Tag cnv [at least 200 articles] Export

Recent papers classified by the tag cnv.

	Human genome variation and pharmacogenetics [My Copy] Human Mutation, Vol. 29, No. 4. (2008), pp. 453-455. by Bruce Gottlieb posted to variation pharmacogenetics genome cnv cancer by songpku on 2009-11-08 02:17:31 as
	Copy number variation and disease. Preface. [My Copy] Cytogenetic and genome research, Vol. 123, No. 1-4. (2008), pp. 5-6. by Hildegard Kehrer-Sawatzki, David N. Cooper posted to treatment pharamacogenetics cnv cancer by songpku on 2009-11-08 02:12:27 as
	Origins and functional impact of copy number variation in the human genome [My Copy] Nature, Vol. advance online publication (07 October 2009) by Donald F. Conrad, Dalila Pinto, Richard Redon, et al.Lars Feuk, Omer Gokcumen, Yujun Zhang, Jan Aerts, T. Daniel Andrews, Chris Barnes, Peter Campbell, Tomas Fitzgerald, Min Hu, Chun H. Ihm, Kati Kristiansson, Daniel G. MacArthur, Jeffrey R. MacDonald, Ifejinelo Onyiah, Andy W. Pang, Sam Robson, Kathy Stirrups, Armand Valsesia, Klaudia Walter, John Wei, Chris Tyler-Smith, Nigel P. Carter, Charles Lee, Stephen W. Scherer, Matthew E. Hurles posted to methods genomics genetics cnv by psique on 2009-11-05 13:02:47 as along with 16 people and 1 group chvlyl daed daforerog zufar jessopher DrRichardBadge operon colinveal frohike sf11 sameersoi polivares dswan qayub bpcusack rdiaz Journal picks
	Global variation in copy number in the human genome [My Copy] Nature, Vol. 444, No. 7118. (23 November 2006), pp. 444-454. by Richard Redon, Shumpei Ishikawa, Karen R. Fitch, et al.Lars Feuk, George H. Perry, T. Daniel Andrews, Heike Fiegler, Michael H. Shapero, Andrew R. Carson, Wenwei Chen, Eun K. Cho, Stephanie Dallaire, Jennifer L. Freeman, Juan R. Gonzalez, Monica Gratacos, Jing Huang, Dimitrios Kalaitzopoulos, Daisuke Komura, Jeffrey R. MacDonald, Christian R. Marshall, Rui Mei, Lyndal Montgomery, Kunihiro Nishimura, Kohji Okamura, Fan Shen, Martin J. Somerville, Joelle Tchinda, Armand Valsesia, Cara Woodwark, Fengtang Yang, Junjun Zhang, Tatiana Zerjal, Jane Zhang, Lluis Armengol, Donald F. Conrad, Xavier Estivill, Chris Tyler-Smith, Nigel P. Carter, Hiroyuki Aburatani, Charles Lee, Keith W. Jones, Stephen W. Scherer, Matthew E. Hurles posted to human genetics cnv by lp2 on 2009-11-05 10:45:01 as along with 40 people and 7 groups ilyashl ajbattle darian jonilaserson jrvalcourt turnersd guhjy daforerog noushin Glires ivanek waszak jo_davies psique bpb jfr balajis pradiptaray dpollard mtagaya adepace aswin rdiaz qfwills ealloza vplagnol giovanni jeremymiller frohike vpschulz raiyar ramensky ccr azazello dbgrant colinveal xingxu srp33 Ema daed parkinson's disease references Bioinformatics EisenLab BioinfoCIPF GeschwindLab steinmetzlab MBLAB
	An Optimization Framework for Unsupervised Identification of Rare Copy Number Variation from SNP Array Data [My Copy] Genome Biology, Vol. 10, No. 10. (22 October 2009), R119. by Gokhan Yavas, Mehmet Koyuturk, Meral Ozsoyoglu, Meetha Gould, Thomas LaFramboise posted to statistics methods genomics cnv by merpublic on 2009-11-04 19:35:06 as
	The theory of discovering rare variants via DNA sequencing [My Copy] BMC Genomics, Vol. 10, No. 1. (2009), 485. by Michael Wendl, Richard Wilson posted to solexa snp-calling short-read-mapping cnv by jasontsai on 2009-11-04 14:07:22 as along with 4 people jsatkosk merpublic n00c druvus
