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Stamatopoulos, K.

Publications and source records attributed to Stamatopoulos, K..

2 recordsLinked to original sources

ParaSurf: A Surface-Based Deep Learning Approach for Paratope-Antigen Interaction Prediction

MotivationIdentifying antibody binding sites, is crucial for developing vaccines and therapeutic antibodies, processes that are time-consuming and costly. Accurate prediction of the paratopes binding site can speed up the development by improving our understanding of antibody-antigen interactions. ResultsWe present ParaSurf, a deep learning model that significantly enhances paratope prediction by incorporating both surface geometric and non-geometric factors. Trained and tested on three prominent antibody-antigen benchmarks, ParaSurf achieves state-of-the-art results across nearly all metrics. Unlike models restricted to the variable region, ParaSurf demonstrates the ability to accurately predict binding scores across the entire Fab region of the antibody. Additionally, we conducted an extensive analysis using the largest of the three datasets employed, focusing on three key components: (1) a detailed evaluation of paratope prediction for each Complementarity-Determining Region loop, (2) the performance of models trained exclusively on the heavy chain, and (3) the results of training models solely on the light chain without incorporating data from the heavy chain. Availability and ImplementationSource code for ParaSurf, along with the datasets used, preprocessing pipeline, and trained model weights, are freely available at https://github.com/aggelos-michael-papadopoulos/ParaSurf. Contactangepapa@iti.gr, axenop@iti.gr Supplementary informationSupplementary data are available at Bioinformatics online.

bioinformatics↗

GLASS: assisted and standardized assessment of gene variations from Sanger sequence trace data

MotivationSanger sequencing remains the reference method for sequence variant detection, especially in a clinical setting. However, chromatogram interpretation often requires manual inspection and in some cases considerable expertise. Additionally, variant reporting and nomenclature is typically left to the user, which can lead to inconsistencies.\n\nResultsWe introduce GLASS, a tool built to assist with the assessment of gene variations in Sanger sequencing data. Critically, it provides a standardized variant output as recommended by the Human Genome Variation Society.\n\nAvailabilityThe program is freely available online at http://bat.infspire.org/genomepd/glass/.\n\nContactnikos.darzentas@gmail.com, malcikova.jitka@fnbrno.cz\n\nSupplementary informationSupplementary data are available at Bioinformatics online.

bioinformatics↗