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Rabsch, D.

Publications and source records attributed to Rabsch, D..

2 recordsLinked to original sources

CRISCross: Integration of Epigenetic Information for Deep-Learning-Based Prediction of CRISPR-Cas9 Off-Targets Across Cell Types

CRISPR-Cas9 enables precise genome editing but remains limited by off-target effects, raising safety concerns and necessitating accurate prediction. Although epigenetic features influence Cas9 binding and cleavage, their predictive signals are often weak, highlyvariable, and context-dependent, limiting the effectiveness of existing machine learning approaches. Cross-cell-type settings are especially challenging: epigenetic landscapes differ substantially, and models trained on one cell type frequently fail to generalize. Here, we systematically investigate the role of epigenetic context in off-target prediction and demonstrate that its utility depends on modeling interactions with sequence features rather than treating it as an independent signal. Tabular and deep learning experiments demonstrate that epigenetic features provide a consistent but modestly complementary signal, and that late-stage fusion strategies are insufficient to effectively exploit this information. To address this, we introduce CRISCross, a cross-attention-based architecture that captures sequence-epigenetic interactions at the nucleotide level, alongside CRISPRAT, a synthetic pretraining strategy that learns transferable representations from genome-derived sgRNA-off-target pairs without relying on dataset-specific pretraining. CRISCross, incorporating AlphaGenome-derived chromatin accessibility signals, shows better predictive performance than sequence-only baselines across three independent test datasets spanning two cell types, demonstrating improved generalization across guide RNAs, datasets, and cellular contexts. This is particularly relevant for therapeutic applications involving cell types or patient-derived contexts that lack dedicated experimental datasets. In such settings, predicted chromatin accessibility may provide scalable contextual information when direct epigenomic profiling is unavailable or impractical. Together, these results show that accurate CRISPR off-target prediction benefits from interaction-aware integration of epigenetic context alongside generalizable pretraining strategies.

bioinformatics↗

RAPDOR: Using Jensen-Shannon Distance for the computational analysis of complex proteomics datasets

The computational analysis of large proteomics datasets, such as those from gradient profiling or spatially resolved proteomics, is often as crucial as the experimental design. We present RAPDOR, a tool for intuitive analyzing and visualizing such datasets, based on the Jensen-Shannon distance and subsequent analysis of similarities between replicates, applied to three datasets. First, we examined the in-gradient distribution profiles of protein complexes with or without RNase treatment (GradR) to identify the set of RNA-binding proteins (RBPs) in the cyanobacterium Synechocystis sp. PCC 6803. RBPs play pivotal regulatory and structural roles; although numerous RBPs have been identified, the complete set is unknown for any species. RAPDOR identified 80 potential RBPs, including ribosomal proteins, likely RNA-modifying enzymes, and several proteins not previously associated with RNA binding. High-ranking putative RBPs, such as the universal stress protein Sll1388, or the translation inhibitor LrtA/RaiA, were predicted by RAPDOR but not the TriPepSVM algorithm, indicating uncharacterized RBP domains. These data are available online at https://synecho-rapdor.biologie.uni-freiburg.de, providing a comprehensive resource for RNase-sensitive protein complexes in cyanobacteria. We then show by reanalyzing existing datasets, that RAPDOR is effective in examining the intracellular redistribution of proteins under stress conditions. RAPDOR is a generic, non-parametric tool for the intuitive and versatile analysis of highly complex data sets such as the study of protein distributions using fractionation protocols.

bioinformatics↗