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An improved approach for accurate and efficient calling of structural variations with low-coverage sequence data
BACKGROUND: Recent advances in sequencing technologies make it possible to comprehensively study structural variations (SVs) using sequence data of large-scale populations. Currently, more efforts have been taken to develop methods that call SVs with exact breakpoints. Among these approaches, split-...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2012
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3358659/ https://www.ncbi.nlm.nih.gov/pubmed/22537045 http://dx.doi.org/10.1186/1471-2105-13-S6-S6 |