daed's cnv [41 articles] Export

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	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
	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
	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 2 people jfr rdiaz
	Origins and functional impact of copy number variation in the human genome [My Copy] Nature In 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 tiling map human cnv array by daed on 2009-10-29 11:53:54 as along with 21 people and 1 group n00c Zephyrus gthorisson vplagnol biovils psique chvlyl daforerog zufar jessopher DrRichardBadge operon colinveal frohike sf11 sameersoi polivares dswan qayub bpcusack rdiaz Journal picks
	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 30 people and 1 group ongenetics chvlyl 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
	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 sequencing cnv by daed on 2009-10-13 15:14:13 as along with 35 people and 2 groups hzoltan n00c 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
	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] 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 sequencing cnv algorithm by daed on 2009-10-13 11:32:42 as along with 13 people and 1 group n00c Leaflet heliopais stubrown 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 16 people and 1 group biovils zufar daforerog pengchy ptrobajo vplagnol waszak caseybrown Zephyrus dakelley buyske misonneh djkt rdiaz Stew guhjy Roswell Cancer Crosstalk
	Rare chromosomal deletions and duplications increase risk of schizophrenia. [My Copy] Nature, Vol. 455, No. 7210. (11 September 2008), pp. 237-241. by International Schizophrenia Consortium posted to rare gwas cnv by daed on 2009-09-29 22:07:25 as along with 2 people daforerog psique
	Gene-Network Analysis Identifies Susceptibility Genes Related to Glycobiology in Autism [My Copy] PLoS ONE, Vol. 4, No. 5. (28 May 2009), e5324. by Bert van der Zwaag, Lude Franke, Martin Poot, et al.Ron Hochstenbach, Henk A. Spierenburg, Jacob A. S. Vorstman, Emma van Daalen, Maretha V. de Jonge, Nienke E. Verbeek, Eva H. Brilstra, Ruben van 't Slot, Roel A. Ophoff, Michael A. van Es, Hylke M. Blauw, Jan H. Veldink, Jacobine E. Buizer-Voskamp, Frits A. Beemer, Leonard H. van den Berg, Cisca Wijmenga, Hans K. van Amstel, Herman van Engeland, Burbach, Wouter G. Staal posted to ranking gene cnv candidate by daed on 2009-09-02 13:51:05 as along with 2 people rdiaz daforerog
	CNV discovery using SNP genotyping arrays. [My Copy] Cytogenetic and genome research, Vol. 123, No. 1-4. (2008), pp. 307-312. by C. Yau, C. C. Holmes posted to calling cnv methods by daed on 2009-06-24 10:55:30 as along with 1 person jdbowes
	Extending genome-wide association studies to copy-number variation. [My Copy] Human molecular genetics, Vol. 17, No. R2. (15 October 2008) by Steven A. McCarroll posted to cnv gwas review by daed on 2009-06-24 10:47:06 as along with 3 people daforerog guhjy cheyloveday
	Genetic association analysis of copy-number variation (CNV) in human disease pathogenesis. [My Copy] Genomics, Vol. 93, No. 1. (23 January 2009), pp. 22-26. by Iuliana Ionita-Laza, Angela J. Rogers, Christoph Lange, Benjamin A. Raby, Charles Lee posted to cnv disease by daed on 2009-06-24 10:46:13 as along with 7 people and 1 group rdiaz sameersoi brianb marywaye guhjy daforerog Zephyrus Roswell Cancer Crosstalk
	A Bayesian segmentation approach to ascertain copy number variations at the population level. [My Copy] Bioinformatics (Oxford, England), Vol. 25, No. 13. (1 July 2009), pp. 1669-1679. by Long Yang Y. Wu, Hugh A. Chipman, Shelley B. Bull, Laurent Briollais, Kesheng Wang posted to algorithm array cnv by daed on 2009-06-22 15:57:22 as along with 2 people rdiaz guhjy
