rdiaz's snp [51 articles] Export

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

	Validation and extension of an empirical Bayes method for SNP calling on Affymetrix microarrays. [My Copy] Genome biology, Vol. 9, No. 4. (3 April 2008), R63. by Shin Lin, Benilton Carvalho, David J. Cutler, Dan E. Arking, Aravinda Chakravarti, Rafael A. Irizarry posted to snp calling bayesian affymetrix by rdiaz on 2009-10-23 14:19:08 as along with 5 people shikin daforerog maren natstreet jfr
	The SNP ratio test: pathway analysis of genome-wide association datasets [My Copy] Bioinformatics, Vol. 25, No. 20. (15 October 2009), pp. 2762-2763. by Colm O'Dushlaine, Elaine Kenny, Elizabeth A. Heron, et al.Ricardo Segurado, Michael Gill, Derek W. Morris, Aiden Corvin posted to snp set pathway gwas gene by rdiaz on 2009-10-09 10:45:52 as along with 8 people shikin zufar liqbbi daforerog natstreet pkonings guhjy druvus
	Segmentation and Estimation for SNP Microarrays: A Bayesian Multiple Change-Point Approach. [My Copy] Biometrics (17 September 2009) by Yu Chuan C. Tai, Mark N. Kvale, John S. Witte posted to snp region recurrent common cnv bayesian by rdiaz on 2009-09-25 13:27:31 as along with 1 person shikin
	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 teaching snp region example common cnv autism by rdiaz on 2009-09-23 17:25:29 as along with 8 people daforerog pkonings fenghezi scjparker dswan neils jbhiatt psique
	Extensions of sparse canonical correlation analysis with applications to genomic data. [My Copy] Statistical applications in genetics and molecular biology, Vol. 8, No. 1. (2009) by Daniela M. Witten, Robert J. Tibshirani posted to snp integration expression coexpression cnv by rdiaz on 2009-09-15 16:55:10 as
	SHARE: an adaptive algorithm to select the most informative set of SNPs for candidate genetic association [My Copy] Biostat, Vol. 10, No. 4. (1 October 2009), pp. 680-693. by James Y. Dai, Michael Leblanc, Nicholas L. Smith, Bruce Psaty, Charles Kooperberg posted to window snp selection recurrent haplotype gwas by rdiaz on 2009-09-15 16:39:04 as along with 1 person djkt
	Potential etiologic and functional implications of genome-wide association loci for human diseases and traits [My Copy] Proceedings of the National Academy of Sciences, Vol. 106, No. 23. (9 June 2009), pp. 9362-9367. by Lucia A. Hindorff, Praveen Sethupathy, Heather A. Junkins, et al.Erin M. Ramos, Jayashri P. Mehta, Francis S. Collins, Teri A. Manolio posted to snp review gwas disease catalog association by rdiaz on 2009-09-11 11:46:25 as along with 6 people liqbbi guhjy zufar daforerog pkonings jsatkosk
	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 integration cnv by rdiaz on 2009-09-09 16:28:41 as along with 1 person and 1 group daed Journal picks
	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 snp modeling cgh by rdiaz on 2009-09-09 12:56:11 as along with 2 people pkonings guhjy
	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 review comparison cnv by rdiaz on 2009-09-08 16:40:37 as along with 2 people daed jsatkosk
	De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot. [My Copy] Nature genetics, Vol. 41, No. 8. (August 2009), pp. 931-935. by Steven C. Greenway, Alexandre C. Pereira, Jennifer C. Lin, et al.Steven R. DePalma, Samuel J. Israel, Sonia M. Mesquita, Emel Ergul, Jessie H. Conta, Joshua M. Korn, Steven A. McCarroll, Joshua M. Gorham, Stacey Gabriel, David M. Altshuler, Maria de Lourdes d. e. . L. Quintanilla-Dieck, Maria Alexandra A. Artunduaga, Roland D. Eavey, Robert M. Plenge, Nancy A. Shadick, Michael E. Weinblatt, Philip L. De Jager, David A. Hafler, Roger E. Breitbart, Jonathan G. Seidman, Christine E. Seidman posted to snp de_novo cnv by rdiaz on 2009-09-08 12:47:47 as along with 1 person misonneh
