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Decoding the effects of synonymous variants

Synonymous single nucleotide variants (sSNVs) are common in the human genome but are often overlooked. However, sSNVs can have significant biological impact and may lead to disease. Existing computational methods for evaluating the effect of sSNVs suffer from the lack of gold-standard training/evalu...

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Detalles Bibliográficos
Autores principales: Zeng, Zishuo, Aptekmann, Ariel A, Bromberg, Yana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8682775/
https://www.ncbi.nlm.nih.gov/pubmed/34850938
http://dx.doi.org/10.1093/nar/gkab1159