Evidence map›Paper›PMID 23866986›Full record

ArticleBMC systems biology2013

A novel function prediction approach using protein overlap networks.

Shide Liang, Dandan Zheng, Daron M Standley, Huarong Guo, Chi Zhang

Abstract read
In one paragraph

Article in BMC systems biology, 2013. 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
–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

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.

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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

5 authors.

Shide LiangSystems Immunology Lab, Immunology Frontier Research Center, Osaka University, Suita, Osaka 565-0871, Japan. shideliang@ifrec.osaka-u.ac.jp
Dandan Zheng
Daron M Standley
Huarong Guo
Chi Zhang

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundConstruction of a reliable network remains the bottleneck for network-based protein function prediction. We built an artificial network model called protein overlap network (PON) for the entire genome of yeast, fly, worm, and human, respectively. Each node of the network represents a protein, and two proteins are connected if they share a domain according to InterPro database.

resultsThe function of a protein can be predicted by counting the occurrence frequency of GO (gene ontology) terms associated with domains of direct neighbors. The average success rate and coverage were 34.3% and 43.9%, respectively, for the test genomes, and were increased to 37.9% and 51.3% when a composite PON of the four species was used for the prediction. As a comparison, the success rate was 7.0% in the random control procedure. We also made predictions with GO term annotations of the second layer nodes using the composite network and obtained an impressive success rate (>30%) and coverage (>30%), even for small genomes. Further improvement was achieved by statistical analysis of manually annotated GO terms for each neighboring protein.

conclusionsThe PONs are composed of dense modules accompanied by a few long distance connections. Based on the PONs, we developed multiple approaches effective for protein function prediction.

Indexed as

AnimalsComputational BiologyDatabases, GeneticGenomicsHumansMolecular Sequence AnnotationProteinsProteins

Identifiers

PMID23866986
PMCPMC3720179

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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.