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sv-callers: a highly portable parallel workflow for structural variant detection in whole-genome sequence data
Structural variants (SVs) are an important class of genetic variation implicated in a wide array of genetic diseases including cancer. Despite the advances in whole genome sequencing, comprehensive and accurate detection of SVs in short-read data still poses some practical and computational challeng...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
PeerJ Inc.
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6951283/ https://www.ncbi.nlm.nih.gov/pubmed/31934500 http://dx.doi.org/10.7717/peerj.8214 |