pkonings's cnv [101 articles] Export

Recent papers added to pkonings's library classified by the tag cnv. You can also see everyone's cnv.

	Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture [My Copy] Hum. Mol. Genet., Vol. 18, No. 19. (1 October 2009), pp. 3579-3593. by Lisenka E. L. M. Vissers, Samarth S. Bhatt, Irene M. Janssen, et al.Zhilian Xia, Seema R. Lalani, Rolph Pfundt, Katarzyna Derwinska, Bert B. A. de Vries, Christian Gilissen, Alexander Hoischen, Monika Nesteruk, Barbara Wisniowiecka-Kowalnik, Marta Smyk, Han G. Brunner, Sau W. Cheung, Ad G. van Kessel, Joris A. Veltman, Pawel Stankiewicz posted to cnv by pkonings on 2009-09-15 10:39:42 as
	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 ngs cnv by pkonings on 2009-09-01 14:41:18 as along with 30 people and 1 group ongenetics chvlyl leemachado daed gbenson n00c bozdagd dakelley sbmontgomery eshirdel merpublic shyamsg scmelton qayub natstreet fenghezi Annab djkt nuin xingxu jamesmorris rdiaz brant torfinnnome jandot danmaclean daforerog frohike rschulz gangcai Journal picks
	Inferring progression models for CGH data [My Copy] Bioinformatics, Vol. 25, No. 17. (1 September 2009), pp. 2208-2215. by Jun Liu, Nirmalya Bandyopadhyay, Sanjay Ranka, M. Baudis, Tamer Kahveci posted to evolution cnv cancer by pkonings on 2009-08-20 09:25:42 as along with 5 people davfre sameersoi rdiaz nuin bgordski
	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 preprocessing cnv affymetrix by pkonings on 2009-08-20 09:24:38 as along with 5 people shikin djkt rdiaz daforerog neils
	Genome-wide copy number variation association study suggested VPS13B gene for osteoporosis in Caucasians [My Copy] Osteoporosis International, Vol. advance access (13 August 2009), pp. x-x. by F. Y. Deng, L. J. Zhao, Y. F. Pei, et al.B. Y. Sha, X. G. Liu, H. Yan, L. Wang, T. L. Yang, R. Recker, C. Papasian, H. W. Deng posted to osteoporosis gwas cnv by pkonings on 2009-08-17 08:54:11 as
	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 cnv by pkonings on 2009-08-14 10:23:30 as along with 7 people rdiaz ericrpaquet jandot guhjy frohike vplagnol daforerog
	Copy number variation influences gene expression and metabolic traits in mice. [My Copy] Human molecular genetics (31 July 2009), ddp360. by Luz D. Orozco, Shawn J. Cokus, Anatole Ghazalpour, et al.Leslie Ingram-Drake, Susanna Wang, Atila van Nas, Nam Che, Jesus A. Araujo, Matteo Pellegrini, Aldons J. Lusis posted to metabolomics expression cnv by pkonings on 2009-08-14 10:21:58 as along with 2 people memerman rdiaz
	Segmental duplications mediate novel, clinically relevant chromosome rearrangements [My Copy] Hum. Mol. Genet., Vol. 18, No. 16. (15 August 2009), pp. 2957-2962. by M. Katharine Rudd, Julia Keene, Brian Bunke, et al.Erin B. Kaminsky, Margaret P. Adam, Jennifer G. Mulle, David H. Ledbetter, Christa L. Martin posted to segmental cnv by pkonings on 2009-08-14 10:20:34 as along with 1 person djkt
	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 cnv sequencing by pkonings on 2009-08-11 09:29:54 as along with 7 people woodson8 scmelton torfinnnome dakelley n00c rdiaz jbhiatt
	Searching genetic risk factors for schizophrenia and bipolar disorder: learn from the past and back to the future. [My Copy] Human mutation, Vol. 30, No. 8. (August 2009), pp. 1139-1152. by Maaike Alaerts, Jurgen Del-Favero posted to cnv gwas by pkonings on 2009-08-04 09:56:12 as along with 1 person daforerog
