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Characterizing linkage disequilibrium and evaluating imputation power of human genomic insertion-deletion polymorphisms

BACKGROUND: Indels are an important cause of human variation and central to the study of human disease. The 1000 Genomes Project Low-Coverage Pilot identified over 1.3 million indels shorter than 50 bp, of which over 890 were identified as potentially disruptive variants. Yet, despite their ubiquity...

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Detalles Bibliográficos
Autores principales: Lu, James T, Wang, Yi, Gibbs, Richard A, Yu, Fuli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3334570/
https://www.ncbi.nlm.nih.gov/pubmed/22377349
http://dx.doi.org/10.1186/gb-2012-13-2-r15