Evidence map›Paper›PMID 18811946›Full record

ArticleBMC bioinformatics2008

Comparison study on k-word statistical measures for protein: from sequence to 'sequence space'.

Qi Dai, Tianming Wang

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Article in BMC bioinformatics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

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16citing papers in PubMed
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3 · Its place in the literature

Who cites it

16 citing papers in PubMed.

  1. Predicting Polymerase Chain Reaction Success: Integrating theCombinatorial chemistry & high throughput screening · 2026
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  2. Review
  3. Comparative Study on Feature Selection in Protein Structure and Function Prediction.Computational and mathematical methods in medicine · 2022
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  8. Clustering of reads with alignment-free measures and quality values.Algorithms for molecular biology : AMB · 2015
    Article
  9. Review
  10. Article
  11. Article
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  14. Article
  15. Article
  16. Using Gaussian model to improve biological sequence comparison.Journal of computational chemistry · 2010
    Article
4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Qi DaiDepartment of Applied Mathematics, Dalian University of Technology, Dalian 116024, PR China. daiailiu2004@yahoo.com.cn
Tianming Wang

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMany proposed statistical measures can efficiently compare protein sequence to further infer protein structure, function and evolutionary information. They share the same idea of using k-word frequencies of protein sequences. Given a protein sequence, the information on its related protein sequences hasn't been used for protein sequence comparison until now. This paper proposed a scheme to construct protein 'sequence space' which was associated with protein sequences related to the given protein, and the performances of statistical measures were compared when they explored the information on protein 'sequence space' or not. This paper also presented two statistical measures for protein: gre.k (generalized relative entropy) and gsm.k (gapped similarity measure).

resultsWe tested statistical measures based on protein 'sequence space' or not with three data sets. This not only offers the systematic and quantitative experimental assessment of these statistical measures, but also naturally complements the available comparison of statistical measures based on protein sequence. Moreover, we compared our statistical measures with alignment-based measures and the existing statistical measures. The experiments were grouped into two sets. The first one, performed via ROC (Receiver Operating Curve) analysis, aims at assessing the intrinsic ability of the statistical measures to discriminate and classify protein sequences. The second set of the experiments aims at assessing how well our measure does in phylogenetic analysis. Based on the experiments, several conclusions can be drawn and, from them, novel valuable guidelines for the use of protein 'sequence space' and statistical measures were obtained.

conclusionAlignment-based measures have a clear advantage when the data is high redundant. The more efficient statistical measure is the novel gsm.k introduced by this article, the cos.k followed. When the data becomes less redundant, gre.k proposed by us achieves a better performance, but all the other measures perform poorly on classification tasks. Almost all the statistical measures achieve improvement by exploring the information on 'sequence space' as word's length increases, especially for less redundant data. The reasonable results of phylogenetic analysis confirm that Gdis.k based on 'sequence space' is a reliable measure for phylogenetic analysis. In summary, our quantitative analysis verifies that exploring the information on 'sequence space' is a promising way to improve the abilities of statistical measures for protein comparison.

Indexed as

AlgorithmsData Interpretation, StatisticalModels, ChemicalSoftwareAmino Acid SequenceComputer SimulationModels, StatisticalMolecular Sequence DataProteinsSequence AlignmentSequence Analysis, ProteinSequence Homology, Amino AcidProteins

Identifiers

PMID18811946
PMCPMC2571980

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LicenceCC BY
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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.