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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...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Research Network of Computational and Structural Biotechnology
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7484502/ https://www.ncbi.nlm.nih.gov/pubmed/32952940 http://dx.doi.org/10.1016/j.csbj.2020.08.011 |