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01.
bioRxiv (Bioinfo) 2026-06-11

DLDN-Bench: A Benchmark Framework for Deep Learning de Novo Peptide Sequencing in Proteomics

De novo peptide sequencing is an essential approach for analyzing mass spectrometry data because it enables the identification of novel peptides without relying on protein sequence databases. Recent advances in deep learning have substantially improved the performance of de novo sequencing methods, but the rapid emergence of new models has led to heterogeneous evaluation practices and limited comparability. To address this, we introduce DLDN-Bench, a benchmark framework including a set of benchmark datasets derived from human muscle biopsy mass spectrometry data retrieved from PRIDE and annotated through consensus across multiple widely used database search engines. Using these datasets, we systematically benchmark recent deep learning-based de novo sequencing tools alongside traditional approaches. Performance is assessed using established metrics, including precision and coverage relative to a pseudo-ground truth defined by cross-engine agreement. To demonstrate the utility of DLDN-Bench, we benchmark four recent deep learning models and make all results publicly available. This benchmark framework provides a standardized basis for comparing state-of-the-art methods and offers an extensible resource for evaluating future tools in de novo peptide sequencing.

02.
medRxiv (Medicine) 2026-06-25

Longitudinal Bundibugyo Virus Glycoprotein Seroreactivity Following rVSVΔG-ZEBOV-GP Vaccination in Outbreak-Affected Populations of the Democratic Republic of the Congo

Background: There are currently no vaccines approved for the prevention or treatment of Orthoebolavirus bundibugyoense (Bundibugyo virus; BDBV). The recombinant vesicular stomatitis virus- Zaire ebolavirus glycoprotein vaccine (rVSV-ZEBOV-GP; ERVEBO) has been widely deployed during Ebola virus disease (EVD) outbreaks caused by Orthoebolavirus zairense (Ebola virus; EBOV). Given the lack of vaccines and medical countermeasures we evaluated development of antibodies to Bundibugyo glycoprotein (GP) following rVSV-ZEBOV-GP vaccination in two EVD outbreak-affected populations in the Democratic Republic of the Congo (DRC). Methods: Between 2018 and 2023, serum samples were collected from vaccine recipients in Mbandaka, Equateur Province (n=482 at baseline), and Beni, North Kivu Province (n=599 at baseline). Antibody reactivity was assessed using a multiplex pan-filovirus immunoassay. We evaluated longitudinal trends in BDBV GP seroreactivity across follow-up visits extending to approximately five years after vaccination. Findings: We collected 2552 samples from 482 participants in Mbandaka and 3297 samples from 599 participants in Beni. BDBV GP responses diverged by location. Baseline BDBV GP seroreactivity differed between sites, with 3.3% of participants reactive in Mbandaka and 10.4% in Beni. In Mbandaka, BDBV GP titers remained unchanged through 6 months post-vaccination but increased markedly between 2.5 and 3.5 years (mean MFI 1,238 to 4,845; p

03.
arXiv (CS.LG) 2026-06-19

Mask-Morph Graph U-Net: A Generalisable Mesh-Based Surrogate for Crashworthiness Field Prediction under Large Geometric Variation

arXiv:2605.15231v2 Announce Type: replace Abstract: Nonlinear finite element crash simulations are accurate but computationally expensive, limiting their use in iterative design optimisation. Machine-learning surrogate models based on graph neural networks (GNNs) offer a faster alternative. Message-passing GNNs are widely used for mesh simulation, and their shared node and edge update functions are relatively generalisable across varying graph structures. By contrast, non-shareable edge-specific aggregation layers can capture nonlinear relationships more accurately but usually require fixed graph connectivity, which limits generalisability. This paper presents Mask-Morph Graph U-Net (MMGUNet), a practical approach to addressing the limitation of hierarchical Graph U-Net architectures that use edge-specific downsampling and upsampling layers. Fixed coarse graph connectivity is required for edge-specific layers. To retain this while improving spatial correspondence, the proposed method morphs the coarsened graph hierarchy to each input mesh using feature-aligned barycentric parameterisation before constructing cross-graph edges. It further applies node masking during supervised pretraining, followed by parameter-efficient fine-tuning in which high-parameter edge-specific layers are frozen. The proposed approach is evaluated in in-distribution, out-of-distribution, and cross-component transfer settings using mean Euclidean distance and maximum intrusion percentage error. Results show that coarse-graph morphing improves test accuracy relative to a fixed-coarse-graph baseline, while masked supervised pretraining reduces the train-test discrepancy and improves data efficiency during transfer. The proposed model also achieves lower prediction error compared with external baselines. These results demonstrate a practical route toward reusable, data-efficient mesh-based surrogate modelling for crashworthiness design exploration.