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Computational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectives
Copy number variation (CNV) is a prevalent form of critical genetic variation that leads to an abnormal number of copies of large genomic regions in a cell. Microarray-based comparative genome hybridization (arrayCGH) or genotyping arrays have been standard technologies to detect large regions subje...
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| Main Authors: | , , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
BioMed Central
2013
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3846878/ https://ncbi.nlm.nih.gov/pubmed/24564169 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-14-S11-S1 |
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