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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Detalles Bibliográficos
Autores principales: David, Matei, Mustafa, Harun, Brudno, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Methods Online
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

Internet

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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