Evidence map›Paper›PMID 29298679›Full record

ArticleBMC bioinformatics2018

Sequence motif finder using memetic algorithm.

Jader M Caldonazzo Garbelini, André Y Kashiwabara, Danilo S Sanches

Abstract read
In one paragraph

Article in BMC bioinformatics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Putative Novel Viruses in the FamiliesAdvances in virology · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Jader M Caldonazzo GarbeliniDepartment of Computer Science, Bioinformatics Graduate Program, Federal University of Technology - Paraná, Cornélio Procópio, PR, Brazil. jadermcg@hotmail.com.ORCID 0000-0003-2289-882X
André Y KashiwabaraDepartment of Computer Science, Bioinformatics Graduate Program, Federal University of Technology - Paraná, Cornélio Procópio, PR, Brazil.
Danilo S SanchesDepartment of Computer Science, Bioinformatics Graduate Program, Federal University of Technology - Paraná, Cornélio Procópio, PR, Brazil.

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 458598/2014-3
6 · The paper itself

Abstract

backgroundDe novo prediction of Transcription Factor Binding Sites (TFBS) using computational methods is a difficult task and it is an important problem in Bioinformatics. The correct recognition of TFBS plays an important role in understanding the mechanisms of gene regulation and helps to develop new drugs.

resultsWe here present Memetic Framework for Motif Discovery (MFMD), an algorithm that uses semi-greedy constructive heuristics as a local optimizer. In addition, we used a hybridization of the classic genetic algorithm as a global optimizer to refine the solutions initially found. MFMD can find and classify overrepresented patterns in DNA sequences and predict their respective initial positions. MFMD performance was assessed using ChIP-seq data retrieved from the JASPAR site, promoter sequences extracted from the ABS site, and artificially generated synthetic data. The MFMD was evaluated and compared with well-known approaches in the literature, called MEME and Gibbs Motif Sampler, achieving a higher f-score in the most datasets used in this work.

conclusionsWe have developed an approach for detecting motifs in biopolymers sequences. MFMD is a freely available software that can be promising as an alternative to the development of new tools for de novo motif discovery. Its open-source software can be downloaded at https://github.com/jadermcg/mfmd .

Indexed as

AlgorithmsBase SequenceBinding SitesInternetTranscription FactorsUser-Computer InterfaceTranscription FactorsEvolutionary algorithmsHeuristicsMemetic algorithmsMotifTranscription factor binding sites

Identifiers

PMID29298679
PMCPMC5751424

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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.