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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: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2011
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| Assuntos: | |
| Acesso em linha: | 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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