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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...
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Gene expression is the process in which DNA directs the synthesis of functional products, that is, proteins. Cells can regulate gene expression at various stages. It allows organisms to generate different cell types and enables cells to adapt to internal and external factors.
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Multiscale Embedded Gene Co-expression Network Analysis.

Won-Min Song1, Bin Zhang1

  • 1Department of Genetics and Genomic Sciences, Icahn Institute of Genomics and Multiscale Biology, Icahn School of Medicine at Mount Sinai, New York, New York, United States of America.

Plos Computational Biology
|December 1, 2015
PubMed
Summary
This summary is machine-generated.

A new framework, Multiscale Embedded Gene Co-expression Network Analysis (MEGENA), identifies gene modules for complex diseases. MEGENA improves upon existing methods by revealing multi-scale gene organizations and novel cancer targets.

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Area of Science:

  • Genomics
  • Bioinformatics
  • Systems Biology

Background:

  • Gene co-expression network analysis is crucial for understanding complex human diseases.
  • Existing methods for constructing co-expression networks have limitations, including requiring predefined parameters and failing to capture complex system properties.

Purpose of the Study:

  • To develop a novel framework, Multiscale Embedded Gene Co-expression Network Analysis (MEGENA), for constructing gene co-expression networks.
  • To address limitations of previous methods, particularly for large-scale genomic data.

Main Methods:

  • MEGENA incorporates quality control for co-expression similarities.
  • It utilizes parallelized embedded network construction.
  • A novel clustering technique identifies multi-scale structures within Planar Filtered Networks (PFNs).

Main Results:

  • MEGENA was applied to simulated data and The Cancer Genome Atlas (TCGA) data for breast carcinoma and lung adenocarcinoma.
  • The framework demonstrated superior performance compared to established methods.
  • MEGENA successfully identified multi-scale organizations of co-expressed gene clusters and novel therapeutic targets.

Conclusions:

  • MEGENA offers an improved approach for gene co-expression network analysis.
  • The framework effectively reveals complex gene organization and identifies potential targets in cancers like breast carcinoma and lung adenocarcinoma.