Literature DB >> 17625973

Integrating domain knowledge with statistical and data mining methods for high-density genomic SNP disease association analysis.

Valentin Dinu1, Hongyu Zhao, Perry L Miller.   

Abstract

Genome-wide association studies can help identify multi-gene contributions to disease. As the number of high-density genomic markers tested increases, however, so does the number of loci associated with disease by chance. Performing a brute-force test for the interaction of four or more high-density genomic loci is unfeasible given the current computational limitations. Heuristics must be employed to limit the number of statistical tests performed. In this paper we explore the use of biological domain knowledge to supplement statistical analysis and data mining methods to identify genes and pathways associated with disease. We describe Pathway/SNP, a software application designed to help evaluate the association between pathways and disease. Pathway/SNP integrates domain knowledge--SNP, gene and pathway annotation from multiple sources--with statistical and data mining algorithms into a tool that can be used to explore the etiology of complex diseases.

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Year:  2007        PMID: 17625973     DOI: 10.1016/j.jbi.2007.06.002

Source DB:  PubMed          Journal:  J Biomed Inform        ISSN: 1532-0464            Impact factor:   6.317


  10 in total

1.  U-statistics-based tests for multiple genes in genetic association studies.

Authors:  Zhi Wei; Mingyao Li; Timothy Rebbeck; Hongzhe Li
Journal:  Ann Hum Genet       Date:  2008-08-06       Impact factor: 1.670

2.  Pathway-based identification of SNPs predictive of survival.

Authors:  Herbert Pang; Michael Hauser; Stéphane Minvielle
Journal:  Eur J Hum Genet       Date:  2011-02-02       Impact factor: 4.246

Review 3.  Gene set analysis of genome-wide association studies: methodological issues and perspectives.

Authors:  Lily Wang; Peilin Jia; Russell D Wolfinger; Xi Chen; Zhongming Zhao
Journal:  Genomics       Date:  2011-04-30       Impact factor: 5.736

4.  Analysis of SLCO1B1 and APOE genetic polymorphisms in a large ethnic Hakka population in southern China.

Authors:  Zhixiong Zhong; Heming Wu; Bin Li; Cunren Li; Zhidong Liu; Min Yang; Qifeng Zhang; Wei Zhong; Pingsen Zhao
Journal:  J Clin Lab Anal       Date:  2018-02-09       Impact factor: 2.352

Review 5.  Risk estimation and risk prediction using machine-learning methods.

Authors:  Jochen Kruppa; Andreas Ziegler; Inke R König
Journal:  Hum Genet       Date:  2012-07-03       Impact factor: 4.132

6.  Pathway based analysis of genotypes in relation to alcohol dependence.

Authors:  M A Reimers; B P Riley; G Kalsi; D A Kertes; K S Kendler
Journal:  Pharmacogenomics J       Date:  2011-04-05       Impact factor: 3.550

7.  Data mining of high density genomic variant data for prediction of Alzheimer's disease risk.

Authors:  Natalia Briones; Valentin Dinu
Journal:  BMC Med Genet       Date:  2012-01-25       Impact factor: 2.103

8.  GLOSSI: a method to assess the association of genetic loci-sets with complex diseases.

Authors:  High-Seng Chai; Hugues Sicotte; Kent R Bailey; Stephen T Turner; Yan W Asmann; Jean-Pierre A Kocher
Journal:  BMC Bioinformatics       Date:  2009-04-03       Impact factor: 3.169

9.  PAPAyA: a platform for breast cancer biomarker signature discovery, evaluation and assessment.

Authors:  Angel Janevski; Sitharthan Kamalakaran; Nilanjana Banerjee; Vinay Varadan; Nevenka Dimitrova
Journal:  BMC Bioinformatics       Date:  2009-09-17       Impact factor: 3.169

10.  Genomic variation in myeloma: design, content, and initial application of the Bank On A Cure SNP Panel to detect associations with progression-free survival.

Authors:  Brian Van Ness; Christine Ramos; Majda Haznadar; Antje Hoering; Jeff Haessler; John Crowley; Susanna Jacobus; Martin Oken; Vincent Rajkumar; Philip Greipp; Bart Barlogie; Brian Durie; Michael Katz; Gowtham Atluri; Gang Fang; Rohit Gupta; Michael Steinbach; Vipin Kumar; Richard Mushlin; David Johnson; Gareth Morgan
Journal:  BMC Med       Date:  2008-09-08       Impact factor: 8.775

  10 in total

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