ClipSV: improving structural variation detection by read extension, spliced alignment and tree-based decision rules

Structural variation (SV), which consists of genomic variation from 50 to millions of base pairs, confers considerable impacts on human diseases, complex traits and evolution. Accurately detecting SV is a fundamental step to characterize the features of individual genomes. Currently, several methods...

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Detalles Bibliográficos
Autores principales: Xu, Peng, chen, Yu, Gao, Min, Chong, Zechen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Methods Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7850140/
https://www.ncbi.nlm.nih.gov/pubmed/33554118
http://dx.doi.org/10.1093/nargab/lqab003

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7850140/
https://www.ncbi.nlm.nih.gov/pubmed/33554118
http://dx.doi.org/10.1093/nargab/lqab003

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