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Recent papers classified by the tag snp.

	Searching for SNPs with cloud computing [My Copy] Genome Biology, Vol. 10, No. 11. (2009), R134. by Ben Langmead, Michael Schatz, Jimmy Lin, Mihai Pop, Steven Salzberg posted to software snp hadoop cloud-computing alignment by neils on 2009-11-22 04:55:28 as along with 1 person n00c
	SNPinfo: integrating GWAS and candidate gene information into functional SNP selection for genetic association studies [My Copy] Nucl. Acids Res., Vol. 37, No. suppl_2. (1 July 2009), pp. W600-605. by Zongli Xu, Jack A. Taylor posted to study-design studies snp selection association by Zephyrus on 2009-11-20 05:48:11 as along with 7 people songpku daed misonneh guhjy psique jdbowes daforerog
	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
	Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease. [My Copy] JAMA : the journal of the American Medical Association, Vol. 302, No. 1. (1 July 2009), pp. 37-48. by Paul Elliott, John C. Chambers, Weihua Zhang, et al.Robert Clarke, Jemma C. Hopewell, John F. Peden, Jeanette Erdmann, Peter Braund, James C. Engert, Derrick Bennett, Lachlan Coin, Deborah Ashby, Ioanna Tzoulaki, Ian J. Brown, Shahrul Mt-Isa, Mark I. McCarthy, Leena Peltonen, Nelson B. Freimer, Martin Farrall, Aimo Ruokonen, Anders Hamsten, Noha Lim, Philippe Froguel, Dawn M. Waterworth, Peter Vollenweider, Gerard Waeber, Marjo-Riitta R. Jarvelin, Vincent Mooser, James Scott, Alistair S. Hall, Heribert Schunkert, Sonia S. Anand, Rory Collins, Nilesh J. Samani, Hugh Watkins, Jaspal S. Kooner posted to snp cv crp by guhjy on 2009-11-18 02:33:46 as along with 3 people Terkko booker djmonstermo
	Genetic Variation and Recent Positive Selection in Worldwide Human Populations: Evidence from Nearly 1 Million SNPs. [My Copy] PloS one, Vol. 4, No. 11. (18 November 2009), e7888. by David López Herráez, Marc Bauchet, Kun Tang, et al.Christoph Theunert, Irina Pugach, Jing Li, Madhusudan R. Nandineni, Arnd Gross, Markus Scholz, Mark Stoneking posted to snp by phoenixzxl on 2009-11-18 01:05:49 as along with 1 person gjuggler
	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 cca by guhjy on 2009-11-17 04:34:05 as along with 3 people and 1 group dswan rdiaz pkonings Bioinformatics
	Single Nucleotide Polymorphisms in Inflammation-related Genes and Mortality in a Community-based Cohort in Washington County, Maryland [My Copy] Am. J. Epidemiol., Vol. 167, No. 7. (7 February 2008), pp. kwm378-813. by Lisa Gallicchio, Howard Chang, Dana K. Christo, et al.Lucy Thuita, Han-Yao Huang, Paul Strickland, Ingo Ruczinski, Sandra C. Hoffman, Kathy J. Helzlsouer posted to snp inflammation by zoex_99 on 2009-11-16 17:31:07 as
	SNP detection for massively parallel whole-genome resequencing [My Copy] Genome Research, Vol. 19, No. 6. (6 June 2009), pp. 1124-1132. by Ruiqiang Li, Yingrui Li, Xiaodong Fang, et al.Huanming Yang, Jian Wang, Karsten Kristiansen, Jun Wang posted to software soap snp short-reads detection by torfinnnome on 2009-11-16 16:41:04 as along with 18 people hzoltan seb1 maren adijr greg jandot guhjy jonilaserson n00c druvus reyez sandfire jasontsai djkt sameersoi natstreet jbhiatt GeeSharpMinor
	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 gene_expression bioconductor by jfr on 2009-11-15 16:09:51 as along with 6 people guhjy druvus nuin rdiaz djkt giovanni
