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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...
Autores principales: | David, Matei, Mustafa, Harun, Brudno, Michael |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3783187/ https://www.ncbi.nlm.nih.gov/pubmed/23921633 http://dx.doi.org/10.1093/nar/gkt612 |
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