Evidence map›Paper›PMID 38528492›Full record

ArticleBMC bioinformatics2024

BIOMAPP::CHIP: large-scale motif analysis.

Jader M Caldonazzo Garbelini, Danilo S Sanches, Aurora T Ramirez Pozo

Abstract read
In one paragraph

Article in BMC bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

The trial behind it

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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 Informatics, Federal University of Parana, XV de Novembro Street, Curitiba, Parana, 80060000, Brazil. jmcgarbelini@inf.ufpr.br.
Danilo S Sanches *Department of Informatics, Federal University of Technology, Alberto Carazzai Avenue, Cornelio Procopio, Parana, 86300000, Brazil.
Aurora T Ramirez Pozo *Department of Informatics, Federal University of Parana, XV de Novembro Street, Curitiba, Parana, 80060000, Brazil.

Funding

Coordination for the Improvement of Higher Education Personnel (CAPES) - Program of Academic Excellence (PROEX) Finance Code 001
6 · The paper itself

Abstract

backgroundDiscovery biological motifs plays a fundamental role in understanding regulatory mechanisms. Computationally, they can be efficiently represented as kmers, making the counting of these elements a critical aspect for ensuring not only the accuracy but also the efficiency of the analytical process. This is particularly useful in scenarios involving large data volumes, such as those generated by the ChIP-seq protocol. Against this backdrop, we introduce BIOMAPP::CHIP, a tool specifically designed to optimize the discovery of biological motifs in large data volumes.

resultsWe conducted a comprehensive set of comparative tests with state-of-the-art algorithms. Our analyses revealed that BIOMAPP::CHIP outperforms existing approaches in various metrics, excelling both in terms of performance and accuracy. The tests demonstrated a higher detection rate of significant motifs and also greater agility in the execution of the algorithm. Furthermore, the SMT component played a vital role in the system's efficiency, proving to be both agile and accurate in kmer counting, which in turn improved the overall efficacy of our tool.

conclusionBIOMAPP::CHIP represent real advancements in the discovery of biological motifs, particularly in large data volume scenarios, offering a relevant alternative for the analysis of ChIP-seq data and have the potential to boost future research in the field. This software can be found at the following address: (https://github.com/jadermcg/biomapp-chip).

Indexed as

AlgorithmsSoftwareBinding SitesChromatin ImmunoprecipitationNucleotide MotifsSequence Analysis, DNAChip-seqKmer countingMotif discoveryOptimization

Identifiers

PMID38528492
PMCPMC10964687

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.