inCNV: An Integrated Analysis Tool for Copy Number Variation on Whole Exome Sequencing

The detection of copy number variations (CNVs) on whole-exome sequencing (WES) represents a cost-effective technique for the study of genetic variants. This approach, however, has encountered an obstacle with high false-positive rates due to biases from exome sequencing capture kits and GC contents....

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Detalles Bibliográficos
Autores principales: Chanwigoon, Saowwapark, Piwluang, Sakkayaphab, Wichadakul, Duangdao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Software or database Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7520931/
https://www.ncbi.nlm.nih.gov/pubmed/33029071
http://dx.doi.org/10.1177/1176934320956577

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7520931/
https://www.ncbi.nlm.nih.gov/pubmed/33029071
http://dx.doi.org/10.1177/1176934320956577

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