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Imputation and quality control steps for combining multiple genome-wide datasets

The electronic MEdical Records and GEnomics (eMERGE) network brings together DNA biobanks linked to electronic health records (EHRs) from multiple institutions. Approximately 51,000 DNA samples from distinct individuals have been genotyped using genome-wide SNP arrays across the nine sites of the ne...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:Front Genet
Päätekijät: Verma, Shefali S., de Andrade, Mariza, Tromp, Gerard, Kuivaniemi, Helena, Pugh, Elizabeth, Namjou-Khales, Bahram, Mukherjee, Shubhabrata, Jarvik, Gail P., Kottyan, Leah C., Burt, Amber, Bradford, Yuki, Armstrong, Gretta D., Derr, Kimberly, Crawford, Dana C., Haines, Jonathan L., Li, Rongling, Crosslin, David, Ritchie, Marylyn D.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Frontiers Media S.A. 2014
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4263197/
https://ncbi.nlm.nih.gov/pubmed/25566314
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2014.00370
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