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Burtsev, M.

Publications and source records attributed to Burtsev, M..

5 recordsLinked to original sources

GENATATORs: ab initio Gene Annotation With DNA Language Models

Inference of gene structure and location from genome sequences - known as de novo gene annotation - is a fundamental task in biological research. However, sequence grammar encoding gene structure is complex and poorly understood, often requiring costly transcriptomic data for accurate gene annotation. In this work, we benchmark current solutions and develop new methods of gene annotation. We show that pre-trained DNA language model (DNA LM) embeddings do not capture the features necessary for precise gene segmentation, and that task-specific fine-tuning remains essential. We comprehensively evaluate the impact of model architecture, training strategy, receptive field size, dataset composition, and data augmentations on gene segmentation performance. We revisit standard evaluation protocols, showing that commonly used per-token and per-sequence metrics fail to capture the challenges of real-world gene annotation. We introduce and theoretically justify new biologically grounded metrics, along with benchmarking datasets that better capture annotation quality. We show that fine-tuned DNA LMs outperform existing annotation tools, generalizing across species separated by hundreds of millions of years from those seen during training, and providing segmentation of previously intractable non-coding transcripts and untranslated regions of protein-coding genes. Our results thus provide a foundation for new biological applications centered on accurate gene annotation.

bioinformatics↗

Back to BERT in 2026: ModernGENA as a Strong, Efficient Baseline for DNA Foundation Models

AO_SCPLOWBSTRACTC_SCPLOWRecent advances in DNA language models have mainly come from building larger and more complex architectures, making it harder to understand the effect of changes to standard components such as the transformer layers widely used in NLP. In this work, we study whether and how a modernized BERT-style back-bone (ModernBERT) can be adapted to genomic sequence modeling to improve computational efficiency, training stability, and downstream performance. Under controlled experimental settings, we benchmark efficiency across a range of sequence lengths and evaluate downstream performance on the Nucleotide Transformer benchmark. The resulting model, ModernGENA, achieves a strong efficiency-quality trade-off and ranks among the top-performing models in our evaluation suite. To support reproducibility and provide a solid default reference point for future architectural work in genomics, we release the full implementation and configuration of ModernGENA as an open, reusable baseline, and make ModernGENA base and ModernGENA large publicly available through the DNA language models collection on Hugging Face.

bioinformatics↗

GENA-Web - GENomic Annotations Web Inference using DNA language models

The advent of advanced sequencing technologies has significantly reduced the cost and increased the feasibility of assembling high-quality genomes. Yet, the annotation of genomic elements remains a complex challenge. Even for species with comprehensively annotated reference genomes, the functional assessment of individual genetic variants is not straightforward. In response to these challenges, recent breakthroughs in machine learning have led to the development of DNA language models. These transformer-based architectures are designed to tackle a wide array of genomic tasks with enhanced efficiency and accuracy. In this context, we introduce GENA-Web, a web-based platform that consolidates a suite of genome annotation tools powered by DNA language models. The version of GENA-Web presented here encompasses a diverse set of models trained on human data, including the prediction of promoter activity, annotation of splice sites, determination of various chromatin features, and a model for scoring of enhancer activity in Drosophila. GENA-Web is accessible online at https://dnalm.airi.net/

bioinformatics↗

GENA-LM: A Family of Open-Source Foundational Models for Long DNA Sequences

Recent advancements in genomics, propelled by artificial intelligence, have unlocked unprecedented capabilities in interpreting genomic sequences, mitigating the need for exhaustive experimental analysis of complex, intertwined molecular processes inherent in DNA function. A significant challenge, however, resides in accurately decoding genomic sequences, which inherently involves comprehending rich contextual information dispersed across thousands of nucleotides. To address this need, we introduce GENA-LM, a suite of transformer-based foundational DNA language models capable of handling input lengths up to 36,000 base pairs. Notably, integrating the newly-developed Recurrent Memory mechanism allows these models to process even larger DNA segments. We provide pre-trained versions of GENA-LM, including multispecies and taxon-specific models, demonstrating their capability for fine-tuning and addressing a spectrum of complex biological tasks with modest computational demands. While language models have already achieved significant breakthroughs in protein biology, GENA-LM showcases a similarly promising potential for reshaping the landscape of genomics and multi-omics data analysis. All models are publicly available on GitHub https://github.com/AIRI-Institute/GENA_LM and HuggingFace https://huggingface.co/AIRI-Institute. In addition, we provide a web-service https://dnalm.airi.net/ allowing user-friendly DNA annotation with GENA-LM models.

bioinformatics↗

Plasticity facilitates rapid evolution

Developmental plasticity enables organisms to cope with new environmental challenges. If deploying such plasticity is costly in terms of time or energy, the same adaptive behavior could subsequently evolve through piecemeal genomic reorganisation that replaces the requirement to acquire that adaptation by individual plasticity. Here we report a new dimension to the way in which plasticity can drive evolutionary change leading to ever greater complexity in biological organization. Our model deploys the concept of partially overlapping functional systems. We found that plasticity accelerated dramatically the evolutionary accumulation of adaptive systems in model organisms with relatively low rates of mutation. The effect of plasticity on the evolutionary growth of complexity was even greater when the number of elements needed to construct a functional system was increased. These results suggest that as the difficulty of challenges from the environment become greater, so plasticity exerts an ever more powerful role in meeting those challenges and in opening up new avenues for the subsequent evolution of complex adaptations.

animal behavior and cognition↗