Identification of genomic indels and structural variations using split reads

BACKGROUND: 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-throughput surveys of SVs on the whole-genome level have...

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Main Authors: Zhang, Zhengdong D, Du, Jiang, Lam, Hugo, Abyzov, Alex, Urban, Alexander E, Snyder, Michael, Gerstein, Mark
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2011
Teme:
Methodology Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC3161018/
https://ncbi.nlm.nih.gov/pubmed/21787423
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-12-375
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