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LUMPY: a probabilistic framework for structural variant discovery
Comprehensive discovery of structural variation (SV) from whole genome sequencing data requires multiple detection signals including read-pair, split-read, read-depth and prior knowledge. Owing to technical challenges, extant SV discovery algorithms either use one signal in isolation, or at best use...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4197822/ https://ncbi.nlm.nih.gov/pubmed/24970577 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gb-2014-15-6-r84 |
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