	Copy-number variation: the end of the human genome? [My Copy] Trends in biotechnology, Vol. 27, No. 8. (01 August 2009), pp. 448-454. by Paul H. Dear posted to cnv by pkonings on 2009-08-04 09:54:36 as along with 2 people rdiaz VGreiff
	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 affymetrix cnv by pkonings on 2009-08-04 09:53:31 as along with 2 people rdiaz guhjy
	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 pkonings on 2009-08-03 15:31:32 as along with 13 people and 1 group biovils Zephyrus sameersoi xingxu qayub nicolesoranzo jandot rdiaz misonneh fenghezi daforerog ppgardne psique Journal picks
	Genomic copy number variation, human health, and disease. [My Copy] Lancet, Vol. 374, No. 9686. (25 June 2009), pp. 340-350. by Louise V. Wain, John A. L. Armour, Martin D. Tobin posted to association cnv by pkonings on 2009-06-22 14:25:18 as along with 5 people psique jandot daforerog guhjy rdiaz
	Complex disease: Autism clues from genome-wide studies [My Copy] Nature Reviews Genetics, Vol. 10, No. 6., pp. 346-347. by Louisa Flintoft posted to cnv gwas networks by pkonings on 2009-06-16 12:03:36 as
	Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. [My Copy] Nature, Vol. 459, No. 7246. (28 May 2009), pp. 569-573. by Joseph T. Glessner, Kai Wang, Guiqing Cai, et al.Olena Korvatska, Cecilia E. Kim, Shawn Wood, Haitao Zhang, Annette Estes, Camille W. Brune, Jonathan P. Bradfield, Marcin Imielinski, Edward C. Frackelton, Jennifer Reichert, Emily L. Crawford, Jeffrey Munson, Patrick M. Sleiman, Rosetta Chiavacci, Kiran Annaiah, Kelly Thomas, Cuiping Hou, Wendy Glaberson, James Flory, Frederick Otieno, Maria Garris, Latha Soorya, Lambertus Klei, Joseph Piven, Kacie J. Meyer, Evdokia Anagnostou, Takeshi Sakurai, Rachel M. Game, Danielle S. Rudd, Danielle Zurawiecki, Christopher J. McDougle, Lea K. Davis, Judith Miller, David J. Posey, Shana Michaels, Alexander Kolevzon, Jeremy M. Silverman, Raphael Bernier, Susan E. Levy, Robert T. Schultz, Geraldine Dawson, Thomas Owley, William M. McMahon, Thomas H. Wassink, John A. Sweeney, John I. Nurnberger, Hilary Coon, James S. Sutcliffe, Nancy J. Minshew, Struan F. Grant, Maja Bucan, Edwin H. Cook, Joseph D. Buxbaum, Bernie Devlin, Gerard D. Schellenberg, Hakon Hakonarson posted to autism cnv by pkonings on 2009-06-15 14:28:00 as along with 8 people rdiaz daforerog fenghezi scjparker dswan neils jbhiatt psique
	Chaos in the embryo [My Copy] Nat Med, Vol. 15, No. 5. (May 2009), pp. 490-491. by David H. Ledbetter posted to cnv single_cell by pkonings on 2009-05-08 09:01:43 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 cnv by pkonings on 2009-04-28 15:31:47 as along with 2 people psique bmenten
	Chromosome instability is common in human cleavage-stage embryos [My Copy] Nature Medicine, Vol. 15, No. 5. (May 2009), pp. 577-583. by Evelyne Vanneste, Thierry Voet, Cédric Le Caignec, et al.Michèle Ampe, Peter Konings, Cindy Melotte, Sophie Debrock, Mustapha Amyere, Miikka Vikkula, Frans Schuit, Jean-Pierre Fryns, Geert Verbeke, Thomas D'Hooghe, Yves Moreau, Joris R. Vermeesch posted to cnv single_cell by pkonings on 2009-04-27 10:08:30 as along with 1 person bmenten
	Smoothing waves in array CGH tumor profiles [My Copy] Bioinformatics, Vol. 25, No. 9. (1 May 2009), pp. 1099-1104. by Mark A. van de Wiel, Rebecca Brosens, Paul H. C. Eilers, et al.Candy Kumps, Gerrit A. Meijer, Bjorn Menten, Erik Sistermans, Frank Speleman, Marieke E. Timmerman, Bauke Ylstra posted to cnv preprocessing wave by pkonings on 2009-04-02 14:27:40 as along with 4 people jfr nuin lwaldron rdiaz
