eVIP2: Expression-based variant impact phenotyping to predict the function of gene variants

While advancements in genome sequencing have identified millions of somatic mutations in cancer, their functional impact is poorly understood. We previously developed the expression-based variant impact phenotyping (eVIP) method to use gene expression data to characterize the function of gene varian...

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Detalles Bibliográficos
Autores principales: Thornton, Alexis M., Fang, Lishan, Lo, April, McSharry, Maria, Haan, David, O’Brien, Casey, Berger, Alice H., Giannakis, Marios, Brooks, Angela N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8281988/
https://www.ncbi.nlm.nih.gov/pubmed/34214079
http://dx.doi.org/10.1371/journal.pcbi.1009132

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8281988/
https://www.ncbi.nlm.nih.gov/pubmed/34214079
http://dx.doi.org/10.1371/journal.pcbi.1009132

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