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Recent papers classified by the tag cgh.

	Integrating chromosomal aberrations and gene expression profiles to dissect rectal tumorigenesis [My Copy] BMC Cancer, Vol. 8, No. 1. (2008), 314. by Esther Lips, Ronald van Eijk, Eelco de Graaf, et al.Jan Oosting, Noel de Miranda, Tom Karsten, Cornelis van de Velde, Paul Eilers, Rob Tollenaar, Tom van Wezel, Hans Morreau posted to tumorigenesis rectal integration expression cgh cancer by dolchan on 2009-10-29 17:10:15 as along with 7 people zufar rdiaz tvanwezel jfr imina ealloza frohike
	Molecular Profiling of Breast Cancer Cell Lines Defines Relevant Tumor Models and Provides a Resource for Cancer Gene Discovery [My Copy] PLoS ONE, Vol. 4, No. 7. (3 July 2009), e6146. by Jessica Kao, Keyan Salari, Melanie Bocanegra, et al.Yoon-La Choi, Luc Girard, Jeet Gandhi, Kevin A. Kwei, Tina Hernandez-Boussard, Pei Wang, Adi F. Gazdar, John D. Minna, Jonathan R. Pollack posted to lines comparison cgh cell by eshirdel on 2009-10-25 15:49:20 as along with 2 people tonamswish chrisamiller
	Accurate confidence aware clustering of array CGH tumor profiles. [My Copy] Bioinformatics (Oxford, England) (21 October 2009), btp603. by Bart P. van Houte, Jaap Heringa posted to cgh by shigepong on 2009-10-24 14:30:29 as along with 1 person frohike
	Integrated Analysis of Copy Number Alterations and Gene Expression: A Bivariate Assessment of Equally Directed Abnormalities [My Copy] Bioinformatics (14 October 2009), btp592. by Martin Schafer, Holger Schwender, Sylvia Merk, Claudia Haferlach, Katja Ickstadt, Martin Dugas posted to integration expression cnv cgh by rdiaz on 2009-10-15 16:56:24 as
	Computation of recurrent minimal genomic alterations from array-CGH data [My Copy] Bioinformatics, Vol. 22, No. 7. (1 April 2006), pp. 849-856. by C. Rouveirol, N. Stransky, Ph Hupe, et al.Ph Rosa, E. Viara, E. Barillot, F. Radvanyi posted to tool pattern mining dna_copy data cgh bioinformatics analysis by dolchan on 2009-10-13 18:58:14 as along with 1 person stharward
	Model-based clustering of array CGH data [My Copy] Bioinformatics, Vol. 25, No. 12. (15 June 2009), pp. i30-38. by Sohrab P. Shah, K-John Cheung, Nathalie A. Johnson, et al.Guillaume Alain, Randy D. Gascoyne, Douglas E. Horsman, Raymond T. Ng, Kevin P. Murphy posted to tool number hidden_markov_model dna_copy copy clustering change cgh bioinformatics by dolchan on 2009-10-13 18:48:12 as along with 4 people jonilaserson rdiaz kdpreter nuin
	Recent advances in array comparative genomic hybridization technologies and their applications in human genetics. [My Copy] European journal of human genetics : EJHG, Vol. 14, No. 2. (February 2006), pp. 139-148. by William W. Lockwood, Raj Chari, Bryan Chi, Wan L. Lam posted to cgh by giovenko on 2009-10-10 13:42:51 as along with 1 person and 1 group rdiaz Bioinformatics
	Analysis of Array-CGH Data Using the R and Bioconductor Software Suite. [My Copy] Comparative and functional genomics (2009) by Winfried A. Hofmann, Anja Weigmann, Marcel Tauscher, et al.Britta Skawran, Tim Focken, Reena Buurman, Luzie U. Wingen, Brigitte Schlegelberger, Doris Steinemann posted to cgh by giovenko on 2009-10-10 13:40:55 as along with 3 people and 1 group shikin rdiaz jandot Journal picks
