Demonstration venue · read-only. Every page can be browsed; the buttons that would change it are switched off. Create an account to run TaxoReview on your own data. A simulation from public publication records: the people listed were not invited and did not agree to review.
? Tutorial for this page

Pablo Acera Mateos

dblp:349/8449 · DBLP profile ↗
← Back
2ranked-venue papers
1as first author
2since 2021 · last 2024
0000-0002-7599-6039ORCID · corroborated

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

Applied, interdisciplinary, general and emerging computing · 2 · 1 first-author · 2 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 2 heaviest of 2, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
transcriptomics
0.812024
R2Dtool: integration and visualization of isoform-resolved RNA features · Bioinform. 2024
Bioinformatics and computational biology › transcriptomics
epitranscriptomics
0.212024
R2Dtool: integration and visualization of isoform-resolved RNA features · Bioinform. 2024

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

visualization · 0.8transcript annotation integration · 0.8
YearPublicationVenuePosition
2024 R2Dtool: integration and visualization of isoform-resolved RNA features
abstract
MOTIVATION: Long-read RNA sequencing enables the mapping of RNA modifications, structures, and protein-interaction sites at the resolution of individual transcript isoforms. To understand the functions of these RNA features, it is critical to analyze them in the context of transcriptomic and genomic annotations, such as open reading frames and splice junctions. RESULTS: We have developed R2Dtool, a bioinformatics tool that integrates transcript-mapped information with transcript and genome annotations, allowing for the isoform-resolved analytics and graphical representation of RNA features in their genomic context. We illustrate R2Dtool's capability to integrate and expedite RNA feature analysis using epitranscriptomics data. R2Dtool facilitates the comprehensive analysis and interpretation of alternative transcript isoforms. AVAILABILITY AND IMPLEMENTATION: R2Dtool is freely available under the MIT license at github.com/comprna/R2Dtool.
Aditya J. Sethi, Pablo Acera Mateos, Rippei Hayashi, Nikolay E. Shirokikh, Eduardo Eyras
Bioinform.2
2023 Concepts and methods for transcriptome-wide prediction of chemical messenger RNA modifications with machine learning
abstract
The expanding field of epitranscriptomics might rival the epigenome in the diversity of biological processes impacted. In recent years, the development of new high-throughput experimental and computational techniques has been a key driving force in discovering the properties of RNA modifications. Machine learning applications, such as for classification, clustering or de novo identification, have been critical in these advances. Nonetheless, various challenges remain before the full potential of machine learning for epitranscriptomics can be leveraged. In this review, we provide a comprehensive survey of machine learning methods to detect RNA modifications using diverse input data sources. We describe strategies to train and test machine learning methods and to encode and interpret features that are relevant for epitranscriptomics. Finally, we identify some of the current challenges and open questions about RNA modification analysis, including the ambiguity in predicting RNA modifications in transcript isoforms or in single nucleotides, or the lack of complete ground truth sets to test RNA modifications. We believe this review will inspire and benefit the rapidly developing field of epitranscriptomics in addressing the current limitations through the effective use of machine learning.
Pablo Acera Mateos, Kathi Zarnack, Eduardo Eyras
Briefings Bioinform.1