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MTR-Viewer: identifying regions within genes under purifying selection

Advances in genomic sequencing have enormous potential to revolutionize personalized medicine, however distinguishing disease-causing from benign variants remains a challenge. The increasing number of human genome and exome sequences available has revealed areas where unfavourable variation is remov...

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Detalhes bibliográficos
Publicado no:Nucleic Acids Res
Main Authors: Silk, Michael, Petrovski, Slavé, Ascher, David B
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2019
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6602522/
https://ncbi.nlm.nih.gov/pubmed/31170280
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkz457
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