Cargando…
Function-driven discovery of disease genes in zebrafish using an integrated genomics big data resource
Whole exome sequencing (WES) accelerates disease gene discovery using rare genetic variants, but further statistical and functional evidence is required to avoid false-discovery. To complement variant-driven disease gene discovery, here we present function-driven disease gene discovery in zebrafish...
Autores principales: | Shim, Hongseok, Kim, Ji Hyun, Kim, Chan Yeong, Hwang, Sohyun, Kim, Hyojin, Yang, Sunmo, Lee, Ji Eun, Lee, Insuk |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5175370/ https://www.ncbi.nlm.nih.gov/pubmed/27903883 http://dx.doi.org/10.1093/nar/gkw897 |
Ejemplares similares
-
COEXPEDIA: exploring biomedical hypotheses via co-expressions associated with medical subject headings (MeSH)
por: Yang, Sunmo, et al.
Publicado: (2017) -
FlyNet: a versatile network prioritization server for the Drosophila community
por: Shin, Junha, et al.
Publicado: (2015) -
RiceNet v2: an improved network prioritization server for rice genes
por: Lee, Tak, et al.
Publicado: (2015) -
Systematic identification of A-to-I RNA editing in zebrafish development and adult organs
por: Buchumenski, Ilana, et al.
Publicado: (2021) -
Primary transcriptome and translatome analysis determines transcriptional and translational regulatory elements encoded in the Streptomyces clavuligerus genome
por: Hwang, Soonkyu, et al.
Publicado: (2019)