Detection of homozygous and hemizygous complete or partial exon deletions by whole-exome sequencing

The detection of copy number variations (CNVs) in whole-exome sequencing (WES) data is important, as CNVs may underlie a number of human genetic disorders. The recently developed HMZDelFinder algorithm can detect rare homozygous and hemizygous (HMZ) deletions in WES data more effectively than other...

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Detalles Bibliográficos
Autores principales: Bigio, Benedetta, Seeleuthner, Yoann, Kerner, Gaspard, Migaud, Mélanie, Rosain, Jérémie, Boisson, Bertrand, Nasca, Carla, Puel, Anne, Bustamante, Jacinta, Casanova, Jean-Laurent, Abel, Laurent, Cobat, Aurelie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Methods Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8140739/
https://www.ncbi.nlm.nih.gov/pubmed/34046589
http://dx.doi.org/10.1093/nargab/lqab037

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8140739/
https://www.ncbi.nlm.nih.gov/pubmed/34046589
http://dx.doi.org/10.1093/nargab/lqab037

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