Article |
PupaSuite: finding functional single nucleotide polymorphisms for large-scale genotyping purposes
1 Department of Bioinformatics, Centro de Investigación Príncipe Felipe (CIPF) Valencia, 46013, Spain 2 Switch laboratory, Flanders Interuniversity Institute for Biotechnology. (VIB), Vrije Universiteit Brussel Pleinlaan 2, 1050 Brussels, Belgium 3 Functional Genomics Node, INB CIPF Valencia 46013, Spain
*To whom correspondence should be addressed. Tel: +34 963289680; Fax: +34 963289701; Email: jdopazo{at}cipf.es
Received February 14, 2006. Revised February 23, 2006. Accepted March 3, 2006.
We have developed a web tool, PupaSuite, for the selection of single nucleotide polymorphisms (SNPs) with potential phenotypic effect, specifically oriented to help in the design of large-scale genotyping projects. PupaSuite uses a collection of data on SNPs from heterogeneous sources and a large number of pre-calculated predictions to offer a flexible and intuitive interface for selecting an optimal set of SNPs. It improves the functionality of PupaSNP and PupasView programs and implements new facilities such as the analysis of user's data to derive haplotypes with functional information. A new estimator of putative effect of polymorphisms has been included that uses evolutionary information. Also SNPeffect database predictions have been included. The PupaSuite web interface is accessible through http://pupasuite.bioinfo.cipf.es and through http://www.pupasnp.org.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
A. Moreno-Estrada, K. Tang, M. Sikora, T. Marques-Bonet, F. Casals, A. Navarro, F. Calafell, J. Bertranpetit, M. Stoneking, and E. Bosch Interrogating 11 Fast-Evolving Genes for Signatures of Recent Positive Selection in Worldwide Human Populations Mol. Biol. Evol., October 1, 2009; 26(10): 2285 - 2297. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Chelala, A. Khan, and N. R Lemoine SNPnexus: a web database for functional annotation of newly discovered and public domain single nucleotide polymorphisms Bioinformatics, March 1, 2009; 25(5): 655 - 661. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. A Reeves, D. Talavera, and J. M Thornton Genome and proteome annotation: organization, interpretation and integration J R Soc Interface, February 6, 2009; 6(31): 129 - 147. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Karchin Next generation tools for the annotation of human SNPs Brief Bioinform, January 1, 2009; 10(1): 35 - 52. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. R. Pico, I. V. Smirnov, J. S. Chang, R.-F. Yeh, J. L. Wiemels, J. K. Wiencke, T. Tihan, B. R. Conklin, and M. Wrensch SNPLogic: an interactive single nucleotide polymorphism selection, annotation, and prioritization system Nucleic Acids Res., January 1, 2009; 37(suppl_1): D803 - D809. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Quaye, S. A. Gayther, S. J. Ramus, R. A. Di Cioccio, V. McGuire, E. Hogdall, C. Hogdall, J. Blaakr, D. F. Easton, B. A.J. Ponder, et al. The Effects of Common Genetic Variants in Oncogenes on Ovarian Cancer Survival Clin. Cancer Res., September 15, 2008; 14(18): 5833 - 5839. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Leng, A. Bernauer, C. A. Stidley, M. A. Picchi, X. Sheng, M. A. Frasco, D. Van Den Berg, F. D. Gilliland, R. E. Crowell, and S. A. Belinsky Association between Common Genetic Variation in Cockayne Syndrome A and B Genes and Nucleotide Excision Repair Capacity among Smokers Cancer Epidemiol. Biomarkers Prev., August 1, 2008; 17(8): 2062 - 2069. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Chen, F. Song, G. A. Calin, Q. Wei, X. Hao, and W. Zhang Polymorphisms in microRNA targets: a gold mine for molecular epidemiology Carcinogenesis, July 1, 2008; 29(7): 1306 - 1311. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. M. Mercader, E. Saus, Z. Aguera, M. Bayes, C. Boni, A. Carreras, E. Cellini, R. de Cid, M. Dierssen, G. Escaramis, et al. Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders Hum. Mol. Genet., May 1, 2008; 17(9): 1234 - 1244. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Leng, C. A. Stidley, R. Willink, A. Bernauer, K. Do, M. A. Picchi, X. Sheng, M. A. Frasco, D. Van Den Berg, F. D. Gilliland, et al. Double-Strand Break Damage and Associated DNA Repair Genes Predispose Smokers to Gene Methylation Cancer Res., April 15, 2008; 68(8): 3049 - 3056. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Bethke, E. Webb, A. Murray, M. Schoemaker, C. Johansen, H. C. Christensen, K. Muir, P. McKinney, S. Hepworth, P. Dimitropoulou, et al. Comprehensive analysis of the role of DNA repair gene polymorphisms on risk of glioma Hum. Mol. Genet., March 15, 2008; 17(6): 800 - 805. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Bethke, A. Murray, E. Webb, M. Schoemaker, K. Muir, P. McKinney, S. Hepworth, P. Dimitropoulou, A. Lophatananon, M. Feychting, et al. Comprehensive Analysis of DNA Repair Gene Variants and Risk of Meningioma J Natl Cancer Inst, February 20, 2008; 100(4): 270 - 276. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Reumers, L. Conde, I. Medina, S. Maurer-Stroh, J. Van Durme, J. Dopazo, F. Rousseau, and J. Schymkowitz Joint annotation of coding and non-coding single nucleotide polymorphisms and mutations in the SNPeffect and PupaSuite databases Nucleic Acids Res., January 11, 2008; 36(suppl_1): D825 - D829. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Ruiz-Llorente, C. Montero-Conde, R. L. Milne, C. M. Moya, A. Cebrian, R. Leton, A. Cascon, F. Mercadillo, I. Landa, S. Borrego, et al. Association Study of 69 Genes in the Ret Pathway Identifies Low-penetrance Loci in Sporadic Medullary Thyroid Carcinoma Cancer Res., October 1, 2007; 67(19): 9561 - 9567. [Abstract] [Full Text] [PDF] |
||||










