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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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Detalhes bibliográficos
Main Authors: Kindt, Alida S D, Navarro, Pau, Semple, Colin A M, Haley, Chris S
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3600003/
https://ncbi.nlm.nih.gov/pubmed/23418889
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-14-108
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