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GIGI-Quick: a fast approach to impute missing genotypes in genome-wide association family data

SUMMARY: Genome-wide association studies have become common over the last ten years, with a shift towards targeting rare variants, especially in pedigree-data. Despite lower costs, sequencing for rare variants still remains expensive. To have a relatively large sample with acceptable cost, imputatio...

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Bibliografiske detaljer
Udgivet i:Bioinformatics
Main Authors: Kunji, Khalid, Ullah, Ehsan, Nato, Alejandro Q, Wijsman, Ellen M, Saad, Mohamad
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 2018
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5925782/
https://ncbi.nlm.nih.gov/pubmed/29267877
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btx782
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