Cargando…
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...
Autores principales: | Liu, Xiangtao, Han, Shizhong, Wang, Zuoheng, Gelernter, Joel, Yang, Bao-Zhu |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3785481/ https://www.ncbi.nlm.nih.gov/pubmed/24086590 http://dx.doi.org/10.1371/journal.pone.0075619 |
Ejemplares similares
-
The Role and Challenges of Exome Sequencing in Studies of Human Diseases
por: Wang, Zuoheng, et al.
Publicado: (2013) -
Pisces: an accurate and versatile variant caller for somatic and germline next-generation sequencing data
por: Dunn, Tamsen, et al.
Publicado: (2019) -
Needlestack: an ultra-sensitive variant caller for multi-sample next generation sequencing data
por: Delhomme, Tiffany M, et al.
Publicado: (2020) -
MetaSV: an accurate and integrative structural-variant caller for next generation sequencing
por: Mohiyuddin, Marghoob, et al.
Publicado: (2015) -
VarDict: a novel and versatile variant caller for next-generation sequencing in cancer research
por: Lai, Zhongwu, et al.
Publicado: (2016)