CiteULike: pkonings's acgh [10 articles]

	Identification of significant regional genetic variations using continuous CNV values in aCGH data. [My Copy] Genomics (19 August 2009) by Ki-Yeol Y. Kim, Gui Youn Y. Lee, Jin Kim, Hei-Cheul C. Jeung, Hyun Cheol C. Chung, Sun Young Y. Rha posted to segmentation acgh by pkonings on 2009-08-26 09:05:44 as along with 1 person rdiaz
	SnoopCGH: software for visualizing comparative genomic hybridization data [My Copy] Bioinformatics, Vol. 25, No. 20. (15 October 2009), pp. 2732-2733. by Jacob Almagro-Garcia, Magnus Manske, Celine Carret, et al.Susana Campino, Sarah Auburn, Bronwyn L. MacInnis, Gareth Maslen, Arnab Pain, Christopher I. Newbold, Dominic P. Kwiatkowski, Taane G. Clark posted to visualization software acgh by pkonings on 2009-08-18 09:37:25 as along with 3 people and 1 group nuin jandot rdiaz Journal picks
	A hypergraph-based learning algorithm for classifying gene expression and arrayCGH data with prior knowledge [My Copy] Bioinformatics, Vol. 25, No. 21. (1 November 2009), pp. 2831-2838. by Ze Tian, TaeHyun Hwang, Rui Kuang posted to acgh by pkonings on 2009-08-17 09:06:13 as along with 5 people tmmurali dolchan rdiaz guhjy nuin
	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
	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
	MSMAD: a computationally efficient method for the analysis of noisy array CGH data. [My Copy] Bioinformatics (Oxford, England), Vol. 25, No. 6. (15 March 2009), pp. 703-713. by Eva Budinska, Eva Gelnarova, Michael G. Schimek posted to acgh by pkonings on 2009-02-03 08:47:17 as along with 5 people jfr nuin rdiaz guhjy dswan
	Genomic copy number determination in cancer cells from single nucleotide polymorphism microarrays based on quantitative genotyping corrected for aneuploidy [My Copy] Genome Research, Vol. advance access (13 January 2009) by Edward F. Attiyeh, Sharon J. Diskin, Marc A. Attiyeh, et al.Yaël P. Mossé, Cuiping Hou, Eric M. Jackson, Cecilia Kim, Joseph Glessner, Hakon Hakonarson, Jaclyn A. Biegel, John M. Maris posted to acgh cnv by pkonings on 2009-01-14 15:27:15 as
	Bayesian DNA copy number analysis [My Copy] BMC Bioinformatics, Vol. 10 (08 January 2009), 10. by Paola M. V. Rancoita, Marcus Hutter, Francesco Bertoni, Ivo Kwee posted to acgh bayesian cnv by pkonings on 2009-01-12 10:37:56 as along with 6 people guhjy noushin nuin mhamada xieminzhu rdiaz
	Estimation of tumor heterogeneity using CGH array data. [My Copy] BMC bioinformatics, Vol. 10, No. 1. (2009) by K. Wang, J. Li, S. Li, L. Bolund, C. Wiuf posted to acgh cnv tumor by pkonings on 2009-01-12 10:36:09 as along with 4 people and 1 group jfr mdharsee rdiaz dswan Bioinformatics
	CNVDetector: locating copy number variations using array CGH data [My Copy] Bioinformatics, Vol. 24, No. 23. (1 December 2008), pp. 2773-2775. by Peng-An Chen, Hsiao-Fei Liu, Kun-Mao Chao posted to acgh cnv by pkonings on 2008-12-10 09:20:17 as along with 4 people jfr dswan rdiaz nuin

pkonings's acgh [10 articles] Export

pkonings's tags

file-import-08-10-29	1718
regression	139
data	125
gwas	105
cnv	101
model	92
analysis	88
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