[ Pakiet źródłowy: snpsift ]
Pakiet: snpsift (5.1+dfsg2-2)
Odnośniki dla snpsift
Zasoby systemu Debian:
- Raporty o błędach
- Developer Information
- Dziennik zmian w systemie Debian
- Informacje nt. praw autorskich
- Śledzenie łatek systemu Debian
Pobieranie pakietu źródłowego snpsift:
Opiekunowie:
Zasoby zewnętrzne:
- Strona internetowa [pcingola.github.io]
Podobne pakiety:
tool to annotate and manipulate genome variants - tool
SnpSift is a toolbox that allows one to filter and manipulate annotated files. Once the genomic variants have been annotated, one needs to filter them out in order to find the "interesting / relevant variants". Given the large data files, this is not a trivial task (e.g. one cannot load all the variants into XLS spreadsheet). SnpSift helps to perform this VCF file manipulation and filtering required at this stage in data processing pipelines.
This package contains the command line tool.
Inne pakiety związane z snpsift
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- dep: default-jre
- Standard Java or Java compatible Runtime
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- dep: libsnpsift-java (= 5.1+dfsg2-2)
- tool to annotate and manipulate genome variants - lib
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- sug: snpeff
- genetic variant annotation and effect prediction toolbox - tool
Pobieranie snpsift
| Architektura | Rozmiar pakietu | Rozmiar po instalacji | Pliki |
|---|---|---|---|
| all | 4,3 KiB | 15,0 KiB | [lista plików] |