	A sequence-level map of chromosomal breakpoints in the MCF-7 breast cancer cell line yields insights into the evolution of a cancer genome [My Copy] Genome Research, Vol. 19, No. 2. (9 February 2009), pp. 167-177. by Oliver A. Hampton, Petra Den Hollander, Christopher A. Miller, et al.David A. Delgado, Jian Li, Cristian Coarfa, Ronald A. Harris, Stephen Richards, Steven E. Scherer, Donna M. Muzny, Richard A. Gibbs, Adrian V. Lee, Aleksandar Milosavljevic posted to sequenc next-gen cgh by burak on 2009-10-08 06:16:44 as along with 6 people and 2 groups chrisamiller myzhang jiezhou renatomilani songpku Zephyrus Roswell Cancer Crosstalk Breast Cancer Reading Club
	Array comparative genomic hybridization copy number profiling: a new tool for translational research in solid malignancies. [My Copy] Seminars in radiation oncology, Vol. 18, No. 2. (April 2008), pp. 98-104. by José Luis L. Costa, Gerrit Meijer, Bauke Ylstra, Carlos Caldas posted to translational classification cgh by rdiaz on 2009-10-01 15:26:23 as along with 1 person abhattac
	BAC array CGH distinguishes mutually exclusive alterations that define clinicogenetic subtypes of gliomas. [My Copy] International journal of cancer. Journal international du cancer, Vol. 122, No. 8. (15 April 2008), pp. 1778-1786. by Ahmed Idbaih, Yannick Marie, Carlo Lucchesi, et al.Gaëlle Pierron, Elodie Manié, Virginie Raynal, Véronique Mosseri, Khê Hoang-Xuan, Michèle Kujas, Isabel Brito, Karima Mokhtari, Marc Sanson, Emmanuel Barillot, Alain Aurias, Jean-Yves Y. Delattre, Olivier Delattre posted to example classification cgh by rdiaz on 2009-10-01 15:24:32 as along with 1 person kdpreter
	Array comparative genome hybridization for tumor classification and gene discovery in mouse models of malignant melanoma. [My Copy] Cancer research, Vol. 63, No. 17. (1 September 2003), pp. 5352-5356. by Rónán C. O'Hagan, Cameron W. Brennan, Andrew Strahs, et al.Xuegong Zhang, Karuppiah Kannan, Melissa Donovan, Craig Cauwels, Norman E. Sharpless, Wing Hung H. Wong, Lynda Chin posted to example classification cgh by rdiaz on 2009-10-01 15:21:50 as
	Detection of recurrent copy number alterations in the genome: taking among-subject heterogeneity seriously [My Copy] BMC Bioinformatics, Vol. 10, No. 1. (23 September 2009), 308. by Oscar Rueda, Ramon D. Uriarte posted to recurrent common cnv cgh acgh by rdiaz on 2009-10-01 11:10:47 as along with 1 person frohike
	Genomic profiling distinguishes familial multiple and sporadic multiple meningiomas [My Copy] BMC Medical Genomics, Vol. 2, No. 1. (2009), 42. by Yiping Shen, Fabio Nunes, Anat S. Rachamimov, et al.Marianne James, Gayatry Mohapatra, Scott Plotkin, Rebecca Betensky, David Engler, Jennifer Roy, Vijaya Ramesh, James Gusella posted to regions instability common cnv classification chromosomal cgh acgh by rdiaz on 2009-10-01 09:26:22 as
	A Latent Class Model with Hidden Markov Dependence for Array CGH Data. [My Copy] Biometrics, Vol. 9999, No. 9999. (7 April 2009) by Stacia M. Desantis, E. Andrés Houseman, Brent A. Coull, David N. Louis, Gayatry Mohapatra, Rebecca A. Betensky posted to hmm cnv classification cgh acgh by rdiaz on 2009-09-28 17:26:48 as along with 1 person kdpreter
	Comparative genomic hybridization: uses and limitations. [My Copy] Seminars in hematology, Vol. 37, No. 4. (October 2000), pp. 348-357. by P. Lichter, S. Joos, M. Bentz, S. Lampel posted to microarray comparative-genomic-hybridization cgh by bertelsen on 2009-09-28 16:12:17 as
