Tag snp [at least 200 articles] Export

Recent papers classified by the tag snp.

	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 mirna_regulation mirna database by jfr to the group microRNA on 2009-11-08 22:08:30 as along with 6 people songpku guhjy pengchy daforerog lwaldron ealloza
	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. (08 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, Rene 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 11 people and 2 groups 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 9 people and 1 group 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
	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 snp mpss by maren on 2009-10-29 21:13:10 as along with 15 people adijr greg jandot guhjy jonilaserson n00c druvus reyez sandfire jasontsai djkt sameersoi natstreet jbhiatt GeeSharpMinor
	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 tool tagsnp snp gwas by songpku on 2009-10-29 19:58:17 as along with 6 people daed misonneh guhjy psique jdbowes daforerog
	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
	High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping. [My Copy] Genome research, Vol. 16, No. 9. (September 2006), pp. 1136-1148. by Daniel A. Peiffer, Jennie M. Le, Frank J. Steemers, et al.Weihua Chang, Tony Jenniges, Francisco Garcia, Kirt Haden, Jiangzhen Li, Chad A. Shaw, John Belmont, Sau Wai W. Cheung, Richard M. Shen, David L. Barker, Kevin L. Gunderson posted to snp microarray illumina cnv by shikin on 2009-10-27 17:24:03 as along with 3 people baizhang jfr jackjackjjj
	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 snp microarray cnv by shikin on 2009-10-27 17:23:18 as along with 12 people and 1 group sameersoi daforerog psique maren pengchy vplagnol waszak caseybrown Zephyrus misonneh rdiaz guhjy Roswell Cancer Crosstalk
	Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays. [My Copy] Genome research, Vol. 16, No. 12. (1 December 2006), pp. 1575-1584. by Daisuke Komura, Fan Shen, Shumpei Ishikawa, et al.Karen R. Fitch, Wenwei Chen, Jane Zhang, Guoying Liu, Sigeo Ihara, Hiroshi Nakamura, Matthew E. Hurles, Charles Lee, Stephen W. Scherer, Keith W. Jones, Michael H. Shapero, Jing Huang, Hiroyuki Aburatani posted to snp microarray cnv by shikin on 2009-10-27 16:51:13 as along with 10 people and 4 groups rdiaz waszak jfr dchughes giovanni jeremymiller frohike vpschulz shigepong debasis Bioinformatics G4ID GeschwindLab Genetics-of-Gambling
	Relative Impact of Nucleotide and Copy Number Variation on Gene Expression Phenotypes [My Copy] Science, 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 Tavare, Panagiotis Deloukas, Matthew E. Hurles, Emmanouil T. Dermitzakis posted to snp phenotype mutation expression_evolution cnv by daveGerrard on 2009-10-27 15:48:48 as along with 31 people and 5 groups lp2 sameersoi timhubbard Zephyrus ajbattle jonilaserson ilyashl emptyhb buyske zufar koller waszak daed 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
	QualitySNP: a pipeline for detecting single nucleotide polymorphisms and insertions/deletions in EST data from diploid and polyploid species [My Copy] BMC Bioinformatics, Vol. 7, No. 1. (09 October 2006), 438. by Jifeng Tang, Ben Vosman, Roeland Voorrips, C. Gerard van der Linden, Jack Leunissen posted to snp_discovery snp single_nucleotide_polymorphisms paralogs by rs on 2009-10-26 19:39:10 as along with 5 people and 1 group orzenil csrocha farhat guhjy Ayest Bioinformatics
	How to interpret a genome-wide association study. [My Copy] JAMA : the journal of the American Medical Association, Vol. 299, No. 11. (19 March 2008), pp. 1335-1344. by Thomas A. Pearson, Teri A. Manolio posted to snp gwa genotyping genomics by operon on 2009-10-26 18:16:23 as along with 11 people and 1 group daforerog kshameer Zephyrus psique ptrobajo qfwills cheyloveday misonneh guhjy BrianTomasik xingxu Roswell Cancer Crosstalk
	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 pathway-analysis by shikin on 2009-10-26 18:15:20 as along with 8 people zufar liqbbi daforerog rdiaz natstreet pkonings guhjy druvus
	A genotype calling algorithm for affymetrix SNP arrays. [My Copy] Bioinformatics (Oxford, England), Vol. 22, No. 1. (1 January 2006), pp. 7-12. by Nusrat Rabbee, Terence P. Speed posted to statistics snp affy by shikin on 2009-10-26 16:13:35 as along with 6 people daforerog pcahan1 jfr beniltoncarvalho ashandanj djkt
	SNPchip: R classes and methods for SNP array data. [My Copy] Bioinformatics (Oxford, England), Vol. 23, No. 5. (1 March 2007), pp. 627-628. by Robert B. Scharpf, Jason C. Ting, Jonathan Pevsner, Ingo Ruczinski posted to snp r by shikin on 2009-10-26 16:11:41 as along with 6 people daforerog guhjy jfr Ayest eckart_bindewald cpnP
	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 bayesian by shikin on 2009-10-26 11:54:02 as along with 5 people rdiaz daforerog maren natstreet jfr
	Large-scale SNP genotyping in crosses between outbred lines: how useful is it\|[quest]\| [My Copy] Heredity (21 October 2009) by M. C. Ledur, N. Navarro, M. Perez-Enciso posted to snp pooled ngs gwa by natstreet on 2009-10-24 16:06:43 as along with 1 person druvus
