Evidence map›Paper›PMID 25420551›Full record

ArticleBMC bioinformatics2014

A statistical approach for 5' splice site prediction using short sequence motifs and without encoding sequence data.

Prabina Kumar Meher, Tanmaya Kumar Sahu, Atmakuri Ramakrishna Rao, Sant Dass Wahi

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 27% of its field
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

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 16 citations in OpenAlex.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Prabina Kumar MeherDivision of Statistical Genetics, Indian Agricultural Statistics Research Institute, New Delhi, 110012, India. meherprabin@yahoo.com.
Tanmaya Kumar SahuCentre for Agricultural Bioinformatics, Indian Agricultural Statistics Research Institute, New Delhi, 110012, India. tanmayabioinfo@gmail.com.
Atmakuri Ramakrishna RaoCentre for Agricultural Bioinformatics, Indian Agricultural Statistics Research Institute, New Delhi, 110012, India. rao.cshl.work@gmail.com.
Sant Dass WahiDivision of Statistical Genetics, Indian Agricultural Statistics Research Institute, New Delhi, 110012, India. sdwahi@iasri.res.in.
Indian Agricultural Statistics Research Institute · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMost of the approaches for splice site prediction are based on machine learning techniques. Though, these approaches provide high prediction accuracy, the window lengths used are longer in size. Hence, these approaches may not be suitable to predict the novel splice variants using the short sequence reads generated from next generation sequencing technologies. Further, machine learning techniques require numerically encoded data and produce different accuracy with different encoding procedures. Therefore, splice site prediction with short sequence motifs and without encoding sequence data became a motivation for the present study.

resultsAn approach for finding association among nucleotide bases in the splice site motifs is developed and used further to determine the appropriate window size. Besides, an approach for prediction of donor splice sites using sum of absolute error criterion has also been proposed. The proposed approach has been compared with commonly used approaches i.e., Maximum Entropy Modeling (MEM), Maximal Dependency Decomposition (MDD), Weighted Matrix Method (WMM) and Markov Model of first order (MM1) and was found to perform equally with MEM and MDD and better than WMM and MM1 in terms of prediction accuracy.

conclusionsThe proposed prediction approach can be used in the prediction of donor splice sites with higher accuracy using short sequence motifs and hence can be used as a complementary method to the existing approaches. Based on the proposed methodology, a web server was also developed for easy prediction of donor splice sites by users and is available at http://cabgrid.res.in:8080/sspred .

Indexed as

AlgorithmsModels, StatisticalArtificial IntelligenceBase SequenceComputational BiologyHigh-Throughput Nucleotide SequencingHumansMolecular Sequence DataNucleotide MotifsRNA Splice SitesRNA SplicingROC CurveSequence Analysis, RNARNA Splice Sites

Identifiers

PMID25420551
PMCPMC4702320
OpenAlexW2101874025

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.