Bioinformatics sits at the exciting intersection where biology meets data science, using powerful computer tools to decode the vast complexity of living systems. From mapping the human genome to tracking how viruses evolve, this field transforms raw biological information into actionable insights that drive modern medicine and research forward without requiring a supercomputer to understand the basics.

On Gist.Science, we ensure you never miss a breakthrough by processing every new preprint in this category directly from bioRxiv. Our team provides both plain-language explanations and detailed technical summaries for each paper, making cutting-edge discoveries accessible to everyone regardless of their background.

Below are the latest bioinformatics papers added from bioRxiv, ready for you to explore with clarity and depth.

💻 bioinformatics

Coding agents author interpretable single-cell embedding models from the literature

This paper demonstrates that coding agents can automatically generate interpretable, zero-shot single-cell embedding models by extracting and composing literature-cited gene programs into named axes, achieving biological quality comparable to data-driven methods while ensuring inherent batch robustness and interpretability without requiring training or prior gene-set databases.

Brunn, N., Krissmer, S. M., Frosch, M., Frick, M., Prinz, M., Binder, H.2026-07-09
💻 bioinformatics

Characterizing dynamic tissue architectures by identifying cell-type-specific spatiotemporal gene programs with stGP

The paper introduces stGP, a statistical framework that decomposes spatiotemporal transcriptomic data into temporal and spatial components to identify interpretable, cell-type-specific gene programs, thereby revealing how dynamic tissue architectures and localized cellular responses evolve across time and anatomical niches.

Yu, B., Tan, Z., Wan, X., Wang, H., Yang, C.2026-07-08
💻 bioinformatics

Residual Multi-Modal Learning for Pan-Breast-Cancer Drug Response Prediction

The paper introduces DL4DR, a two-tower residual late-fusion deep learning model that predicts pan-breast-cancer drug responses by encoding cell lines as genomic images and combining molecular representations, thereby achieving superior generalization to unseen cell lines and cancer types while identifying novel genomic drivers without relying on cell line identities.

Huang, B., Tasaka, L., Li, J., Islam, T., Zhang, S.2026-07-08
💻 bioinformatics

Scanning transcriptomes for nonlinear, domain-level similarities using hmSEEKR

The paper introduces hmSEEKR, a k-mer-based hidden Markov model that scans transcriptomes to identify non-linear, domain-level sequence similarities in long noncoding RNAs, thereby enabling the discovery of functionally related RNA domains and their associated protein interaction networks without requiring prior knowledge of sequence alignment.

Li, S., Sprague, D. A., Eberhard, Q. E., Boyson, S. P., Laederach, A., Calabrese, J. M.2026-07-08
💻 bioinformatics

AllTheBacteria: a community resource empowers biology and discovers novel peptide antibiotics

The paper introduces AllTheBacteria, a comprehensive community resource that uniformly processes nearly 2.5 million public bacterial genomes to enable large-scale biological research and successfully demonstrates its utility by discovering and validating novel peptide antibiotics through AI-driven mining.

Hunt, M., Torres, M. D. T., Alikhan, N.-F., Anderson, D., Andreani, M. L., Blom, J., Bouras, G., Brinkman, F., Carroll (…)2026-07-07
💻 bioinformatics

PHI: A Galaxy-based workflow for reproducible prophage-host interaction analysis and standardized viral-genomics reporting

The paper introduces PHI, a user-friendly and automated Galaxy-based workflow that streamlines reproducible prophage identification, host interaction prediction, and functional characterization while generating standardized reports to lower barriers for both experts and non-experts in viral genomics research.

Saraiva, J. P., Borim Correa, F., Bernt, M., Ghanem, N., Nieto, E., Brizola Toscan, R., Y. Wick, L., Chatzinotas, A.2026-07-07
💻 bioinformatics

Scop3P in 2026: an expanded proteomics-informed resource contextualizing phosphorylation sites through sequence, structure, mutation, and experimental provenance

The 2026 update to Scop3P presents a major expansion of this proteomics-informed knowledgebase by integrating 152,350 uniformly reprocessed human phosphorylation sites with comprehensive structural, biophysical, evolutionary, and mutational annotations to provide a scalable, provenance-aware resource for interpreting phosphorylation in functional and disease contexts.

Ramasamy, P., Tichshenko, N., Diaz, A., Velghe, K., Massignani, E., Vranken, W. F., Martens, L.2026-07-06