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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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書目詳細資料
Main Authors: Dering, Carmen, Schillert, Arne, König, Inke R, Ziegler, Andreas
格式: Artigo
語言:Inglês
出版: BioMed Central 2014
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在線閱讀: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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