Literature DB >> 18241193

Quantifying the association between gene expressions and DNA-markers by penalized canonical correlation analysis.

Sandra Waaijenborg1, Philip C Verselewel de Witt Hamer, Aeilko H Zwinderman.   

Abstract

Multiple changes at the DNA level are at the basis of complex diseases. Identifying the genetic networks that are influenced by these changes might help in understanding the development of these diseases. Canonical correlation analysis is used to associate gene expressions with DNA-markers and thus reveals sets of co-expressed and co-regulated genes and their associating DNA-markers. However, when the number of variables gets high, e.g. in the case of microarray studies, interpretation of these results can be difficult. By adapting the elastic net to canonical correlation analysis the number of variables reduces, and interpretation becomes easier, moreover, due to the grouping effect of the elastic net co-regulated and co-expressed genes cluster. Additionally, our adaptation works well in situations where the number of variables exceeds by far the number of subjects.

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Year:  2008        PMID: 18241193     DOI: 10.2202/1544-6115.1329

Source DB:  PubMed          Journal:  Stat Appl Genet Mol Biol        ISSN: 1544-6115


  54 in total

1.  Simultaneous analysis of multiple data types in pharmacogenomic studies using weighted sparse canonical correlation analysis.

Authors:  Prabhakar Chalise; Anthony Batzler; Ryan Abo; Liewei Wang; Brooke L Fridley
Journal:  OMICS       Date:  2012-06-26

2.  Sparse partial least squares classification for high dimensional data.

Authors:  Dongjun Chung; Sunduz Keles
Journal:  Stat Appl Genet Mol Biol       Date:  2010-03-03

3.  A penalized matrix decomposition, with applications to sparse principal components and canonical correlation analysis.

Authors:  Daniela M Witten; Robert Tibshirani; Trevor Hastie
Journal:  Biostatistics       Date:  2009-04-17       Impact factor: 5.899

Review 4.  Extensions of sparse canonical correlation analysis with applications to genomic data.

Authors:  Daniela M Witten; Robert J Tibshirani
Journal:  Stat Appl Genet Mol Biol       Date:  2009-06-09

5.  Simulating systems genetics data with SysGenSIM.

Authors:  Andrea Pinna; Nicola Soranzo; Ina Hoeschele; Alberto de la Fuente
Journal:  Bioinformatics       Date:  2011-07-06       Impact factor: 6.937

6.  SPARSE INTEGRATIVE CLUSTERING OF MULTIPLE OMICS DATA SETS.

Authors:  Ronglai Shen; Sijian Wang; Qianxing Mo
Journal:  Ann Appl Stat       Date:  2013-04-09       Impact factor: 2.083

7.  Improved heterosis prediction by combining information on DNA- and metabolic markers.

Authors:  Tanja Gärtner; Matthias Steinfath; Sandra Andorf; Jan Lisec; Rhonda C Meyer; Thomas Altmann; Lothar Willmitzer; Joachim Selbig
Journal:  PLoS One       Date:  2009-04-16       Impact factor: 3.240

8.  Sparse canonical correlation analysis for identifying, connecting and completing gene-expression networks.

Authors:  Sandra Waaijenborg; Aeilko H Zwinderman
Journal:  BMC Bioinformatics       Date:  2009-09-28       Impact factor: 3.169

9.  Predicting qualitative phenotypes from microarray data - the Eadgene pig data set.

Authors:  Christèle Robert-Granié; Kim-Anh Lê Cao; Magali Sancristobal
Journal:  BMC Proc       Date:  2009-07-16

10.  Associating multiple longitudinal traits with high-dimensional single-nucleotide polymorphism data: application to the Framingham Heart Study.

Authors:  Sandra Waaijenborg; Aeilko H Zwinderman
Journal:  BMC Proc       Date:  2009-12-15
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