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UMI-Gen: A UMI-based read simulator for variant calling evaluation in paired-end sequencing NGS libraries
MOTIVATION: With Next Generation Sequencing becoming more affordable every year, NGS technologies asserted themselves as the fastest and most reliable way to detect Single Nucleotide Variants (SNV) and Copy Number Variations (CNV) in cancer patients. These technologies can be used to sequence DNA at...
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| 出版年: | Comput Struct Biotechnol J |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Research Network of Computational and Structural Biotechnology
2020
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7484502/ https://ncbi.nlm.nih.gov/pubmed/32952940 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.csbj.2020.08.011 |
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