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Gencore: an efficient tool to generate consensus reads for error suppressing and duplicate removing of NGS data

BACKGROUND: Removing duplicates might be considered as a well-resolved problem in next-generation sequencing (NGS) data processing domain. However, as NGS technology gains more recognition in clinical application, researchers start to pay more attention to its sequencing errors, and prefer to remove...

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Detalles Bibliográficos
Publicado en:BMC Bioinformatics
Main Authors: Chen, Shifu, Zhou, Yanqing, Chen, Yaru, Huang, Tanxiao, Liao, Wenting, Xu, Yun, Li, Zhicheng, Gu, Jia
Formato: Artigo
Idioma:Inglês
Publicado: BioMed Central 2019
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6933617/
https://ncbi.nlm.nih.gov/pubmed/31881822
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-019-3280-9
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