	Defensins and the dynamic genome: what we can learn from structural variation at human chromosome band 8p23.1. [My Copy] Genome research, Vol. 18, No. 11. (November 2008), pp. 1686-1697. by Edward J. Hollox, John C. Barber, Anthony J. Brookes, John A. Armour posted to human_adaptation evolution cnv by sameersoi on 2009-11-04 05:54:43 as
	CNV-seq, a new method to detect copy number variation using high-throughput sequencing. [My Copy] BMC bioinformatics, Vol. 10, No. 1. (2009), 80. by Chao Xie, Martti T. Tammi posted to whole-genome-seq nextgen cnv bioinformatics by stubrown on 2009-11-03 16:26:43 as along with 16 people and 1 group cthachuk GustavoLacerda n00c darian bmenten natstreet sameersoi svenrahmann xiechao semrich pkonings rdiaz dswan sleepingcell neils magusina Bioinformatics
	A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology. [My Copy] Cytogenetic and genome research, Vol. 124, No. 1. (2009), pp. 94-101. by B. A. Talseth-Palmer, N. A. Bowden, C. Meldrum, et al.J. Nicholl, E. Thompson, K. Friend, J. Liebelt, D. Bratkovic, E. Haan, S. Yu, R. J. Scott posted to translocation snp-chip snp mutations genotyping deletions cnv bioinformatics by stubrown on 2009-11-03 16:21:23 as
	Computational methods for discovering structural variation with next-generation sequencing [My Copy] Nature Methods, Vol. 6, No. 11s. (15 October 2009), pp. S13-S20. by Paul Medvedev, Monica Stanciu, Michael Brudno posted to statistics sequencing cnv by sameersoi on 2009-11-03 16:15:29 as along with 9 people and 1 group jasontsai heliopais druvus GeeSharpMinor Peiyong n00c gdv desany qayub Journal picks
	Rapid identification of homologous recombinants and determination of gene copy number with reference/query pyrosequencing (RQPS) [My Copy] Genome Research, Vol. 19, No. 11. (November 2009), pp. 2081-2089. by Zhenyi Liu, Anna C. Obenauf, Michael R. Speicher, Raphael Kopan posted to sequencing cnv by sameersoi on 2009-11-02 19:37:05 as
	Ultrasome: efficient aberration caller for copy number studies of ultra-high resolution. [My Copy] Bioinformatics (Oxford, England), Vol. 25, No. 8. (15 April 2009), pp. 1078-1079. by Björn Nilsson, Mikael Johansson, Fatima Al-Shahrour, Anne E. Carpenter, Benjamin L. Ebert posted to segmentation cnv by daed on 2009-11-02 13:40:50 as along with 3 people jfr rdiaz pkonings
	Mapping and sequencing of structural variation from eight human genomes [My Copy] Nature, Vol. 453, No. 7191. (01 May 2008), pp. 56-64. by Jeffrey M. Kidd, Gregory M. Cooper, William F. Donahue, et al.Hillary S. Hayden, Nick Sampas, Tina Graves, Nancy Hansen, Brian Teague, Can Alkan, Francesca Antonacci, Eric Haugen, Troy Zerr, N. Alice Yamada, Peter Tsang, Tera L. Newman, Eray Tuzun, Ze Cheng, Heather M. Ebling, Nadeem Tusneem, Robert David, Will Gillett, Karen A. Phelps, Molly Weaver, David Saranga, Adrianne Brand, Wei Tao, Erik Gustafson, Kevin McKernan, Lin Chen, Maika Malig, Joshua D. Smith, Joshua M. Korn, Steven A. McCarroll, David A. Altshuler, Daniel A. Peiffer, Michael Dorschner, John Stamatoyannopoulos, David Schwartz, Deborah A. Nickerson, James C. Mullikin, Richard K. Wilson, Laurakay Bruhn, Maynard V. Olson, Rajinder Kaul, Douglas R. Smith, Evan E. Eichler posted to variant structure sequencing mapping genome cnv by n00c on 2009-10-30 19:28:05 as along with 34 people and 2 groups daed fstrozzi sameersoi jonilaserson ilyashl rdiaz dakelley xingxu alweber APRegier Annab smiddha daforerog vkwn frohike waszak matthewsuderman jfr hpaces Ema bpb dchughes djkt balicea shikin psique kintoki kaniko aprasad vplagnol maximilianh chrisamiller guhjy skoch3 GeneGo Koch_Lab
