Search bioRxiv⌕ Search

bioRxiv · 10.64898/2026.10.01.752299

RiboWin: A computational framework to identify non-canonical open reading frames

Abstract

Abstract Ribosome profiling is widely used to map translation across the genome, yet current sORF discovery pipelines are constrained by their reliance on annotated protein coding regions and by treating biological replicates primarily as tools for quantification rather than as strict filters for reproducibility. This results in two major issues, the systematic exclusion of pseudogene derived loci from analysis and the generation of extremely large candidate sets in which true translation events are difficult to distinguish from noise. To overcome these limitations, a five-stage framework was developed that expands the search space to include pseudogene loci while enforcing dual biological replicate concordance as a hard binary filter. When applied to four human cell lines with matched replicates and benchmarked against existing tools, the framework produces dramatically smaller and more reliable candidate sets, reducing thousands to millions of predicted sORFs down to a small number of high confidence concordant loci. Across HeLa cell cycle conditions, a limited set of unique concordant sORFs was identified spanning multiple transcript classes including upstream ORFs, retained introns, and nonsense mediated decay transcripts, along with a pseudogene derived candidate. Notably, the pseudogene encoded sORF RPL26P19 was detected consistently in HeLa cells but missed or inconsistently identified by existing tools, while a separate pseudogene sORF from UBE3AP2 was observed specifically in normal primary cell types and absent in HeLa. Both candidates were later found to be supported by entries in OpenProt, even though this was not known during the analysis, which gives added confidence that the results are genuine and not biased by prior expectations. Overall, these findings suggest that pseudogenes are not just inactive remnants in the genome but can act as real, functional sources of translated sORFs in a cell type specific manner. At the same time, it becomes clear that most current tools are not designed to detect these signals effectively. This highlights the need for approaches that both broaden the regions being searched and apply stricter reproducibility checks, so that truly meaningful translation events can be identified more reliably.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

D, V., N, A., Yadav, B. K., Phadnis, S., Verma, B., YS, R.. 2026-10-08. RiboWin: A computational framework to identify non-canonical open reading frames. https://doi.org/10.64898/2026.10.01.752299

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

StableProt: Structure-Aware Deep Learning for Protein Thermostability (Tm) and Environmental Adaptation (OGT) Prediction

Predicting protein melting temperature (Tm) and organismal optimal growth temperature (OGT) is essential for enzyme engineering, biocatalyst design, and metagenomic bioprospecting, yet computational prediction faces several fundamental bottlenecks: sequence-only representations miss tertiary packing; dual-task coupling induces destructive gradient conflict; natural database skew (>87% mesophiles) drives mesophilic collapse; and existing tools produce uncalibrated point predictions. To address these challenges, we present StableProt, a structure-aware framework that couples amino acid sequences with Foldseek 3Di structural tokens via a frozen SaProt backbone to capture 3D contacts. Disjoint heads condition thermodynamic stability on ecological context without gradient conflict, while targeted 14% mesophilic subsampling expands thermophile representation to eliminate mesophilic collapse. Calibrated ensemble modeling reduces calibration error to 1.92%, providing dependable 95% confidence intervals. Evaluating models across 10{degrees}C temperature intervals reveals severe baseline collapse at thermal extremes, whereas StableProt maintains robust accuracy across regimes. On ProThermDB and zero-shot FireProtDB, StableProt achieves state-of-the-art probabilistic accuracy (CRPS = 4.52{degrees}C and 8.71{degrees}C) while recovering 92.0% of hyperthermophiles ([≥]80{degrees}C), and in prospective validation, its calibrated intervals capture both enzyme stability (75.3% coverage) and host environmental growth temperatures (78.1% coverage). StableProt is freely accessible as an interactive web server at https://stableprot.dixitlab.org/.

bioinformatics↗

RoDPAA: A Robust Dissimilarity-Based Principal Angle Analysis Framework for Multi-View Microbiome Data Integration

Multiview microbiome studies profile the same participants across body sites or molecular layers, but integration is hampered by sparse, compositional data, modest sample sizes and methods that recognize only exact sharing. We present RoDPAA (Robust Dissimilarity-based Principal Angle Analysis), a framework that represents each view through any data-appropriate dissimilarity, such as Bray--Curtis, without log-ratio transformation or likelihood assumptions. RoDPAA aligns view-specific signal subspaces through principal angles, captures complete and partial sharing, and tests by permutation how many components are shared, using only eigendecomposition and little tuning. In Gaussian simulations, RoDPAA matched JIVE and MOFA given true ranks, ran faster and alone recovered the shared dimension in every replicate. In two inflammatory bowel disease (IBD) cohorts with sparse, zero-inflated data, Bray--Curtis-based RoDPAA recovered shared structure that was stable to prevalence filtering, whereas log-ratio-based alternatives were not. Its leading microbiome--metabolome factors, learned without disease labels, were the only ones associated with IBD.

bioinformatics↗

Deducing splicing events from transcript sets with splicelogic

Long-read RNA sequencing captures a greater proportion of full-length transcripts, enabling more accurate isoform identification, discovery of novel isoforms, and more precise differential transcript usage analysis. However, comparing transcripts, whether between conditions or between sets such as novel and annotated isoforms, yields complex isoform changes that are hard to manipulate, summarize, and visualize. This is compounded by vertical integration of some tools, where downstream analysis depends on the specific output of a particular upstream tool. To address this gap, we have developed splicelogic, an R/Bioconductor package that makes transcript-set comparisons biologically interpretable by turning them into discrete splicing events, such as exon skipping, alternative splice sites, intron retention, and alternative transcription start and end sites. We designed splicelogic to integrate easily with existing RNA-seq workflows and tools. The splicelogic functions are modular, readable, and extensible, making it easy for users to adapt core logic to their own custom scientific questions or novel splicing definitions. By obtaining interpretable splicing events from transcript changes, splicelogic enables downstream analyses, including annotation of RNA-binding protein recognition sites, alongside summary statistics and visualization. The splicelogic package is publicly available and distributed through Bioconductor.

bioinformatics↗