Tag cnv [at least 200 articles] Export

Recent papers classified by the tag cnv.

	Integrated analysis of DNA copy number and gene expression microarray data using gene sets [My Copy] BMC Bioinformatics, Vol. 10, No. 1. (29 June 2009), 203. by Renee Menezes, Marten Boetzer, Melle Sieswerda, Gert J. van Ommen, Judith Boer posted to integration expr cnv by daed on 2009-11-23 14:04:58 as along with 8 people and 1 group zufar ptrobajo rdiaz dswan guhjy lwaldron shikin barriot Bioinformatics
	Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patients. [My Copy] Human mutation, Vol. 27, No. 9. (September 2006), pp. 914-920. by Arvid Suls, Kristl G. Claeys, Dirk Goossens, et al.Boris Harding, Rob Van Luijk, Stefaan Scheers, Liesbet Deprez, Dominique Audenaert, Tine Van Dyck, Sabine Beeckmans, Iris Smouts, Berten Ceulemans, Lieven Lagae, Gunnar Buyse, Nina Barisic, Jean-Paul P. Misson, Jan Wauters, Jurgen Del-Favero, Peter De Jonghe, Lieve R. Claes posted to genotyping cnv by daforerog on 2009-11-20 13:20:23 as
	Segmental copy number variation shapes tissue transcriptomes. [My Copy] Nature genetics (8 March 2009) by Charlotte N N. Henrichsen, Nicolas Vinckenbosch, Sebastian Zöllner, et al.Evelyne Chaignat, Sylvain Pradervand, Frédéric Schütz, Manuel Ruedi, Henrik Kaessmann, Alexandre Reymond posted to cnv by leemachado on 2009-11-20 11:36:14 as along with 11 people stubrown absterga lwaldron psique bertrandservin fenghezi megraw djkt rdiaz daforerog buyske
	Comprehensive genomic characterization defines human glioblastoma genes and core pathways [My Copy] Nature, Vol. 455, No. 7216. (04 September 2008), pp. 1061-1068. posted to tcga pathway microarrays methylation human genomics expression exon cnv cgh cancer aberration by ealloza on 2009-11-20 11:20:24 as along with 24 people and 2 groups iskathy srp33 dolchan ajbattle aezrin myzhang chrisamiller fenghezi jessopher jfr zufar wimufi jbhiatt frohike huiminC renatomilani ptrobajo cchand Zephyrus nuin brianb oelemento shikin shigepong Roswell Cancer Crosstalk GeneGo
	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 review impact genome cnv by Zephyrus on 2009-11-20 05:48:37 as along with 20 people and 1 group gthorisson vplagnol biovils psique chvlyl daed daforerog zufar jessopher DrRichardBadge operon colinveal frohike sf11 sameersoi polivares dswan qayub bpcusack rdiaz Journal picks
	Genome Alteration Print (GAP): a tool to visualize and mine complex cancer genomic profiles obtained by SNP arrays [My Copy] Genome Biology, Vol. 10, No. 11. (2009), R128. by Tatiana Popova, Elodie Manie, Dominique S. Lyonnet, Guillem Rigaill, Emmanuel Barillot, Marc H. Stern posted to snp microarray cnv by shikin on 2009-11-19 18:00:46 as
	Rapid and simple prenatal diagnosis of common chromosome disorders: advantages and disadvantages of the molecular methods FISH and QF-PCR. [My Copy] Reproduction (Cambridge, England), Vol. 126, No. 3. (September 2003), pp. 279-297. by Maj A. Hultén, Seema Dhanjal, Barbara Pertl posted to genotyping cnv by daforerog on 2009-11-19 17:13:19 as
	Gene dosage methods as diagnostic tools for the identification of chromosome abnormalities. [My Copy] Pathologie-biologie, Vol. 56, No. 6. (September 2008), pp. 345-353. by L. Gouas, C. Goumy, L. Véronèse, A. Tchirkov, P. Vago posted to humgen genotyping genomics cnv by daforerog on 2009-11-18 15:57:41 as
	The population genetics of structural variation. [My Copy] Nature genetics, Vol. 39, No. 7 Suppl. (July 2007) by Donald F. Conrad, Matthew E. Hurles posted to population_genetics cnv by sameersoi on 2009-11-18 12:50:08 as along with 5 people APRegier guhjy mrkrause rdiaz jlangdon