	Copy number variation at 1q21.1 associated with neuroblastoma [My Copy] Nature, Vol. 459, No. 7249. (18 June 2009), pp. 987-991. by Sharon J. Diskin, Cuiping Hou, Joseph T. Glessner, et al.Edward F. Attiyeh, Marci Laudenslager, Kristopher Bosse, Kristina Cole, Yael P. Mosse, Andrew Wood, Jill E. Lynch, Katlyn Pecor, Maura Diamond, Cynthia Winter, Kai Wang, Cecilia Kim, Elizabeth A. Geiger, Patrick W. Mcgrady, Alexandra I. F. Blakemore, Wendy B. London, Tamim H. Shaikh, Jonathan Bradfield, Struan F. A. Grant, Hongzhe Li, Marcella Devoto, Eric R. Rappaport, Hakon Hakonarson, John M. Maris posted to cnv gwas by daed on 2009-06-22 14:58:04 as along with 3 people rdiaz kdpreter lwaldron
	In vivo differentiation and genomic evolution in adult male germ cell tumors. [My Copy] Genes, chromosomes & cancer, Vol. 47, No. 1. (January 2008), pp. 43-55. by J. E. Korkola, S. Heck, A. B. Olshen, et al.V. E. Reuter, G. J. Bosl, J. Houldsworth, R. S. Chaganti posted to cancer cnv testis by daed on 2009-06-16 12:19:00 as
	Functional copy-number alterations in cancer. [My Copy] PloS one, Vol. 3, No. 9. (11 September 2008), e3179. by Barry S. Taylor, Jordi Barretina, Nicholas D. Socci, et al.Penelope Decarolis, Marc Ladanyi, Matthew Meyerson, Samuel Singer, Chris Sander posted to functional detection cnv by daed on 2009-04-16 09:20:04 as along with 5 people and 1 group chrisamiller jfr huiminC oelemento Zephyrus Roswell Cancer Crosstalk
	Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing. [My Copy] Nature genetics, Vol. 40, No. 6. (27 June 2008), pp. 722-729. by Peter J. Campbell, Philip J. Stephens, Erin D. Pleasance, et al.Sarah O'Meara, Heng Li, Thomas Santarius, Lucy A. Stebbings, Catherine Leroy, Sarah Edkins, Claire Hardy, Jon W. Teague, Andrew Menzies, Ian Goodhead, Daniel J. Turner, Christopher M. Clee, Michael A. Quail, Antony Cox, Clive Brown, Richard Durbin, Matthew E. Hurles, Paul A. Edwards, Graham R. Bignell, Michael R. Stratton, P. Andrew Futreal posted to cancer cnv sequencing by daed on 2008-11-19 13:31:04 as along with 12 people chvlyl dakelley APRegier myzhang jessopher frohike smiddha xingxu matthewsuderman jfr caseybrown chrisamiller
	A faster circular binary segmentation algorithm for the analysis of array CGH data. [My Copy] Bioinformatics (18 January 2007) by E S S. Venkatraman, A B B. Olshen posted to algorithm cnv by daed on 2008-10-28 10:42:29 as along with 4 people and 1 group noushin rdiaz shigepong ellakat Bioinformatics
	A fast and flexible method for the segmentation of aCGH data. [My Copy] Bioinformatics (Oxford, England), Vol. 24, No. 16. (15 August 2008) by E. Ben-Yaacov, Y. C. Eldar posted to algorithm cnv by daed on 2008-10-28 10:40:39 as along with 6 people noushin jfr rdiaz nuin talponer aviad_work
	Computation of recurrent minimal genomic alterations from array-CGH data. [My Copy] Bioinformatics (24 January 2006) by C Rouveirol, N Stransky, Ph Hupé, et al.Ph La Rosa, E Viara, E Barillot, F Radvanyi posted to algorithm cnv by daed on 2008-10-28 10:38:15 as along with 3 people archroad rdiaz OscarRueda
	Localization to Xq27 of a susceptibility gene for testicular germ-cell tumours. [My Copy] Nature genetics, Vol. 24, No. 2. (February 2000), pp. 197-200. by E. A. Rapley, G. P. Crockford, D. Teare, et al.P. Biggs, S. Seal, R. Barfoot, S. Edwards, R. Hamoudi, K. Heimdal, S. D. Fossâ, K. Tucker, J. Donald, F. Collins, M. Friedlander, D. Hogg, P. Goss, A. Heidenreich, W. Ormiston, P. A. Daly, D. Forman, T. D. Oliver, M. Leahy, R. Huddart, C. S. Cooper, J. G. Bodmer, D. F. Easton, M. R. Stratton, D. T. Bishop posted to cnv tgct by daed on 2008-10-13 17:02:57 as
	Cytogenetic and molecular analysis of a family with three brothers afflicted with germ-cell cancer. [My Copy] Clinical genetics, Vol. 65, No. 1. (January 2004), pp. 32-39. by A. M. Ottesen, E. Rajpert-De Meyts, M. Holm, et al.I. L. Andersen, P. H. Vogt, C. Lundsteen, N. E. Skakkebaek posted to cnv tgct by daed on 2008-10-13 16:57:19 as
