Evidence map›Paper›PMID 19542155›Full record

ArticleBioinformatics (Oxford, England)2009

Reconstruct modular phenotype-specific gene networks by knowledge-driven matrix factorization.

Xuerui Yang, Yang Zhou, Rong Jin, Christina Chan

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
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  5. Review
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  9. Matrix Factorization for Transcriptional Regulatory Network Inference.IEEE Symposium on Computational Intelligence in Bioinformatics and Computational Biology proceedings. IEEE Symposium on Computational Intelligence in Bioinformatics and Computational Biology · 2012
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Xuerui YangDepartment of Chemical Engineering and Materials Science, Michigan State University, East Lansing, MI 48824, USA.
Yang Zhou
Rong Jin
Christina Chan
Michigan State University · US

Funding

Develop a Dynamic Model that Incoporates Text-mining to Reconstruct NetworksR01GM079688 · NIGMS · MICHIGAN STATE UNIVERSITY · PI CHAN, CHRISTINA · 2007 to 2012
$1.2M
Development of a parallel, array-based transcription factor expression assayR21RR024439 · NCRR · MICHIGAN STATE UNIVERSITY · PI WALTON, STEPHEN PATRICK · 2008 to 2010
$540k
Aptamer-based Proteomic Analysis for Cancer SignaturesR21CA126136 · NCI · MICHIGAN STATE UNIVERSITY · PI WALTON, STEPHEN PATRICK · 2006 to 2007
$354k
NCI NIH HHS R21CA126136-01NCRR NIH HHS R21RR024439NIGMS NIH HHS R01 GM079688NIGMS NIH HHS R01GM079688-01
6 · The paper itself

Abstract

motivationReconstructing gene networks from microarray data has provided mechanistic information on cellular processes. A popular structure learning method, Bayesian network inference, has been used to determine network topology despite its shortcomings, i.e. the high-computational cost when analyzing a large number of genes and the inefficiency in exploiting prior knowledge, such as the co-regulation information of the genes. To address these limitations, we are introducing an alternative method, knowledge-driven matrix factorization (KMF) framework, to reconstruct phenotype-specific modular gene networks.

resultsConsidering the reconstruction of gene network as a matrix factorization problem, we first use the gene expression data to estimate a correlation matrix, and then factorize the correlation matrix to recover the gene modules and the interactions between them. Prior knowledge from Gene Ontology is integrated into the matrix factorization. We applied this KMF algorithm to hepatocellular carcinoma (HepG2) cells treated with free fatty acids (FFAs). By comparing the module networks for the different conditions, we identified the specific modules that are involved in conferring the cytotoxic phenotype induced by palmitate. Further analysis of the gene modules of the different conditions suggested individual genes that play important roles in palmitate-induced cytotoxicity. In summary, KMF can efficiently integrate gene expression data with prior knowledge, thereby providing a powerful method of reconstructing phenotype-specific gene networks and valuable insights into the mechanisms that govern the phenotype.

Indexed as

AlgorithmsGene Regulatory NetworksKnowledgeCell DeathCell Line, TumorComputational BiologyGene Expression Regulation, NeoplasticGenes, NeoplasmHumansPalmitatesPhenotypePalmitates

Identifiers

PMID19542155
PMCPMC2800351
OpenAlexW2165952829

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

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.