	Estimating the number of unseen variants in the human genome. [My Copy] Proceedings of the National Academy of Sciences of the United States of America, Vol. 106, No. 13. (31 March 2009), pp. 5008-5013. by I. Ionita-Laza, C. Lange, N. M Laird posted to cnv by pkonings on 2009-04-02 13:56:08 as along with 5 people jsatkosk giovanni TRHvidsten guhjy benjaminsb
	The genetics of chronic inflammatory diseases [My Copy] Hum. Mol. Genet., Vol. 18, No. R1. (15 April 2009), pp. R101-106. by Graham A. Heap, David A. van Heel posted to cnv crohn by pkonings on 2009-03-31 12:19:36 as along with 2 people jdbowes kochhan
	Human genetic variation and its contribution to complex traits. [My Copy] Nature reviews. Genetics, Vol. 10, No. 4. (01 April 2009), pp. 241-251. by Kelly A. Frazer, Sarah S. Murray, Nicholas J. Schork, Eric J. Topol posted to cnv complex gwa by pkonings on 2009-03-30 16:52:58 as along with 18 people and 1 group ongenetics PabloMarin songpku guhjy ilyashl roys JoeSabatini Zephyrus jbhiatt daforerog welliegirl dbk psique zufar misonneh fenghezi rdiaz dchughes Roswell Cancer Crosstalk
	The complex relationship of gene duplication and essentiality [My Copy] Trends in Genetics, Vol. advance access (13 March 2009) by Takashi Makino, Karsten Hokamp, Aoife Mclysaght posted to cnv by pkonings on 2009-03-30 16:45:11 as along with 3 people maximilianh dchughes djkt
	Copy number variants, diseases and gene expression [My Copy] Hum. Mol. Genet., Vol. 18, No. R1. (15 April 2009), pp. R1-8. by Charlotte N. Henrichsen, Evelyne Chaignat, Alexandre Reymond posted to cnv expression by pkonings on 2009-03-26 14:33:05 as along with 5 people stubrown guhjy jdbowes giovanni rdiaz
	Copy number variation in African Americans [My Copy] BMC Genetics, Vol. 10 (24 March 2009), 15. by Joseph P. Mcelroy, Mathew R. Nelson, Stacy J. Caillier, Jorge R. Oksenberg posted to cnv population_stratification by pkonings on 2009-03-26 11:06:43 as
	Joint estimation of copy number variation and reference intensities on multiple DNA arrays using GADA. [My Copy] Bioinformatics (Oxford, England), Vol. 25, No. 10. (15 May 2009), pp. 1223-1230. by R. Pique-Regi, A. Ortega, S. Asgharzadeh posted to cnv by pkonings on 2009-03-18 13:24:41 as along with 5 people jfr guhjy jsatkosk humburg rdiaz
	Segmental copy number variation shapes tissue transcriptomes [My Copy] Nature Genetics, Vol. advance access (8 March 2009), pp. x-x. by Charlotte N. Henrichsen, Nicolas Vinckenbosch, Sebastian Zöllner, et al.Evelyne Chaignat, Sylvain Pradervand, Frédéric Schütz, Manuel Ruedi, Henrik Kaessmann, Alexandre Reymond posted to cnv by pkonings on 2009-03-18 13:23:09 as
	The impact of copy number variation on local gene expression in mouse hematopoietic stem and progenitor cells [My Copy] Nature Genetics, Vol. advance access (8 March 2009), pp. x-x. by Patrick Cahan, Yedda Li, Masayo Izumi, Timothy A. Graubert posted to cnv expression by pkonings on 2009-03-18 13:20:09 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 cnv sequencing by pkonings on 2009-03-18 13:17:48 as along with 18 people and 1 group hzoltan biovils stubrown cthachuk GustavoLacerda n00c darian bmenten natstreet sameersoi svenrahmann xiechao semrich rdiaz dswan sleepingcell neils magusina Bioinformatics
	Copy-number-variation and copy-number-alteration region detection by cumulative plots. [My Copy] BMC bioinformatics, Vol. 10 Suppl 1 (2009) by Wentian Li, Annette Lee, Peter K. Gregersen posted to cnv by pkonings on 2009-03-18 13:16:33 as along with 3 people rdiaz noushin jdbowes
