Bioinformatics Advance Access originally published online on September 20, 2004
Bioinformatics 2004 20(18):3413-3422; doi:10.1093/bioinformatics/bth418
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Bioinformatics vol. 20 issue 18 © Oxford University Press 2004; all rights reserved.
Analysis of array CGH data: from signal ratio to gain and loss of DNA regions
1 Service Bioinformatique and 2 UMR 144 CNRS/Institut Curie, 26, rue d'Ulm, Paris, 75248 cedex 05, France
Received on March 19, 2004; revised on June 18, 2004; accepted on July 12, 2004
Advance Access Publication September 30, 2004
Motivation: Genomic DNA regions are frequently lost or gained during tumor progression. Array Comparative Genomic Hybridization (array CGH) technology makes it possible to assess these changes in DNA in cancers, by comparison with a normal reference. The identification of systematically deleted or amplified genomic regions in a set of tumors enables biologists to identify genes involved in cancer progression because tumor suppressor genes are thought to be located in lost genomic regions and oncogenes, in gained regions. Array CGH profiles should also improve the classification of tumors. The achievement of these goals requires a methodology for detecting the breakpoints delimiting altered regions in genomic patterns and assigning a status (normal, gained or lost) to each chromosomal region.
Results: We have developed a methodology for the automatic detection of breakpoints from array CGH profile, and the assignment of a status to each chromosomal region. The breakpoint detection step is based on the Adaptive Weights Smoothing (AWS) procedure and provides highly convincing results: our algorithm detects 97, 100 and 94% of breakpoints in simulated data, karyotyping results and manually analyzed profiles, respectively. The percentage of correctly assigned statuses ranges from 98.9 to 99.8% for simulated data and is 100% for karyotyping results. Our algorithm also outperforms other solutions on a public reference dataset.
Availability: The R package GLAD (Gain and Loss Analysis of DNA) is available upon request
Contact: glad{at}curie.fr
* To whom correspondence should be addressed.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
A. Magi, M. Benelli, G. Marseglia, G. Nannetti, M. R. Scordo, and F. Torricelli A shifting level model algorithm that identifies aberrations in array-CGH data Biostat., November 30, 2009; (2009) kxp051v1. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Ernst, S. Hofmann, R. Ahmadi, N. Becker, A. Korshunov, F. Engel, C. Hartmann, J. Felsberg, M. Sabel, H. Peterziel, et al. Genomic and Expression Profiling of Glioblastoma Stem Cell-Like Spheroid Cultures Identifies Novel Tumor-Relevant Genes Associated with Survival Clin. Cancer Res., November 1, 2009; 15(21): 6541 - 6550. [Abstract] [Full Text] [PDF] |
||||
![]() |
O. M. Rueda and R. Diaz-Uriarte RJaCGH: Bayesian analysis of aCGH arrays for detecting copy number changes and recurrent regions Bioinformatics, August 1, 2009; 25(15): 1959 - 1960. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Daines, H. Wang, Y. Li, Y. Han, R. Gibbs, and R. Chen High-Throughput Multiplex Sequencing to Discover Copy Number Variants in Drosophila Genetics, August 1, 2009; 182(4): 935 - 941. [Abstract] [Full Text] [PDF] |
||||
![]() |
M B K Lambros, D S P Tan, R L Jones, R Vatcheva, K Savage, N Tamber, K Fenwick, A Mackay, A Ashworth, and J S Reis-Filho Genomic profile of a secretory breast cancer with an ETV6-NTRK3 duplication J. Clin. Pathol., July 1, 2009; 62(7): 604 - 612. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Di Vizio, J. Kim, M. H. Hager, M. Morello, W. Yang, C. J. Lafargue, L. D. True, M. A. Rubin, R. M. Adam, R. Beroukhim, et al. Oncosome Formation in Prostate Cancer: Association with a Region of Frequent Chromosomal Deletion in Metastatic Disease Cancer Res., July 1, 2009; 69(13): 5601 - 5609. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Trolet, P. Hupe, I. Huon, I. Lebigot, C. Decraene, O. Delattre, X. Sastre-Garau, S. Saule, J.-P. Thiery, C. Plancher, et al. Genomic Profiling and Identification of High-Risk Uveal Melanoma by Array CGH Analysis of Primary Tumors and Liver Metastases Invest. Ophthalmol. Vis. Sci., June 1, 2009; 50(6): 2572 - 2580. