Evidence map›Paper›PMID 28383059›Full record

ArticleScientific reports2017

An improved method for identification of small non-coding RNAs in bacteria using support vector machine.

Ranjan Kumar Barman, Anirban Mukhopadhyay, Santasabuj Das

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Prevalence of small base-pairing RNAs derived from diverse genomic loci.Biochimica et biophysica acta. Gene regulatory mechanisms · 2020
    Review
  5. Article
  6. Article
  7. Article
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

Ranjan Kumar BarmanBiomedical Informatics Centre, National Institute Of Cholera and Enteric Diseases, Kolkata, West Bengal, India.
Anirban MukhopadhyayDepartment of Computer Science and Engineering, University of Kalyani, Kalyani, West Bengal, India.
Santasabuj DasBiomedical Informatics Centre, National Institute Of Cholera and Enteric Diseases, Kolkata, West Bengal, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacterial small non-coding RNAs (sRNAs) are not translated into proteins, but act as functional RNAs. They are involved in diverse biological processes like virulence, stress response and quorum sensing. Several high-throughput techniques have enabled identification of sRNAs in bacteria, but experimental detection remains a challenge and grossly incomplete for most species. Thus, there is a need to develop computational tools to predict bacterial sRNAs. Here, we propose a computational method to identify sRNAs in bacteria using support vector machine (SVM) classifier. The primary sequence and secondary structure features of experimentally-validated sRNAs of Salmonella Typhimurium LT2 (SLT2) was used to build the optimal SVM model. We found that a tri-nucleotide composition feature of sRNAs achieved an accuracy of 88.35% for SLT2. We validated the SVM model also on the experimentally-detected sRNAs of E. coli and Salmonella Typhi. The proposed model had robustly attained an accuracy of 81.25% and 88.82% for E. coli K-12 and S. Typhi Ty2, respectively. We confirmed that this method significantly improved the identification of sRNAs in bacteria. Furthermore, we used a sliding window-based method and identified sRNAs from complete genomes of SLT2, S. Typhi Ty2 and E. coli K-12 with sensitivities of 89.09%, 83.33% and 67.39%, respectively.

Indexed as

Support Vector MachineComputational BiologyDatabases, GeneticGenome, BacterialMachine LearningReproducibility of ResultsRNA, BacterialRNA, Small UntranslatedRNA, BacterialRNA, Small Untranslated

Identifiers

PMID28383059
PMCPMC5382675

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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.