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Bruno Thiago de Lima Nichio

dblp:245/1127 · DBLP profile ↗
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2ranked-venue papers
1as first author
1since 2021 · last 2026
0000-0002-0196-6486ORCID · corroborated

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 2 · 1 first-author · 1 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 1 heaviest of 1, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
RNA biology
1.012026
mirtronDB 2.0: enhanced database with novel mirtron discoveries · Bioinform. 2026

Methods — techniques the papers use, named apart from their topics

machine learning · 1.0bioinformatics pipeline · 1.0
YearPublicationVenuePosition
2026 mirtronDB 2.0: enhanced database with novel mirtron discoveries
abstract
MOTIVATION: MirtronDB provides a comprehensive and up-to-date resource for advancing mirtron research within RNA biology. Therefore, maintaining a specialized and continuously updated resource for mirtrons is essential to support ongoing discoveries and to serve as a key reference for researchers investigating the roles of mirtrons. RESULTS: Here, we present mirtronDB 2.0, an enhanced version that expands both content and functionality. This version integrates mirtron data published between 2017 and 2025, increasing the number of documented mirtrons across various species. In addition, it incorporates newly predicted mirtrons identified through a robust pipeline that combines advanced bioinformatics and machine learning approaches, with specific coverage of six mammalian species. We have introduced new website features, including an interactive dashboard to enhance usability and facilitate intuitive data exploration. These rigorous updates consolidate mirtronDB as a key resource for mirtron to the RNA biology community. AVAILABILITY AND IMPLEMENTATION: mirtronDB can be found under http://mirtrondb.cp.utfpr.edu.br/. The complete content of Database 2.0 and the source code for the analyses are also freely available in the FigShare repository: https://figshare.com/articles/dataset/MirtronDB_version2/29344775.
Fabiana Rodrigues de Góes, Matheus Fujimura Soares, Vitor Gregorio, Bruno Thiago de Lima Nichio, Alisson Gaspar Chiquitto, Flavia Lombardi Lopes, Mark Basham, Douglas Silva Domingues, Alexandre Rossi Paschoal
Bioinform.4
2019 RAFTS3G: an efficient and versatile clustering software to analyses in large protein datasets
abstract
Clustering methods are essential to partitioning biological samples being useful to minimize the information complexity in large datasets. Tools in this context usually generates data with greed algorithms that solves some Data Mining difficulties which can degrade biological relevant information during the clustering process. The lack of standardization of metrics and consistent bases also raises questions about the clustering efficiency of some methods. Benchmarks are needed to explore the full potential of clustering methods - in which alignment-free methods stand out - and the good choice of dataset makes it essentials. Here we present a new approach to Data Mining in large protein sequences datasets, the Rapid Alignment Free Tool for Sequences Similarity Search to Groups (RAFTS 3 G), a method to clustering aiming of losing less biological information in the processes of generation groups. The strategy developed in our algorithm is optimized to be more astringent which reflects increase in accuracy and sensitivity in the generation of clusters in a wide range of similarity. RAFTS 3 G is the better choice compared to three main methods when the user wants more reliable result even ignoring the ideal threshold to clustering. In general, RAFTS 3 G is able to group up to millions of biological sequences into large datasets, which is a remarkable option of efficiency in clustering. RAFTS 3 G compared to other “standard-gold” methods in the clustering of large biological data maintains the balance between the reduction of biological information redundancy and the creation of consistent groups. We bring the binary search concept applied to grouped sequences which shows maintaining sensitivity/accuracy relation and up to minimize the time of data generated with RAFTS 3 G process.
Bruno Thiago de Lima Nichio, Aryel Marlus Repula de Oliveira, Camilla Reginatto de Pierri, Leticia Graziela Costa Santos, Alexandre Quadros Lejambre, Ricardo Assunção Vialle, Nilson Antônio da Rocha Coimbra, Dieval Guizelini, Jeroniza Nunes Marchaukoski, Fábio de Oliveira Pedrosa, Roberto Tadeu Raittz
BMC Bioinform.1