	Screening for copy-number alterations and loss of heterozygosity in chronic lymphocytic leukemia--a comparative study of four differently designed, high resolution microarray platforms. [My Copy] Genes, chromosomes & cancer, Vol. 47, No. 8. (August 2008), pp. 697-711. by Rebeqa Gunnarsson, Johan Staaf, Mattias Jansson, et al.Anne Marie M. Ottesen, Hanna Göransson, Ulrika Liljedahl, Ulrik Ralfkiaer, Mahmoud Mansouri, Anne Mette M. Buhl, Karin Ekström E. Smedby, Henrik Hjalgrim, Ann-Christine C. Syvänen, Ake Borg, Anders Isaksson, Jesper Jurlander, Gunnar Juliusson, Richard Rosenquist posted to snp illumina cnv affy by shikin on 2009-10-29 18:51:56 as along with 1 person jfr
	High-resolution analysis of copy number alterations and associated expression changes in ovarian tumors. [My Copy] BMC medical genomics, Vol. 2 (2009) by Peter M. Haverty, Lawrence S. Hon, Joshua S. Kaminker, John Chant, Zemin Zhang posted to expression cnv cancer by daed on 2009-10-29 14:23:34 as along with 1 person rdiaz
	Personalized copy number and segmental duplication maps using next-generation sequencing. [My Copy] Nature genetics, Vol. 41, No. 10. (30 October 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 seq cnv by daed on 2009-10-29 11:49:32 as along with 28 people and 1 group leemachado gbenson n00c bozdagd dakelley sbmontgomery eshirdel merpublic shyamsg scmelton qayub natstreet fenghezi Annab djkt nuin xingxu jamesmorris rdiaz brant torfinnnome jandot pkonings danmaclean daforerog frohike rschulz gangcai Journal picks
	Statistical issues in the analysis of DNA Copy Number Variations. [My Copy] International journal of computational biology and drug design, Vol. 1, No. 4. (1 January 2008), pp. 368-395. by Nathan E. Wineinger, Richard E. Kennedy, Stephen W. Erickson, Mary K. Wojczynski, Carl E. Bruder, Hemant K. Tiwari posted to statistics cnv by shikin on 2009-10-28 14:14:31 as
	Comparison of comparative genomic hybridization technologies across microarray platforms. [My Copy] Journal of biomolecular techniques : JBT, Vol. 20, No. 2. (April 2009), pp. 135-151. by Susan D. Hester, Laura Reid, Norma Nowak, et al.Wendell D. Jones, Joel S. Parker, Kevin Knudtson, William Ward, Jay Tiesman, Nancy D. Denslow posted to cnv by shikin on 2009-10-27 17:49:24 as along with 2 people rdiaz idonaldson
	A single-array preprocessing method for estimating full-resolution raw copy numbers from all Affymetrix genotyping arrays including GenomeWideSNP 5 & 6. [My Copy] Bioinformatics (Oxford, England), Vol. 25, No. 17. (1 September 2009), pp. 2149-2156. by Henrik Bengtsson, Pratyaksha Wirapati, Terence P. Speed posted to snp r cnv affy by shikin on 2009-10-27 17:36:28 as along with 5 people djkt pkonings rdiaz daforerog neils
	High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping. [My Copy] Genome research, Vol. 16, No. 9. (September 2006), pp. 1136-1148. by Daniel A. Peiffer, Jennie M. Le, Frank J. Steemers, et al.Weihua Chang, Tony Jenniges, Francisco Garcia, Kirt Haden, Jiangzhen Li, Chad A. Shaw, John Belmont, Sau Wai W. Cheung, Richard M. Shen, David L. Barker, Kevin L. Gunderson posted to snp microarray illumina cnv by shikin on 2009-10-27 17:24:03 as along with 3 people baizhang jfr jackjackjjj
