Difference between revisions of "Vt"
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=== Location === | === Location === | ||
− | + | The source files are housed in github. | |
git clone https://github.com/atks/vt.git | git clone https://github.com/atks/vt.git |
Revision as of 16:26, 21 October 2013
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.
-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.
Normalization
Normalize variants in a VCF file.
vt normalize -i mills.vcf -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