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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Publicado en:Comput Struct Biotechnol J
Autores principales: Sater, Vincent, Viailly, Pierre-Julien, Lecroq, Thierry, Ruminy, Philippe, Bérard, Caroline, Prieur-Gaston, Élise, Jardin, Fabrice
Formato: Artigo
Lenguaje:Inglês
Publicado: Research Network of Computational and Structural Biotechnology 2020
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Research Article
Acceso en línea: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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