	Systematic assessment of copy number variant detection via genome-wide SNP genotyping. [My Copy] Nature genetics, Vol. 40, No. 10. (7 October 2008), pp. 1199-1203. by Gregory M. Cooper, Troy Zerr, Jeffrey M. Kidd, Evan E. Eichler, Deborah A. Nickerson posted to snp microarray cnv by shikin on 2009-10-27 17:23:18 as along with 12 people and 1 group sameersoi daforerog psique maren pengchy vplagnol waszak caseybrown Zephyrus misonneh rdiaz guhjy Roswell Cancer Crosstalk
	Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays. [My Copy] Genome research, Vol. 16, No. 12. (1 December 2006), pp. 1575-1584. by Daisuke Komura, Fan Shen, Shumpei Ishikawa, et al.Karen R. Fitch, Wenwei Chen, Jane Zhang, Guoying Liu, Sigeo Ihara, Hiroshi Nakamura, Matthew E. Hurles, Charles Lee, Stephen W. Scherer, Keith W. Jones, Michael H. Shapero, Jing Huang, Hiroyuki Aburatani posted to snp microarray cnv by shikin on 2009-10-27 16:51:13 as along with 10 people and 4 groups rdiaz waszak jfr dchughes giovanni jeremymiller frohike vpschulz shigepong debasis Bioinformatics G4ID GeschwindLab Genetics-of-Gambling
	Relative Impact of Nucleotide and Copy Number Variation on Gene Expression Phenotypes [My Copy] Science, Vol. 315, No. 5813. (9 February 2007), pp. 848-853. by Barbara E. Stranger, Matthew S. Forrest, Mark Dunning, et al.Catherine E. Ingle, Claude Beazley, Natalie Thorne, Richard Redon, Christine P. Bird, Anna de Grassi, Charles Lee, Chris Tyler-Smith, Nigel Carter, Stephen W. Scherer, Simon Tavare, Panagiotis Deloukas, Matthew E. Hurles, Emmanouil T. Dermitzakis posted to snp phenotype mutation expression_evolution cnv by daveGerrard on 2009-10-27 15:48:48 as along with 31 people and 5 groups lp2 sameersoi timhubbard Zephyrus ajbattle jonilaserson ilyashl emptyhb buyske zufar koller waszak daed psique jo_davies srp33 guhjy jfr dpollard balicea rdiaz qfwills djkt vplagnol shigepong jlangdon xingxu cisevol caseybrown frohike jandot Roswell Cancer Crosstalk Visiting Position Bioinformatics EisenLab cis-regulatory-evolution
	Microduplications of 16p11.2 are associated with schizophrenia [My Copy] Nature Genetics, Vol. 41, No. 11. (25 October 2009), pp. 1223-1227. by Shane E. McCarthy, Vladimir Makarov, George Kirov, et al.Anjene M. Addington, Jon McClellan, Seungtai Yoon, Diana O. Perkins, Diane E. Dickel, Mary Kusenda, Olga Krastoshevsky, Verena Krause, Ravinesh A. Kumar, Detelina Grozeva, Dheeraj Malhotra, Tom Walsh, Elaine H. Zackai, Paige Kaplan, Jaya Ganesh, Ian D. Krantz, Nancy B. Spinner, Patricia Roccanova, Abhishek Bhandari, Kevin Pavon, B. Lakshmi, Anthony Leotta, Jude Kendall, Yoon-ha Lee, Vladimir Vacic, Sydney Gary, Lilia M. Iakoucheva, Timothy J. Crow, Susan L. Christian, Jeffrey A. Lieberman, T. Scott Stroup, Terho Lehtimaki, Kaija Puura, Chad Haldeman-Englert, Justin Pearl, Meredith Goodell, Virginia L. Willour, Pamela DeRosse, Jo Steele, Layla Kassem, Jessica Wolff, Nisha Chitkara, Francis J. McMahon, Anil K. Malhotra, James B. Potash, Thomas G. Schulze, Markus M. Nothen, Sven Cichon, Marcella Rietschel, Ellen Leibenluft, Vlad Kustanovich, Clara M. Lajonchere, James S. Sutcliffe, David Skuse, Michael Gill, Louise Gallagher, Nancy R. Mendell, Nick Craddock, Michael J. Owen, Michael C. O'Donovan, Tamim H. Shaikh, Ezra Susser, Lynn E. DeLisi, Patrick F. Sullivan, Curtis K. Deutsch, Judith Rapoport, Deborah L. Levy, Mary-Claire King, Jonathan Sebat posted to schizophrenia cnv association by vplagnol on 2009-10-27 11:48:46 as along with 2 people dchughes daforerog
