Evidence map›Paper›PMID 21342580›Full record

ArticleBMC bioinformatics2011

Fast and accurate clustering of noncoding RNAs using ensembles of sequence alignments and secondary structures.

Yutaka Saito, Kengo Sato, Yasubumi Sakakibara

Abstract read
In one paragraph

Article in BMC bioinformatics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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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.

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3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Review
  2. Reference-based read clustering improves theComputational and structural biotechnology journal · 2023
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

Yutaka SaitoDepartment of Biosciences and Informatics, Keio University, 3-14-1 Hiyoshi, Kohoku-ku, Yokohama, Kanagawa 223-8522, Japan. saito@dna.bio.keio.ac.jp
Kengo Sato
Yasubumi Sakakibara

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundClustering of unannotated transcripts is an important task to identify novel families of noncoding RNAs (ncRNAs). Several hierarchical clustering methods have been developed using similarity measures based on the scores of structural alignment. However, the high computational cost of exact structural alignment requires these methods to employ approximate algorithms. Such heuristics degrade the quality of clustering results, especially when the similarity among family members is not detectable at the primary sequence level.

resultsWe describe a new similarity measure for the hierarchical clustering of ncRNAs. The idea is that the reliability of approximate algorithms can be improved by utilizing the information of suboptimal solutions in their dynamic programming frameworks. We approximate structural alignment in a more simplified manner than the existing methods. Instead, our method utilizes all possible sequence alignments and all possible secondary structures, whereas the existing methods only use one optimal sequence alignment and one optimal secondary structure. We demonstrate that this strategy can achieve the best balance between the computational cost and the quality of the clustering. In particular, our method can keep its high performance even when the sequence identity of family members is less than 60%.

conclusionsOur method enables fast and accurate clustering of ncRNAs. The software is available for download at http://bpla-kernel.dna.bio.keio.ac.jp/clustering/.

Indexed as

AlgorithmsNucleic Acid ConformationBase SequenceCluster AnalysisComputational BiologyRNA, UntranslatedSequence AlignmentSequence Analysis, RNASoftwareRNA, Untranslated

Identifiers

PMID21342580
PMCPMC3044305

What OpenQuestion holds

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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.