	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 variation software sequencing human genetic_architecture cnv by ongenetics on 2009-11-16 13:17:28 as along with 30 people and 1 group chvlyl leemachado daed 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
	VarScan: variant detection in massively parallel sequencing of individual and pooled samples [My Copy] Bioinformatics, Vol. 25, No. 17. (1 September 2009), pp. 2283-2285. by Daniel C. Koboldt, Ken Chen, Todd Wylie, et al.David E. Larson, Michael D. McLellan, Elaine R. Mardis, George M. Weinstock, Richard K. Wilson, Li Ding posted to variant cnv by Peiyong on 2009-11-15 07:48:50 as along with 15 people and 3 groups hzoltan darian seb1 heliopais mkiyer dakelley djkt PabloMarin guhjy n00c orzenil natstreet druvus stajich malcook Journal picks Mycology SIMR bioinformatics
	Integrated detection and population-genetic analysis of SNPs and copy number variation. [My Copy] Nature genetics, Vol. 40, No. 10. (7 October 2008), pp. 1166-1174. by Steven A. McCarroll, Finny G. Kuruvilla, Joshua M. Korn, et al.Simon Cawley, James Nemesh, Alec Wysoker, Michael H. Shapero, Paul I. de Bakker, Julian B. Maller, Andrew Kirby, Amanda L. Elliott, Melissa Parkin, Earl Hubbell, Teresa Webster, Rui Mei, James Veitch, Patrick J. Collins, Robert Handsaker, Steve Lincoln, Marcia Nizzari, John Blume, Keith W. Jones, Rich Rava, Mark J. Daly, Stacey B. Gabriel, David Altshuler posted to snp cnv affy by shikin on 2009-11-13 17:42:47 as along with 20 people and 1 group vplagnol buyske turnersd sameersoi gruberjd Hans45 pdexheimer madreach waszak caseybrown rsantana Zephyrus psique jbsaltz Ema misonneh djkt daed rdiaz guhjy Roswell Cancer Crosstalk
	BreakDancer: an algorithm for high-resolution mapping of genomic structural variation [My Copy] Nature Methods, 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 whole-genome-seq translocation somatic_mutations software nextgen gene-fusion deletions cnv bioinformatics by stubrown on 2009-11-13 14:44:29 as along with 12 people and 1 group Leaflet heliopais dakelley fenghezi daed natstreet druvus sitalange qayub gdb jasontsai danmaclean 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 population_genetics cnv by sameersoi on 2009-11-12 21:57:35 as along with 41 people and 7 groups lp2 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
	Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs. [My Copy] Nature genetics, Vol. 40, No. 10. (7 October 2008), pp. 1253-1260. by Joshua M. Korn, Finny G. Kuruvilla, Steven A. McCarroll, et al.Alec Wysoker, James Nemesh, Simon Cawley, Earl Hubbell, Jim Veitch, Patrick J. Collins, Katayoon Darvishi, Charles Lee, Marcia M. Nizzari, Stacey B. Gabriel, Shaun Purcell, Mark J. Daly, David Altshuler posted to snp method cnv affy by shikin on 2009-11-12 18:02:50 as along with 14 people sameersoi fenghezi psique buyske maren guhjy pdexheimer pengchy caseybrown dakelley djkt daed rdiaz vplagnol
	The role of DNA copy number variation in schizophrenia. [My Copy] Biological psychiatry, Vol. 66, No. 11. (1 December 2009), pp. 1005-1012. by Gloria W. Tam, Richard Redon, Nigel P. Carter, Seth G. Grant posted to schizophrenia cnv by vplagnol on 2009-11-12 18:00:36 as along with 2 people Leaflet daforerog
	A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes. [My Copy] Nature genetics (8 November 2009) by Marwan Shinawi, Christian P. Schaaf, Samarth S. Bhatt, et al.Zhilian Xia, Ankita Patel, Sau Wai W. Cheung, Brendan Lanpher, Sandra Nagl, Heinrich Stephan S. Herding, Claudia Nevinny-Stickel, Ladonna L. Immken, Gayle Simpson S. Patel, Jennifer Ruth R. German, Arthur L. Beaudet, Pawel Stankiewicz posted to psychgen mr cnv by daforerog on 2009-11-12 15:49:43 as
