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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Detalles Bibliográficos
Autores principales: Zhang, Zhengdong D, Du, Jiang, Lam, Hugo, Abyzov, Alex, Urban, Alexander E, Snyder, Michael, Gerstein, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3161018/
https://www.ncbi.nlm.nih.gov/pubmed/21787423
http://dx.doi.org/10.1186/1471-2164-12-375

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3161018/
https://www.ncbi.nlm.nih.gov/pubmed/21787423
http://dx.doi.org/10.1186/1471-2164-12-375

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