	Targeted Interrogation of Copy Number Variation using SCIMMkit. [My Copy] Bioinformatics (Oxford, England) (21 October 2009), btp606. by Troy Zerr, Gregory M. Cooper, Evan E. Eichler, Deborah A. Nickerson posted to population_genetics cnv by sameersoi on 2009-10-26 00:37:23 as along with 2 people and 1 group leemachado ppgardne Journal picks
	Copy number variation in the human genome and its implication in autoimmunity. [My Copy] Clinical and experimental immunology, Vol. 156, No. 1. (April 2009), pp. 12-16. by H. Schaschl, T. J. Aitman, T. J. Vyse posted to cnv by leemachado on 2009-10-22 10:45:46 as along with 6 people shikin sahrazanetti rdiaz noushin Zephyrus pkonings
	An integrated approach for measuring copy number variation at the FCGR3 (CD16) locus. [My Copy] Human mutation, Vol. 30, No. 3. (March 2009), pp. 477-484. by Edward J. Hollox, Jan-Christoph C. Detering, Tushna Dehnugara posted to cnv by leemachado on 2009-10-21 18:25:10 as along with 1 person pkonings
	Oncogene Mutations, Copy Number Gains and Mutant Allele Specific Imbalance (MASI) Frequently Occur Together in Tumor Cells [My Copy] PLoS ONE, Vol. 4, No. 10. (14 October 2009), e7464. by Junichi Soh, Naoki Okumura, William W. Lockwood, et al.Hiromasa Yamamoto, Hisayuki Shigematsu, Wei Zhang, Raj Chari, David S. Shames, Ximing Tang, Calum MacAulay, Marileila Varella-Garcia, Tõnu Vooder, Ignacio I. Wistuba, Stephen Lam, Rolf Brekken, Shinichi Toyooka, John D. Minna, Wan L. Lam, Adi F. Gazdar posted to tumor metastasis integration cnv by rdiaz on 2009-10-15 18:29:34 as
	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
	Integrated study of copy number states and genotype calls using high-density SNP arrays [My Copy] Nucl. Acids Res., Vol. 37, No. 16. (1 September 2009), pp. 5365-5377. by Wei Sun, Fred A. Wright, Zhengzheng Tang, et al.Silje H. Nordgard, Peter V. Loo, Tianwei Yu, Vessela N. Kristensen, Charles M. Perou posted to snp detection cnv array by daed on 2009-10-13 11:47:58 as along with 1 person and 1 group rdiaz Journal picks
	Comparing CNV detection methods for SNP arrays [My Copy] Brief Funct Genomic Proteomic, Vol. 8, No. 5. (8 September 2009), pp. elp017-366. by Laura Winchester, Christopher Yau, Jiannis Ragoussis posted to snp methods detection cnv arrays by daed on 2009-10-13 11:46:04 as along with 2 people jsatkosk rdiaz
	BreakDancer: an algorithm for high-resolution mapping of genomic structural variation [My Copy] Nat Meth, Vol. 6, No. 9. (09 August 2009), pp. 677-681. by Ken Chen, John W. Wallis, Michael D. McLellan, et al.David E. Larson, Joelle M. Kalicki, Craig S. Pohl, Sean D. McGrath, Michael C. Wendl, Qunyuan Zhang, Devin P. Locke, Xiaoqi Shi, Robert S. Fulton, Timothy J. Ley, Richard K. Wilson, Li Ding, Elaine R. Mardis posted to sequencing cnv algorithm by daed on 2009-10-13 11:32:42 as along with 9 people and 1 group dakelley fenghezi natstreet druvus sitalange qayub gdb jasontsai danmaclean Journal picks
	Completing the map of human genetic variation [My Copy] Nature, Vol. 447, No. 7141. (09 May 2007), pp. 161-165. posted to sequencing cnv by daed on 2009-10-13 11:21:17 as along with 5 people and 3 groups guhjy dchughes rdiaz massivemayhem jlangdon Bioinformatics G4ID Genetics-of-Gambling