	Oligonucleotide Array-CGH Identifies Genomic Subgroups and Prognostic Markers for Tumor Stage Mycosis Fungoides [My Copy] J Invest Dermatol (17 September 2009) by Rocio Salgado, Octavio Servitje, Fernando Gallardo, et al.Maarten H. Vermeer, Pablo L. Ortiz-Romero, Maria B. Karpova, Marie C. Zipser, Cristina Muniesa, Maria P. Garcia-Muret, Teresa Estrach, Marta Salido, Julia Sanchez-Schmidt, Marta Herrera, Vicenc Romagosa, Javier Suela, Bibiana I. Ferreira, Juan C. Cigudosa, Carlos Barranco, Sergio Serrano, Reinhard Dummer, Cornelis P. Tensen, Francesc Sole, Ramon M. Pujol, Blanca Espinet posted to survival stability region instability genomic example common cgh acgh by rdiaz on 2009-09-28 15:19:34 as
	High Resolution Genome-Wide Analysis of Chromosomal Alterations in Burkitt's Lymphoma [My Copy] PLoS ONE, Vol. 4, No. 9. (17 September 2009), e7089. by Saloua Toujani, Philippe Dessen, Nathalie Ithzar, et al.Gisèle Danglot, Catherine Richon, Yegor Vassetzky, Thomas Robert, Vladimir Lazar, Jacques Bosq, Lydie Da Costa, Christine Pérot, Vincent Ribrag, Catherine Patte, Jöelle Wiels, Alain Bernheim posted to region recurrent mcr example common cgh by rdiaz on 2009-09-28 11:21:53 as
	Integrative clustering of multiple genomic data types using a joint latent variable model with application to breast and lung cancer subtype analysis [My Copy] Bioinformatics, Vol. 25, No. 22. (15 November 2009), pp. 2906-2912. by Ronglai Shen, Adam B. Olshen, Marc Ladanyi posted to integrative integration expression cnv cluster cgh by rdiaz on 2009-09-17 11:19:37 as along with 1 person dswan
	Submicroscopic genomic alterations in Silver-Russell syndrome and Silver-Russell-like patients. [My Copy] Journal of medical genetics (14 September 2009) by Sara Bruce, Katariina Hannula-Jouppi, Mari Puoskari, et al.Ingegerd Fransson, Kalle Oj O. Simola, Marita Lipsanen-Nyman, Juha Kere posted to srs microarray human epigenetics disease cgh affymetrix by rschulz on 2009-09-16 12:44:58 as along with 1 person Terkko
	Algorithms for Calling Gains and Losses in Array CGH Data. [My Copy] Methods in molecular biology (Clifton, N.J.), Vol. 556 (2009), pp. 99-116. by Pei Wang posted to review method cgh by rdiaz on 2009-09-15 17:56:27 as along with 1 person shikin
	Comparative Genomic Hybridization on BAC Arrays. [My Copy] Methods in molecular biology (Clifton, N.J.), Vol. 556 (2009), pp. 7-19. by Bradley P. Coe, William W. Lockwood, Raj Chari, Wan L. Lam posted to review cgh bac by rdiaz on 2009-09-15 17:48:27 as
	Comparative genomic hybridization on spotted oligonucleotide microarrays. [My Copy] Methods in molecular biology (Clifton, N.J.), Vol. 556 (2009), pp. 21-32. by Young H. Kim, Jonathan R. Pollack posted to review oligonucleotide cgh by rdiaz on 2009-09-15 17:48:07 as
	High-throughput Multiplex Sequencing to Discover Copy Number Variants in Drosophila [My Copy] Genetics, Vol. 182, No. 4. (15 June 2009), pp. genetics.109.103218-941. by Bryce Daines, Hui Wang, Yumei Li, Yi Han, Richard Gibbs, Rui Chen posted to sequencing number copy cgh by rdiaz on 2009-09-11 10:50:39 as along with 1 person operon
