D. Pinkel, R. Segraves, D. Sudar, S. Clark, I. Poole et al., High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays, Nature Genetics, vol.20, issue.2, pp.207-211, 1998.
DOI : 10.1038/2524

D. Albertson, C. Collins, F. Mccormick, and J. Gray, Chromosome aberrations in solid tumors, Nature Genetics, vol.34, issue.4, pp.369-76, 2003.
DOI : 10.1038/ng1215

J. Fridlyand, A. Snijders, D. Pinkel, D. Albertson, and A. Jain, Application of Hidden Markov Models to the analysis of the array CGH data, Journal of Multivariate Analysis Special Issue on Multivariate Methods in Genomic Data Analysis, vol.4, 2004.

P. Hupé, N. Stransky, J. Thiery, F. Radvanyi, and E. Barillot, Analysis of array CGH data: from signal ratio to gain and loss of DNA regions, Bioinformatics, vol.20, issue.18, pp.3413-3422, 2004.
DOI : 10.1093/bioinformatics/bth418

K. Jong, E. Marchiori, A. Van-der-vaart, B. Ylstra, M. Weiss et al., Chromosomal Breakpoint Detection in Human Cancer, Applications of Evolutionary Computing, EvoWorkshops2003: EvoBIO, pp.54-65
DOI : 10.1007/3-540-36605-9_6

A. Olshen, E. Venkatraman, R. Lucito, and M. Wigler, Circular binary segmentation for the analysis of array-based DNA copy number data, Biostatistics, vol.5, issue.4, pp.557-572, 2004.
DOI : 10.1093/biostatistics/kxh008

F. Picard, R. S. Lavielle, M. Vaisse, C. Daudin, and J. , A statistical approach for array CGH data analysis, BMC Bioinformatics, vol.6, issue.1, p.27, 2005.
DOI : 10.1186/1471-2105-6-27

URL : https://hal.archives-ouvertes.fr/hal-00427846

J. Pollack, T. Sorlie, C. Perou, A. Rees, S. Jeffreys et al., Microarray analysis reveals a major direct role of DNA copy number alteration in the transcriptional program of human breast tumors, Proceedings of the National Academy of Sciences, vol.340, issue.26, 2002.
DOI : 10.1073/pnas.94.26.14506

J. Wang, L. Meza-zepeda, S. Kresse, and O. Myklebost, Analysing microarray-based CGH experiments, BMC Bioinformatics, vol.5, issue.1, p.74, 2004.
DOI : 10.1186/1471-2105-5-74

Y. Yang, S. Dudoit, P. Luu, D. Lin, V. Pend et al., Normalization for cDNA microarray data: a robust composite method addressing single and multiple slide systematic variation, Nucleic Acids Research, vol.30, issue.4, pp.15-16, 2002.
DOI : 10.1093/nar/30.4.e15

URL : http://doi.org/10.1093/nar/30.4.e15

M. Khojasteh, W. Lam, R. Ward, and C. Macaulay, A stepwise framework for the normalization of array CGH data, BMC Bioinformatics, vol.6, issue.1, p.274, 2005.
DOI : 10.1186/1471-2105-6-274

C. Billerey, D. Chopin, M. Aubriot-lorton, D. Ricol, S. Gil et al., Frequent FGFR3 Mutations in Papillary Non-Invasive Bladder (pTa) Tumors, The American Journal of Pathology, vol.158, issue.6, pp.955-1959, 2001.
DOI : 10.1016/S0002-9440(10)64665-2

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1891972

A. Snijders, N. Nowak, R. Segraves, S. Blackwood, N. Brown et al., Assembly of microarrays for genome-wide measurement of DNA copy number, Nature Genetics, vol.29, issue.3, pp.263-267, 2001.
DOI : 10.1038/ng754