isoCNV: in silico optimization of copy number variant detection from targeted or exome sequencing data
Abstract Background Accurate copy number variant (CNV) detection is especially challenging for both targeted sequencing (TS) and whole‐exome sequencing (WES) data. To maximize the performance, the parameters of the CNV calling algorithms should be optimized for each specific dataset. This requires o...
Uloženo v:
| Hlavní autoři: | , , |
|---|---|
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BMC
2021-10-01
|
| Edice: | BMC Bioinformatics |
| Témata: | |
| On-line přístup: | https://doi.org/10.1186/s12859-021-04452-6 |
| Tagy: |
Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!
|