CNV Detection from Exome Sequencing Data in Routine Diagnostics of Rare Genetic Disorders: Opportunities and Limitations

To assess the potential of detecting copy number variations (CNVs) directly from exome sequencing (ES) data in diagnostic settings, we developed a CNV-detection pipeline based on ExomeDepth software and applied it to ES data of 450 individuals. Initially, only CNVs affecting genes in the requested d...

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Detalles Bibliográficos
Autores principales: Royer-Bertrand, Beryl, Cisarova, Katarina, Niel-Butschi, Florence, Mittaz-Crettol, Laureane, Fodstad, Heidi, Superti-Furga, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8472439/
https://www.ncbi.nlm.nih.gov/pubmed/34573409
http://dx.doi.org/10.3390/genes12091427

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8472439/
https://www.ncbi.nlm.nih.gov/pubmed/34573409
http://dx.doi.org/10.3390/genes12091427

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