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SeqTailor: a user-friendly webserver for the extraction of DNA or protein sequences from next-generation sequencing data
Human whole-genome-sequencing reveals about 4 000 000 genomic variants per individual. These data are mostly stored as VCF-format files. Although many variant analysis methods accept VCF as input, many other tools require DNA or protein sequences, particularly for splicing prediction, sequence align...
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| Publicado no: | Nucleic Acids Res |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6602489/ https://ncbi.nlm.nih.gov/pubmed/31045209 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkz326 |
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