	GRIMP: a web- and grid-based tool for high-speed analysis of large-scale genome-wide association using imputed data [My Copy] Bioinformatics, Vol. 25, No. 20. (15 October 2009), pp. 2750-2752. by Karol Estrada, Anis Abuseiris, Frank G. Grosveld, Andre G. Uitterlinden, Tobias A. Knoch, Fernando Rivadeneira posted to software snp imputation gwas grid computing by rdiaz on 2009-09-08 10:54:40 as along with 2 people daforerog pkonings
	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. [My Copy] Human molecular genetics, Vol. 18, No. 23. (1 December 2009), pp. 4650-4661. by Anna C. Need, Deborah K. Attix, Jill M. McEvoy, et al.Elizabeth T. Cirulli, Kristen L. Linney, Priscilla Hunt, Dongliang Ge, Erin L. Heinzen, Jessica M. Maia, Kevin V. Shianna, Michael E. Weale, Lynn F. Cherkas, Gail Clement, Tim D. Spector, Greg Gibson, David B. Goldstein posted to snp example disease cgh association by rdiaz on 2009-09-07 11:41:51 as along with 1 person daforerog
	Correlating multiple SNPs and multiple disease phenotypes: penalized non-linear canonical correlation analysis. [My Copy] Bioinformatics (Oxford, England), Vol. 25, No. 21. (1 November 2009), pp. 2764-2771. by Sandra Waaijenborg, Aeilko H. Zwinderman posted to snp phenotype correlation canonical by rdiaz on 2009-08-21 11:41:26 as along with 3 people and 1 group guhjy dswan pkonings Bioinformatics
	Hidden Markov models for the assessment of chromosomal alterations using high-throughput SNP arrays. [My Copy] The annals of applied statistics, Vol. 2, No. 2. (1 June 2008), pp. 687-713. by Robert B. Scharpf, Giovanni Parmigiani, Jonathan Pevsner, Ingo Ruczinski posted to snp hmm cnv cgh by rdiaz on 2009-08-18 19:35:04 as
	Single nucleotide polymorphism arrays: a decade of biological, computational and technological advances [My Copy] Nucl. Acids Res., Vol. 37, No. 13. (1 July 2009), pp. 4181-4193. by Thomas Laframboise posted to review snp teaching by rdiaz on 2009-07-31 16:25:12 as along with 4 people and 1 group pkonings GeeSharpMinor daforerog guhjy Journal picks
	QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data. [My Copy] Nucleic Acids Res (27 March 2007) by Stefano Colella, Christopher Yau, Jennifer M M. Taylor, et al.Ghazala Mirza, Helen Butler, Penny Clouston, Anne S S. Bassett, Anneke Seller, Christopher C C. Holmes, Jiannis Ragoussis posted to cnv hmm recurrent region snp by rdiaz on 2009-07-24 16:38:29 as along with 6 people and 2 groups qfwills druvus waszak psique caldavis jfr parkinson's disease references Bioinformatics
	PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data [My Copy] Genome Research, Vol. 17, No. 11. (5 November 2007), pp. 1665-1674. by Kai Wang, Mingyao Li, Dexter Hadley, et al.Rui Liu, Joseph Glessner, Struan F. A. Grant, Hakon Hakonarson, Maja Bucan posted to acgh cgh penncnv snp by rdiaz on 2009-07-20 18:01:49 as along with 2 people vplagnol jfr
	A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease [My Copy] Genome Research, Vol. 19, No. 9. (8 September 2009), pp. 1579-1585. by Heather C. Mefford, Gregory M. Cooper, Troy Zerr, et al.Joshua D. Smith, Carl Baker, Neil Shafer, Erik C. Thorland, Cindy Skinner, Charles E. Schwartz, Deborah A. Nickerson, Evan E. Eichler posted to cnv example snp by rdiaz on 2009-07-16 10:55:34 as along with 1 person daforerog
	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 affymetrix cgh normalization snp by rdiaz on 2009-06-29 17:29:02 as along with 5 people shikin djkt pkonings daforerog neils
	A flexible and accurate genotype imputation method for the next generation of genome-wide association studies. [My Copy] PLoS genetics, Vol. 5, No. 6. (19 June 2009), e1000529. by Bryan N. Howie, Peter Donnelly, Jonathan Marchini posted to software snp multiple imputation by rdiaz on 2009-06-29 15:13:02 as along with 8 people and 1 group talponer engelhardt maren xingxu kimorley daforerog reyez djkt Journal picks
