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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Detalles Bibliográficos
Autores principales: Dering, Carmen, Schillert, Arne, König, Inke R, Ziegler, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Proceedings
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143760/
https://www.ncbi.nlm.nih.gov/pubmed/25519408
http://dx.doi.org/10.1186/1753-6561-8-S1-S8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143760/
https://www.ncbi.nlm.nih.gov/pubmed/25519408
http://dx.doi.org/10.1186/1753-6561-8-S1-S8

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