Evidence map›Paper›PMID 30373534›Full record

ArticleBMC bioinformatics2018

Feature related multi-view nonnegative matrix factorization for identifying conserved functional modules in multiple biological networks.

Peizhuo Wang, Lin Gao, Yuxuan Hu, Feng Li

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

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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.

Peizhuo WangSchool of Computer Science and Technology, Xidian University, Xi'an, 710071, China.
Lin GaoSchool of Computer Science and Technology, Xidian University, Xi'an, 710071, China. lgao@mail.xidian.edu.cn.ORCID http://orcid.org/0000-0001-6396-0787
Yuxuan HuSchool of Computer Science and Technology, Xidian University, Xi'an, 710071, China.
Feng LiSchool of Computer Science and Technology, Xidian University, Xi'an, 710071, China.
Xidian University · CN

Funding

National Natural Science Foundation of China 61432010National Natural Science Foundation of China 61532014National Natural Science Foundation of China 61702397
6 · The paper itself

Abstract

backgroundComprehensive analyzing multi-omics biological data in different conditions is important for understanding biological mechanism in system level. Multiple or multi-layer network model gives us a new insight into simultaneously analyzing these data, for instance, to identify conserved functional modules in multiple biological networks. However, because of the larger scale and more complicated structure of multiple networks than single network, how to accurate and efficient detect conserved functional biological modules remains a significant challenge.

resultsHere, we propose an efficient method, named ConMod, to discover conserved functional modules in multiple biological networks. We introduce two features to characterize multiple networks, thus all networks are compressed into two feature matrices. The module detection is only performed in the feature matrices by using multi-view non-negative matrix factorization (NMF), which is independent of the number of input networks. Experimental results on both synthetic and real biological networks demonstrate that our method is promising in identifying conserved modules in multiple networks since it improves the accuracy and efficiency comparing with state-of-the-art methods. Furthermore, applying ConMod to co-expression networks of different cancers, we find cancer shared gene modules, the majority of which have significantly functional implications, such as ribosome biogenesis and immune response. In addition, analyzing on brain tissue-specific protein interaction networks, we detect conserved modules related to nervous system development, mRNA processing, etc.

conclusionsConMod facilitates finding conserved modules in any number of networks with a low time and space complexity, thereby serve as a valuable tool for inference shared traits and biological functions of multiple biological system.

Indexed as

AlgorithmsGene Expression Regulation, NeoplasticGene Regulatory NetworksProtein Interaction MapsCluster AnalysisComputational BiologyGene Expression ProfilingHumansNeoplasmsConserved modulesFeaturesMatrix factorizationMultiple biological networks

Identifiers

PMID30373534
PMCPMC6206826
OpenAlexW2899003199

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.