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Perez Gallardo, Y.

Publications and source records attributed to Perez Gallardo, Y..

2 recordsLinked to original sources

REDIRECTION: Generating drug repurposing hypotheses using link prediction with DISNET data

In the recent years and due to COVID-19 pandemic, drug repurposing or repositioning has been placed in the spotlight. Giving new therapeutic uses to already existing drugs, this discipline allows to streamline the drug discovery process, reducing the costs and risks inherent to de novo development. Computational approaches have gained momentum, and emerging techniques from the machine learning domain have proved themselves as highly exploitable means for repurposing prediction. Against this backdrop, one can find that biomedical data can be represented in terms of graphs, which allow depicting in a very expressive manner the underlying structure of the information. Combining these graph data structures with deep learning models enhances the prediction of new links, such as potential disease-drug connections. In this paper, we present a new model named REDIRECTION, which aim is to predict new disease-drug links in the context of drug repurposing. It has been trained with a part of the DISNET biomedical graph, formed by diseases, symptoms, drugs, and their relationships. The reserved testing graph for the evaluation has yielded to an AUROC of 0.93 and an AUPRC of 0.90. We have performed a secondary validation of REDIRECTION using RepoDB data as the testing set, which has led to an AUROC of 0.87 and a AUPRC of 0.83. In the light of these results, we believe that REDIRECTION can be a meaningful and promising tool to generate drug repurposing hypotheses.

bioinformatics↗

Analysis of new nosological models from disease similarities using clustering

While classical disease nosology is based on phenotypical characteristics, the increasing availability of biological and molecular data is providing new understanding of diseases and their underlying relationships, that could lead to a more comprehensive paradigm for modern medicine. In the present work, similarities between diseases are used to study the generation of new possible disease nosologic models that include both phenotypical and biological information. To this aim, disease similarity is measured in terms of disease feature vectors, that stood for genes, proteins, metabolic pathways and PPIs in the case of biological similarity, and for symptoms in the case of phenotypical similarity. An improvement in similarity computation is proposed, considering weighted instead of Booleans feature vectors. Unsupervised learning methods were applied to these data, specifically, density-based DBSCAN clustering algorithm. As evaluation metric silhouette coefficient was chosen, even though the number of clusters and the number of outliers were also considered. As a results validation, a comparison with randomly distributed data was performed. Results suggest that weighted biological similarities based on proteins, and computed according to cosine index, may provide a good starting point to rearrange disease taxonomy and nosology.

bioinformatics↗