Evidence map›Paper›PMID 31918656›Full record

ArticleBMC bioinformatics2020

Bayesian differential analysis of gene regulatory networks exploiting genetic perturbations.

Yan Li, Dayou Liu, Tengfei Li, Yungang Zhu

Abstract read
In one paragraph

Article in BMC bioinformatics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Analysis of Variance of Multiple Causal Networks.Advances in neural information processing systems · 2023
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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Yan LiCollege of Computer Science and Technology, Jilin University, Changchun, 130012, China.
Dayou LiuCollege of Computer Science and Technology, Jilin University, Changchun, 130012, China. liudy@jlu.edu.cn.
Tengfei LiCollege of Computer Science and Technology, Jilin University, Changchun, 130012, China.
Yungang ZhuCollege of Computer Science and Technology, Jilin University, Changchun, 130012, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGene regulatory networks (GRNs) can be inferred from both gene expression data and genetic perturbations. Under different conditions, the gene data of the same gene set may be different from each other, which results in different GRNs. Detecting structural difference between GRNs under different conditions is of great significance for understanding gene functions and biological mechanisms.

resultsIn this paper, we propose a Bayesian Fused algorithm to jointly infer differential structures of GRNs under two different conditions. The algorithm is developed for GRNs modeled with structural equation models (SEMs), which makes it possible to incorporate genetic perturbations into models to improve the inference accuracy, so we name it BFDSEM. Different from the naive approaches that separately infer pair-wise GRNs and identify the difference from the inferred GRNs, we first re-parameterize the two SEMs to form an integrated model that takes full advantage of the two groups of gene data, and then solve the re-parameterized model by developing a novel Bayesian fused prior following the criterion that separate GRNs and differential GRN are both sparse.

conclusionsComputer simulations are run on synthetic data to compare BFDSEM to two state-of-the-art joint inference algorithms: FSSEM and ReDNet. The results demonstrate that the performance of BFDSEM is comparable to FSSEM, and is generally better than ReDNet. The BFDSEM algorithm is also applied to a real data set of lung cancer and adjacent normal tissues, the yielded normal GRN and differential GRN are consistent with the reported results in previous literatures. An open-source program implementing BFDSEM is freely available in Additional file 1.

Indexed as

AlgorithmsGene Regulatory NetworksBayes TheoremComputer SimulationHumansBayesian inferenceDifferential GRNGene expressionGene regulatory networksGenetic perturbationsStructural equation models

Identifiers

PMID31918656
PMCPMC6953167

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.