vipR: variant identification in pooled DNA using R

Motivation: High-throughput-sequencing (HTS) technologies are the method of choice for screening the human genome for rare sequence variants causing susceptibility to complex diseases. Unfortunately, preparation of samples for a large number of individuals is still very cost- and labor intensive. Th...

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Detalles Bibliográficos
Autores principales: Altmann, Andre, Weber, Peter, Quast, Carina, Rex-Haffner, Monika, Binder, Elisabeth B., Müller-Myhsok, Bertram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2011
Materias:
Ismb/Eccb 2011 Proceedings Papers Committee July 17 to July 19, 2011, Vienna, Austria
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3117388/
https://www.ncbi.nlm.nih.gov/pubmed/21685105
http://dx.doi.org/10.1093/bioinformatics/btr205

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3117388/
https://www.ncbi.nlm.nih.gov/pubmed/21685105
http://dx.doi.org/10.1093/bioinformatics/btr205

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