	Tag SNP selection for Finnish individuals based on the CEPH Utah HapMap database [My Copy] Genetic Epidemiology, Vol. 30, No. 2. (2006), pp. 180-190. by Cristen J. Willer, Laura J. Scott, Lori L. Bonnycastle, et al.Anne U. Jackson, Peter Chines, Randall Pruim, Craig W. Bark, Ya-Yu Tsai, Elizabeth W. Pugh, Kimberly F. Doheny, Leena Kinnunen, Karen L. Mohlke, Timo T. Valle, Richard N. Bergman, Jaakko Tuomilehto, Francis S. Collins, Michael Boehnke posted to snp hapmap database by wwalke on 2009-11-13 23:40:08 as along with 1 person ashandanj
	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
	Genome-wide autozygosity mapping in human populations. [My Copy] Genetic epidemiology, Vol. 33, No. 2. (February 2009), pp. 172-180. by Shuang Wang, Chad Haynes, Francis Barany, Jurg Ott posted to snp roh population human homozygosity genome-wide autozigosity by ealloza on 2009-11-12 18:34:23 as along with 2 people psique daforerog
	Long contiguous stretches of homozygosity in the human genome. [My Copy] Human mutation, Vol. 27, No. 11. (November 2006), pp. 1115-1121. by Ling-Hui H. Li, Sheng-Feng F. Ho, Chien-Hsiun H. Chen, et al.Chun-Yu Y. Wei, Wan-Ching C. Wong, Li-Ying Y. Li, Shuen-Iu I. Hung, Wen-Hung H. Chung, Wen-Han H. Pan, Ming-Ta T. Lee, Fuu-Jen J. Tsai, Ching-Fen F. Chang, Jer-Yuarn Y. Wu, Yuan-Tsong T. Chen posted to snp loh human homozygosity by ealloza on 2009-11-12 18:31:30 as along with 2 people daforerog psique
	Extended tracts of homozygosity in outbred human populations. [My Copy] Human molecular genetics, Vol. 15, No. 5. (1 March 2006), pp. 789-795. by Jane Gibson, Newton E. Morton, Andrew Collins posted to snp roh population loh homozygosity hapmap by ealloza on 2009-11-12 18:27:19 as along with 3 people daforerog psique ashandanj
	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
	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
	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 snp review human genetic_architecture complex_traits by ongenetics on 2009-11-11 13:13:12 as along with 18 people and 1 group PabloMarin songpku guhjy ilyashl roys JoeSabatini pkonings Zephyrus jbhiatt daforerog welliegirl dbk psique zufar misonneh fenghezi rdiaz dchughes Roswell Cancer Crosstalk
	Common Variants of Inflammatory Cytokine Genes Are Associated with Risk of Nephropathy in Type 2 Diabetes among Asian Indians [My Copy] PLoS ONE, Vol. 4, No. 4. (9 April 2009), e5168. by Tarunveer S. Ahluwalia, Madhu Khullar, Monica Ahuja, et al.Harbir S. Kohli, Anil Bhansali, Viswanathan Mohan, Radha Venkatesan, Taranjit S. Rai, Kamal Sud, Pawan K. Singal posted to tnf snp dn cytokine by guhjy on 2009-11-11 04:19:08 as
	Mapping short DNA sequencing reads and calling variants using mapping quality scores [My Copy] Genome Research, Vol. 18, No. 11. (19 November 2008), pp. 1851-1858. by Heng Li, Jue Ruan, Richard Durbin posted to snv snp ngs alignment by cthachuk on 2009-11-09 19:12:52 as along with 37 people and 2 groups heliopais hzoltan darshan adijr darian bozdagd jmanning2k stubrown APRegier ghattem jbhiatt mmartin michaelbarton polivares jonilaserson humburg n00c jessopher maren GeeSharpMinor vmsr vplagnol natstreet poschm jfr druvus dandaman xingxu rschulz jmcq inesdesantiago Neeperando nmohelli matthewsuderman bpb gdb farhat SIMR bioinformatics BergmanLab
