Identification of genomic indels and structural variations using split reads

Identification of genomic indels and structural variations using split reads

<p>Abstract</p> <p>Background</p> <p>Recent studies have demonstrated the genetic significance of insertions, deletions, and other more complex structural variants (SVs) in the human population. With the development of the next-generation sequencing technologies, high-t...

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Détails bibliographiques
Auteurs principaux: Urban Alexander E, Abyzov Alex, Lam Hugo, Du Jiang, Zhang Zhengdong D, Snyder Michael, Gerstein Mark
Format: Article
Langue:English
Publié: BMC 2011-07-01
Collection:BMC Genomics
Sujets:
insertion
deletion
structure variation
split read
high-throughput sequencing
Accès en ligne:http://www.biomedcentral.com/1471-2164/12/375

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http://www.biomedcentral.com/1471-2164/12/375

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