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A Hidden Markov Model for Copy Number Variant prediction from whole genome resequencing data
MOTIVATION: Copy Number Variants (CNVs) are important genetic factors for studying human diseases. While high-throughput whole genome re-sequencing provides multiple lines of evidence for detecting CNVs, computational algorithms need to be tailored for different type or size of CNVs under different...
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| Autori principali: | , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2011
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3194192/ https://ncbi.nlm.nih.gov/pubmed/21989326 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-12-S6-S4 |
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