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Related Experiment Video

Updated: Jul 9, 2026

Generating the Transcriptional Regulation View of Transcriptomic Features for Prediction Task and Dark Biomarker Detection on Small Datasets
03:37

Generating the Transcriptional Regulation View of Transcriptomic Features for Prediction Task and Dark Biomarker Detection on Small Datasets

Published on: March 1, 2024

Tail posterior probability for inference in pairwise and multiclass gene expression data.

N Bochkina1, S Richardson

  • 1Centre for Biostatistics, Imperial College, London W2 1PG, UK. n.bochkina@imperial.ac.uk

Biometrics
|December 15, 2007
PubMed
Summary

This study introduces a new Bayesian method, tail posterior probability, for identifying differentially expressed genes in microarray data. It offers a robust approach for analyzing gene expression differences between conditions and in multiclass settings.

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Last Updated: Jul 9, 2026

Generating the Transcriptional Regulation View of Transcriptomic Features for Prediction Task and Dark Biomarker Detection on Small Datasets
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07:35

Selecting Multiple Biomarker Subsets with Similarly Effective Binary Classification Performances

Published on: October 11, 2018

Area of Science:

  • Bioinformatics
  • Statistical genetics
  • Computational biology

Background:

  • Microarray data analysis is crucial for understanding gene expression.
  • Identifying differentially expressed genes between conditions is a key challenge.
  • Bayesian frameworks offer a powerful approach for statistical inference in genomics.

Purpose of the Study:

  • To introduce a novel Bayesian rule, tail posterior probability, for identifying differentially expressed genes.
  • To develop a frequentist estimator for the false discovery rate associated with the new rule.
  • To extend the tail posterior probability rule for multiclass data analysis.

Main Methods:

  • Bayesian inference with a noninformative prior distribution.
  • Utilizing the posterior distribution of the standardized difference.
  • Deriving a frequentist estimator for the false discovery rate.
  • Extending the rule for compound null hypotheses in multiclass settings.

Main Results:

  • The tail posterior probability rule effectively identifies differentially expressed genes.
  • The derived frequentist false discovery rate estimator is associated with the new rule.
  • The method demonstrates comparable or superior performance to existing Bayesian rules.
  • The tail posterior probability rule is adaptable to complex multiclass comparisons.

Conclusions:

  • The tail posterior probability offers a statistically sound and effective method for differential gene expression analysis.
  • This approach provides a reliable way to control false discoveries in genomic studies.
  • The extension to multiclass data enhances its applicability in diverse biological research scenarios.