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...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Hang, Wang, Ke, Zhou, Juan, Chen, Jianhua, Xu, Yizhou, Wang, Dong, Li, Xiaoqi, Sun, Renliang, Zhang, Mancang, Wang, Zhuo, Shi, Yongyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6936113/
https://www.ncbi.nlm.nih.gov/pubmed/31888441
http://dx.doi.org/10.1186/s12859-019-3226-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6936113/
https://www.ncbi.nlm.nih.gov/pubmed/31888441
http://dx.doi.org/10.1186/s12859-019-3226-2

Ejemplares similares