	High-resolution copy number and gene expression microarray analyses of head and neck squamous cell carcinoma cell lines of tongue and larynx. [My Copy] Genes Chromosomes Cancer (3 March 2008) by Anna-Kaarina K. Järvinen, Reija Autio, Sami Kilpinen, et al.Matti Saarela, Ilmo Leivo, Reidar Grénman, Antti A A. Mäkitie, Outi Monni posted to association_study cnv relaxin by daed on 2008-10-06 16:23:52 as along with 1 person Terkko
	Detection of large-scale variation in the human genome. [My Copy] Nature genetics, Vol. 36, No. 9. (September 2004), pp. 949-951. by A. John Iafrate, Lars Feuk, Miguel N. Rivera, et al.Marc L. Listewnik, Patricia K. Donahoe, Ying Qi, Stephen W. Scherer, Charles Lee posted to cnv global segmental_duplications by daed on 2008-10-06 15:42:04 as along with 7 people and 2 groups daforerog psique pcahan1 dchughes ealloza bioguru2000 Ema G4ID Genetics-of-Gambling
	Recent segmental duplications in the human genome. [My Copy] Science, Vol. 297, No. 5583. (9 August 2002), pp. 1003-1007. by J. A. Bailey, Z. Gu, R. A. Clark, et al.K. Reinert, R. V. Samonte, S. Schwartz, M. D. Adams, E. W. Myers, P. W. Li, E. E. Eichler posted to cnv segmental_duplications by daed on 2008-10-06 15:40:13 as along with 5 people dakelley APRegier pcahan1 balicea bioguru2000
	Segmental duplications and copy-number variation in the human genome. [My Copy] American journal of human genetics, Vol. 77, No. 1. (July 2005), pp. 78-88. by A. J. Sharp, D. P. Locke, S. D. McGrath, et al.Z. Cheng, J. A. Bailey, R. U. Vallente, L. M. Pertz, R. A. Clark, S. Schwartz, R. Segraves, V. V. Oseroff, D. G. Albertson, D. Pinkel, E. E. Eichler posted to cnv segmental_duplications by daed on 2008-10-06 15:38:25 as along with 6 people and 4 groups stharward dakelley pcahan1 balicea dchughes giovanni Bioinformatics G4ID GeschwindLab Genetics-of-Gambling
	FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity. [My Copy] Nature genetics, Vol. 39, No. 6. (21 June 2007), pp. 721-723. by Manuela Fanciulli, Penny J. Norsworthy, Enrico Petretto, et al.Rong Dong, Lorraine Harper, Lavanya Kamesh, Joanne M. Heward, Stephen C. Gough, Adam de Smith, Alexandra I. Blakemore, Philippe Froguel, Catherine J. Owen, Simon H. Pearce, Luis Teixeira, Loic Guillevin, Deborah Cunninghame S. Graham, Charles D. Pusey, H. Terence Cook, Timothy J. Vyse, Timothy J. Aitman posted to association_study cnv by daed on 2008-10-06 15:29:56 as along with 3 people leemachado yanicem vplagnol
	Psoriasis is associated with increased beta-defensin genomic copy number. [My Copy] Nature genetics, Vol. 40, No. 1. (2 January 2008), pp. 23-25. by Edward J. Hollox, Ulrike Huffmeier, Patrick L. Zeeuwen, et al.Raquel Palla, Jesús Lascorz, Diana Rodijk-Olthuis, Peter C. van de Kerkhof, Heiko Traupe, Gys de Jongh, Martin den Heijer, André Reis, John A. Armour, Joost Schalkwijk posted to association_study cnv by daed on 2008-10-06 15:27:43 as along with 5 people leemachado jo_davies bootsy caseybrown vplagnol
	Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans. [My Copy] Nature, Vol. 439, No. 7078. (16 February 2006), pp. 851-855. by Timothy J. Aitman, Rong Dong, Timothy J. Vyse, et al.Penny J. Norsworthy, Michelle D. Johnson, Jennifer Smith, Jonathan Mangion, Cheri Roberton-Lowe, Amy J. Marshall, Enrico Petretto, Matthew D. Hodges, Gurjeet Bhangal, Sheetal G. Patel, Kelly Sheehan-Rooney, Mark Duda, Paul R. Cook, David J. Evans, Jan Domin, Jonathan Flint, Joseph J. Boyle, Charles D. Pusey, H. Terence Cook posted to association_study cnv by daed on 2008-10-06 15:25:06 as along with 7 people and 2 groups leemachado cscweb ccots cmm breden vplagnol guhjy FAB-lab SFUAntibodyResearch
	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 affymetrix cnv by daed on 2008-09-30 14:09:22 as along with 20 people and 1 group shikin vplagnol buyske turnersd sameersoi gruberjd Hans45 pdexheimer madreach waszak caseybrown rsantana Zephyrus psique jbsaltz Ema misonneh djkt rdiaz guhjy Roswell Cancer Crosstalk
