REMAG: recovery of eukaryotic genomes from metagenomic data using non-contrastive self-supervised learning

Metagenome-assembled genomes (MAGs) are central to exploring microbial communities. Yet, despite the relevance of protists and fungi to diverse ecosystems, eukaryotic MAG recovery lags behind that of prokaryotes. A major bottleneck is that most state-of-the-art binning pipelines exclusively rely on prokaryotic single-copy core gene reference databases and are optimized for smaller genomes. To address this gap, we present REMAG (Recovery of Eukaryotic MAGs), a tool designed to recover high-quality eukaryotic genomes suited for long-read metagenomic data. REMAG uses a fine-tuned HyenaDNA genomic foundation model to efficiently filter eukaryotic contigs. It then employs a dual-encoder Siamese network trained with the non-contrastive Barlow Twins loss to learn a shared embedding space by integrating contig composition and differential coverage. Finally, high-quality bins are extracted using greedy iterative Leiden clustering optimized with eukaryotic single-copy core gene constraints. In benchmarks based on simulated mixed prokaryotic/eukaryotic communities and real datasets of varying sizes and origin, we demonstrate REMAG's ability to recover more near-complete eukaryotic genomes than existing state-of-the-art tools, which often produce highly fragmented eukaryotic bins. REMAG provides an automated eukaryotic binning method that scales effectively with the increasing size and sequencing depth of metagenomic datasets.