MSeq-CNV: accurate detection of Copy Number Variation from Sequencing of Multiple samples

Currently a few tools are capable of detecting genome-wide Copy Number Variations (CNVs) based on sequencing of multiple samples. Although aberrations in mate pair insertion sizes provide additional hints for the CNV detection based on multiple samples, the majority of the current tools rely only on...

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Detalles Bibliográficos
Autores principales: Malekpour, Seyed Amir, Pezeshk, Hamid, Sadeghi, Mehdi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5838159/
https://www.ncbi.nlm.nih.gov/pubmed/29507384
http://dx.doi.org/10.1038/s41598-018-22323-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5838159/
https://www.ncbi.nlm.nih.gov/pubmed/29507384
http://dx.doi.org/10.1038/s41598-018-22323-8

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