Bibliography

Hupé, P., Stransky, N., Thiery, J. P., Radvanyi, F., and Barillot, E. (2004).

Analysis of array CGH data: from signal ratio to gain and loss of DNA regions.
Bioinformatics, Advance Access published on September 20, 2004; doi: 10.1093/bioinformatics/bth418.

Jong, K., Marchiori, E., van der Vaart, A., Ylstra, B., Weiss, M., and Meijer, G. (2003).

Chromosomal breakpoint detection in human cancer.
In Raidl, G. R., Cagnoni, S., Cardalda, J. J. R., Corne, D. W., Gottlieb, J., Guillot, A., Hart, E., Johnson, C. G., Marchiori, E., Meyer, J.-A., and Middendorf, M., editors, Applications of Evolutionary Computing, EvoWorkshops2003: EvoBIO, EvoCOP, EvoIASP, EvoMUSART, EvoROB, EvoSTIM, volume 2611 of LNCS, pages 54-65, University of Essex, England, UK. Springer-Verlag.

Pinkel, D., Segraves, R., Sudar, D., Clark, S., Poole, I., Kowbel, D., Collins, C., Kuo, W. L., Chen, C., Zhai, Y., Dairkee, S. H., Ljung, B. M., Gray, J. W., and Albertson, D. G. (1998).

High resolution analysis of dna copy number variation using comparative genomic hybridization to microarrays.
Nat. Genet., 20:207-211.

Polzehl, J. and Spokoiny, S. (2002).

Local likelihood modelling by adaptive weights smoothing.
WIAS-Preprint 787.

Snijders, A. M., Nowak, N., Segraves, R., Blackwood, S., Brown, N., Conroy, J., Hamilton, G., Hindle, A. K., Huey, B., Kimura, K., S, S. L., Myambo, K., Palmer, J., Ylstra, B., Yue, J. P., Gray, J. W., Jain, A. N., Pinkel, D., and Albertson, D. G. (2001).

Assembly of microarrays for genome-wide measurement of dna copy number.
Nat. Genet., 29:263-4.

Solinas-Toldo, S., Lampel, S., Stilgenbauer, S., Nickolenko, J., Benner, A., Dohner, H., Cremer, T., and Lichter, P. (1997).

Matrix-based comparative genomic hybridization: Biochips to screen for genomic imbalances.
Genes Chromosomes Cancer, 20:399-407.