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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...
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| 出版年: | ACM BCB |
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| 主要な著者: | , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2019
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| 主題: | |
| オンライン･アクセス: | 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 |
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