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Detecting common copy number variants in high-throughput sequencing data by using JointSLM algorithm
The discovery of genomic structural variants (SVs), such as copy number variants (CNVs), is essential to understand genetic variation of human populations and complex diseases. Over recent years, the advent of new high-throughput sequencing (HTS) platforms has opened many opportunities for SVs disco...
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| Autori principali: | , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Oxford University Press
2011
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3105418/ https://ncbi.nlm.nih.gov/pubmed/21321017 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkr068 |
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