	VarScan: variant detection in massively parallel sequencing of individual and pooled samples [My Copy] Bioinformatics, Vol. 25, No. 17. (1 September 2009), pp. 2283-2285. by Daniel C. Koboldt, Ken Chen, Todd Wylie, et al.David E. Larson, Michael D. McLellan, Elaine R. Mardis, George M. Weinstock, Richard K. Wilson, Li Ding posted to varient snp sequencing next_generation massively_parallel_sequencing detection by mkiyer on 2009-10-22 20:24:51 as along with 12 people and 3 groups seb1 heliopais dakelley djkt PabloMarin guhjy n00c orzenil natstreet druvus stajich malcook Journal picks Mycology SIMR bioinformatics
	From the detection of population structure to the reconstruction of population history: the historical reading of the human genome [My Copy] Heredity, Vol. 103, No. 5. (22 July 2009), pp. 362-363. by H. Laayouni, J. Bertranpetit posted to snp population_structure population_history human_genome by Geknitics on 2009-10-22 15:34:08 as along with 1 person psique
	Pathway and network-based analysis of genome-wide association studies in multiple sclerosis. [My Copy] Human molecular genetics, Vol. 18, No. 11. (1 June 2009), pp. 2078-2090. by S. E. Baranzini, N. W. Galwey, J. Wang, et al.P. Khankhanian, R. Lindberg, D. Pelletier, W. Wu, B. M. Uitdehaag, L. Kappos, C. H. Polman, P. M. Matthews, S. L. Hauser, R. A. Gibson, J. R. Oksenberg, M. R. Barnes posted to snp by zufar on 2009-10-21 19:47:10 as along with 3 people shikin daforerog jdbowes
	The theory of discovering rare variants via DNA sequencing [My Copy] BMC Genomics, Vol. 10, No. 1. (2009), 485. by Michael Wendl, Richard Wilson posted to variant snp-discovery snp sequencing by n00c on 2009-10-21 18:35:21 as along with 4 people jasontsai jsatkosk merpublic druvus
	Comprehensive analysis of the impact of SNPs and CNVs on human microRNAs and their regulatory genes. [My Copy] RNA biology, Vol. 6, No. 4. (23 October 2009) by Shiwei Duan, Shuangli Mi, Wei Zhang, Eileen E. Dolan posted to snp microrna by heliopais on 2009-10-20 14:30:32 as along with 5 people and 2 groups guhjy samgj ealloza daforerog ppgardne microRNA Journal picks
	Large scale single nucleotide polymorphism discovery in unsequenced genomes using second generation high throughput sequencing technology: applied to turkey [My Copy] BMC Genomics, Vol. 10, No. 1. (2009), 479. by Hindrik Kerstens, Richard Crooijmans, Albertine Veenendaal, et al.Bert Dibbits, Thomas Chin, Johan den Dunnen, Martien Groenen posted to snp ngs by natstreet on 2009-10-20 13:31:50 as
	Cancer-Specific High-Throughput Annotation of Somatic Mutations: Computational Prediction of Driver Missense Mutations [My Copy] Cancer Res, Vol. 69, No. 16. (15 August 2009), pp. 6660-6667. by Hannah Carter, Sining Chen, Leyla Isik, et al.Svitlana Tyekucheva, Victor E. Velculescu, Kenneth W. Kinzler, Bert Vogelstein, Rachel Karchin posted to somatic snp prediction mutation function cancer bioinformatics annotation by chrisamiller on 2009-10-20 00:31:42 as along with 5 people zufar kshameer burak ericrpaquet frohike
	Slider--maximum use of probability information for alignment of short sequence reads and SNP detection [My Copy] Bioinformatics, Vol. 25, No. 1. (1 January 2009), pp. 6-13. by Nawar Malhis, Yaron S. N. Butterfield, Martin Ester, Steven J. M. Jones posted to software snp short-read sequencing probability mapping illumina alignment by torfinnnome on 2009-10-19 16:06:43 as along with 7 people seb1 orzenil jsatkosk n00c mdimon druvus jmeppley
	Interrogating a High-Density SNP Map for Signatures of Natural Selection [My Copy] Genome Research, Vol. 12, No. 12. (1 December 2002), pp. 1805-1814. by Joshua M. Akey, Ge Zhang, Kun Zhang, Li Jin, Mark D. Shriver posted to snp signatures printed positiveselection naturalselection fst by Garamonfok on 2009-10-19 14:59:40 as along with 5 people and 1 group renewang kieran101 hdopazo JBEgwa01 iris42 BioinfoCIPF

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cancer	114
software	107
cnv	106
genetics	84
gwas	80
human	76
association	74
mirna	72
genomics	66
bioinformatics	61
dn	61
pcr	57
ace	56
genome	55
microarray	49
sequencing	48
disease	46
genotyping	44
hapmap	44
humgen	44
gwa	43
haplotype	42
polymorphism	42
evolution	41
tw	40
ma	39
oral	39
review	39
methods	37
selection	35
statistics	33
dm	32
ckd	31
detection	31
expression	30
variation	30
stats	29
assoc	27
linkage	27
primer	26
r	26
cv	25
mining	25
db	21
hd	21
meta-analysis	21
gene	20
japan	20
silico	20
454	19
algorithm	19
resequencing	19
seq	19
snp-discovery	19
breast	18
classification	18
database	18
method	18
protein	18
cancer-crosstalk	17
chicken	17
cost	17
lab	17
p53	17
phenotype	17
bp	16
china	16
dna	16
eqtl	16
genetic	16
genotype	16
mutation	16
pooling	16
population	16
prediction	16
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
microrna	14
snp-calling	14
tool	14
ua	14
alignment	13
apoe	13
array	13
il6	13
imputation	13
indel	13
mouse	13
rca	13

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