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Related Concept Videos

Regulation of Expression at Multiple Steps01:23

Regulation of Expression at Multiple Steps

The gene expression in cells is regulated at different stages: (i) transcription, (ii) RNA processing, (iii) RNA localization, and (iv) translation. Transcriptional regulation is mediated by regulatory proteins such as transcription factors, activators, or repressors—these control gene expression by initiating or inhibiting the transcription of genes. Once a precursor or pre-mRNA is produced, it undergoes post-transcriptional modification, including 5' capping, splicing, and the addition of a...
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Structure of a Gene

A gene is the fundamental unit of heredity. Every individual has two copies of each gene, one inherited from each parent. Although most people contain the same genes, there is a small fraction that is slightly different amongst people. A gene with a small difference in its sequence of DNA bases forms different alleles, contributing to different phenotypes.
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Gene expression can be regulated at almost every step from gene to protein. Transcription is the step that is most commonly regulated. This involves the binding of proteins to short regulatory sequences on the DNA. This association can either promote or inhibit the transcription of a gene associated with the respective sequence.
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This lesson introduces two critical methods in pharmacokinetics, the Wagner-Nelson and Loo-Riegelman methods, used for estimating the absorption rate constant (ka) for drugs administered via non-intravenous routes. The Wagner-Nelson method relates ka to the plasma concentration derived from the slope of a semilog percent unabsorbed time plot. However, it is limited to drugs with one-compartment kinetics and can be impacted by factors like gastrointestinal motility or enzymatic degradation.
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Generating the Transcriptional Regulation View of Transcriptomic Features for Prediction Task and Dark Biomarker Detection on Small Datasets
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Published on: March 1, 2024

A three-stage framework for gene expression data analysis by L1-norm support vector regression.

Hyunsoo Kim1, Jeff X Zhou, Herbert C Morse

  • 1Department of Computer Science, University of Minnesota, Minneapolis, MN 55455, USA. hskim@cs.umn.edu

International Journal of Bioinformatics Research and Applications
|December 1, 2007
PubMed
Summary

A new three-stage gene selection framework effectively identifies genes for continuous phenotypes in gene expression data. This method improves upon existing approaches for biological data analysis.

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Three Differential Expression Analysis Methods for RNA Sequencing: limma, EdgeR, DESeq2
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Three Differential Expression Analysis Methods for RNA Sequencing: limma, EdgeR, DESeq2

Published on: September 18, 2021

Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • Gene expression data analysis traditionally focuses on categorical phenotypes for disease diagnosis.
  • Continuous phenotypes, such as apoptosis levels measured by caspase 3 enzyme, require specialized gene selection methods.
  • Existing methods may not optimally handle the complexity of continuous biological data.

Purpose of the Study:

  • To develop an effective gene selection method for continuous phenotypes in gene expression data.
  • To introduce a novel three-stage framework for analyzing gene expression data with continuous outcomes.
  • To improve the accuracy and efficiency of identifying relevant genes for biological processes.

Main Methods:

  • A three-stage framework utilizing L1-norm support vector regression (L1-SVR) was developed.
  • Stage 1: Recursive multiple feature elimination based on L1-SVR for gene ranking.
  • Stage 2: Kernel regression to determine minimal genes by minimizing ten-fold cross-validation error.
  • Stage 3: Leave-one-out cross-validation to build the final non-linear regression model.

Main Results:

  • The proposed three-stage framework demonstrated significant improvements over current state-of-the-art methods.
  • The method effectively selected relevant genes for continuous phenotypes.
  • The final non-linear regression model achieved optimal performance with selected genes and parameters.

Conclusions:

  • The novel three-stage gene selection framework provides a robust approach for analyzing gene expression data with continuous phenotypes.
  • This method offers a significant advancement for understanding biological processes and potential disease mechanisms.
  • The framework enhances the identification of discriminative genes, outperforming existing two-stage approaches.