	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 affymetrix cnv by daed on 2008-09-30 14:09:04 as along with 14 people shikin sameersoi fenghezi psique buyske maren guhjy pdexheimer pengchy caseybrown dakelley djkt rdiaz vplagnol
	Improved detection of global copy number variation using high density, non-polymorphic oligonucleotide probes [My Copy] BMC Genetics, Vol. 9 (28 March 2008), 27. by Fan Shen, Jing Huang, Karen R. Fitch, et al.Vivi B. Truong, Andrew Kirby, Wenwei Chen, Jane Zhang, Guoying Liu, Steven A. Mccarroll, Keith W. Jones, Michael H. Shapero posted to affymetrix cnv by daed on 2008-09-30 14:08:37 as along with 2 people maren guhjy
	Mutational and selective effects on copy-number variants in the human genome. [My Copy] Nat Genet, Vol. 39, No. 7 Suppl. (July 2007) by G. M. Cooper, D. A. Nickerson, E. E. Eichler posted to cnv segmental_duplications by daed on 2008-09-30 12:56:29 as along with 3 people and 1 group waszak mrkrause rdiaz Bioinformatics
	Relative impact of nucleotide and copy number variation on gene expression phenotypes. [My Copy] Science (New York, N.Y.), 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 Tavaré, Panagiotis Deloukas, Matthew E. Hurles, Emmanouil T. Dermitzakis posted to cnv expression snp by daed on 2008-09-30 12:34:04 as along with 32 people and 5 groups biovils lp2 daveGerrard sameersoi timhubbard Zephyrus ajbattle jonilaserson ilyashl emptyhb buyske zufar koller waszak 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
	The fine-scale and complex architecture of human copy-number variation. [My Copy] American journal of human genetics, Vol. 82, No. 3. (24 March 2008), pp. 685-695. by George H. Perry, Amir Ben-Dor, Anya Tsalenko, et al.Nick Sampas, Laia Rodriguez-Revenga, Charles W. Tran, Alicia Scheffer, Israel Steinfeld, Peter Tsang, N. Alice Yamada, Han Soo S. Park, Jong-Il I. Kim, Jeong-Sun S. Seo, Zohar Yakhini, Stephen Laderman, Laurakay Bruhn, Charles Lee posted to cnv by daed on 2008-09-30 12:23:47 as along with 4 people psique daforerog vplagnol guhjy
	aCGHViewer: A Generic Visualization Tool For aCGH data. [My Copy] Cancer informatics, Vol. 2 (2006), pp. 36-43. by G. Shankar, M. R. Rossi, D. E. McQuaid, et al.J. M. Conroy, D. G. Gaile, J. K. Cowell, N. J. Nowak, P. Liang posted to application cgh cnv by daed on 2008-06-17 12:45:44 as
	ADaCGH: A parallelized web-based application and R package for the analysis of aCGH data. [My Copy] PLoS ONE, Vol. 2, No. 1. (2007) by R. Díaz-Uriarte, O. M. Rueda posted to application cgh cnv r by daed on 2008-06-17 12:44:16 as along with 1 person guhjy

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cnv	41
cancer	20
gwas	14
snp	14
tgct	12
expression	10
tds	9
association_study	8
pathway	8
sequencing	7
testis	7
algorithm	6
disease	6
ngs	6
functional	6
review	6
integration	5
genome	5
multiloci	5
gene	5
glp1	5
rna-seq	5
phenome	4
relaxin	4
prevalence	4
affymetrix	4
network	4
segmental_duplications	4
human	4
multisnp	3
detection	3
transcriptomics	3
application	3
similarity	3
array	3
454	2
phenotype	2
cgh	2
rat	2
interactome	2
infertility	2
methods	2
systems	2
data	2
familial	2
biology	2
genetics	2
webtool	2
protocol	2
design	2
tool	2
kinome	2
technology	2
sensitivity	1
arrays	1
calling	1
connectivity	1
loci	1
and	1
variation	1
ranking	1
reference	1
rxpf2	1
integrative	1
gene-gene	1
linkage	1
hapmap	1
expr	1
sample	1
rare	1
transcription	1
genomewide	1
clustering	1
epistasis	1
digital	1
omics	1
relationships	1
cisplatin	1
transfac	1
primer	1
common	1
statistics	1
map	1
overfitting	1
seq	1
protein	1
aroma	1
encode	1
ppi	1
kinases	1
tools	1
mutation	1
pcr	1
cryptorchidism	1
segmentation	1
association	1
mice	1
spermatogenesis	1
ensembl	1
microrna	1
r	1
comparison	1
microlithias	1
environment	1
acgh	1
candidate	1
genomic	1
rxfp2	1
definition	1
nn	1
male	1
drug-drug	1
web	1
atlas	1
tiling	1
development	1
2008	1
enrichment	1
resources	1
polymorphisms	1
interactions	1
analysis	1
global	1

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