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Detection and characterization of novel sequence insertions using paired-end next-generation sequencing
Motivation: In the past few years, human genome structural variation discovery has enjoyed increased attention from the genomics research community. Many studies were published to characterize short insertions, deletions, duplications and inversions, and associate copy number variants (CNVs) with di...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2865866/ https://ncbi.nlm.nih.gov/pubmed/20385726 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btq152 |
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