Biology subjects

Bian, B.

Publications and source records attributed to Bian, B..

7 recordsLinked to original sources

bioRxiv2026

TRACE: a framework for traceable biomedical resource construction demonstrated through single-cell glaucoma data

The growing availability of public omics datasets presents opportunities for biomedical research, yet constructing research question-driven resources from distributed studies remains challenging due to heterogeneous data, incomplete metadata and limited documentation of curation decisions. Here, we present TRACE (Traceable Resource Assembly and Curation Ecosystem), a general framework that links systematic knowledge discovery, data curation and resource delivery while preserving provenance throughout resource construction. We demonstrate TRACE through TRACE-scGlaucoma, a curated single-cell transcriptomics resource for glaucoma and optic nerve biology. Systematic screening identified 57 eligible studies, of which 42 provided accessible datasets comprising approximately 3.3 million cells. The resource provides harmonised metadata, standardised cell-type annotations and reusable expression objects while retaining original study information and curation provenance. We demonstrate its analytical utility through cellular enrichment of glaucoma GWAS-associated genes, comparing candidate drug-repurposing signals across distinct biological contexts and assessment of cell-type annotation reliability. TRACE provides a systematic and traceable approach to transforming fragmented public datasets into reusable biomedical resources, supporting reproducible analyses and future extensions across disease areas and data modalities.

bioinformatics↗

bioRxiv2026

Generalisable tissue-wide molecular reconstruction from histology

Spatial transcriptomics technologies measure gene expression within intact tissues but remain difficult to scale across large tissue sections and patient cohorts. Consequently, many studies rely on tissue microarrays (TMAs) or sparse spatial profiling designs, where molecular measurements are available for only limited tissue regions and are often generated using heterogeneous gene panels. Existing H&E to spatial gene expression prediction methods remain challenged by sparse molecular measurements, partially overlapping gene panels and tissue-wide reconstruction across heterogeneous spatial datasets. Here, we present GHIST+, a framework for tissue-wide reconstruction of single-cell molecular states from H&E histology. GHIST+ integrates cellular morphology, local tissue context and shared tissue representations to extend sparse molecular measurements into tissue-wide molecular maps across heterogeneous spatial datasets. Across multiple cancer types and GTEx breast tissues, GHIST+ reconstructs biologically meaningful tissue-wide molecular organisation from sparse TMA-derived measurements while preserving spatial tissue structure, cell-type organisation and age-associated tissue states across cancer and non-cancer settings. GHIST+ establishes a scalable framework for transforming sparse spatial profiling experiments into tissue-wide molecular maps, enabling cohort-scale molecular reconstruction from routine histology under heterogeneous spatial transcriptomic settings.

bioinformatics↗

bioRxiv2026

Designing mRNA coding sequence via multimodal reverse translation language modeling with Pro2RNA

mRNA coding sequence design is a critical component in the development of mRNA vaccines, nucleic acid therapeutics, and heterologous gene expression systems. While large language models have recently been successfully applied to protein design and RNA modeling, designing optimal mRNA coding sequences for a given protein, particularly in a species-specific manner, remains a major challenge. Here, we present Pro2RNA, a multimodal reverse-translation language model that generates mRNA coding sequences from their corresponding protein sequences while explicitly conditioning on host organism taxonomy information. Pro2RNA integrates multiple pretrained language models across different modalities, including ESM2 for protein representation, SciBERT for taxonomy understanding, and a generative RNA language model for mRNA codon-level sequence generation. By training on mRNA-protein pairs from eukaryote and bacteria datasets respectively, Pro2RNA learns species-dependent genetic codes and codon usage patterns, enabling the generation of host-adapted and natural-like mRNA coding sequences. Across multiple benchmark evaluations, Pro2RNA matches or surpasses existing optimization methods, demonstrating its potential as a powerful and flexible framework for species-aware mRNA coding sequence design.

bioinformatics↗

bioRxiv2025

Large generative mRNA language foundation model for efficient coding sequence generation and design with mRNA-GPT