	A network model of a cooperative genetic landscape in brain tumors. [My Copy] JAMA : the journal of the American Medical Association, Vol. 302, No. 3. (15 July 2009), pp. 261-275. by Markus Bredel, Denise M. Scholtens, Griffith R. Harsh, et al.Claudia Bredel, James P. Chandler, Jaclyn J. Renfrow, Ajay K. Yadav, Hannes Vogel, Adrienne C. Scheck, Robert Tibshirani, Branimir I. Sikic posted to network landscape expression cnv cgh by rdiaz on 2009-09-09 12:58:51 as along with 3 people srp33 burak daforerog
	Hybridization modeling of oligonucleotide SNP arrays for accurate DNA copy number estimation. [My Copy] Nucleic acids research (7 July 2009), gkp559. by Lin Wan, Kelian Sun, Qi Ding, et al.Yuehua Cui, Ming Li, Yalu Wen, Robert C. Elston, Minping Qian, Wenjiang J. Fu posted to snp modeling cgh by rdiaz on 2009-09-09 12:56:11 as along with 2 people pkonings guhjy
	Transcriptional landscape estimation from tiling array data using a model of signal shift and drift. [My Copy] Bioinformatics (Oxford, England), Vol. 25, No. 18. (15 September 2009), pp. 2341-2347. by Pierre Nicolas, Aurélie Leduc, Stéphane Robin, Simon Rasmussen, Hanne Jarmer, Philippe Bessières posted to landscape hmm cgh by rdiaz on 2009-09-07 15:41:10 as along with 1 person humburg
	Identification of significant regional genetic variations using continuous CNV values in aCGH data. [My Copy] Genomics (19 August 2009) by Ki-Yeol Y. Kim, Gui Youn Y. Lee, Jin Kim, Hei-Cheul C. Jeung, Hyun Cheol C. Chung, Sun Young Y. Rha posted to statistics region recurrent common cnv cgh anova by rdiaz on 2009-09-07 14:57:47 as along with 1 person pkonings
	A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery. [My Copy] Human molecular genetics (4 September 2009), ddp413. by Anna C. Need, Deborah K. Attix, Jill M. McEvoy, et al.Elizabeth T. Cirulli, Kristen L. Linney, Priscilla Hunt, Dongliang Ge, Erin L. Heinzen, Jessica M. Maia, Kevin V. Shianna, Michael E. Weale, Lynn F. Cherkas, Gail Clement, Tim D. Spector, Greg Gibson, David B. Goldstein posted to snp example disease cgh association by rdiaz on 2009-09-07 11:41:51 as along with 1 person daforerog
	Copy Number Variation in Human Health, Disease, and Evolution [My Copy] Annual Review of Genomics and Human Genetics, Vol. 10, No. 1. (2009), pp. 451-481. by Feng Zhang, Wenli Gu, Matthew E. Hurles, James R. Lupski posted to review cnv cgh by rdiaz on 2009-09-03 14:01:38 as along with 2 people sf11 scmelton
	Personalized copy number and segmental duplication maps using next-generation sequencing [My Copy] Nat Genet, Vol. 41, No. 10. (30 August 2009), pp. 1061-1067. by Can Alkan, Jeffrey M. Kidd, Tomas Marques-Bonet, et al.Gozde Aksay, Francesca Antonacci, Fereydoun Hormozdiari, Jacob O. Kitzman, Carl Baker, Maika Malig, Onur Mutlu, S. Cenk Sahinalp, Richard A. Gibbs, Evan E. Eichler posted to sequencing cnv cgh acgh by rdiaz on 2009-09-03 14:01:24 as along with 28 people and 1 group leemachado daed gbenson n00c bozdagd dakelley sbmontgomery eshirdel merpublic shyamsg scmelton qayub natstreet fenghezi Annab djkt nuin xingxu jamesmorris brant torfinnnome jandot pkonings danmaclean daforerog frohike rschulz gangcai Journal picks
	CGHnormaliter: an iterative strategy to enhance normalization of array CGH data with imbalanced aberrations [My Copy] BMC Genomics, Vol. 10, No. 1. (26 August 2009), 401. by Bart van Houte, Thomas Binsl, Hannes Hettling, Walter Pirovano, Jaap Heringa posted to normalization cgh acgh by rdiaz on 2009-09-03 14:00:27 as