	A robust statistical method for case-control association testing with copy number variation. [My Copy] Nature genetics, Vol. 40, No. 10. (7 October 2008), pp. 1245-1252. by Chris Barnes, Vincent Plagnol, Tomas Fitzgerald, et al.Richard Redon, Jonathan Marchini, David Clayton, Matthew E. Hurles posted to cnv association by daed on 2009-10-13 11:04:19 as along with 15 people and 1 group zufar daforerog pengchy ptrobajo vplagnol waszak caseybrown Zephyrus dakelley buyske misonneh djkt rdiaz Stew guhjy Roswell Cancer Crosstalk
	Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen [My Copy] The Lancet Neurology, Vol. 7, No. 4. (April 2008), pp. 319-326. by Hylke M. Blauw, Jan H. Veldink, Michael A. van Es, et al.Paul W. van Vught, Christiaan G. J. Saris, Bert van der Zwaag, Lude Franke, Burbach, John H. Wokke, Roel A. Ophoff posted to gwas genomics cnv als by psique on 2009-10-12 11:02:59 as
	DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources [My Copy] Vol. 84, No. 4. (10 April 2009), pp. 524-533. by Helen V. Firth, Shola M. Richards, A. Paul Bevan, et al.Stephen Clayton, Manuel Corpas, Diana Rajan, Steven V. Vooren, Yves Moreau, Roger M. Pettett, Nigel P. Carter posted to genomics database cnv bioinformatics by psique on 2009-10-12 10:49:26 as along with 2 people bmenten pkonings
	Common variants conferring risk of schizophrenia [My Copy] Nature, Vol. 460, No. 7256. (01 July 2009), pp. 744-747. by Hreinn Stefansson, Roel A. Ophoff, Stacy Steinberg, et al.Ole A. Andreassen, Sven Cichon, Dan Rujescu, Thomas Werge, Olli P. H. Pietilainen, Ole Mors, Preben B. Mortensen, Engilbert Sigurdsson, Omar Gustafsson, Mette Nyegaard, Annamari Tuulio-Henriksson, Andres Ingason, Thomas Hansen, Jaana Suvisaari, Jouko Lonnqvist, Tiina Paunio, Anders D. Borglum, Annette Hartmann, Anders Fink-Jensen, Merete Nordentoft, David Hougaard, Bent Norgaard-Pedersen, Yvonne Bottcher, Jes Olesen, Rene Breuer, Hans-Jurgen Moller, Ina Giegling, Henrik B. Rasmussen, Sally Timm, Manuel Mattheisen, Istvan Bitter, Janos M. Rethelyi, Brynja B. Magnusdottir, Thordur Sigmundsson, Pall Olason, MassonGisli, Jeffrey R. Gulcher, Magnus Haraldsson, Ragnheidur Fossdal, Thorgeir E. Thorgeirsson, Unnur Thorsteinsdottir, Mirella Ruggeri, Sarah Tosato, Barbara Franke, Eric Strengman, Lambertus A. Kiemeney, Ingrid Melle, Srdjan Djurovic, Lilia Abramova, Vasily Kaleda, Julio Sanjuan, Rosa de Frutos, Elvira Bramon, Evangelos Vassos, Gillian Fraser, Ulrich Ettinger, Marco Picchioni, Nicholas Walker, Timi Toulopoulou, Anna C. Need, Dongliang Ge, Joeng Lim Yoon, Kevin V. Shianna, Nelson B. Freimer, Rita M. Cantor, Robin Murray, Augustine Kong, Vera Golimbet, Angel Carracedo, Celso Arango, Javier Costas, Erik G. Jonsson, Lars Terenius, Ingrid Agartz, Hannes Petursson, Markus M. Nothen, Marcella Rietschel, Paul M. Matthews, Pierandrea Muglia, Leena Peltonen, David St Clair, David B. Goldstein, Kari Stefansson, David A. Collier posted to schizo gwas genomics cnv by psique on 2009-10-11 11:54:20 as along with 5 people and 1 group pkonings djkt jbhiatt Terkko daforerog Journal picks
	Recurrent copy number alterations in BRCA1-mutated ovarian tumors alter biological pathways. [My Copy] Human mutation (2 October 2009) by Karin Leunen, Olivier Gevaert, Anneleen Daemen, et al.Vanessa Vanspauwen, Geneviève Michils, Bart De Moor, Philippe Moerman, Ignace Vergote, Eric Legius posted to recurrent method hmm example cnv acgh by rdiaz on 2009-10-09 10:06:13 as along with 1 person frohike
