Finding type 2 diabetes causal single nucleotide polymorphism combinations and functional modules from genome-wide association data

BACKGROUND: Due to the low statistical power of individual markers from a genome-wide association study (GWAS), detecting causal single nucleotide polymorphisms (SNPs) for complex diseases is a challenge. SNP combinations are suggested to compensate for the low statistical power of individual marker...

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Detalles Bibliográficos
Autores principales: Kang, Chiyong, Yu, Hyeji, Yi, Gwan-Su
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Proceedings
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3618247/
https://www.ncbi.nlm.nih.gov/pubmed/23566118
http://dx.doi.org/10.1186/1472-6947-13-S1-S3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3618247/
https://www.ncbi.nlm.nih.gov/pubmed/23566118
http://dx.doi.org/10.1186/1472-6947-13-S1-S3

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