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Copy number variation genotyping using family information
BACKGROUND: In recent years there has been a growing interest in the role of copy number variations (CNV) in genetic diseases. Though there has been rapid development of technologies and statistical methods devoted to detection in CNVs from array data, the inherent challenges in data quality associa...
Sparad:
| Huvudupphovsmän: | , , , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
BioMed Central
2013
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3668900/ https://ncbi.nlm.nih.gov/pubmed/23656838 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-14-157 |
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