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This paper presents BlockFormer, a transformer-based model designed to solve the inverse problem of inferring genomic features from Hi-C contact maps. By leveraging shared structural patterns and synthetic data generation, it effectively handles variability in chromosome sizes across species for tasks like centromere localization. The work demonstrates how advanced machine learning architectures can be adapted to complex biological inverse problems without relying on traditional physics-based simulations.
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$\textit{BlockFormer}$: Transformer-based inference from genomic contact maps

arXiv2 min read

arXiv:2605.21617v3 Announce Type: replace Abstract: Locating genomic features from genomic contact maps, such as centromere identification from genome-wide chromosome conformation capture techniques, notably Hi-C, can be formulated as an inverse problem: infer one parameter per entity given a map summarizing pairwise interactions through blocks of variable numbers and sizes. In this work, we introduce a data-driven approach that leverages shared structure between these contact maps, such as global alignment between localized patterns, while handling the variability in number and size of chromosomes arising in real-world data. Our approach relies on a transformer architecture capable of handling such variability and a custom simulator to generate abundant, yet computationally cheap synthetic data for training. Applied to the problem of centromere localization, the method recovers genomic positions at or below the map resolution across species with various genome sizes using a coarse-to-fine refinement step when chromosome sizes fall outside the training range. We concentrate our evaluation on Hi-C data, where the block structure is well characterized and ground truth is available.

Abstract:Locating genomic features from genomic contact maps, such as centromere identification from genome-wide chromosome conformation capture techniques, notably Hi-C, can be formulated as an inverse problem: infer one parameter per entity given a map summarizing pairwise interactions through blocks of variable numbers and sizes. In this work, we introduce a data-driven approach that leverages shared structure between these contact maps, such as global alignment between localized patterns, while handling the variability in number and size of chromosomes arising in real-world data. Our approach relies on a transformer architecture capable of handling such variability and a custom simulator to generate abundant, yet computationally cheap synthetic data for training. Applied to the problem of centromere localization, the method recovers genomic positions at or below the map resolution across species with various genome sizes using a coarse-to-fine refinement step when chromosome sizes fall outside the training range. We concentrate our evaluation on Hi-C data, where the block structure is well characterized and ground truth is available.

Machine Learning (cs.LG); Quantitative Methods (q-bio.QM)

arXiv:2605.21617 [cs.LG]

(or arXiv:2605.21617v3 [cs.LG] for this version)

https://doi.org/10.48550/arXiv.2605.21617 Focus to learn more arXiv-issued DOI via DataCite

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Full text under the publisher's open licence · 258 words

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