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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...
Shranjeno v:
| izdano v: | ACM BCB |
|---|---|
| Main Authors: | , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2019
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| Teme: | |
| Online dostop: | 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 |
| Oznake: |
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