Literature DB >> 16873516

SNP Function Portal: a web database for exploring the function implication of SNP alleles.

Pinglang Wang1, Manhong Dai, Weijian Xuan, Richard C McEachin, Anne U Jackson, Laura J Scott, Brian Athey, Stanley J Watson, Fan Meng.   

Abstract

MOTIVATION: Finding the potential functional significance of SNPs is a major bottleneck in understanding genome-wide SNP scanning results, as the related functional data are distributed across many different databases. The SNP Function Portal is designed to be a clearing house for all public domain SNP functional annotation data, as well as in-house functional annotations derived from different data sources. It currently contains SNP functional annotations in six major categories including genomic elements, transcription regulation, protein function, pathway, disease and population genetics. Besides extensive SNP functional annotations, the SNP Function Portal includes a powerful search engine that accepts different types of genetic markers as input and identifies all genetically related SNPs based on the HapMap Phase II data as well as the relationship of different markers to known genes. As a result, our system allows users to identify the potential biological impact of genetic markers and complex relationships among genetic markers and genes, and it greatly facilitates knowledge discovery in genome-wide SNP scanning experiments. AVAILABILITY: http://brainarray.mbni.med.umich.edu/Brainarray/Database/SearchSNP/snpfunc.aspx.

Mesh:

Year:  2006        PMID: 16873516     DOI: 10.1093/bioinformatics/btl241

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  38 in total

1.  Path to facilitate the prediction of functional amino acid substitutions in red blood cell disorders--a computational approach.

Authors:  Rajith B; George Priya Doss C
Journal:  PLoS One       Date:  2011-09-13       Impact factor: 3.240

2.  Genetic variations in the homologous recombination repair pathway genes modify risk of glioma.

Authors:  Haishi Zhang; Yanhong Liu; Keke Zhou; Chengcheng Zhou; Renke Zhou; Chunxia Cheng; Qingyi Wei; Daru Lu; Liangfu Zhou
Journal:  J Neurooncol       Date:  2015-10-29       Impact factor: 4.130

3.  Next generation tools for the annotation of human SNPs.

Authors:  Rachel Karchin
Journal:  Brief Bioinform       Date:  2009-01       Impact factor: 11.622

4.  The novel genetic variant predisposing to coronary artery disease in the region of the PSRC1 and CELSR2 genes on chromosome 1 associates with serum cholesterol.

Authors:  Nilesh J Samani; Peter S Braund; Jeanette Erdmann; Anika Götz; Maciej Tomaszewski; Patrick Linsel-Nitschke; Cother Hajat; Massimo Mangino; Christian Hengstenberg; Klaus Stark; Andreas Ziegler; Mark Caulfield; Paul R Burton; Heribert Schunkert; Martin D Tobin
Journal:  J Mol Med (Berl)       Date:  2008-07-23       Impact factor: 4.599

5.  Genetic Modulation of Neurocognitive Function in Glioma Patients.

Authors:  Yanhong Liu; Renke Zhou; Erik P Sulman; Michael E Scheurer; Nicholas Boehling; Georgina N Armstrong; Spiridon Tsavachidis; Fu-Wen Liang; Carol J Etzel; Charles A Conrad; Mark R Gilbert; Terri S Armstrong; Melissa L Bondy; Jeffrey S Wefel
Journal:  Clin Cancer Res       Date:  2015-04-22       Impact factor: 12.531

6.  Natural variability of minimotifs in 1092 people indicates that minimotifs are targets of evolution.

Authors:  Kenneth F Lyon; Christy L Strong; Steve G Schooler; Richard J Young; Nervik Roy; Brittany Ozar; Mark Bachmeier; Sanguthevar Rajasekaran; Martin R Schiller
Journal:  Nucleic Acids Res       Date:  2015-06-11       Impact factor: 16.971

7.  In silico functional profiling of human disease-associated and polymorphic amino acid substitutions.

Authors:  Matthew Mort; Uday S Evani; Vidhya G Krishnan; Kishore K Kamati; Peter H Baenziger; Angshuman Bagchi; Brandon J Peters; Rakesh Sathyesh; Biao Li; Yanan Sun; Bin Xue; Nigam H Shah; Maricel G Kann; David N Cooper; Predrag Radivojac; Sean D Mooney
Journal:  Hum Mutat       Date:  2010-03       Impact factor: 4.878

8.  FunctSNP: an R package to link SNPs to functional knowledge and dbAutoMaker: a suite of Perl scripts to build SNP databases.

Authors:  Stephen J Goodswen; Cedric Gondro; Nathan S Watson-Haigh; Haja N Kadarmideen
Journal:  BMC Bioinformatics       Date:  2010-06-09       Impact factor: 3.169

9.  From SNPs to pathways: integration of functional effect of sequence variations on models of cell signalling pathways.

Authors:  Anna Bauer-Mehren; Laura I Furlong; Michael Rautschka; Ferran Sanz
Journal:  BMC Bioinformatics       Date:  2009-08-27       Impact factor: 3.169

10.  GWAS analyzer: integrating genotype, phenotype and public annotation data for genome-wide association study analysis.

Authors:  Christine Fong; Dennis C Ko; Michael Wasnick; Matthew Radey; Samuel I Miller; Mitchell Brittnacher
Journal:  Bioinformatics       Date:  2010-01-06       Impact factor: 6.937

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