	A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2 [My Copy] Nat Genet, Vol. 41, No. 9. (September 2009), pp. 996-1000. by Honglin Song, Susan J. Ramus, Jonathan Tyrer, et al.Kelly L. Bolton, Aleksandra Gentry-Maharaj, Eva Wozniak, Hoda Anton-Culver, Jenny Chang-Claude, Daniel W. Cramer, Richard Dicioccio, Thilo Dork, Ellen L. Goode, Marc T. Goodman, Joellen M. Schildkraut, Thomas Sellers, Laura Baglietto, Matthias W. Beckmann, Jonathan Beesley, Jan Blaakaer, Michael E. Carney, Stephen Chanock, Zhihua Chen, Julie M. Cunningham, Ed Dicks, Jennifer A. Doherty, Matthias Durst, Arif B. Ekici, David Fenstermacher, Brooke L. Fridley, Graham Giles, Martin E. Gore, Immaculata De Vivo, Peter Hillemanns, Claus Hogdall, Estrid Hogdall, Edwin S. Iversen, Ian J. Jacobs, Anna Jakubowska, Dong Li, Jolanta Lissowska, Jan Lubinski, Galina Lurie, Valerie Mcguire, John Mclaughlin, Krzysztof Medrek, Patricia G. Moorman, Kirsten Moysich, Steven Narod, Catherine Phelan, Carole Pye, Harvey Risch, Ingo B. Runnebaum, Gianluca Severi, Melissa Southey, Daniel O. Stram, Falk C. Thiel, Kathryn L. Terry, Ya-Yu Tsai, Shelley S. Tworoger, David J. Van Den Berg, Robert A. Vierkant, Shan Wang-Gohrke, Penelope M. Webb, Lynne R. Wilkens, Anna H. Wu, Hannah Yang, Wendy Brewster, Argyrios Ziogas, Richard Houlston, Ian Tomlinson, Alice S. Whittemore, Mary A. Rossing, Bruce A. J. Ponder, Celeste L. Pearce, Roberta B. Ness, Usha Menon, Susanne K. Kjaer, Jacek Gronwald, Montserrat Garcia-Closas, Peter A. Fasching, Douglas F. Easton, Georgia Chenevix-Trench, Andrew Berchuck, Paul D. P. Pharoah, Simon A. Gayther posted to uk snp ovarian_cancer gwas cgh by frohike on 2009-08-27 11:38:31 as along with 1 person jamesmorris
	Cancer gene discovery in mouse and man [My Copy] Biochimica et Biophysica Acta (BBA) - Reviews on Cancer (12 March 2009) by Jenny Mattison, Louise van der Weyden, Tim Hubbard, David J. Adams posted to rjacgh review examples cgh cancer by rdiaz on 2009-08-21 17:15:10 as along with 1 person timhubbard
	Aneuploidy prediction and tumor classification with heterogeneous hidden conditional random fields [My Copy] Bioinformatics, Vol. 25, No. 10. (15 May 2009), pp. 1307-1313. by Zafer Barutcuoglu, Edoardo M. Airoldi, Vanessa Dumeaux, Robert E. Schapire, Olga G. Troyanskaya posted to recurrent markov hmm field disease cgh association by rdiaz on 2009-08-21 15:34:00 as along with 3 people jfr pkonings Zephyrus
	RJaCGH: Bayesian analysis of aCGH arrays for detecting copy number changes and recurrent regions [My Copy] Bioinformatics, Vol. 25, No. 15. (1 August 2009), pp. 1959-1960. by Oscar M. Rueda, Ramon Diaz-Uriarte posted to rjacgh hmm cgh bayesian by rdiaz on 2009-08-21 11:52:04 as along with 2 people and 1 group Stew nuin Bioinformatics - CRUK
	SnoopCGH: software for visualizing comparative genomic hybridization data [My Copy] Bioinformatics, Vol. 25, No. 20. (15 October 2009), pp. 2732-2733. by Jacob Almagro-Garcia, Magnus Manske, Celine Carret, et al.Susana Campino, Sarah Auburn, Bronwyn L. MacInnis, Gareth Maslen, Arnab Pain, Christopher I. Newbold, Dominic P. Kwiatkowski, Taane G. Clark posted to visualization cgh by nuin on 2009-08-20 22:21:27 as along with 3 people and 1 group jandot rdiaz pkonings Journal picks
