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A method for scoring the cell type-specific impacts of noncoding variants in personal genomes

A person’s genome typically contains millions of variants which represent the differences between this personal genome and the reference human genome. The interpretation of these variants, i.e., the assessment of their potential impact on a person’s phenotype, is currently of great interest in human...

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Detalhes bibliográficos
Publicado no:Proc Natl Acad Sci U S A
Main Authors: Li, Wenran, Duren, Zhana, Jiang, Rui, Wong, Wing Hung
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 2020
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7474608/
https://ncbi.nlm.nih.gov/pubmed/32817564
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1922703117
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