	dbSMR: a novel resource of genome-wide SNPs affecting microRNA mediated regulation [My Copy] BMC Bioinformatics, Vol. 10, No. 1. (2009), 108. by Manoj Hariharan, Vinod Scaria, Samir Brahmachari posted to snp microrna database by heliopais on 2009-11-09 17:32:11 as along with 7 people and 1 group jfr songpku guhjy pengchy daforerog lwaldron ealloza microRNA
	Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia. [My Copy] Nature genetics, Vol. 41, No. 10. (06 October 2009), pp. 1110-1115. by Johan Rung, Stéphane Cauchi, Anders Albrechtsen, et al.Lishuang Shen, Ghislain Rocheleau, Christine Cavalcanti-Proença, François Bacot, Beverley Balkau, Alexandre Belisle, Knut Borch-Johnsen, Guillaume Charpentier, Christian Dina, Emmanuelle Durand, Paul Elliott, Samy Hadjadj, Marjo-Riitta R. Järvelin, Jaana Laitinen, Torsten Lauritzen, Michel Marre, Alexander Mazur, David Meyre, Alexandre Montpetit, Charlotta Pisinger, Barry Posner, Pernille Poulsen, Anneli Pouta, Marc Prentki, Rasmus Ribel-Madsen, Aimo Ruokonen, Anelli Sandbaek, David Serre, Jean Tichet, Martine Vaxillaire, Jørgen F. Wojtaszewski, Allan Vaag, Torben Hansen, Constantin Polychronakos, Oluf Pedersen, Philippe Froguel, Robert Sladek posted to snp irs1 irs dm by guhjy on 2009-11-09 05:16:13 as along with 1 person sf11
	Allelic imbalance sequencing reveals that single-nucleotide polymorphisms frequently alter microRNA-directed repression [My Copy] Nature Biotechnology, Vol. 27, No. 5. (26 April 2009), pp. 472-477. by Jinkuk Kim, David P. Bartel posted to snp mirna_regulation mirna by jfr to the group microRNA on 2009-11-08 23:34:10 as along with 7 people guhjy fenghezi giovanni jbhiatt daforerog samgj valeriehilgers
	The colorectal cancer risk at 18q21 is caused by a novel variant altering SMAD7 expression [My Copy] Genome Research, Vol. 19, No. 6. (June 2009), pp. 987-993. by Alan M. Pittman, Silvia Naranjo, Emily Webb, et al.Peter Broderick, Esther H. Lips, Tom van Wezel, Hans Morreau, Kate Sullivan, Sarah Fielding, Philip Twiss, Jayaram Vijayakrishnan, Fernando Casares, Mobshra Qureshi, José L. Gómez-Skarmeta, Richard S. Houlston posted to snp smad7 colon_cancer by jfr on 2009-11-08 23:32:50 as along with 1 person neils
	Common genetic variants in pre-microRNAs are associated with risk of coal workers' pneumoconiosis. [My Copy] Journal of human genetics (30 October 2009) by Meilin Wang, Yang Ye, Haiyang Qian, et al.Zhifang Song, Xiaomin Jia, Zhengdong Zhang, Jianwei Zhou, Chunhui Ni posted to snp pre-microrna polymorphism mirna microrna by songpku on 2009-11-07 17:56:34 as
	GLIDERS - A web-based search engine for genome-wide linkage disequilibrium between HapMap SNPs [My Copy] BMC Bioinformatics, Vol. 10, No. 1. (2009), 367. by Robert Lawrence, Aaron D. Williams, Richard Mott, John Broxholme, Lon Cardon, Eleftheria Zeggini posted to web-server snp hapmap genome-analysis by kshameer on 2009-11-06 08:42:09 as along with 1 person daforerog
	Distinct inherited metastasis susceptibility exists for different breast cancer subtypes: a prognosis study. [My Copy] Breast cancer research : BCR, Vol. 11, No. 5. (13 October 2009), R75. by Szu-Min M. Hsieh, Maxime P. Look, Anieta M. Sieuwerts, John A. Foekens, Kent W. Hunter posted to snp sipa polymorphism metastasis cancer breast by songpku on 2009-11-05 16:25:48 as along with 1 person merpublic