	Association of a Germ-Line Copy Number Variation at 2p24.3 and Risk for Aggressive Prostate Cancer [My Copy] Cancer Res, Vol. 69, No. 6. (15 March 2009), pp. 2176-2179. by Wennuan Liu, Jishan Sun, Ge Li, et al.Yi Zhu, Scott Zhang, Seong-Tae Kim, Jielin Sun, Fredrik Wiklund, Kathleen Wiley, Sarah D. Isaacs, Par Stattin, Jianfeng Xu, David Duggan, John D. Carpten, William B. Isaacs, Henrik Gronberg, Lilly S. Zheng, Bao-Li Chang posted to cnv tumor by pkonings on 2009-03-18 13:00:31 as
	Replication Stress Induces Genome-wide Copy Number Changes in Human Cells that Resemble Polymorphic and Pathogenic Variants [My Copy] The American Journal of Human Genetics (19 February 2009) by Martin F. Arlt, Jennifer G. Mulle, Valerie M. Schaibley, et al.Ryan L. Ragland, Sandra G. Durkin, Stephen T. Warren, Thomas W. Glover posted to cnv by pkonings on 2009-02-23 11:08:19 as
	Paired-End Mapping Reveals Extensive Structural Variation in the Human Genome [My Copy] Science, Vol. 318, No. 5849. (19 October 2007), pp. 420-426. by Jan O. Korbel, Alexander E. Urban, Jason P. Affourtit, et al.Brian Godwin, Fabian Grubert, Jan F. Simons, Philip M. Kim, Dean Palejev, Nicholas J. Carriero, Lei Du, Bruce E. Taillon, Zhoutao Chen, Andrea Tanzer, A. C. Eugenia Saunders, Jianxiang Chi, Fengtang Yang, Nigel P. Carter, Matthew E. Hurles, Sherman M. Weissman, Timothy T. Harkins, Mark B. Gerstein, Michael Egholm, Michael Snyder posted to cnv by pkonings on 2009-02-20 12:50:27 as along with 22 people and 2 groups torfinnnome jandot n00c jonilaserson jrvalcourt APRegier jessopher hpaces Zephyrus orzenil stuetz matthewsuderman dpollard dchughes AaronDarling rdiaz giovanni jlangdon annacarina07 Neeperando jfr caseybrown Journal picks EisenLab
	CGAS: comparative genomic analysis server. [My Copy] Bioinformatics (Oxford, England), Vol. 25, No. 7. (1 April 2009), pp. 958-959. by Masumi Itoh, Hidemi Watanabe posted to cnv by pkonings on 2009-02-20 09:23:33 as along with 7 people n00c dswan behindtherabbit guhjy nuin natstreet druvus
	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 calling cnv by pkonings on 2009-02-20 09:22:54 as along with 3 people jfr daed rdiaz
	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 autoimmunity cnv crohn by pkonings on 2009-02-18 14:49:42 as along with 6 people leemachado shikin sahrazanetti rdiaz noushin Zephyrus
	A burst of segmental duplications in the genome of the African great ape ancestor [My Copy] Nature, Vol. 457, No. 7231. (12 February 2009), pp. 877-881. by Tomas Marques-Bonet, Jeffrey M. Kidd, Mario Ventura, et al.Tina A. Graves, Ze Cheng, Ladeana W. Hillier, Zhaoshi Jiang, Carl Baker, Ray Malfavon-Borja, Lucinda A. Fulton, Can Alkan, Gozde Aksay, Santhosh Girirajan, Priscillia Siswara, Lin Chen, Maria F. Cardone, Arcadi Navarro, Elaine R. Mardis, Richard K. Wilson, Evan E. Eichler posted to cnv evolution by pkonings on 2009-02-12 09:00:59 as along with 8 people psique dakelley provero shoshin anphony treangen djkt jbhiatt
	Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants [My Copy] Nature Genetics, Vol. advance access (8 February 2009), pp. x-x. by Myocardial Infarction Genetics Consortium posted to cnv gwas snp by pkonings on 2009-02-11 08:34:11 as
	A flexible rank-based framework for detecting copy number aberrations from array data [My Copy] Bioinformatics, Vol. 25, No. 6. (15 March 2009), pp. 722-728. by Thomas LaFramboise, Wendy Winckler, Roman K. Thomas posted to acgh cnv by pkonings on 2009-02-09 11:46:20 as along with 5 people jfr djkt rdiaz dswan guhjy