	Human genetics: Sharp focus on the variable genome [My Copy] Nature, Vol. 461, No. 7265. (07 October 2009), pp. 735-736. by John A. L. Armour posted to cnv by bpcusack on 2009-10-08 18:19:26 as along with 4 people josepe rdiaz carolep merpublic
	Computational methods for identification of recurrent copy number alteration patterns by array CGH. [My Copy] Cytogenetic and genome research, Vol. 123, No. 1-4. (2008), pp. 343-351. by S. P. Shah posted to cnv by shikin on 2009-10-08 15:24:35 as along with 1 person rdiaz
	Genotype, haplotype and copy-number variation in worldwide human populations. [My Copy] Nature, Vol. 451, No. 7181. (21 February 2008), pp. 998-1003. by Mattias Jakobsson, Sonja W. Scholz, Paul Scheet, et al.J. Raphael Gibbs, Jenna M. VanLiere, Hon-Chung C. Fung, Zachary A. Szpiech, James H. Degnan, Kai Wang, Rita Guerreiro, Jose M. Bras, Jennifer C. Schymick, Dena G. Hernandez, Bryan J. Traynor, Javier Simon-Sanchez, Mar Matarin, Angela Britton, Joyce van de Leemput, Ian Rafferty, Maja Bucan, Howard M. Cann, John A. Hardy, Noah A. Rosenberg, Andrew B. Singleton posted to haplotype gwas genetics epidemiology cnv association by misonneh on 2009-10-07 03:05:13 as along with 15 people and 2 groups vplagnol turnersd daforerog sameersoi psique ilyashl Zephyrus djkt ramensky mailund thomaskelder Archaeogenetics jo_davies guhjy frohike Roswell Cancer Crosstalk Fasting, food and evolution
	Sensitive and accurate detection of copy number variants using read depth of coverage [My Copy] Genome Research, Vol. 19, No. 9. (5 September 2009), pp. 1586-1592. by Seungtai Yoon, Zhenyu Xuan, Vladimir Makarov, Kenny Ye, Jonathan Sebat posted to sequencing coverage cnv by woodson8 on 2009-10-03 15:55:36 as along with 7 people scmelton torfinnnome dakelley n00c rdiaz jbhiatt pkonings
	Complete Resequencing of 40 Genomes Reveals Domestication Events and Genes in Silkworm (Bombyx) [My Copy] Science, Vol. 326, No. 5951. (16 October 2009), pp. 433-436. by Qingyou Xia, Yiran Guo, Ze Zhang, et al.Dong Li, Zhaoling Xuan, Zhuo Li, Fangyin Dai, Yingrui Li, Daojun Cheng, Ruiqiang Li, Tingcai Cheng, Tao Jiang, Celine Becquet, Xun Xu, Chun Liu, Xingfu Zha, Wei Fan, Ying Lin, Yihong Shen, Lan Jiang, Jeffrey Jensen, Ines Hellmann, Si Tang, Ping Zhao, Hanfu Xu, Chang Yu, Guojie Zhang, Jun Li, Jianjun Cao, Shiping Liu, Ningjia He, Yan Zhou, Hui Liu, Jing Zhao, Chen Ye, Zhouhe Du, Guoqing Pan, Aichun Zhao, Haojing Shao, Wei Zeng, Ping Wu, Chunfeng Li, Minhui Pan, Jingjing Li, Xuyang Yin, Dawei Li, Juan Wang, Huisong Zheng, Wen Wang, Xiuqing Zhang, Songgang Li, Huanming Yang, Cheng Lu, Rasmus Nielsen, Zeyang Zhou, Jian Wang, Zhonghuai Xiang, Jun Wang posted to cnv by fstrozzi on 2009-10-02 09:57:13 as along with 6 people and 2 groups venancio cisevol dinnes operon natstreet biomcgary BergmanLab Journal picks
	Elucidating the genetic architecture of familial schizophrenia using rare copy number variant and linkage scans. [My Copy] Proceedings of the National Academy of Sciences of the United States of America, Vol. 106, No. 39. (29 September 2009), pp. 16746-16751. by Bin Xu, Abigail Woodroffe, Laura Rodriguez-Murillo, et al.J. Louw Roos, Elizabeth J. van Rensburg, Gonçalo R. Abecasis, Joseph A. Gogos, Maria Karayiorgou posted to schizophrenia linkage genomics cnv by daforerog on 2009-10-02 08:49:22 as along with 1 person rdiaz
