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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Salvato in:
Dettagli Bibliografici
Pubblicato in:Nucleic Acids Res
Autori principali: Zhang, Peng, Boisson, Bertrand, Stenson, Peter D, Cooper, David N, Casanova, Jean-Laurent, Abel, Laurent, Itan, Yuval
Natura: Artigo
Lingua:Inglês
Pubblicazione: Oxford University Press 2019
Soggetti:
Web Server Issue
Accesso online: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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