	MicroRNA Expression, Chromosomal Alterations, and Immunoglobulin Variable Heavy Chain Hypermutations in Mantle Cell Lymphomas [My Copy] Cancer Res, Vol. 69, No. 17. (1 September 2009), pp. 7071-7078. by Alba Navarro, Silvia Bea, Veronica Fernandez, et al.Miriam Prieto, Itziar Salaverria, Pedro Jares, Elena Hartmann, Anna Mozos, Armando Lopez-Guillermo, Neus Villamor, Dolors Colomer, Xavier Puig, German Ott, Francesc Sole, Sergi Serrano, Andreas Rosenwald, Elias Campo, Luis Hernandez posted to mirna microrna cgh by rdiaz on 2009-08-20 10:27:09 as along with 1 person wmatsui
	Hidden Markov models for the assessment of chromosomal alterations using high-throughput SNP arrays. [My Copy] The annals of applied statistics, Vol. 2, No. 2. (1 June 2008), pp. 687-713. by Robert B. Scharpf, Giovanni Parmigiani, Jonathan Pevsner, Ingo Ruczinski posted to snp hmm cnv cgh by rdiaz on 2009-08-18 19:35:04 as
	Integrating sequencing technologies in personal genomics: optimal low cost reconstruction of structural variants. [My Copy] PLoS computational biology, Vol. 5, No. 7. (10 July 2009), e1000432. by Jiang Du, Robert D. Bjornson, Zhengdong D. Zhang, Yong Kong, Michael Snyder, Mark B. Gerstein posted to sequencing cnv cgh by rdiaz on 2009-08-18 17:38:11 as along with 5 people operon nuin natstreet dakelley guhjy
	A continuous-index hidden Markov jump process for modeling DNA copy number data [My Copy] Biostat, Vol. 10, No. 4. (1 October 2009), pp. 773-778. by Susann Stjernqvist, Tobias Ryden posted to hmm cgh by rdiaz on 2009-08-18 17:01:44 as along with 1 person djkt
	Oncogenic Activating Mutations Are Associated with Local Copy Gain [My Copy] Molecular Cancer Research (11 August 2009) by Barmak Modrek, Lin Ge, Ajay Pandita, et al.Eva Lin, Sankar Mohan, Peng Yue, Steve Guerrero, William M. Lin, Thinh Pham, Zora Modrusan, Somasekar Seshagiri, Howard M. Stern, Paul Waring, Levi A. Garraway, John Chant, David Stokoe, Guy Cavet posted to teaching phenotype examples cgh cancer by rdiaz on 2009-08-18 13:55:19 as
	A hypergraph-based learning algorithm for classifying gene expression and arrayCGH data with prior knowledge [My Copy] Bioinformatics, Vol. 25, No. 21. (1 November 2009), pp. 2831-2838. by Ze Tian, TaeHyun Hwang, Rui Kuang posted to cgh software by guhjy on 2009-08-09 05:39:23 as along with 5 people tmmurali dolchan rdiaz pkonings nuin
	High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications [My Copy] Genome Research, Vol. 19, No. 9. (10 September 2009), pp. 1682-1690. by Tamim H. Shaikh, Xiaowu Gai, Juan C. Perin, et al.Joseph T. Glessner, Hongbo Xie, Kevin Murphy, Ryan O'Hara, Tracy Casalunovo, Laura K. Conlin, Monica D'Arcy, Edward C. Frackelton, Elizabeth A. Geiger, Chad Haldeman-Englert, Marcin Imielinski, Cecilia E. Kim, Livija Medne, Kiran Annaiah, Jonathan P. Bradfield, Elvira Dabaghyan, Andrew Eckert, Chioma C. Onyiah, Svetlana Ostapenko, F. George Otieno, Erin Santa, Julie L. Shaner, Robert Skraban, Ryan M. Smith, Josephine Elia, Elizabeth Goldmuntz, Nancy B. Spinner, Elaine H. Zackai, Rosetta M. Chiavacci, Robert Grundmeier, Eric F. Rappaport, Struan F. A. Grant, Peter S. White, Hakon Hakonarson posted to for:pkonings databases database_genomic_variants copy_number_variation cnv cgh by frohike on 2009-08-06 10:07:27 as along with 7 people rdiaz pkonings ericrpaquet jandot guhjy vplagnol daforerog
	Discovering Combinations of Genomic Aberrations Associated With Cancer [My Copy] Journal of the American Statistical Association, Vol. 97, No. 460. (December 2002), pp. 931-942. by Michael A. Newton posted to copy-number computational cgh cancer by stharward on 2009-07-23 17:33:51 as along with 1 person srp33
