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Juhasz, J.

Publications and source records attributed to Juhasz, J..

2 recordsLinked to original sources

ProkBERT PhaStyle: Accurate Phage Lifestyle Prediction with Pretrained Genomic Language Models

BackgroundPhage lifestyle prediction, i.e. classifying phage sequences as virulent or temperate, is crucial in biomedical and ecological applications. Phage sequences from metagenome or metavirome assemblies are often fragmented, and the diversity of environmental phages is not well known. Current computational approaches often rely on database comparisons and machine learning algorithms that require significant effort and expertise to update. We propose using genomic language models for phage lifestyle classification, allowing efficient direct analysis from nucleotide sequences without the need for sophisticated preprocessing pipelines or manually curated databases. MethodsWe trained three genomic language models (DNABERT-2, Nucleotide Transformer, and ProkBERT) on datasets of short, fragmented sequences. These models were then compared with dedicated phage lifestyle prediction methods (PhaTYP, DeePhage, BACPHLIP) in terms of accuracy, prediction speed, and generalization capability. ResultsProkBERT PhaStyle consistently outperforms existing models in various scenarios. It generalizes well for out-of-sample data, accurately classifies phages from extreme environments, and also demonstrates high inference speed. Despite having up to 20 times fewer parameters, it proved to be better performing than much larger genomic language models. ConclusionsGenomic language models offer a simple and computationally efficient alternative for solving complex classification tasks, such as phage lifestyle prediction. ProkBERT PhaStyles simplicity, speed, and performance suggest its utility in various ecological and clinical applications.

bioinformatics↗

ProkBERT Family: Genomic Language Models for Microbiome Applications

Machine learning offers transformative capabilities in microbiology and microbiome analysis, deciphering intricate microbial interactions, predicting functionalities, and unveiling novel patterns in vast datasets. This enriches our comprehension of microbial ecosystems and their influence on health and disease. However, the integration of machine learning in these fields contends with issues like the scarcity of labeled datasets, the immense volume and complexity of microbial data, and the subtle interactions within microbial communities. Addressing these challenges, we introduce the ProkBERT model family. Built on transfer learning and self-supervised methodologies, ProkBERT models capitalize on the abundant available data, demonstrating adaptability across diverse scenarios. The models learned representations align with established biological understanding, shedding light on phylogenetic relationships. With the novel Local Context-Aware (LCA) tokenization, the ProkBERT family overcomes the context size limitations of traditional transformer models without sacrificing performance or the information rich local context. In bioinformatics tasks like promoter prediction and phage identification, ProkBERT models excel. For promoter predictions, the best performing model achieved an MCC of 0.74 for E. coli and 0.62 in mixed-species contexts. In phage identification, they all consistently outperformed tools like VirSorter2 and DeepVirFinder, registering an MCC of 0.85. Compact yet powerful, the ProkBERT models are efficient, generalizable, and swift. They cater to both supervised and unsupervised tasks, providing an accessible tool for the community. The models are available on GitHub and HuggingFace.

bioinformatics↗