VariFAST: a variant filter by automated scoring based on tagged-signatures

BACKGROUND: Variant calling and refinement from whole genome/exome sequencing data is a fundamental task for genomics studies. Due to the limited accuracy of NGS sequencing and variant callers, IGV-based manual review is required for further false positive variant filtering, which costs massive labo...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:BMC Bioinformatics
Egile Nagusiak: Zhang, Hang, Wang, Ke, Zhou, Juan, Chen, Jianhua, Xu, Yizhou, Wang, Dong, Li, Xiaoqi, Sun, Renliang, Zhang, Mancang, Wang, Zhuo, Shi, Yongyong
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2019
Gaiak:
Research
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC6936113/
https://ncbi.nlm.nih.gov/pubmed/31888441
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-019-3226-2
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