Literature DB >> 17267436

SNPassoc: an R package to perform whole genome association studies.

Juan R González1, Lluís Armengol, Xavier Solé, Elisabet Guinó, Josep M Mercader, Xavier Estivill, Víctor Moreno.   

Abstract

UNLABELLED: The popularization of large-scale genotyping projects has led to the widespread adoption of genetic association studies as the tool of choice in the search for single nucleotide polymorphisms (SNPs) underlying susceptibility to complex diseases. Although the analysis of individual SNPs is a relatively trivial task, when the number is large and multiple genetic models need to be explored it becomes necessary a tool to automate the analyses. In order to address this issue, we developed SNPassoc, an R package to carry out most common analyses in whole genome association studies. These analyses include descriptive statistics and exploratory analysis of missing values, calculation of Hardy-Weinberg equilibrium, analysis of association based on generalized linear models (either for quantitative or binary traits), and analysis of multiple SNPs (haplotype and epistasis analysis). AVAILABILITY: Package SNPassoc is available at CRAN from http://cran.r-project.org. SUPPLEMENTARY INFORMATION: A tutorial is available on Bioinformatics online and in http://davinci.crg.es/estivill_lab/snpassoc.

Mesh:

Year:  2007        PMID: 17267436     DOI: 10.1093/bioinformatics/btm025

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


  251 in total

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Journal:  J Cereb Blood Flow Metab       Date:  2012-03-28       Impact factor: 6.200

3.  No association between genetic ancestry and susceptibility to asthma or atopy in Canary Islanders.

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Journal:  Immunogenetics       Date:  2012-06-19       Impact factor: 2.846

Review 4.  Genome-wide association studies--data generation, storage, interpretation, and bioinformatics.

Authors:  Guillaume Pare
Journal:  J Cardiovasc Transl Res       Date:  2010-04-08       Impact factor: 4.132

5.  Exploring epistatic relationships of NO biosynthesis pathway genes in susceptibility to CHD.

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Journal:  Acta Pharmacol Sin       Date:  2010-06-28       Impact factor: 6.150

6.  Inference of biogeographical ancestry across central regions of Eurasia.

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Journal:  Int J Legal Med       Date:  2015-08-20       Impact factor: 2.686

7.  Association of vitamin D receptor gene polymorphisms with disc degeneration.

Authors:  Adam Biczo; Julia Szita; Iain McCall; Peter Pal Varga; Aron Lazary
Journal:  Eur Spine J       Date:  2019-11-25       Impact factor: 3.134

8.  The effects of a MAP2K5 microRNA target site SNP on risk for anxiety and depressive disorders.

Authors:  Kevin P Jensen; Henry R Kranzler; Murray B Stein; Joel Gelernter
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2014-01-16       Impact factor: 3.568

9.  Strong effect of SNP rs4988300 of the LRP5 gene on bone phenotype of Caucasian postmenopausal women.

Authors:  Péter Horváth; Bernadett Balla; János P Kósa; Bálint Tóbiás; Balázs Szili; Gyöngyi Kirschner; Gabriella Győri; Karina Kató; Péter Lakatos; István Takács
Journal:  J Bone Miner Metab       Date:  2015-03-12       Impact factor: 2.626

10.  Tag-SNP analysis of the GFI1-EVI5-RPL5-FAM69 risk locus for multiple sclerosis.

Authors:  Antonio Alcina; Oscar Fernández; Juan Ramón Gonzalez; Antonio Catalá-Rabasa; María Fedetz; Dorothy Ndagire; Laura Leyva; Miguel Guerrero; Carmen Arnal; Concepción Delgado; Miguel Lucas; Guillermo Izquierdo; Fuencisla Matesanz
Journal:  Eur J Hum Genet       Date:  2010-01-20       Impact factor: 4.246

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