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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....
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
SAGE Publications
2020
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| 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 |