	inGAP: an integrated next-generation genome analysis pipeline [My Copy] Bioinformatics (30 October 2009), btp615. by Ji Qi, Fangqing Zhao, Anne Buboltz, Stephan C. Schuster posted to software snp ngs indel by natstreet on 2009-11-04 07:22:01 as along with 4 people jasontsai n00c heliopais druvus
	Single nucleotide polymorphism associated with mature miR-125a alters the processing of pri-miRNA [My Copy] Hum. Mol. Genet., Vol. 16, No. 9. (1 May 2007), pp. 1124-1131. by Ranhui Duan, ChangHui Pak, Peng Jin posted to snp pri-mirna polymophirsm mirna microrna by songpku on 2009-11-03 20:16:50 as along with 2 people and 1 group daforerog tardigrade Bioinformatics
	Single Nucleotide Polymorphisms of microRNA Machinery Genes Modify the Risk of Renal Cell Carcinoma [My Copy] Clinical Cancer Research, Vol. 14, No. 23. (1 December 2008), pp. 7956-7962. by Yohei Horikawa, Christopher G. Wood, Hushan Yang, et al.Hua Zhao, Yuanqing Ye, Jian Gu, Jie Lin, Tomonori Habuchi, Xifeng Wu posted to snp renal mirna microrna cell carcinoma cancer by songpku on 2009-11-03 19:59:37 as along with 1 person daforerog
	Functional genetic variation of human miRNAs and phenotypic consequences [My Copy] Mammalian Genome, Vol. 19, No. 7. (1 August 2008), pp. 503-509. by Christelle Borel, Stylianos Antonarakis posted to snp polymorphism mirna microrna genetic by songpku on 2009-11-03 19:57:20 as along with 1 person daforerog
	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
	An Open Access Database of Genome-wide Association Results [My Copy] BMC Medical Genetics, Vol. 10, No. 1. (22 January 2009), 6. by Andrew Johnson, Christopher O'Donnell posted to snp human gwas databases by ongenetics on 2009-11-03 02:17:25 as along with 11 people and 2 groups farhat gderwin daforerog guhjy lptolik A_Olympia Zephyrus neils mchelen djkt akmanning logics of knowledge Roswell Cancer Crosstalk
	Mutational evolution in a lobular breast tumour profiled at single nucleotide resolution. [My Copy] Nature, Vol. 461, No. 7265. (8 October 2009), pp. 809-813. by Sohrab P. Shah, Ryan D. Morin, Jaswinder Khattra, et al.Leah Prentice, Trevor Pugh, Angela Burleigh, Allen Delaney, Karen Gelmon, Ryan Guliany, Janine Senz, Christian Steidl, Robert A. Holt, Steven Jones, Mark Sun, Gillian Leung, Richard Moore, Tesa Severson, Greg A. Taylor, Andrew E. Teschendorff, Kane Tse, Gulisa Turashvili, Richard Varhol, René L. Warren, Peter Watson, Yongjun Zhao, Carlos Caldas, David Huntsman, Martin Hirst, Marco A. Marra, Samuel Aparicio posted to snp sequencing cancer breast by chvlyl on 2009-11-02 06:55:07 as along with 13 people and 2 groups misonneh pst jwfoley stubrown giovenko frohike brianb Zephyrus jsuchit mkiyer torfinnnome merpublic djkt Chinnaiyan Lab Journal picks
	Predictive rule inference for epistatic interaction detection in genome-wide association studies [My Copy] Bioinformatics (30 October 2009), btp622. by Xiang Wan, Can Yang, Qiang Yang, Hong Xue, Nelson L. S. Tang, Weichuan Yu posted to snp prediction interaction gwa epistasis by neils on 2009-11-02 04:16:37 as
	Pro12Ala polymorphism in the PPARG gene contributes to the development of diabetic nephropathy in Chinese type 2 diabetes. [My Copy] Diabetes care (16 October 2009) by Limei Liu, Taishan Zheng, Feng Wang, et al.Niansong Wang, Yanyan Song, Ming Li, Lifang Li, Jiamei Jiang, Weijing Zhao posted to snp pparg dn chinese by guhjy on 2009-11-02 02:18:53 as
