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Detecting Alu insertions from high-throughput sequencing data
High-throughput sequencing technologies have allowed for the cataloguing of variation in personal human genomes. In this manuscript, we present alu-detect, a tool that combines read-pair and split-read information to detect novel Alus and their precise breakpoints directly from either whole-genome o...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3783187/ https://ncbi.nlm.nih.gov/pubmed/23921633 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkt612 |
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