MARV: a tool for genome-wide multi-phenotype analysis of rare variants

BACKGROUND: Genome-wide association studies have enabled identification of thousands of loci for hundreds of traits. Yet, for most human traits a substantial part of the estimated heritability is unexplained. This and recent advances in technology to produce high-dimensional data cost-effectively ha...

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Detalles Bibliográficos
Autores principales: Kaakinen, Marika, Mägi, Reedik, Fischer, Krista, Heikkinen, Jani, Järvelin, Marjo-Riitta, Morris, Andrew P., Prokopenko, Inga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5311849/
https://www.ncbi.nlm.nih.gov/pubmed/28209135
http://dx.doi.org/10.1186/s12859-017-1530-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5311849/
https://www.ncbi.nlm.nih.gov/pubmed/28209135
http://dx.doi.org/10.1186/s12859-017-1530-2

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