Evidence map›Paper›PMID 21034431›Full record

ArticleBMC bioinformatics2010

Semi-supervised prediction of protein subcellular localization using abstraction augmented Markov models.

Cornelia Caragea, Doina Caragea, Adrian Silvescu, Vasant Honavar

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In one paragraph

Article in BMC bioinformatics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Cornelia CarageaArtificial Intelligence Research Laboratory, Department of Computer Science,Iowa State University, Ames, IA 50010, USA. cornelia@cs.iastate.edu
Doina Caragea
Adrian Silvescu
Vasant Honavar

Funding

Discovery of Protein Seq.Struct.Func.RelationshipsR33GM066387 · NIGMS · IOWA STATE UNIVERSITY · PI HONAVAR, VASANT G. · 2005 to 2006
$545k
Protein Sequence Structure Function RelationshipsR21GM066387 · NIGMS · IOWA STATE UNIVERSITY · PI HONAVAR, VASANT G. · 2003 to 2004
$291k
NIGMS NIH HHS R21 GM066387NIGMS NIH HHS R33 GM066387
6 · The paper itself

Abstract

backgroundDetermination of protein subcellular localization plays an important role in understanding protein function. Knowledge of the subcellular localization is also essential for genome annotation and drug discovery. Supervised machine learning methods for predicting the localization of a protein in a cell rely on the availability of large amounts of labeled data. However, because of the high cost and effort involved in labeling the data, the amount of labeled data is quite small compared to the amount of unlabeled data. Hence, there is a growing interest in developing semi-supervised methods for predicting protein subcellular localization from large amounts of unlabeled data together with small amounts of labeled data.

resultsIn this paper, we present an Abstraction Augmented Markov Model (AAMM) based approach to semi-supervised protein subcellular localization prediction problem. We investigate the effectiveness of AAMMs in exploiting unlabeled data. We compare semi-supervised AAMMs with: (i) Markov models (MMs) (which do not take advantage of unlabeled data); (ii) an expectation maximization (EM); and (iii) a co-training based approaches to semi-supervised training of MMs (that make use of unlabeled data).

conclusionsThe results of our experiments on three protein subcellular localization data sets show that semi-supervised AAMMs: (i) can effectively exploit unlabeled data; (ii) are more accurate than both the MMs and the EM based semi-supervised MMs; and (iii) are comparable in performance, and in some cases outperform, the co-training based semi-supervised MMs.

Indexed as

Markov ChainsAlgorithmsArtificial IntelligenceCluster AnalysisComputational BiologyDatabases, ProteinModels, BiologicalPlant ProteinsProteinsReproducibility of ResultsSubcellular FractionsPlant ProteinsProteins

Identifiers

PMID21034431
PMCPMC2966293

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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.