bcftools singularity container
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Updated
Nov 8, 2018 - Shell
bcftools singularity container
convert genotype array output into annotated IBD segments
Scripts used on a cluster that demonstrate vcf file manipulation and preparation.
Analysis pipeline for processing paired-end Illumina reads obtained after ancient mtDNA target enrichment capture.
A Nextflow variant normalization pipeline based on vt and bcftools
Merge in parallel, speeding up bcftools merge
Here we are going to discuss variant calling on human datasets using GATK Best practices pipeline
1,674 S.cerevisiae genomics data
A collection of scripts for filtering annotated variant call format files
This script filters false positive alleles from poolseq VCF file created with bcftools.
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