Evidence map›Paper›PMID 24085567›Full record

ArticleBioinformatics (Oxford, England)2014

Functional module identification in protein interaction networks by interaction patterns.

Yijie Wang, Xiaoning Qian

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

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3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

  1. Article
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  3. Review
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  12. Bayesian module identification from multiple noisy networks.EURASIP journal on bioinformatics & systems biology · 2016
    Article
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  14. Article
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

2 authors.

Yijie WangDepartment of Computer Science and Engineering, University of South Florida, Tampa, FL 33620, USA and Department of Electrical and Computer Engineering, Texas A&M University, College Station, TX 77843, USA.
Xiaoning Qian

Funding

Identifying Risk Factors and Interactions for Type 1 Diabetes in Large StudiesR21DK092845 · NIDDK · UNIVERSITY OF SOUTH FLORIDA · PI QIAN, XIAONING · 2011 to 2012
$375k
NIDDK NIH HHS R21 DK092845NIDDK NIH HHS R21DK092845
6 · The paper itself

Abstract

motivationIdentifying functional modules in protein-protein interaction (PPI) networks may shed light on cellular functional organization and thereafter underlying cellular mechanisms. Many existing module identification algorithms aim to detect densely connected groups of proteins as potential modules. However, based on this simple topological criterion of 'higher than expected connectivity', those algorithms may miss biologically meaningful modules of functional significance, in which proteins have similar interaction patterns to other proteins in networks but may not be densely connected to each other. A few blockmodel module identification algorithms have been proposed to address the problem but the lack of global optimum guarantee and the prohibitive computational complexity have been the bottleneck of their applications in real-world large-scale PPI networks.

resultsIn this article, we propose a novel optimization formulation LCP(2) (low two-hop conductance sets) using the concept of Markov random walk on graphs, which enables simultaneous identification of both dense and sparse modules based on protein interaction patterns in given networks through searching for LCP(2) by random walk. A spectral approximate algorithm SLCP(2) is derived to identify non-overlapping functional modules. Based on a bottom-up greedy strategy, we further extend LCP(2) to a new algorithm (greedy algorithm for LCP(2)) GLCP(2) to identify overlapping functional modules. We compare SLCP(2) and GLCP(2) with a range of state-of-the-art algorithms on synthetic networks and real-world PPI networks. The performance evaluation based on several criteria with respect to protein complex prediction, high level Gene Ontology term prediction and especially sparse module detection, has demonstrated that our algorithms based on searching for LCP(2) outperform all other compared algorithms. AVAILABILITY AND IMPLEMENTATION: All data and code are available at http://www.cse.usf.edu/~xqian/fmi/slcp2hop/.

Indexed as

Protein Interaction MapsAlgorithmsCluster AnalysisHumansProtein Interaction MappingProteinsSignal TransductionProteins

Identifiers

PMID24085567
PMCPMC3924044

What OpenQuestion holds

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Registered trials

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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.