[ Fonte: snpsift ]
Pacote: snpsift (5.2.e+dfsg-2)
Links para snpsift
Recursos de Debian:
- Relatórios de bug
- Informação de desenvolvedor(a)
- Debian Changelog
- Arquivo de copyright
- Rastreador de patch Debian
Baixe o pacote-fonte snpsift:
Mantenedores(as):
Fontes externas:
- Pagina principal [pcingola.github.io]
Pacotes similares:
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.
Outros pacotes relacionados a snpsift
|
|
|
|
-
- dep: default-jre
- ambiente de execução Java padrão ou compatível com Java
-
- dep: libsnpsift-java (= 5.2.e+dfsg-2)
- tool to annotate and manipulate genome variants - lib
-
- sug: snpeff
- genetic variant annotation and effect prediction toolbox - tool
Download de snpsift
| Arquitetura | Tamanho do pacote | Tamanho instalado | Arquivos |
|---|---|---|---|
| all | 4.6 kB | 15.0 kB | [lista de arquivos] |