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Rocha, M.

Publications and source records attributed to Rocha, M..

21 records · Page 2Linked to original sources

HABIT - a webserver for interactive T cell neoepitope discovery

Neoepitopes generated by amino acid variants specifically found in pathogens or cancer cells are gaining momentum in immunotherapy development. HABIT (HLA Binding InTelligence) is a web platform designed to generate and analyse machine learning-based T cell epitope predictions for improved neoepitope discovery. Availability and ImplementationHABIT is available at http://habit.evobiomed.com. Peptide-HLA binding predictions by NetMHCpan 4.0 and NetMHCIIpan 3.1 were implemented in a web application for interactive data exploration using shiny package powered by RStudio. Contactnosorio@med.uminho.pt Supplementary informationSupplementary data and video tutorials are available online.

bioinformatics↗

Vocal motor experiences consolidate the vocal motor circuitry and accelerate future vocal skill development

Complex motor skills take considerable time and practice to learn. Without continued practice the level of skill performance quickly degrades, posing a problem for the timely utilization of skilled motor responses. Here we quantified the recurring development of vocal motor skills and the accompanying changes in synaptic connectivity in the brain of a songbird, while manipulating skill performance by consecutively administrating and withdrawing testosterone. We demonstrate that a songbird with prior singing experience can significantly accelerate the re-acquisition of vocal performance. We further demonstrate that an increase in vocal performance is accompanied by a pronounced synaptic pruning in the forebrain vocal motor area HVC, a reduction that is not reversed when birds stop singing. These results provide evidence that lasting synaptic changes in the motor circuitry are associated with the savings of motor skills, enabling a rapid recovery of motor performance under environmental time constraints.

animal behavior and cognition↗

Reconstruction of consensus tissue-specific metabolic models

Genome-Scale Metabolic Models have shown promising results in biomedical applications, such as understanding cancer metabolism and drug discovery. However, to take full advantage of these models there is the need to address the representation and simulation of the metabolic phenotypes of distinct cell types. With this aim, several algorithms have been recently proposed to reconstruct tissue-specific metabolic models based on available data. Here, the most promising were implemented and used to reconstruct models for two case studies, using omics data from distinct sources. The set of obtained models were compared and analyzed, being shown they are highly variable and that no combination of algorithm and data source can achieve models with acceptable phenotype predictions. We propose an algorithm to achieve a consensus model from the set of models available for a given tissue/cell line, and to improve it given functional data (e.g. known metabolic tasks). The results show that the resulting models are more accurate, both considering the prediction of known metabolic phenotypes and of experimental data not used in the model construction. Two case studies used for model validation consider healthy hepatocytes and a glioblastoma cell line. The open-source implementation of the algorithms is provided, together with the models built, in a software container, allowing full reproducibility, and representing by itself a contribution for the community.

systems biology↗