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...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
izdano v:BMC Bioinformatics
Main Authors: Chen, Shifu, Zhou, Yanqing, Chen, Yaru, Huang, Tanxiao, Liao, Wenting, Xu, Yun, Li, Zhicheng, Gu, Jia
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2019
Teme:
Software
Online dostop: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
Oznake: Označite
Brez oznak, prvi označite!

Podobne knjige/članki