Literature DB >> 16646860

Empirical bayes microarray ANOVA and grouping cell lines by equal expression levels.

Ingrid Lönnstedt1, Rebecca Rimini, Peter Nilsson.   

Abstract

In the exploding field of gene expression techniques such as DNA microarrays, there are still few general probabilistic methods for analysis of variance. Linear models and ANOVA are heavily used tools in many other disciplines of scientific research. The usual F-statistic is unsatisfactory for microarray data, which explore many thousand genes in parallel, with few replicates. We present three potential one-way ANOVA statistics in a parametric statistical framework. The aim is to separate genes that are differently regulated across several treatment conditions from those with equal regulation. The statistics have different features and are evaluated using both real and simulated data. Our statistic B1 generally shows the best performance, and is extended for use in an algorithm that groups cell lines by equal expression levels for each gene. An extension is also outlined for more general ANOVA tests including several factors. The methods presented are implemented in the freely available statistical language R. They are available at http://www.math.uu.se/staff/pages/?uname=ingrid.

Year:  2005        PMID: 16646860     DOI: 10.2202/1544-6115.1125

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


  8 in total

1.  baySeq: empirical Bayesian methods for identifying differential expression in sequence count data.

Authors:  Thomas J Hardcastle; Krystyna A Kelly
Journal:  BMC Bioinformatics       Date:  2010-08-10       Impact factor: 3.169

2.  The simple classification of multiple cancer types using a small number of significant genes.

Authors:  Tae Young Yang
Journal:  Mol Diagn Ther       Date:  2007       Impact factor: 4.074

3.  Batch correction of microarray data substantially improves the identification of genes differentially expressed in rheumatoid arthritis and osteoarthritis.

Authors:  Peter Kupfer; Reinhard Guthke; Dirk Pohlers; Rene Huber; Dirk Koczan; Raimund W Kinne
Journal:  BMC Med Genomics       Date:  2012-06-08       Impact factor: 3.063

4.  Missing channels in two-colour microarray experiments: combining single-channel and two-channel data.

Authors:  Andy G Lynch; David E Neal; John D Kelly; Glyn J Burtt; Natalie P Thorne
Journal:  BMC Bioinformatics       Date:  2007-01-25       Impact factor: 3.169

5.  PMC42, a breast progenitor cancer cell line, has normal-like mRNA and microRNA transcriptomes.

Authors:  Anna Git; Inmaculada Spiteri; Cherie Blenkiron; Mark J Dunning; Jessica C M Pole; Suet-Feung Chin; Yanzhong Wang; James Smith; Frederick J Livesey; Carlos Caldas
Journal:  Breast Cancer Res       Date:  2008-06-27       Impact factor: 6.466

6.  Novel application of multi-stimuli network inference to synovial fibroblasts of rheumatoid arthritis patients.

Authors:  Peter Kupfer; René Huber; Michael Weber; Sebastian Vlaic; Thomas Häupl; Dirk Koczan; Reinhard Guthke; Raimund W Kinne
Journal:  BMC Med Genomics       Date:  2014-07-03       Impact factor: 3.063

7.  Metabolomics of ApcMin/+ mice genetically susceptible to intestinal cancer.

Authors:  Jean-Eudes J Dazard; Yana Sandlers; Stephanie K Doerner; Nathan A Berger; Henri Brunengraber
Journal:  BMC Syst Biol       Date:  2014-06-23

8.  Metabolomic Analysis of Liver Tissue from the VX2 Rabbit Model of Secondary Liver Tumors.

Authors:  R Ibarra; J-E Dazard; Y Sandlers; F Rehman; R Abbas; R Kombu; G-F Zhang; H Brunengraber; J Sanabria
Journal:  HPB Surg       Date:  2014-03-02
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.