	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 variants snp number copy cnv by chvlyl on 2009-11-12 01:50:08 as along with 1 person merpublic
	The DNA replication FoSTeS/MMBIR mechanism can generate genomic, genic and exonic complex rearrangements in humans. [My Copy] Nature genetics, Vol. 41, No. 7. (July 2009), pp. 849-853. by Feng Zhang, Mehrdad Khajavi, Anne M. Connolly, Charles F. Towne, Sat Dev D. Batish, James R. Lupski posted to cnv by sameersoi on 2009-11-11 07:36:35 as along with 2 people dbikard fenghezi
	A Microhomology-Mediated Break-Induced Replication Model for the Origin of Human Copy Number Variation [My Copy] PLoS Genet, Vol. 5, No. 1. (30 January 2009), e1000327. by P. J. Hastings, Grzegorz Ira, James R. Lupski posted to evolution cnv by sameersoi on 2009-11-11 06:07:39 as along with 3 people ahornby jdbowes djkt
	What a difference copy number variation makes [My Copy] BioEssays, Vol. 29, No. 4. (2007), pp. 311-313. by Hildegard Kehrer-Sawatzki posted to cnv by biovils on 2009-11-09 15:21:38 as along with 6 people and 3 groups Zephyrus balicea dchughes rdiaz cerami guhjy Bioinformatics G4ID Genetics-of-Gambling
	Mechanisms of change in gene copy number [My Copy] Nature Reviews Genetics, Vol. 10, No. 8. (01 August 2009), pp. 551-564. by P. J. Hastings, James R. Lupski, Susan M. Rosenberg, Grzegorz Ira posted to cnv by biovils on 2009-11-09 15:21:18 as along with 13 people and 1 group Zephyrus sameersoi xingxu qayub nicolesoranzo pkonings jandot rdiaz misonneh fenghezi daforerog ppgardne psique Journal picks
	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
	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 18 people and 1 group hzoltan biovils 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 17 people and 2 groups seb1 pst owenlancaster robertrentzsch oannes74 toszko kiekyon michaelbarton jasontsai heliopais druvus GeeSharpMinor Peiyong n00c gdv desany qayub Orengo Group Journal Picks 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 35 people and 2 groups hzoltan 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
	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 32 people and 5 groups biovils 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
	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

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genomics	115
snp	110
humgen	67
expression	60
review	60
sequencing	56
cgh	51
human	49
gwas	48
genetics	45
cancer	43
variation	42
evolution	39
acgh	35
association	35
genome	34
integration	34
schizophrenia	30
genotyping	29
microarray	29
researchmethods	29
population_genetics	27
psychgen	27
autism	26
cancer-crosstalk	26
methods	21
recurrent	21
assoc	19
hmm	18
software	18
statistics	17
classification	16
hapmap	16
0-useful	15
example	15
bioinformatics	14
breast	13
common	13
copy	13
number	13
affymetrix	12
algorithm	12
disease	12
haplotype	12
method	12
mr	12
population	12
sv	12
database	11
duplication	11
neurogen	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
nextgen	7
phenotype	7
prediction	7
silico	7
vegf	7
analysis	6
anticipation	6
arraycgh	6
bayesian	6
eeg	6
eqtl	6
erp	6
gene-expression	6
human_adaptation	6
ld	6
network	6
structural	6
time	6
cnvbook	5
copy-number-variation	5
genotype	5
gru	5
gwasneuro	5
illumina	5
impact	5
lab	5
methylation	5
mouse	5
neuropsygen	5
pem	5
segmental	5
segmental_duplications	5
teaching	5
worldwide	5

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