Medical Journals

An Adaptation of the Lms Method to Determine Expression Variations in Profiling Data.

Authors:
  • Chuchana Paul
  • Marchand Dorian
  • Nugoli Mélanie
  • Rodriguez Carmen
  • Molinari Nicolas
  • Garcia-Sanz Jose A

From: EMI 229 INSERM, Génotypes et Phénotypes Tumoraux, CRLC Val d’Aurelle-Paul Lamarque, Montpellier, France.

Nucleic acids research

  • Publish Date: 2007
  • ISSN: 1362-4962
  • Volume: 35
  • Issue: 9
  • Pages: e71
  • Medium: Internet
  • Language: English
  • Citation (JAMA): Chuchana Paul, Marchand Dorian, Nugoli Mélanie, et al. An Adaptation of the Lms Method to Determine Expression Variations in Profiling Data.. Nucleic Acids Res. 2007;35:e71

Abstract

One of the major issues in expression profiling analysis still is to outline proper thresholds to determine differential expression, while avoiding false positives. The problem being that the variance is inversely proportional to the log of signal intensities. Aiming to solve this issue, we describe a model, expression variation (EV), based on the LMS method, which allows data normalization and to construct confidence bands of gene expression, fitting cubic spline curves to the Box-Cox transformation. The confidence bands, fitted to the actual variance of the data, include the genes devoid of significant variation, and allow, based on the confidence bandwidth, to calculate EVs. Each outlier is positioned according to the dispersion space (DS) and a P-value is statistically calculated to determine EV. This model results in variance stabilization. Using two Affymetrix-generated datasets, the sets of differentially expressed genes selected using EV and other classical methods were compared. The analysis suggests that EV is more robust on variance stabilization and on selecting differential expression from both rare and strongly expressed genes.

Mesh Headings (Keywords): Animals, Clone Cells, Confidence Intervals, Gene Expression Profiling, Mice, Models, Statistical, Oligonucleotide Array Sequence Analysis


Check for Full Text / PubMed Unique Identifier (PMID): 17459890


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.

The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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