Showing: vcfreset
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Consensus VCF file from several variant callers
vcf variant calling freebayes gatk written 18 hours ago by ajuiwl30 • updated 18 hours ago by Pierre Lindenbaum115k
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Common SNPs among all populations
vcf snp written 1 day ago by mostafarafiepour60 • updated 22 hours ago by zx87546.1k
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Genotype Extraction Format from VCF file
vcf terminal sequencing written 4 days ago by MK20000 • updated 4 days ago by WouterDeCoster35k
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python Mac run vcf ModuleNotFoundError: No module named 'model'
vcf pyvcf written 6 days ago by haoz0210 • updated 6 days ago by Vijay Lakhujani3.4k
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VCFtools calculate SNP density
vcf bioinformatics snp density vcftools snp written 7 days ago by christinachavez0 • updated 7 days ago by finswimmer8.0k
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Annotate VCF on specific transcripts (ANN field)
vcf snpsift snpeff written 8 days ago by FGV100 • updated 8 days ago by Pierre Lindenbaum115k
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Download Tumor VCF files
vcf varients written 15 days ago by sara_wasl0 • updated 15 days ago by jared.andrews071.7k
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Error in bcftools view -bvcg command
vcf samtools bcftools snp written 15 days ago by hafiz.talhamalik30 • updated 14 days ago by WouterDeCoster35k
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Count variants between two samples within a multi-sample VCF
vcf vcftools written 17 days ago by rc1695550 • updated 17 days ago by chrchang5234.3k
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how to identify disease variants from bam file ?
atacseq vcf bam disease variants written 17 days ago by masaver0 • updated 17 days ago by Garan540
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split vcf by individual
vcf vcf-subset vcftools snp written 18 days ago by sonia.olaechea50 • updated 17 days ago by Paul1.2k
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sql to vcf
vcf database sql written 21 days ago by fmail12210
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Filtering of VCF, INFO DP or FORMAT DP
vcf next-gen dp snp sequencing written 21 days ago by waqasnayab170 • updated 21 days ago by Pierre Lindenbaum115k
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ID and Variants in VCF
vcf genome variants written 22 days ago by sanna.aizad10 • updated 22 days ago by Erin_Ensembl220
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Bcftools merge sample order
vcf dna bcftools multisample htslib written 23 days ago by Chadi Saad50 • updated 22 days ago by paolo002100
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Get genotype GT from multi-sample VCF (per chromosome)
vcf bcftools genotype subset written 23 days ago by zx87546.1k • updated 23 days ago by Pierre Lindenbaum115k
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Difference between . and ./. for missing genotype in VCF
vcf written 23 days ago by William4.3k • updated 23 days ago by Santosh Anand4.3k
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Create a Venn diagram for 5 VCF Files (each VCF file is a population)
vcf venn snp written 24 days ago by mostafarafiepour60 • updated 24 days ago by zx87546.1k
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Relatedness software for 20,000 exome sequencing datasets.
vcf relatedness vcf.gz written 24 days ago by rjobmc0 • updated 24 days ago by Shicheng Guo7.3k
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