Bcftools
From BITS wiki
The canonical samtools follower
: GATK
suggests : VCFtools
bcftools (HTSlib)[1].
Note: A fast HTSlib C version of a filtering tool is now available (see bcftools filter and bcftools view).
Tool page: http://vcftools.sourceforge.net/htslib.html [2]
bcftools Program: bcftools (Tools for variant calling and manipulating VCFs and BCFs) Version: 0.2.0-rc6-37-g17d49cf (using htslib 0.2.0-rc6-32-g20df6b9) Usage: bcftools <command> <argument> Commands: -- Indexing: index index VCF/BCF files -- Core VCF/BCF tools: annotate annotate and edit VCF/BCF files call SNP/indel calling (former "view") filter filter VCF/BCF files using fixed thresholds gtcheck check sample concordance, detect sample swaps and contamination isec intersections of VCF/BCF files merge merge VCF/BCF files (one-sample files yield multi-sample file) norm left-align normalize indels query transform VCF/BCF into user-defined formats stats produce VCF/BCF stats (former vcfcheck) view VCF/BCF conversion, view, subset and filter VCF/BCF files -- Other/Experimental tools: roh identify runs of autozygosity (HMM) som filter using Self-Organized Maps (experimental) Notes: Most commands accept VCF, bgzipped VCF and BCF with filetype detected automatically even when streaming from a pipe. Indexed VCF and BCF will work in all situations. Un-indexed VCF and BCF and streams will work in most, but not all situations.
References:
- ↑
Heng Li
A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data.
Bioinformatics: 2011, 27(21);2987-93
[PubMed:21903627] ##WORLDCAT## [DOI] (I p) - ↑ http://vcftools.sourceforge.net/htslib.html