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A comparison of two collapsing methods in different approaches

Sequencing technologies have enabled the investigation of whole genomes of many individuals in parallel. Studies have shown that the joint consideration of multiple rare variants may explain a relevant proportion of the genetic basis for disease so that grouping of rare variants, termed collapsing,...

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Bibliografiske detaljer
Main Authors: Dering, Carmen, Schillert, Arne, König, Inke R, Ziegler, Andreas
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2014
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4143760/
https://ncbi.nlm.nih.gov/pubmed/25519408
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1753-6561-8-S1-S8
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