MSeq-CNV: accurate detection of Copy Number Variation from Sequencing of Multiple samples
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-018-22323-8.pdf
Reference50 articles.
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2. Aitman, T. J. et al. Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans. Nature 439, 851–855, https://doi.org/10.1038/nature04489 (2006).
3. Albertson, D. G. & Pinkel, D. Genomic microarrays in human genetic disease and cancer. Hum Mol Genet 12(Spec No 2), R145–152, https://doi.org/10.1093/hmg/ddg261 (2003).
4. Cook, E. H. Jr. & Scherer, S. W. Copy-number variations associated with neuropsychiatric conditions. Nature 455, 919–923, https://doi.org/10.1038/nature07458 (2008).
5. Fridlyand, J., Snijders, A. M., Pinkel, D., Albertson, D. G. & Jain, A. N. Hidden Markov models approach to the analysis of array CGH data. Journal of Multivariate Analysis 90, 132–153, https://doi.org/10.1016/j.jmva.2004.02.008 (2004).
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