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Comparative analysis of copy number variation detection methods and database construction
BACKGROUND: Array-based detection of copy number variations (CNVs) is widely used for identifying disease-specific genetic variations. However, the accuracy of CNV detection is not sufficient and results differ depending on the detection programs used and their parameters. In this study, we evaluate...
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| Huvudupphovsmän: | , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
BioMed Central
2011
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3058066/ https://ncbi.nlm.nih.gov/pubmed/21385384 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2156-12-29 |
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