Variant callers for next-generation sequencing data: a comparison study.
Next generation sequencing (NGS) has been leading the genetic study of human disease into an era of unprecedented productivity. Many bioinformatics pipelines have been developed to call variants from NGS data. The performance of these pipelines depends crucially on the variant caller used and on the...
Main Authors: | Xiangtao Liu, Shizhong Han, Zuoheng Wang, Joel Gelernter, Bao-Zhu Yang |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2013-01-01
|
Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC3785481?pdf=render |
Similar Items
-
The Role and Challenges of Exome Sequencing in Studies of Human Diseases
by: Zuoheng eWang, et al.
Published: (2013-08-01) -
NextSV: a meta-caller for structural variants from low-coverage long-read sequencing data
by: Li Fang, et al.
Published: (2018-05-01) -
MAFsnp: A Multi-Sample Accurate and Flexible SNP Caller Using Next-Generation Sequencing Data.
by: Jiyuan Hu, et al.
Published: (2015-01-01) -
Psi-Caller: A Lightweight Short Read-Based Variant Caller With High Speed and Accuracy
by: Yadong Liu, et al.
Published: (2021-08-01) -
Variant Detection Using Next Generation Sequencing Data
by: Pyon, Yoon Soo
Published: (2013)