Evidence map›Paper›PMID 24266903›Full record

ArticleBMC genomics2013

Predicting gene function using similarity learning.

Tu Phuong, Ngo Nhung

Abstract read
In one paragraph

Article in BMC genomics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

2 citing papers in PubMed.

  1. Expression ofTranslational cancer research · 2022
    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

2 authors.

Tu Phuong
Ngo Nhung

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundComputational methods that make use of heterogeneous biological datasets to predict gene function provide a cost-effective and rapid way for annotating genomes. A common framework shared by many such methods is to construct a combined functional association network from multiple networks representing different sources of data, and use this combined network as input to network-based or kernel-based learning algorithms. In these methods, a key factor contributing to the prediction accuracy is the network quality, which is the ability of the network to reflect the functional relatedness of gene pairs. To improve the network quality, a large effort has been spent on developing methods for network integration. These methods, however, produce networks, which then remain unchanged, and nearly no effort has been made to optimize the networks after their construction.

resultsHere, we propose an alternative method to improve the network quality. The proposed method takes as input a combined network produced by an existing network integration algorithm, and reconstructs this network to better represent the co-functionality relationships between gene pairs. At the core of the method is a learning algorithm that can learn a measure of functional similarity between genes, which we then use to reconstruct the input network. In experiments with yeast and human, the proposed method produced improved networks and achieved more accurate results than two other leading gene function prediction approaches.

conclusionsThe results show that it is possible to improve the accuracy of network-based gene function prediction methods by optimizing combined networks with appropriate similarity measures learned from data. The proposed learning procedure can handle noisy training data and scales well to large genomes.

Indexed as

AlgorithmsArtificial IntelligenceComputational BiologyFungal ProteinsGenome, HumanGenome, MicrobialHumansModels, GeneticMolecular Sequence AnnotationSoftwareFungal Proteins

Identifiers

PMID24266903
PMCPMC3849496

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.