Using DIVAN to assess disease/trait-associated single nucleotide variants in genome-wide scale

OBJECTIVE: The majority of sequence variants identified by Genome-wide association studies (GWASs) fall outside of the protein-coding regions. Unlike coding variants, it is challenging to connect these noncoding variants to the pathophysiology of complex diseases/traits due to the lack of functional...

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Detalles Bibliográficos
Autores principales: Chen, Li, Qin, Zhaohui S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research Note
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663107/
https://www.ncbi.nlm.nih.gov/pubmed/29084591
http://dx.doi.org/10.1186/s13104-017-2851-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663107/
https://www.ncbi.nlm.nih.gov/pubmed/29084591
http://dx.doi.org/10.1186/s13104-017-2851-y

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