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Increasing mapping precision of genome-wide association studies: to genotype and impute, sequence, or both?

Fine-mapping to identify causal variants in genome-wide association studies remains challenging. A recent study provides guidance for future research.

Detalles Bibliográficos
Autores principales:	Wang, Zhaoming, Chatterjee, Nilanjan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2017
Materias:	Research Highlight
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5474869/ https://www.ncbi.nlm.nih.gov/pubmed/28629446 http://dx.doi.org/10.1186/s13059-017-1255-6

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