bioRxivBioinformaticsPreprint
Direct CCUT: A Versatile and Standardized Framework to Train 3C Deep Restoration Models
Stanislav SysiD, Alejandro Ceron‐NoriegaiD, Anne Kerber, Stephan WeißbachiD, Susann SchweigeriD, Michael WandiD, Karin Everschor‐SitteiD, Susanne GerberiD
Abstract
Chromatin Capture Experiments such as Hi-C and Micro-C have become popular methods for genome architecture exploration. Recently, also a protocol for long read sequencing, Pore-C, was introduced, allowing the characterization of three-dimensional chromatin structures using Oxford Nanopore Sequencing Technology. Here, we present a framework that focuses on the efficient reconstruction of low-resolution Pore-C data but can also process all other 3C data, such as Hi-C and Micro-C matrices, using models that can be trained on a consumer GPU. Furthermore, we integrate building blocks of popular super-resolution methods such as SWIN-Transformer or residual-in-residual-blocks to modify or build customized networks on the fly. Pre-built models were trained and evaluated on multiple publicly available gold-standard Micro-C and Pore-C datasets, allowing for fine-scale structure prediction. Our work aims to overcome the drawback of high sequencing costs to construct high resolution contact matrices, as well as the problem of mapping low-coverage libraries to high-resolution structures in the genome. Although there have been major breakthroughs regarding NGS-based methods for the reconstruction of high-resolution chromatin interaction matrices from low-resolution data, for data obtained by long-read sequencing, there is currently no solution to reconstruct missing and sparse information and to improve the quality. AvailabilityThe tool is available at (https://github.com/stasys-hub/CCUT)
- assay: Hi-C
- assay: long-read sequencing
- assay: spatial transcriptomics
- research focus: dimensionality reduction
- approach: deep learning
- Citations
- 0
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