An improved approach for accurate and efficient calling of structural variations with low-coverage sequence data

BACKGROUND: Recent advances in sequencing technologies make it possible to comprehensively study structural variations (SVs) using sequence data of large-scale populations. Currently, more efforts have been taken to develop methods that call SVs with exact breakpoints. Among these approaches, split-...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Jin, Wang, Jiayin, Wu, Yufeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Proceedings
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3358659/
https://www.ncbi.nlm.nih.gov/pubmed/22537045
http://dx.doi.org/10.1186/1471-2105-13-S6-S6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3358659/
https://www.ncbi.nlm.nih.gov/pubmed/22537045
http://dx.doi.org/10.1186/1471-2105-13-S6-S6

Ejemplares similares