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Filtering genetic variants and placing informative priors based on putative biological function

High-density genetic marker data, especially sequence data, imply an immense multiple testing burden. This can be ameliorated by filtering genetic variants, exploiting or accounting for correlations between variants, jointly testing variants, and by incorporating informative priors. Priors can be ba...

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Bibliografske podrobnosti
izdano v:BMC Genet
Main Authors: Friedrichs, Stefanie, Malzahn, Dörthe, Pugh, Elizabeth W., Almeida, Marcio, Liu, Xiao Qing, Bailey, Julia N.
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2016
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4895695/
https://ncbi.nlm.nih.gov/pubmed/26866982
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12863-015-0313-x
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