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DB(2): a probabilistic approach for accurate detection of tandem duplication breakpoints using paired-end reads
BACKGROUND: With the advent of paired-end high throughput sequencing, it is now possible to identify various types of structural variation on a genome-wide scale. Although many methods have been proposed for structural variation detection, most do not provide precise boundaries for identified varian...
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| Опубликовано в: : | BMC Genomics |
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| Главные авторы: | , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
BioMed Central
2014
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4234483/ https://ncbi.nlm.nih.gov/pubmed/24597945 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-15-175 |
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