Literature DB >> 18046768

Multivariate analysis of complex gene expression and clinical phenotypes with genetic marker data.

Joseph Beyene1, David Tritchler, Shelley B Bull, Kevin C Cartier, Gudrun Jonasdottir, Aldi T Kraja, Na Li, Nora L Nock, Elena Parkhomenko, J Sunil Rao, Catherine M Stein, Rinku Sutradhar, Sandra Waaijenborg, Ke-Sheng Wang, Yuanjia Wang, Pavel Wolkow.   

Abstract

This paper summarizes contributions to group 12 of the 15th Genetic Analysis Workshop. The papers in this group focused on multivariate methods and applications for the analysis of molecular data including genotypic data as well as gene expression microarray measurements and clinical phenotypes. A range of multivariate techniques have been employed to extract signals from the multi-feature data sets that were provided by the workshop organizers. The methods included data reduction techniques such as principal component analysis and cluster analysis; latent variable models including structural equations and item response modeling; joint multivariate modeling techniques as well as multivariate visualization tools. This summary paper categorizes and discusses individual contributions with regard to multiple classifications of multivariate methods. Given the wide variety in the data considered, the objectives of the analysis and the methods applied, direct comparison of the results of the various papers is difficult. However, the group was able to make many interesting comparisons and parallels between the various approaches. In summary, there was a consensus among authors in group 12 that the genetic research community should continue to draw experiences from other fields such as statistics, econometrics, chemometrics, computer science and linear systems theory. (c) 2007 Wiley-Liss, Inc.

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Year:  2007        PMID: 18046768     DOI: 10.1002/gepi.20286

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  8 in total

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4.  Phenomics: the systematic study of phenotypes on a genome-wide scale.

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Journal:  Neuroscience       Date:  2009-01-20       Impact factor: 3.590

5.  Canonical correlation analysis for gene-based pleiotropy discovery.

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6.  Decision tree-based method for integrating gene expression, demographic, and clinical data to determine disease endotypes.

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Review 8.  Obtaining Reliable RT-qPCR Results in Molecular Diagnostics-MIQE Goals and Pitfalls for Transcriptional Biomarker Discovery.

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Journal:  Life (Basel)       Date:  2022-03-07
  8 in total

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