Inferring copy number and genotype in tumour exome data
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Biotechnology
Link
https://link.springer.com/content/pdf/10.1186/1471-2164-15-732.pdf
Reference32 articles.
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3. Fridlyand J, Snijders AM, Pinkel D, Albertson DG, Jain AN: Hidden Markov models approach to the analysis of array CGH data. J Multivariate Anal. 2004, 90 (1): 132-153. 10.1016/j.jmva.2004.02.008.
4. Li A, Liu Z, Lezon-Geyda K, Sarkar S, Lannin D, Schulz V, Krop I, Winer E, Harris L, Tuck D: GPHMM: an integrated hidden Markov model for identification of copy number alteration and loss of heterozygosity in complex tumor samples using whole genome SNP arrays. Nucleic Acids Res. 2011, 39 (12): 4928-4941. 10.1093/nar/gkr014.
5. Olshen AB, Venkatraman ES, Lucito R, Wigler M: Circular binary segmentation for the analysis of array‒based DNA copy number data. Biostatistics. 2004, 5 (4): 557-572. 10.1093/biostatistics/kxh008.
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