Evidence map›Paper›PMID 31046665›Full record

ArticleBMC bioinformatics2019

Integrating data and knowledge to identify functional modules of genes: a multilayer approach.

Lifan Liang, Vicky Chen, Kunju Zhu, Xiaonan Fan, Xinghua Lu, Songjian Lu

Abstract read
In one paragraph

Article in BMC bioinformatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Lifan LiangDepartment of Biomedical Informatics, University of Pittsburgh, Pittsburgh, PA, USA.
Vicky ChenDepartment of Biomedical Informatics, University of Pittsburgh, Pittsburgh, PA, USA.
Kunju ZhuDepartment of Biomedical Informatics, University of Pittsburgh, Pittsburgh, PA, USA.
Xiaonan FanDepartment of Biomedical Informatics, University of Pittsburgh, Pittsburgh, PA, USA.
Xinghua LuDepartment of Biomedical Informatics, University of Pittsburgh, Pittsburgh, PA, USA.
Songjian LuDepartment of Biomedical Informatics, University of Pittsburgh, Pittsburgh, PA, USA. songjian@pitt.edu.

Funding

TrainingU54HG008540 · NHGRI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BAHAR, IVET, BERG, JEREMY M · 2014 to 2018
$12.8M
Developing Graph Models and Efficient Algorithms for the Study of Cancer DiseaseR00LM011673 · NLM · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LU, SONGJIAN · 2015 to 2017
$656k
NHGRI NIH HHS U54 HG008540NLM NIH HHS R00 LM011673
6 · The paper itself

Abstract

backgroundCharacterizing the modular structure of cellular network is an important way to identify novel genes for targeted therapeutics. This is made possible by the rising of high-throughput technology. Unfortunately, computational methods to identify functional modules were limited by the data quality issues of high-throughput techniques. This study aims to integrate knowledge extracted from literature to further improve the accuracy of functional module identification.

resultsOur new model and algorithm were applied to both yeast and human interactomes. Predicted functional modules have covered over 90% of the proteins in both organisms, while maintaining a comparable overall accuracy. We found that the combination of both mRNA expression information and biomedical knowledge greatly improved the performance of functional module identification, which is better than those only using protein interaction network weighted with transcriptomic data, literature knowledge, or simply unweighted protein interaction network. Our new algorithm also achieved better performance when comparing with some other well-known methods, especially in terms of the positive predictive value (PPV), which indicated the confidence of novel discovery.

conclusionHigher PPV with the multiplex approach suggested that information from both sources has been effectively integrated to reduce false positive. With protein coverage higher than 90%, our algorithm is able to generate more novel biological hypothesis with higher confidence.

Indexed as

AlgorithmsCluster AnalysisGene Expression ProfilingGenes, FungalHumansProtein Interaction MappingSaccharomyces cerevisiae ProteinsSaccharomyces cerevisiae ProteinsFunctional moduleGene expressionGraph clusteringMultiplexProtein complexProtein-protein interactionRandom walkTopic modeling

Identifiers

PMID31046665
PMCPMC6498600

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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.