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. A. van de Wiel, R. Brosens, P. H. C. Eilers, C. Kumps, G. A. Meijer, B. Menten, E. Sistermans, F. Speleman, M. E. Timmerman, and B. Ylstra Smoothing waves in array CGH tumor profiles Bioinformatics, May 1, 2009; 25(9): 1099 - 1104. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Sheffer, M. D. Bacolod, O. Zuk, S. F. Giardina, H. Pincas, F. Barany, P. B. Paty, W. L. Gerald, D. A. Notterman, and E. Domany Association of survival and disease progression with chromosomal instability: A genomic exploration of colorectal cancer PNAS, April 28, 2009; 106(17): 7131 - 7136. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Nilsson, M. Johansson, F. Al-Shahrour, A. E. Carpenter, and B. L. Ebert Ultrasome: efficient aberration caller for copy number studies of ultra-high resolution Bioinformatics, April 15, 2009; 25(8): 1078 - 1079. [Abstract] [Full Text] [PDF] |
||||
![]() |
X. Hu, H. M. Stern, L. Ge, C. O'Brien, L. Haydu, C. D. Honchell, P. M. Haverty, B. A. Peters, T. D. Wu, L. C. Amler, et al. Genetic Alterations and Oncogenic Pathways Associated with Breast Cancer Subtypes Mol. Cancer Res., April 1, 2009; 7(4): 511 - 522. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Bengtsson, A. Ray, P. Spellman, and T. P. Speed A single-sample method for normalizing and combining full-resolution copy numbers from multiple platforms, labs and analysis methods Bioinformatics, April 1, 2009; 25(7): 861 - 867. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Eckstein, K. Servan, B. Hildebrandt, A. Politz, G. v. Jonquieres, S. Wolf-Kummeth, I. Napierski, A. Hamacher, M. U. Kassack, J. Budczies, et al. Hyperactivation of the Insulin-like Growth Factor Receptor I Signaling Pathway Is an Essential Event for Cisplatin Resistance of Ovarian Cancer Cells Cancer Res., April 1, 2009; 69(7): 2996 - 3003. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. S.P. Tan, M. B.K. Lambros, S. Rayter, R. Natrajan, R. Vatcheva, Q. Gao, C. Marchio, F. C. Geyer, K. Savage, S. Parry, et al. PPM1D Is a Potential Therapeutic Target in Ovarian Clear Cell Carcinomas Clin. Cancer Res., April 1, 2009; 15(7): 2269 - 2280. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Budinska, E. Gelnarova, and M. G. Schimek MSMAD: a computationally efficient method for the analysis of noisy array CGH data Bioinformatics, March 15, 2009; 25(6): 703 - 713. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. LaFramboise, W. Winckler, and R. K. Thomas A flexible rank-based framework for detecting copy number aberrations from array data Bioinformatics, March 15, 2009; 25(6): 722 - 728. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. Janoueix-Lerosey, G. Schleiermacher, E. Michels, V. Mosseri, A. Ribeiro, D. Lequin, J. Vermeulen, J. Couturier, M. Peuchmaur, A. Valent, et al. Overall Genomic Pattern Is a Predictor of Outcome in Neuroblastoma J. Clin. Oncol., March 1, 2009; 27(7): 1026 - 1033. [Abstract] [Full Text] [PDF] |
||||
![]() |
L.-y. Wang, A. Abyzov, J. O. Korbel, M. Snyder, and M. Gerstein MSB: A mean-shift-based approach for the analysis of structural variation in the genome Genome Res., January 1, 2009; 19(1): 106 - 117. [Abstract] [Full Text] [PDF] |
||||
![]() |
P.-A. Chen, H.-F. Liu, and K.-M. Chao CNVDetector: locating copy number variations using array CGH data Bioinformatics, December 1, 2008; 24(23): 2773 - 2775. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Erdman and J. W. Emerson A fast Bayesian change point analysis for the segmentation of microarray data Bioinformatics, October 1, 2008; 24(19): 2143 - 2148. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. O'Brien, G. Cavet, A. Pandita, X. Hu, L. Haydu, S. Mohan, K. Toy, C. S. Rivers, Z. Modrusan, L. C. Amler, et al. Functional Genomics Identifies ABCC3 as a Mediator of Taxane Resistance in HER2-Amplified Breast Cancer Cancer Res., July 1, 2008; 68(13): 5380 - 5389. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Cahan, L. E. Godfrey, P. S. Eis, T. A. Richmond, R. R. Selzer, M. Brent, H. L. McLeod, T. J. Ley, and T. A. Graubert wuHMM: a robust algorithm to detect DNA copy number variation using long oligonucleotide microarray data Nucleic Acids Res., April 1, 2008; 36(7): e41 - e41. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. L. Lai, H. Xing, and N. Zhang Stochastic segmentation models for array-based comparative genomic hybridization data analysis Biostat., April 1, 2008; 9(2): 290 - 307. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Vincent-Salomon, C. Lucchesi, N. Gruel, V. Raynal, G. Pierron, R. Goudefroye, F. Reyal, F. Radvanyi, R. Salmon, J.-P. Thiery, et al. Integrated Genomic and Transcriptomic Analysis of Ductal Carcinoma In situ of the Breast Clin. Cancer Res., April 1, 2008; 14(7): 1956 - 1965. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Andersson, C. E. G. Bruder, A. Piotrowski, U. Menzel, H. Nord, J. Sandgren, T. R. Hvidsten, T. Diaz de Stahl, J. P. Dumanski, and J. Komorowski A segmental maximum a posteriori approach to genome-wide copy number profiling Bioinformatics, March 15, 2008; 24(6): 751 - 758. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Rigaill, P. Hupe, A. Almeida, P. La Rosa, J.-P. Meyniel, C. Decraene, and E. Barillot ITALICS: an algorithm for normalization and DNA copy number calling for Affymetrix SNP arrays Bioinformatics, March 15, 2008; 24(6): 768 - 774. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. M. Lin, A. C. Baker, R. Beroukhim, W. Winckler, W. Feng, J. M. Marmion, E. Laine, H. Greulich, H. Tseng, C. Gates, et al. Modeling Genomic Diversity and Tumor Dependency in Malignant Melanoma Cancer Res., February 1, 2008; 68(3): 664 - 673. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Pique-Regi, J. Monso-Varona, A. Ortega, R. C. Seeger, T. J. Triche, and S. Asgharzadeh Sparse representation and Bayesian detection of genome copy number alterations from microarray data Bioinformatics, February 1, 2008; 24(3): 309 - 318. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. G. Durkin, R. L. Ragland, M. F. Arlt, J. G. Mulle, S. T. Warren, and T. W. Glover Replication stress induces tumor-like microdeletions in FHIT/FRA3B PNAS, January 8, 2008; 105(1): 246 - 251. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. A. Bollet, N. Servant, P. Neuvial, C. Decraene, I. Lebigot, J.-P. Meyniel, Y. De Rycke, A. Savignoni, G. Rigaill, P. Hupe, et al. High-Resolution Mapping of DNA Breakpoints to Define True Recurrences Among Ipsilateral Breast Cancers J Natl Cancer Inst, January 2, 2008; 100(1): 48 - 58. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Cutler, L. A. Marshall, N. Chin, H. Baribault, and P. D. Kassner Significant gene content variation characterizes the genomes of inbred mouse strains Genome Res., December 1, 2007; 17(12): 1743 - 1754. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Huang, A. Gusnanto, K. O'Sullivan, J. Staaf, A. Borg, and Y. Pawitan Robust smooth segmentation approach for array CGH data analysis Bioinformatics, September 15, 2007; 23(18): 2463 - 2469. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Barbaro, M. Oscarson, J. Schoumans, J. Staaf, S. A. Ivarsson, and A. Wedell Isolated 46,XY Gonadal Dysgenesis in Two Sisters Caused by a Xp21.2 Interstitial Duplication Containing the DAX1 Gene J. Clin. Endocrinol. Metab., August 1, 2007; 92(8): 3305 - 3313. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Conde, D. Montaner, J. Burguet-Castell, J. Tarraga, I. Medina, F. Al-Shahrour, and J. Dopazo ISACGH: a web-based environment for the analysis of Array CGH and gene expression which includes functional profiling Nucleic Acids Res., July 13, 2007; 35(suppl_2): W81 - W85. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Xing, C. M. T. Greenwood, and S. B. Bull A hierarchical clustering method for estimating copy number variation Biostat., July 1, 2007; 8(3): 632 - 653. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Vincent-Salomon, C. Ganem-Elbaz, E. Manie, V. Raynal, X. Sastre-Garau, D. Stoppa-Lyonnet, M.-H. Stern, and E. Heard X Inactive-Specific Transcript RNA Coating and Genetic Instability of the X Chromosome in BRCA1 Breast Tumors Cancer Res., June 1, 2007; 67(11): 5134 - 5140. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Di Palma, M. B K Lambros, K. Savage, C. Jones, A. Mackay, T. Dexter, M. Iravani, K. Fenwick, A. Ashworth, and J. S Reis-Filho Oncocytic change in pleomorphic adenoma: molecular evidence in support of an origin in neoplastic cells J. Clin. Pathol., May 1, 2007; 60(5): 492 - 499. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Tischkowitz, B. Xia, N. Sabbaghian, J. S. Reis-Filho, N. Hamel, G. Li, E. H. van Beers, L. Li, T. Khalil, L. A. Quenneville, et al. Analysis of PALB2/FANCN-associated breast cancer families PNAS, April 17, 2007; 104(16): 6788 - 6793. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Stjernqvist, T. Ryden, M. Skold, and J. Staaf Continuous-index hidden Markov modelling of array CGH copy number data Bioinformatics, April 15, 2007; 23(8): 1006 - 1014. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Laframboise, D. Harrington, and B. A. Weir PLASQ: a generalized linear model-based procedure to determine allelic dosage in cancer cells from SNP array data Biostat., April 1, 2007; 8(2): 323 - 336. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Hu, J.-B. Gao, Y. Cao, E. Bottinger, and W. Zhang Exploiting noise in array CGH data to improve detection of DNA copy number change Nucleic Acids Res., March 12, 2007; 35(5): e35 - e35. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. P. Kratz, D. Steinemann, C. M. Niemeyer, B. Schlegelberger, E. Koscielniak, U. Kontny, and M. Zenker Uniparental disomy at chromosome 11p15.5 followed by HRAS mutations in embryonal rhabdomyosarcoma: lessons from Costello syndrome Hum. Mol. Genet., February 15, 2007; 16(4): 374 - 379. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. L. Rosa, E. Viara, P. Hupe, G. Pierron, S. Liva, P. Neuvial, I. Brito, S. Lair, N. Servant, N. Robine, et al. VAMP: Visualization and analysis of array-CGH, transcriptome and other molecular profiles Bioinformatics, September 1, 2006; 22(17): 2066 - 2073. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. A. Engler, G. Mohapatra, D. N. Louis, and R. A. Betensky A pseudolikelihood approach for simultaneous analysis of array comparative genomic hybridizations Biostat., July 1, 2006; 7(3): 399 - 421. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Liva, P. Hupe, P. Neuvial, I. Brito, E. Viara, P. L. Rosa, and E. Barillot CAPweb: a bioinformatics CGH array Analysis Platform. Nucleic Acids Res., July 1, 2006; 34(Web Server issue): W477 - W481. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. C. Marioni, N. P. Thorne, and S. Tavare BioHMM: a heterogeneous hidden Markov model for segmenting array CGH data Bioinformatics, May 1, 2006; 22(9): 1144 - 1146. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Rouveirol, N. Stransky, Ph. Hupe, Ph. L. Rosa, E. Viara, E. Barillot, and F. Radvanyi Computation of recurrent minimal genomic alterations from array-CGH data Bioinformatics, April 1, 2006; 22(7): 849 - 856. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Mendrzyk, A. Korshunov, A. Benner, G. Toedt, S. Pfister, B. Radlwimmer, and P. Lichter Identification of gains on 1q and epidermal growth factor receptor overexpression as independent prognostic markers in intracranial ependymoma. Clin. Cancer Res., April 1, 2006; 12(7): 2070 - 2079. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. E. Stange, B. Radlwimmer, F. Schubert, F. Traub, A. Pich, G. Toedt, F. Mendrzyk, U. Lehmann, R. Eils, H. Kreipe, et al. High-Resolution Genomic Profiling Reveals Association of Chromosomal Aberrations on 1q and 16p with Histologic and Genetic Subgroups of Invasive Breast Cancer Clin. Cancer Res., January 15, 2006; 12(2): 345 - 352. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Willenbrock and J. Fridlyand A comparison study: applying segmentation to array CGH data for downstream analyses Bioinformatics, November 15, 2005; 21(22): 4084 - 4091. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. R. Lai, M. D. Johnson, R. Kucherlapati, and P. J. Park Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data Bioinformatics, October 1, 2005; 21(19): 3763 - 3770. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Y. Kim, S. W. Nam, S. H. Lee, W. S. Park, N. J. Yoo, J. Y. Lee, and Y.-J. Chung ArrayCyGHt: a web application for analysis and visualization of array-CGH data Bioinformatics, May 15, 2005; 21(10): 2554 - 2555. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Bilke, Q.-R. Chen, C. C. Whiteford, and J. Khan Detection of low level genomic alterations by comparative genomic hybridization based on cDNA micro-arrays Bioinformatics, April 1, 2005; 21(7): 1138 - 1145. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. H. C. Eilers and R. X. de Menezes Quantile smoothing of array CGH data Bioinformatics, April 1, 2005; 21(7): 1146 - 1153. [Abstract] [Full Text] [PDF] |
||||














