packages
[ 原始碼： snippy ]
套件： snippy (4.6.0+dfsg-5) [universe]
snippy 的相關超連結
Ubuntu 的資源：
下載原始碼套件 snippy：
維護者：
Please consider filing a bug or asking a question via Launchpad before contacting the maintainer directly.
Original Maintainers (usually from Debian):
- Debian Med Packaging Team (郵件存檔)
- Andreas Tille
It should generally not be necessary for users to contact the original maintainer.
外部的資源：
- 主頁 [github.com]
相似套件：
rapid haploid variant calling and core genome alignment
其他與 snippy 有關的套件
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- dep: any2fasta
- convert various sequence formats to FASTA
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- dep: bcftools
- genomic variant calling and manipulation of VCF/BCF files
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- dep: bedtools
- suite of utilities for comparing genomic features
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- dep: bwa
- Burrows-Wheeler Aligner
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- dep: freebayes (>= 1.3.6-2)
- Bayesian haplotype-based polymorphism discovery and genotyping
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- dep: libbio-perl-perl
- BioPerl core perl modules
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- dep: libvcflib-tools
- C++ library for parsing and manipulating VCF files (tools)
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- dep: minimap2
- versatile pairwise aligner for genomic and spliced nucleotide sequences
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- dep: parallel
- build and execute command lines from standard input in parallel
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- dep: perl
- Larry Wall's Practical Extraction and Report Language
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- dep: samclip
- filter SAM file for soft and hard clipped alignments
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- dep: samtools
- processing sequence alignments in SAM, BAM and CRAM formats
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- dep: seqtk
- Fast and lightweight tool for processing sequences in the FASTA or FASTQ format
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- dep: snp-sites
- Binary code for the package snp-sites
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- dep: snpeff
- genetic variant annotation and effect prediction toolbox - tool
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- dep: vt
- toolset for short variant discovery in genetic sequence data