	Representational Oligonucleotide Microarray Analysis: A High-Resolution Method to Detect Genome Copy Number Variation [My Copy] Genome Research, Vol. 13, No. 10. (October 2003), pp. 2291-2305. by Robert Lucito, John Healy, Joan Alexander, et al.Andrew Reiner, Diane Esposito, Maoyen Chi, Linda Rodgers, Amy Brady, Jonathan Sebat, Jennifer Troge, Joseph A. West, Seth Rostan, Ken C. Q. Nguyen, Scott Powers, Kenneth Q. Ye, Adam Olshen, Ennapadam Venkatraman, Larry Norton, Michael Wigler posted to copy-number cgh cancer by stharward on 2009-07-23 17:31:18 as along with 4 people oilcan rdiaz bioguru2000 joule
	Copy number variations and cancer. [My Copy] Genome medicine, Vol. 1, No. 6. (2009) by A. Shlien, D. Malkin posted to cancer cgh cnv review by rdiaz on 2009-07-23 15:50:19 as
	Population Analysis of Large Copy Number Variants and Hotspots of Human Genetic Disease [My Copy] Vol. 84, No. 2. (13 February 2009), pp. 148-161. by Andy Itsara, Gregory M. Cooper, Carl Baker, et al.Santhosh Girirajan, Jun Li, Devin Absher, Ronald M. Krauss, Richard M. Myers, Paul M. Ridker, Daniel I. Chasman, Heather Mefford, Phyllis Ying, Deborah A. Nickerson, Evan E. Eichler posted to cgh hotspot population variation by rdiaz on 2009-07-23 15:21:54 as
	Unsupervised segmentation of continuous genomic data. [My Copy] Bioinformatics (Oxford, England), Vol. 23, No. 11. (1 June 2007), pp. 1424-1426. by Nathan Day, Andrew Hemmaplardh, Robert E. Thurman, John A. Stamatoyannopoulos, William S. Noble posted to cgh segmentation by rdiaz on 2009-07-23 15:10:47 as along with 4 people and 3 groups polivares Eroslavochka waszak ealloza JLab BergmanLab BioinfoCIPF
	PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data [My Copy] Genome Research, Vol. 17, No. 11. (5 November 2007), pp. 1665-1674. by Kai Wang, Mingyao Li, Dexter Hadley, et al.Rui Liu, Joseph Glessner, Struan F. A. Grant, Hakon Hakonarson, Maja Bucan posted to acgh cgh penncnv snp by rdiaz on 2009-07-20 18:01:49 as along with 2 people vplagnol jfr

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cancer	66
cnv	50
microarray	34
expression	28
review	25
acgh	16
breast	16
human	16
analysis	15
array	15
thelist	15
aberration	14
hmm	14
recurrent	13
chromosome	12
copy-number	12
software	12
common	11
integration	11
classification	10
algorithm	9
copy	9
copy_number	9
heterogeneity	9
number	9
database	8
snp	8
superlist	8
normalization	7
cytogenetics	6
dcis	6
example	6
fish	6
methods	6
r	6
rearrangement	6
statistics	6
bioinformatics	5
clinical	5
clustering	5
data-preprocessing	5
genomic	5
sequencing	5
amplification	4
chromosomal	4
cnp	4
computational	4
data	4
disease	4
dna_copy	4
genetic	4
iims	4
instability	4
karyotype	4
method	4
pre-malignant	4
region	4
regions	4
rjacgh	4
segmentation	4
tool	4
17	3
20q	3
affymetrix	3
application	3
arraycgh	3
change	3
gene	3
genetics	3
gwas	3
integrative	3
loh	3
mcr	3
meta_analysis	3
microrna	3
mouse	3
neuroblastoma	3
oncogenetic	3
primer	3
resolution	3
snps	3
stratification	3
tiling	3
tree	3
tumour	3
variation	3
16q	2
association	2
benchmark	2
characterization	2
comparative-genomic-hybridization	2
cross-platform	2
embedded	2
estimation	2
lcis	2
mapping	2
sky	2
tiling-array	2
translational	2
worms	2

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