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Zacharopoulou, E.

Publications and source records attributed to Zacharopoulou, E..

2 recordsLinked to original sources

Discriminative learning of substitution matrices and gap penalties for pairwise alignment of biological sequences

Pairwise alignment scores are used to classify pairs of sequences in many areas of bioinformatics, including homology search, predicting interactions, or read mapping. The relative scores of different pairs strongly depend on the choice of a substitution matrix and gap penalties, but the existing approaches for the estimation of these parameters do not directly optimize them for the task of classification. In this work, we present DiscrimAlign, a statistical model for discriminative learning of substitution matrices and gap penalties from a dataset of positive and negative pairs of unaligned biological sequences. The model links the alignment score of a sequence pair with the associated binary label through a logistic function and learns the parameters by likelihood maximization. We analyze theoretical properties of the model, derive and implement a learning procedure, study its performance in simulated experiments, and apply it to predict microRNA-target interactions. We show that sequence alignment with discriminative substitution matrices and gap penalties predicts the interactions comparably to state-of-the-art neural network classifiers while being more interpretable. An implementation of the model and reproducibility workflows are available at https://github.com/BioGeMT/DiscrimAlign.

bioinformatics↗

Agentomics: An Agentic System that Autonomously Develops Novel State-of-the-art Solutions for Biomedical Machine Learning Tasks

MotivationExtracting knowledge from biomedical data is crucial for advancing our understanding of biological systems and developing novel therapeutics. The quantity, quality, and resolution of biomedical data constantly evolves, requiring the automation of biomedical machine learning (ML). Existing Automated ML tools lack flexibility, while Large Language Models (LLMs) struggle to consistently deliver reproducible machine learning codebases, and existing LLM Agent-powered solutions lag behind human-engineered ML models. ResultsHere, we introduce Agentomics, an autonomous LLM-powered agentic system for end-to-end ML experimentation. Given a biomedical dataset, Agentomics implements various ML modeling strategies, and produces a ready-to-use ML model. Agentomics introduces strict validation checkpoints for standard ML development steps, allowing gradual development on top of working code with defined interfaces and validated artifacts. Further, it offers native support for biomedical foundation models that can be leveraged during experimentation. The generic nature of Agentomics allows the user to create ML solutions for a large variety of datasets and use various LLMs. We evaluate Agentomics across 20 datasets from the domains of Protein Engineering, Drug Discovery, and Regulatory Genomics. When benchmarked against other agentic systems, Agentomics outperformed them in all tested domains. When benchmarked against human expert solutions, Agentomics generated novel state-of-the-art models for 11/20 established benchmark datasets. Availability and ImplementationAgentomics is implemented in Python. Source code and documentation are freely available at: https://github.com/BioGeMT/Agentomics-ML. Contactpanagiotis.alexiou@um.edu.mt

bioinformatics↗