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CNV-TV: A robust method to discover copy number variation from short sequencing reads
BACKGROUND: Copy number variation (CNV) is an important structural variation (SV) in human genome. Various studies have shown that CNVs are associated with complex diseases. Traditional CNV detection methods such as fluorescence in situ hybridization (FISH) and array comparative genomic hybridizatio...
Autores principales: | Duan, Junbo, Zhang, Ji-Gang, Deng, Hong-Wen, Wang, Yu-Ping |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3679874/ https://www.ncbi.nlm.nih.gov/pubmed/23634703 http://dx.doi.org/10.1186/1471-2105-14-150 |
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