	Accounting for uncertainty when assessing association between copy number and disease: a latent class model. [My Copy] BMC bioinformatics, Vol. 10 (06 June 2009), 172. by Juan R. González, Isaac Subirana, Geòrgia Escaramís, et al.Solymar Peraza, Alejandro Cáceres, Xavier Estivill, Lluís Armengol posted to association case-control cnv snp by rdiaz on 2009-06-18 13:26:46 as along with 2 people vplagnol sameersoi
	An integrative scoring system for ranking SNPs by their potential deleterious effects. [My Copy] Bioinformatics (Oxford, England), Vol. 25, No. 8. (15 April 2009), pp. 1048-1055. by Phil Hyoun H. Lee, Hagit Shatkay posted to gwas snp by rdiaz on 2009-04-14 13:55:29 as along with 6 people and 1 group jandot daforerog george_g djkt Zephyrus pkonings Roswell Cancer Crosstalk
	Data structures and algorithms for analysis of genetics of gene expression with Bioconductor: GGtools 3.x [My Copy] Bioinformatics, Vol. 25, No. 11. (1 June 2009), pp. 1447-1448. by Vincent J. Carey, Adam R. Davis, Michael F. Lawrence, Robert Gentleman, Benjamin A. Raby posted to software snp integration expression bioconductor by rdiaz on 2009-04-14 12:47:32 as along with 6 people jfr guhjy druvus nuin djkt giovanni
	SNP imputation in association studies. [My Copy] Nature biotechnology, Vol. 27, No. 4. (April 2009), pp. 349-351. by Eran Halperin, Dietrich A. Stephan posted to imputation snp by rdiaz on 2009-04-14 11:49:00 as along with 4 people daforerog guhjy lwaldron psique
	Association of survival and disease progression with chromosomal instability: A genomic exploration of colorectal cancer [My Copy] Proceedings of the National Academy of Sciences, Vol. 106, No. 17. (28 April 2009), pp. 7131-7136. by Michal Sheffer, Manny D. Bacolod, Or Zuk, et al.Sarah F. Giardina, Hanna Pincas, Francis Barany, Philip B. Paty, William L. Gerald, Daniel A. Notterman, Eytan Domany posted to survival snp integration instability expression cnv chromosomal by rdiaz on 2009-04-14 11:32:37 as along with 2 people jfr kdpreter
	Markov Models for Inferring Copy Number Variations from Genotype Data on Illumina Platforms. [My Copy] Human heredity, Vol. 68, No. 1. (1 April 2009), pp. 1-22. by Hui Wang, Jan H H. Veldink, Hylke Blauw, Leonard H H. van den Berg, Roel A A. Ophoff, Chiara Sabatti posted to association cnv hmm illumina recurrent snp by rdiaz on 2009-04-14 11:18:36 as
	Combining information from related meta-analyses of genetic association studies [My Copy] Journal of the Royal Statistical Society: Series C (Applied Statistics), Vol. 57, No. 1. (2008), pp. 103-115. by J. R. Thompson, C. Minelli, K. R. Abrams, A. Thakkinstian, J. Attia posted to meta-analysis snp by rdiaz on 2009-04-13 10:20:25 as
	Programs for calculating the statistical powers of detecting susceptibility genes in case-control studies based on multistage designs. [My Copy] Bioinformatics (Oxford, England), Vol. 25, No. 2. (15 January 2009), pp. 272-273. by Nobutaka Kitamura, Kouhei Akazawa, Akinori Miyashita, et al.Ryozo Kuwano, Shin-ichi Toyabe, Junichiro Nakamura, Norihito Nakamura, Tatsuhiko Sato, M. Aminul Hoque posted to gwas power snp wgas by rdiaz on 2009-03-23 17:04:36 as along with 3 people daforerog guhjy pkonings
	MegaSNPHunter: a learning approach to detect disease predisposition SNPs and high level interactions in genome wide association study. [My Copy] BMC bioinformatics, Vol. 10, No. 1. (2009) by Xiang Wan, Can Yang, Qiang Yang, Hong Xue, Nelson L. Tang, Weichuan Yu posted to association interaction snp by rdiaz on 2009-03-23 16:36:48 as along with 6 people daed maren daforerog TRHvidsten guhjy pkonings
	Reference Alignment of SNP Microarray Signals for Copy Number Analysis of Tumors [My Copy] Bioinformatics (3 December 2008), btn624. by Stan Pounds, Cheng Cheng, Charles Mullighan, Susana C. Raimondi, Sheila Shurtleff, James R. Downing posted to cnv normalization snp by rdiaz on 2009-03-23 14:53:48 as along with 3 people and 1 group jfr dswan nuin Bioinformatics
