The genomic signature of trait-associated variants

BACKGROUND: Genome-wide association studies have identified thousands of SNP variants associated with hundreds of phenotypes. For most associations the causal variants and the molecular mechanisms underlying pathogenesis remain unknown. Exploration of the underlying functional annotations of trait-a...

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Detalles Bibliográficos
Autores principales: Kindt, Alida S D, Navarro, Pau, Semple, Colin A M, Haley, Chris S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3600003/
https://www.ncbi.nlm.nih.gov/pubmed/23418889
http://dx.doi.org/10.1186/1471-2164-14-108

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3600003/
https://www.ncbi.nlm.nih.gov/pubmed/23418889
http://dx.doi.org/10.1186/1471-2164-14-108

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