	Copy number variations of chromosome 16p13.1 region associated with schizophrenia. [My Copy] Molecular psychiatry (29 September 2009) by A. Ingason, D. Rujescu, S. Cichon, et al.E. Sigurdsson, T. Sigmundsson, O. P. Pietiläinen, J. E. Buizer-Voskamp, E. Strengman, C. Francks, P. Muglia, A. Gylfason, O. Gustafsson, P. I. Olason, S. Steinberg, T. Hansen, K. D. Jakobsen, H. B. Rasmussen, I. Giegling, H-J J. Möller, A. Hartmann, C. Crombie, G. Fraser, N. Walker, J. Lonnqvist, J. Suvisaari, A. Tuulio-Henriksson, E. Bramon, L. A. Kiemeney, B. Franke, R. Murray, E. Vassos, T. Toulopoulou, T. W. Mühleisen, S. Tosato, M. Ruggeri, S. Djurovic, O. A. Andreassen, Z. Zhang, T. Werge, R. A. Ophoff, GROUP Investigators, M. Rietschel, M. M. Nöthen, H. Petursson, H. Stefansson, L. Peltonen, D. Collier, K. Stefansson, St M. Clair posted to schizophrenia psychgen humgen cnv by daforerog on 2009-10-01 17:23:14 as along with 1 person Terkko
	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
	Identification of Copy Number Variants Defining Genomic Differences among Major Human Groups [My Copy] PLoS ONE, Vol. 4, No. 9. (30 September 2009), e7230. by Lluís Armengol, Sergi Villatoro, Juan R. González, et al.Lorena Pantano, Manel García-Aragonés, Raquel Rabionet, Mario Cáceres, Xavier Estivill posted to variation population cnv by rdiaz on 2009-10-01 09:57:24 as
	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
	Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease. [My Copy] Journal of Alzheimer's disease : JAD (11 September 2009) by Erin L. Heinzen, Anna C. Need, Kathleen M. Hayden, et al.Ornit Chiba-Falek, Allen D. Roses, Warren J. Strittmatter, James R. Burke, Christine M. Hulette, Kathleen A. Welsh-Bohmer, David B. Goldstein posted to neurogen humgen gwasneuro gwas find cnv assoc adpdgenrev ad by daforerog on 2009-09-30 21:58:02 as
	Genomewide SNP assay reveals mutations underlying Parkinson disease. [My Copy] Human mutation, Vol. 29, No. 2. (February 2008), pp. 315-322. by Javier Simon-Sanchez, Sonja Scholz, Maria del Mar d. e. l. . M. Matarin, et al.Hon-Chung C. Fung, Dena Hernandez, J. Raphael Gibbs, Angela Britton, John Hardy, Andrew Singleton posted to parkinsons methods genotyping gene_dosage cnv by psique on 2009-09-30 11:33:26 as

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genomics	113
snp	106
humgen	66
expression	59
review	59
sequencing	54
cgh	50
gwas	48
human	47
genetics	45
cancer	42
variation	41
evolution	38
acgh	35
association	35
genome	33
integration	33
researchmethods	29
schizophrenia	29
microarray	28
autism	26
cancer-crosstalk	26
genotyping	26
psychgen	26
population_genetics	25
methods	21
recurrent	21
assoc	19
hmm	18
statistics	17
classification	16
hapmap	16
software	16
0-useful	15
example	15
bioinformatics	13
breast	13
common	13
affymetrix	12
algorithm	12
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haplotype	12
population	12
sv	12
copy	11
database	11
duplication	11
method	11
mr	11
neurogen	11
number	11
amd	10
copy-number	10
gene_expression	10
ma	10
r	10
gwa	9
region	9
cnp	8
detection	8
highly	8
korbel	8
mining	8
popul	8
linkage	7
mutation	7
phenotype	7
prediction	7
silico	7
vegf	7
analysis	6
anticipation	6
arraycgh	6
bayesian	6
copy_number_variation	6
eeg	6
eqtl	6
erp	6
gene-expression	6
human_adaptation	6
ld	6
network	6
nextgen	6
structural	6
time	6
cnvbook	5
genotype	5
gru	5
gwasneuro	5
illumina	5
lab	5
mouse	5
neuropsygen	5
pem	5
segmental	5
segmental_duplications	5
teaching	5
worldwide	5
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