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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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Detalhes bibliográficos
Publicado no:NAR Genom Bioinform
Main Authors: Xu, Peng, chen, Yu, Gao, Min, Chong, Zechen
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2021
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7850140/
https://ncbi.nlm.nih.gov/pubmed/33554118
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nargab/lqab003
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