bcftools

genomic variant calling and manipulation of VCF/BCF files

Install

All systems
curl cmd.cat/bcftools.sh
Debian Debian
apt-get install bcftools
Ubuntu
apt-get install bcftools
image/svg+xml Kali Linux
apt-get install bcftools
Fedora
dnf install bcftools
Windows (WSL2)
sudo apt-get update sudo apt-get install bcftools
OS X
brew install bcftools
Raspbian
apt-get install bcftools

bcftools

genomic variant calling and manipulation of VCF/BCF files

BCFtools is a set of utilities that manipulate variant calls in the Variant Call Format (VCF) and its binary counterpart BCF. All commands work transparently with both VCFs and BCFs, both uncompressed and BGZF-compressed.

samtools

processing sequence alignments in SAM and BAM formats

Samtools is a set of utilities that manipulate nucleotide sequence alignments in the binary BAM format. It imports from and exports to the ascii SAM (Sequence Alignment/Map) format, does sorting, merging and indexing, and allows one to retrieve reads in any regions swiftly. It is designed to work on a stream, and is able to open a BAM (not SAM) file on a remote FTP or HTTP server.