	Support for the involvement of large copy number variants in the pathogenesis of schizophrenia. [My Copy] Human molecular genetics, Vol. 18, No. 8. (15 April 2009), pp. 1497-1503. by George Kirov, Detelina Grozeva, Nadine Norton, et al.Dobril Ivanov, Kiran K. Mantripragada, Peter Holmans, International Schizophrenia Consortium, Wellcome Trust Case Control Consortium, Nick Craddock, Michael J. Owen, Michael C. O'Donovan posted to cnv schizophrenia by pkonings on 2009-02-09 11:40:23 as along with 1 person daforerog
	CCL3L Copy Number Variation and the Co-Evolution of Primate and Viral Genomes. [My Copy] PLoS genetics, Vol. 5, No. 1. (January 2009) by G. Gornalusse, S. Mummidi, W. He, G. Silvestri, M. Bamshad, S. K. Ahuja posted to cnv evolution by pkonings on 2009-02-09 11:39:17 as along with 1 person jdbowes
	A genome-wide investigation of SNPs and CNVs in schizophrenia. [My Copy] PLoS genetics, Vol. 5, No. 2. (6 February 2009), e1000373. by Anna C. Need, Dongliang Ge, Michael E. Weale, et al.Jessica Maia, Sheng Feng, Erin L. Heinzen, Kevin V. Shianna, Woohyun Yoon, Dalia Kasperaviciūte, Massimo Gennarelli, Warren J. Strittmatter, Cristian Bonvicini, Giuseppe Rossi, Karu Jayathilake, Philip A. Cola, Joseph P. McEvoy, Richard S. Keefe, Elizabeth M. Fisher, Pamela L. St Jean, Ina Giegling, Annette M. Hartmann, Hans-Jürgen J. Möller, Andreas Ruppert, Gillian Fraser, Caroline Crombie, Lefkos T. Middleton, David St Clair, Allen D. Roses, Pierandrea Muglia, Clyde Francks, Dan Rujescu, Herbert Y. Meltzer, David B. Goldstein posted to cnv gwas schizophrenia snp by pkonings on 2009-02-09 11:31:08 as along with 7 people fenghezi xingxu rdiaz skembel daforerog psique djkt
	DNA variations in human and medical genetics: 25 years of my experience [My Copy] J Hum Genet, Vol. 54, No. 1. (January 2009), pp. 1-8. by Yusuke Nakamura posted to cnv gwas snp str by pkonings on 2009-02-09 10:16:17 as along with 2 people guhjy psique
	Population analysis of large copy number variants and hotspots of human genetic disease. [My Copy] American journal of human genetics, Vol. advance access, No. 2. (22 January 2009), pp. x-x. by A. Itsara, G. Cooper, C. Baker, et al.S. Girirajan, J. Li, D. Absher, R. Krauss, R. Myers, P. Ridker, D. Chasman posted to cnv gwas by pkonings on 2009-02-09 10:13:07 as along with 8 people and 1 group daforerog jsatkosk turnersd sameersoi guhjy Zephyrus jdbowes psique Roswell Cancer Crosstalk
	"GenotypeColour": colour visualisation of SNPs and CNVs. [My Copy] BMC bioinformatics, Vol. 10, No. 1. (2009) by Sergio Barlati, Sergio Chiesa, Chiara Magri posted to cnv snp visualization by pkonings on 2009-02-09 10:07:55 as along with 4 people daforerog guhjy skap nuin
	A single-sample method for normalizing and combining full-resolution copy numbers from multiple platforms, labs and analysis methods. [My Copy] Bioinformatics (Oxford, England), Vol. 25, No. 7. (1 April 2009), pp. 861-867. by H. Bengtsson, A. Ray, P. Spellman, T. P. Speed posted to acgh agilent cnv snp by pkonings on 2009-02-09 09:54:32 as along with 5 people and 1 group zufar jfr djkt guhjy rdiaz Bioinformatics
	Allelic recombination between distinct genomic locations generates copy number diversity in human β-defensins [My Copy] Proceedings of the National Academy of Sciences, Vol. 106, No. 3. (20 January 2009), pp. 853-858. by Suhaili A. Bakar, Edward J. Hollox, John A. Armour posted to betadefensin cnv crohn evolution psoriasis by pkonings on 2009-01-21 10:23:21 as
	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 inference by pkonings on 2009-01-16 09:48:24 as along with 1 person leemachado
