Efficient identification of rare variants in large populations: deep re-sequencing the CRP locus in the CARDIA study

Effect sizes of many common single nucleotide polymorphisms identified in genome-wide association studies generally explain only a modest fraction of the total estimated heritability in a variety of traits. One hypothesis is that rare variants with larger effects might account for the missing herita...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Christina T. L., McDavid, Andrew N., Kahsai, Orsalem J., Zebari, Ahmad S., Carlson, Christopher S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Methods Online
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3627584/
https://www.ncbi.nlm.nih.gov/pubmed/23408856
http://dx.doi.org/10.1093/nar/gkt092

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3627584/
https://www.ncbi.nlm.nih.gov/pubmed/23408856
http://dx.doi.org/10.1093/nar/gkt092

Ejemplares similares