[ questing ] [ resolute ] [ stonking ]

Paquet source : snippy (4.6.0+dfsg-6) [universe]

Liens pour snippy

Please consider filing a bug or asking a question via Launchpad before contacting the maintainer directly.

It should generally not be necessary for users to contact the original maintainer.

Les paquets binaires suivants sont compilés à partir de ce paquet source :

snippy: rapid haploid variant calling and core genome alignment
snippy-examples: rapid haploid variant calling and core genome alignment (examples)

adep: debhelper-compat (= 13)

Paquet indisponible
adep: any2fasta

convert various sequence formats to FASTA
adep: bcftools

genomic variant calling and manipulation of VCF/BCF files
adep: bedtools

suite of utilities for comparing genomic features
adep: bwa

Burrows-Wheeler Aligner
adep: freebayes

Bayesian haplotype-based polymorphism discovery and genotyping
adep: libbio-perl-perl

BioPerl core perl modules
adep: libvcflib-tools

C++ library for parsing and manipulating VCF files (tools)
adep: minimap2

versatile pairwise aligner for genomic and spliced nucleotide sequences
adep: parallel

build and execute command lines from standard input in parallel
adep: samtools

processing sequence alignments in SAM, BAM and CRAM formats
adep: samclip

filter SAM file for soft and hard clipped alignments
adep: seqtk

Fast and lightweight tool for processing sequences in the FASTA or FASTQ format
adep: snp-sites

Binary code for the package snp-sites
adep: snpeff

genetic variant annotation and effect prediction toolbox - tool
adep: vt

toolset for short variant discovery in genetic sequence data

Dépôt Debian des paquets source (VCS: Git): https://salsa.debian.org/med-team/snippy.git
Dépôt Debian des paquets source (interface web): https://salsa.debian.org/med-team/snippy