	Copy number variation showers in schizophrenia: an emerging hypothesis [My Copy] Molecular Psychiatry, Vol. advance online (13 January 2009), pp. x-x. by S. M. Singh, C. A. Castellani, R. L. O'Reilly posted to cnv meiosis mitosis by pkonings on 2009-01-15 11:32:56 as

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file-import-08-10-29	1718
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hla	7
incomplete	7
interval	7
item	7
jsm	7
local	7
log	7
lung	7
molecular	7
network	7
ordinal	7
overdispersion	7
partitioning	7
procedure	7
pseudolikelihood	7
r	7
section	7
segmentation	7
standard	7
stepwise	7
two-stage	7
validation	7
weighted	7
antigen	6
asymptotic	6
averaging	6
causal	6
cgh	6
closed	6
cluster	6
colitis	6
correlated	6
criteria	6
datasets	6
descent	6
discrete	6
errors	6
exploratory	6
functional	6
gibbs	6
gllamm	6
graphics	6
identical	6
imperfect	6
inequality	6
ld	6
leukocyte	6
lod	6
low	6
mapping	6
multiallelic	6
multipoint	6
ngs	6
parameter	6
pedigree	6
personal_genomics	6
procedures	6
process	6
pruning	6
robustness	6
shrinkage	6
single	6
spline	6
structural	6
structure	6
transmissiondisequilibrium	6
ulcerative	6
adjusted	5
admixture	5
akaike	5
anaemia	5
biomarker	5
colon	5
conditional	5
cytogenetics	5
decision	5
diagnosis	5
effectiveness	5
experiments	5
frequency	5
functions	5
genes	5
gold	5
growth	5
hiv	5
ibd	5
intraclass	5
joint	5
learning	5
level	5
loci	5
loss	5
management	5
markers	5
measurement	5
medical	5
misclassification	5
mixed-effects	5
nucleotide	5
pathway	5
pca	5
permutation	5
piecewise	5
point	5
pooling	5
positive	5
prior	5
program	5
rankings	5
reduction	5
reference	5
review	5
robust	5
semiparametric	5
single_cell	5
splines	5
squares	5
stage	5
subgroup	5
teaching	5
underdispersion	5
values	5
weight	5
aic	4
applications	4
autism	4
baseline	4
bic	4
birth	4
boundary	4
calculation	4
calculations	4
calling	4
care	4
casecontrol	4
censoring	4
change	4
choice	4
class	4
computation	4
cost	4
count	4
cox	4
crohn-disease	4
database	4
decomposition	4
detection	4
diabetes	4
diagnostics	4
discrimination	4
dropout	4
early	4
ecological	4
endpoint	4
endpoints	4
estimates	4
expected	4
failure	4
familywise	4
fitting	4
gee	4
gene-gene	4
genomic	4
genotype	4
genotypes	4
hapmap	4
heritability	4
iii	4
independence	4
index	4
infant	4
inflation	4
intensity	4
interactions	4
least	4
limit	4
measure	4
measurements	4
modelling	4
mortality	4
multiple_testing	4
nominal	4
nonignorable	4
non-parametric	4
nonproportional	4
normal	4
numerical	4
one-sided	4
outcomes	4
outliers	4
p	4
partial	4
pattern-mixture	4
permutations	4
phenotype	4
phenotypes	4
polymorphism	4
polytomous	4
population_stratification	4
profile	4
quasi-likelihood	4
randomization	4
randomized	4
recursive	4
relatedness	4
replication	4
resampling	4
residual	4
sampler	4
simulated	4
simultaneous	4
small	4
spatial	4
stratification	4
strd	4
surface	4
susceptibility	4
table	4
tables	4
the	4
time-dependent	4
to	4
trait	4
transplantation	4
treatment	4
trends	4
tumor	4
under	4
water	4
2	3
adjustment	3
adjuvant	3
affymetrix	3
agents	3
alzheimers	3
analyses	3
aneuploidy	3
atmospheric	3
bagging	3
bandwidth	3
based	3
biased	3
biomarkers	3
biometric	3
board	3
bowel	3
canonical	3
cell	3
col3a1	3
color	3
comparison	3
condition	3
conjugate	3
controls	3
copula	3
covariate	3
dimensionality	3
dirichlet	3
display	3
distance	3
distributions	3
dna	3
doe	3
drug	3
ehlers-danlos	3
environmental	3
erythropoietin	3
event	3
exact	3
explained	3
exponential	3
exposure	3
fdr	3
frailty	3
gene-disease	3
graph	3
graphical	3
guidelines	3
history	3
image	3

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