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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2021
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| Materias: | |
| 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 |