Vt

Introduction

vt is a variant tool set that discovers short variants from Next Generation Sequencing data. The features are being rolled out to github as major rewriting is being undertaken.

Location

The source files are housed in github.

 git clone https://github.com/atks/vt.git

Common options

   -i   multiple intervals in <seq>:<start>-<end> format delimited by commas.

   -I   multiple intervals in <seq>:<start>-<end> format listed in a text file line by line.

   -o  defines the out file which and has the STDOUT set as the default.
         You may modify the STDOUT to output the binary version of the format.

Programs

Normalization

Normalize variants in a VCF file.

Normalized variants may have their positions changed; in such cases, the normalized variants are reordered and output in an ordered fashion. The local reordering takes place over a window of 10000 base pairs.

  vt normalize <input.vcf> -r <sequence.fa> -o <output.vcf>

  #
  vt normalize mills.vcf -r seq.fa -o - 
  vt normalize mills.vcf -r seq.fa -o mills.normalized.vcf
  vt normalize mills.vcf -r seq.fa -o mills.normalized.vcf

Merge duplicate variants

Merges duplicate variants by position with the option of considering alleles. (This just discards the duplicate variant that appears later in the VCF file)

  Options:
  -i,  --input-vcf <string>  : Input VCF file
  -o,  --output-vcf <string> : Output VCF file [-]
  -p,  --merge-by-position   : Merge by position [false]

  Example:
  e.g. vt merge_duplicate_variants -i 8904indels.dups.genotypes.vcf -o out.vcf
  e.g. vt merge_duplicate_variants -p -i 8904indels.dups.genotypes.vcf -o out.vcf

Maintained by

This page is maintained by Adrian