Načítá se...
Copy Number Variation Detection Using Total Variation
Next-generation sequencing (NGS) technologies offer new opportunities for precise and accurate identification of genomic aberrations, including copy number variations (CNVs). For high-throughput NGS data, using depth of coverage has become a major approach to identify CNVs, especially for whole exom...
Uloženo v:
| Vydáno v: | ACM BCB |
|---|---|
| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2019
|
| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7278034/ https://ncbi.nlm.nih.gov/pubmed/32515750 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1145/3307339.3342181 |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|