi.e8910 • updated 3 days ago by Pierre Lindenbaum117k
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PLINK: Error: Invalid chromosome code 'chr11_KI0721v1_random'
vcf plink written 3 days ago by bsmith030465140 • updated 3 days ago by chrchang5234.8k
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Tool: CuteVariant : A GUI to filter VCF file
vcf annotation gui qt tool written 18 months ago by sacha1.7k • updated 5 days ago by richardcaseyhpc0
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What does CSQ means in a VCF file annotated by VEP ?
vcf csq written 6 days ago by badredda70 • updated 6 days ago by WouterDeCoster37k
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VCF modifications before plink analysis
vcf written 13 days ago by hrora0 • updated 13 days ago by Kevin Blighe39k
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SNP Calling Parameter Settings
vcf gatk snp written 7 weeks ago by mcclintock10 • updated 14 days ago by Biostar ♦♦ 20
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VCFParseError: ploidy > 2 not supported
vcf gatk ploidy written 11 weeks ago by always_learning960 • updated 15 days ago by tpoterba40
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Depth of coverage
genome vcf next-gen snp sequence written 18 days ago by jaafari.omid40
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How to extract filename and change text in the same file
vcf sequence script written 19 days ago by Inquisitive899550 • updated 18 days ago by Malcolm.Cook1.0k
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Calling CNV using bcftools
vcf bcftools cnv written 19 days ago by Raheleh50 • updated 19 days ago by Pierre Lindenbaum117k
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Creation of a VCF file from scratch with python
vcf python written 26 days ago by carolina.santiago.t0 • updated 26 days ago by finswimmer11k
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vcfR for Whole Genome Data
genome R vcf snp vcfr written 26 days ago by jaafari.omid40
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Merging vcf files ?
vcf written 2.7 years ago by Picasa390 • updated 27 days ago by jaybee10
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