mRNA design plays a central role in synthetic biology, nucleic acid therapeutics, and vaccine development. Although large language models are applied in many biological fields, generative language models for de novo mRNA design remains largely unexplored. Here, we introduce mRNA-GPT, a series of generative mRNA language models which for the first time covers the three domains of life as pretraining datasets. Based on a GPT-2 transformer architecture with 302 million parameters, we pre-trained three separate models on 19,676 bacterial, 4,688 eukaryotic, and 702 archaeal species, leveraging 80 million, 83 million, and 2 million mRNA coding sequences, respectively. Distinct clustering of mRNA coding sequence embeddings from animals, plants, and fungi in the pretrained mRNA-GPT-eukaryote indicates that the model captures organism-specific sequence features. Following unsupervised pre-training, we fine-tuned mRNA-GPT on a translation-efficiency dataset to generate high-performance mRNA sequence. Compared to the pretrained model, the fine-tuned mRNA-GPT produced mRNA sequences with significantly higher translation efficiency scores, demonstrating the ability of mRNA-GPT to capture sequence features underlying high translation efficiency. We further fine-tuned mRNA-GPT on datasets for mRNA stability and mRNA expression, where it likewise produced high-performance mRNA sequences. Our pretrained models are publicly available, enabling other researchers to adapt mRNA-GPT to specialized tasks such as tissue-specific mRNA expression or stability by fine-tuning on their own data. Together, our study demonstrates that generative mRNA language modeling as a promising approach for accelerating mRNA design across diverse biological fields.

bioinformatics↗

bioRxiv2025

Large mRNA language foundation modeling with NUWA for unified sequence perception and generation

The mRNA serves as a crucial bridge between DNA and proteins. Compared to DNA, mRNA sequences are much more concise and information-dense, which makes mRNA an ideal language through which to explore various biological principles. In this study, we present NUWA, a large mRNA language foundation model leveraging a BERT-like architecture, trained with curriculum masked language modeling and supervised contrastive loss for unified mRNA sequence perception and generation. For pretraining, we utilized large-scale mRNA coding sequences comprising approximately 80 million sequences from 19,676 bacterial species, 33 million from 4,688 eukaryotic species, and 2.1 million from 702 archaeal species, and pre-trained three domain-specific models respectively. This enables NUWA to learn coding sequence patterns across the entire tree of life. The fine-tuned NUWA demonstrates strong performance across a variety of downstream tasks, excelling not only in RNA-related perception tasks but also exhibiting robust capability in cross-modal protein-related tasks. On the generation front, NUWA pioneers an entropy-guided strategy that enables BERT-like models in generating mRNA sequences, producing natural-like sequences that accurately recapitulate species-specific codon usage patterns. Moreover, NUWA can be effectively fine-tuned on small, task-specific datasets to generate functional mRNAs with desired properties, including sequences that do not exist in nature, and to design coding sequences for diverse proteins in biomanufacturing, vaccine development, and therapeutic applications. To our knowledge, NUWA represents the first mRNA language model for unified sequence perception and generation, providing a versatile and programmable platform for mRNA design.

bioinformatics↗

bioRxiv2024

Spatial gene expression at single-cell resolution from histology using deep learning with GHIST

The increased use of spatially resolved transcriptomics provides new biological insights into disease mechanisms. However, the high cost and complexity of these methods are barriers to broad clinical adoption. Consequently, methods have been created to predict spot-based gene expression from routinely-collected histology images. Recent benchmarking showed that current methodologies have limited accuracy and spatial resolution, constraining translational capacity. Here, we introduce GHIST, a deep learning-based framework that predicts spatial gene expression at single-cell resolution by leveraging subcellular spatial transcriptomics and synergistic relationships between multiple layers of biological information. We validated GHIST using public datasets and The Cancer Genome Atlas data, demonstrating its flexibility across different spatial resolutions and superior performance. Our results underscore the utility of in silico generation of single-cell spatial gene expression measurements and the capacity to enrich existing datasets with a spatially resolved omics modality, paving the way for scalable multi-omics analysis and new biomarker discoveries.

bioinformatics↗

bioRxiv2019

Graph Embedding Method Based Genetical Trajectory Reveals Migration History Among East Asians

An important issue in human population genetics is the ancestry. By extracting the ancestral information retained in the single nucleotide polymorphism (SNP) of genomic DNA, the history of migration and reproduction of the population can be reconstructed. Since the SNP data of population are multidimensional, their dimensionality reduction can demonstrate their potential internal connections. In this study, the graph and structure learning based Graph Embedding method commonly used in single cell mRNA sequencing was applied to human population genetics research to decrease the data dimension. As a result, the human population trajectory of East Asia based on 1000 Genomes Project was reconstructed to discover the inseparable relationship between the Chinese population and other East Asian populations. These results are visualized from various ancestry calculators such as E11 and K12B. Finally, the unique SNPs along the psudotime of trajectory were found by differential analysis. Bioprocess enrichment analysis was also used to reveal that the genes of these SNPs may be related to neurological diseases. These results will lay the data foundation for precision medicine.

genetics↗