	Mutation Patterns in the Human Genome: More Variable Than Expected [My Copy] PLoS Biol, Vol. 7, No. 2. (3 February 2009), e1000028. by Laurent Duret posted to cnv mutation review snp by rdiaz on 2009-03-23 11:41:59 as along with 7 people and 2 groups Garamonfok barry leelarcombe idoerg aprasad djkt gjuggler structural_bioinformatics Bioinformatics
	Capturing the spectrum of interaction effects in genetic association studies by simulated evaporative cooling network analysis. [My Copy] PLoS genetics, Vol. 5, No. 3. (20 March 2009), e1000432. by Brett A. McKinney, James E. Crowe, Jingyu Guo, Dehua Tian posted to interaction network snp by rdiaz on 2009-03-23 10:12:24 as along with 4 people and 1 group daforerog guhjy dpollard jdbowes RockmanLab
	A Genome-Wide Association Study of Pulmonary Function Measures in the Framingham Heart Study [My Copy] PLoS Genet, Vol. 5, No. 3. (20 March 2009), e1000429. by Jemma B. Wilk, Ting-Hsu Chen, Daniel J. Gottlieb, et al.Robert E. Walter, Michael W. Nagle, Brian J. Brandler, Richard H. Myers, Ingrid B. Borecki, Edwin K. Silverman, Scott T. Weiss, George T. O'Connor posted to copd epoc snp by rdiaz on 2009-03-23 10:10:24 as along with 1 person oelemento
	Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants [My Copy] Nat Genet, Vol. 41, No. 3. (8 March 2009), pp. 334-341. posted to cnv gwas snp wgas by rdiaz on 2009-03-20 14:20:27 as along with 3 people PabloMarin ilyashl Terkko
	AssociationViewer: a scalable and integrated software tool for visualization of large-scale variation data in genomic context. [My Copy] Bioinformatics (Oxford, England), Vol. 25, No. 5. (1 March 2009), pp. 662-663. by Olivier Martin, Armand Valsesia, Amalio Telenti, Ioannis Xenarios, Brian J. Stevenson posted to annotation snp software visualization by rdiaz on 2009-03-20 14:11:42 as along with 6 people nuin ilyashl guhjy pkonings jmeppley daforerog
	Genotyping and inflated type I error rate in genome-wide association case/control studies [My Copy] BMC Bioinformatics, Vol. 10 (23 February 2009), 68. by Joshua N. Sampson, Hongyu Zhao posted to snp by rdiaz on 2009-03-18 15:06:00 as along with 2 people guhjy pkonings
	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 genetic heterogeneity integration review snp variation by rdiaz on 2009-03-18 13:57:41 as along with 18 people and 1 group ongenetics PabloMarin songpku guhjy ilyashl roys JoeSabatini pkonings Zephyrus jbhiatt daforerog welliegirl dbk psique zufar misonneh fenghezi dchughes Roswell Cancer Crosstalk
	Performance of random forest when SNPs are in linkage disequilibrium [My Copy] BMC Bioinformatics, Vol. 10 (05 March 2009), 78. by Yan, Kathryn L. Lunetta posted to forest random snp by rdiaz on 2009-03-18 13:29:37 as along with 2 people guhjy neils
	Beyond odds ratios--communicating disease risk based on genetic profiles. [My Copy] Nature reviews. Genetics, Vol. 10, No. 4. (24 April 2009), pp. 264-269. by P. Kraft, S. Wacholder, M. C. Cornelis, et al.F. B. Hu, R. B. Hayes, G. Thomas, R. Hoover, D. J. Hunter, S. Chanock posted to gwas snp statistics wgas by rdiaz on 2009-03-17 17:26:13 as along with 10 people and 1 group zufar Zephyrus PabloMarin lwaldron pkonings roys daforerog psique misonneh guhjy Roswell Cancer Crosstalk
	Maximizing power in association studies. [My Copy] Nature biotechnology, Vol. 27, No. 3. (March 2009), pp. 255-256. by Eran Halperin, Dietrich A. Stephan posted to association gwas snp by rdiaz on 2009-03-17 16:52:19 as along with 4 people daforerog Zephyrus guhjy psique
	Genome-wide association analysis by lasso penalized logistic regression [My Copy] Bioinformatics, Vol. 25, No. 6. (15 March 2009), pp. 714-721. by Tong T. Wu, Yi F. Chen, Trevor Hastie, Eric Sobel, Kenneth Lange posted to classification snp by rdiaz on 2009-03-17 15:16:06 as along with 2 people jessopher guhjy