	A rare haplotype of the vitamin D receptor gene is protective against diabetic nephropathy. [My Copy] Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association (27 September 2009) by Rosalind J. Martin, Amy J. McKnight, Christopher C. Patterson, Denise M. Sadlier, Alexander P. Maxwell, The Warren 3/UK GoKinD Study Group posted to vdr snp dn by guhjy on 2009-11-02 02:17:25 as
	Exploring design-related bias in clinical studies on receptor genetic polymorphism of hypertension [My Copy] Journal of Clinical Epidemiology, Vol. 60, No. 1. (January 2007), pp. 1.e1-1.e11. by P. Farahani, L. Dolovich, M. Levine posted to snp bias aii by guhjy on 2009-10-31 10:01:52 as
	Global patterns of cis variation in human cells revealed by high-density allelic expression analysis [My Copy] Nature Genetics, Vol. 41, No. 11. (18 October 2009), pp. 1216-1222. by Bing Ge, Dmitry K. Pokholok, Tony Kwan, et al.Elin Grundberg, Lisanne Morcos, Dominique J. Verlaan, Jennie Le, Vonda Koka, Kevin C. L. Lam, Vincent Gagne, Joana Dias, Rose Hoberman, Alexandre Montpetit, Marie-Michele Joly, Edward J. Harvey, Daniel Sinnett, Patrick Beaulieu, Robert Hamon, Alexandru Graziani, Ken Dewar, Eef Harmsen, Jacek Majewski, Harald H. H. Goring, Anna K. Naumova, Mathieu Blanchette, Kevin L. Gunderson, Tomi Pastinen posted to variant snp expression cis allelic by songpku on 2009-10-30 20:11:58 as along with 10 people and 1 group bpcusack fenghezi gderwin djkt qayub dill2009 zufar psique daforerog vplagnol Journal picks
	Estimating population haplotype frequencies from pooled SNP data using incomplete database information. [My Copy] Bioinformatics (Oxford, England) (27 October 2009) by Matti Pirinen posted to snp population pooling haplotype frequency bayesian by n00c on 2009-10-30 19:22:48 as
	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
	SNPLogic: an interactive single nucleotide polymorphism selection, annotation, and prioritization system. [My Copy] Nucleic acids research, Vol. 37, No. Database issue. (4 January 2009), gkn756. by Alexander R. Pico, Ivan V. Smirnov, Jeffrey S. Chang, et al.Ru-Fang F. Yeh, Joseph L. Wiemels, John K. Wiencke, Tarik Tihan, Bruce R. Conklin, Margaret Wrensch posted to tool snp functional by daed on 2009-10-29 11:40:25 as along with 2 people and 1 group guhjy AlexanderPico ConklinLab
	Next generation tools for the annotation of human SNPs. [My Copy] Briefings in bioinformatics, Vol. 10, No. 1. (1 January 2009), pp. 35-52. by Rachel Karchin posted to tools snp review functional by daed on 2009-10-29 11:38:35 as along with 5 people djkt tanglingfung guhjy daforerog pkonings
	Analytical methods for inferring functional effects of single base pair substitutions in human cancers. [My Copy] Human genetics, Vol. 126, No. 4. (October 2009), pp. 481-498. by William Lee, Peng Yue, Zemin Zhang posted to snp review functional by daed on 2009-10-29 11:37:42 as
	Geography and genography: prediction of continental origin using randomly selected single nucleotide polymorphisms. [My Copy] BMC genomics, Vol. 8 (10 March 2007), 68. by Dominic J. Allocco, Qing Song, Gary H. Gibbons, Marco F. Ramoni, Isaac S. Kohane posted to snps snp forensic ethnicity aims by dchughes on 2009-10-29 08:23:19 as along with 4 people shoshin yife fmacciardi pradiptaray
	Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios. [My Copy] BMC bioinformatics, Vol. 9, No. 1. (02 October 2008), 409. by Johan Staaf, Johan Vallon-Christersson, David Lindgren, et al.Gunnar Juliusson, Richard Rosenquist, Mattias Höglund, Ake Borg, Markus Ringnér posted to snp normalization illumina by shikin on 2009-10-28 17:58:16 as along with 1 person vplagnol
	High-throughput SNP genotyping on universal bead arrays. [My Copy] Mutation research, Vol. 573, No. 1-2. (3 June 2005), pp. 70-82. by Richard Shen, Jian-Bing B. Fan, Derek Campbell, et al.Weihua Chang, Jing Chen, Dennis Doucet, Jo Yeakley, Marina Bibikova, Eliza Wickham Garcia, Celeste McBride, Frank Steemers, Francisco Garcia, Bahram G. Kermani, Kevin Gunderson, Arnold Oliphant posted to snp microarray illumina by shikin on 2009-10-28 16:31:07 as along with 1 person stsaft
	High-resolution copy number analysis of paraffin-embedded archival tissue using SNP BeadArrays. [My Copy] Genome research, Vol. 17, No. 3. (31 March 2007), pp. 368-376. by Jan Oosting, Esther H. Lips, Ronald van Eijk, et al.Paul H. Eilers, Károly Szuhai, Cisca Wijmenga, Hans Morreau, Tom van Wezel posted to snp illumina by shikin on 2009-10-28 14:30:41 as along with 2 people jfr shigepong
	SNP_tools: A compact tool package for analysis and conversion of genotype data for MS-Excel [My Copy] BMC Research Notes, Vol. 2, No. 1. (2009), 214. by Bowang Chen, Stefan Wilkening, Marion Drechsel, Kari Hemminki posted to snp_genotyping snp computer_software by Geknitics on 2009-10-28 13:01:52 as
	Tri-allelic SNP markers enable analysis of mixed and degraded DNA samples [My Copy] Forensic Science International: Genetics, Vol. 3, No. 4. (September 2009), pp. 233-241. by Antoinette A. Westen, Anuska S. Matai, Jeroen F. J. Laros, et al.Hugo C. Meiland, Mandy Jasper, Wiljo J. F. de Leeuw, Peter de Knijff, Titia Sijen posted to snps snp forensic-snp forensic disaster_victim_identification by dchughes on 2009-10-27 22:33:59 as
	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

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cancer	114
cnv	110
software	110
genetics	84
gwas	80
human	79
mirna	77
association	75
genomics	66
dn	62
bioinformatics	61
pcr	57
ace	56
genome	55
microarray	50
sequencing	48
disease	47
hapmap	47
genotyping	44
humgen	44
gwa	43
polymorphism	43
haplotype	42
evolution	41
review	40
tw	40
ma	39
oral	39
methods	37
selection	36
dm	33
statistics	33
detection	32
ckd	31
expression	30
variation	30
stats	29
assoc	27
linkage	27
cv	26
primer	26
r	26
mining	25
database	22
db	21
hd	21
meta-analysis	21
gene	20
japan	20
silico	20
snp-discovery	20
454	19
algorithm	19
method	19
resequencing	19
seq	19
breast	18
classification	18
phenotype	18
population	18
protein	18
cancer-crosstalk	17
chicken	17
cost	17
lab	17
p53	17
bp	16
china	16
dna	16
eqtl	16
genetic	16
genotype	16
microrna	16
mutation	16
pooling	16
prediction	16
alignment	15
discovery	15
dna-damage	15
epistasis	15
est	15
function	15
gst	15
illumina	15
lead	15
pathway	15
affymetrix	14
analysis	14
hcc	14
mapping	14
snp-calling	14
tool	14
ua	14
array	13
crp	13
il6	13
indel	13
mouse	13
parkinsons	13
rca	13

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