	Interpretation of Genetic Association Studies: Markers with Replicated Highly Significant Odds Ratios May Be Poor Classifiers [My Copy] PLoS Genet, Vol. 5, No. 2. (6 February 2009), e1000337. by Johanna Jakobsdottir, Michael B. Gorin, Yvette P. Conley, Robert E. Ferrell, Daniel E. Weeks posted to roc sensitivity snp specificity teaching classification gwas by rdiaz on 2009-02-18 16:55:45 as along with 9 people and 1 group xingxu sg45653 jessopher pkonings Zephyrus psique mdharsee wimufi djkt Roswell Cancer Crosstalk
	A general approach to simultaneous model fitting and variable elimination in response models for biological data with many more variables than observations. [My Copy] BMC bioinformatics, Vol. 9, No. 1. (2008) by Harri T. Kiiveri posted to classification gwas snp wgas by rdiaz on 2009-02-18 10:49:46 as along with 6 people shigepong joaocarrico osilander iceman2995 akastrin guhjy
	Modeling genetic inheritance of copy number variations [My Copy] Nucl. Acids Res., Vol. 36, No. 21. (1 December 2008), e138. by Kai Wang, Zhen Chen, Mahlet G. Tadesse, et al.Joseph Glessner, Struan F. A. Grant, Hakon Hakonarson, Maja Bucan, Mingyao Li posted to association classification cnv family inheritance mendelian snp by rdiaz on 2008-10-13 10:28:50 as along with 3 people sameersoi psique noushin
	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. M. Korn, Finny G. G. Kuruvilla, Steven A. A. Mccarroll, et al.Alec Wysoker, James Nemesh, Simon Cawley, Earl Hubbell, Jim Veitch, Patrick J. J. Collins, Katayoon Darvishi, Charles Lee, Marcia M. M. Nizzari, Stacey B. B. Gabriel, Shaun Purcell, Mark J. J. Daly, David Altshuler posted to cnv hmm snp by rdiaz on 2008-09-29 15:09:50 as along with 14 people shikin sameersoi fenghezi psique buyske maren guhjy pdexheimer pengchy caseybrown dakelley djkt daed vplagnol
	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 cnv gwas method snp by rdiaz on 2008-09-29 15:08:44 as along with 12 people and 1 group shikin sameersoi daforerog psique maren pengchy vplagnol waszak caseybrown Zephyrus misonneh guhjy Roswell Cancer Crosstalk
	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. E. Hurles posted to cnv gwas method snp by rdiaz on 2008-09-29 15:08:42 as along with 16 people and 1 group biovils daed zufar daforerog pengchy ptrobajo vplagnol waszak caseybrown Zephyrus dakelley buyske misonneh djkt Stew guhjy Roswell Cancer Crosstalk
	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 cnv gwas snp by rdiaz on 2008-09-29 15:06:03 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 daed guhjy Roswell Cancer Crosstalk
	Detecting genetic variation in microarray expression data [My Copy] Genome Res. (3 July 2007), gr.6307307. by Jennifer A. Greenhall, Matthew A. Zapala, Mario Caceres, et al.Ondrej Libiger, Carrolee Barlow, Nicholas J. Schork, David J. Lockhart posted to affymetrix arrays genetic snp variation by rdiaz on 2007-07-19 17:16:22 as along with 7 people and 2 groups askrajiv guhjy jfr eckart_bindewald giovanni qmwwallace msomel Bioinformatics GeschwindLab

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editorial	2
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array	2
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binary	1
stochastic	1
integrity	1
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grant	1
nework	1
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window	1
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unit	1
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covariables	1
confidence	1
book	1
propagation	1
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union	1
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dynamics	1
analysis	1
p-values	1
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ai	1
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python	1
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shrinkage	1
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5	1
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mobby	1
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signs	1
tumor	1
programmable	1
family	1

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