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Zhang, S.

Publications and source records attributed to Zhang, S..

At least 145 records · Page 8Linked to original sources

Interpretable Biological Sequence Clustering with iClust

Biological sequence clustering is a fundamental problem in bioinformatics, yet most existing methods mainly optimize clustering quality or efficiency while offering limited insight into why sequences are grouped together. This restricts their usefulness in downstream analysis, where representative sequences and clear cluster boundaries are often needed. To address this issue, we propose iClust, an interpretable clustering method that characterizes each cluster by a representative prototype and an adaptive radius. By adapting to local sequence structure rather than relying on a single global threshold, iClust produces clusters that are both meaningful and explainable. A final consolidation step further reduces tiny fragments and improves structural stability. Experiments on simulated and real biological sequence datasets show that iClust achieves competitive clustering performance while providing clearer cluster-level explanations than conventional threshold-based methods. In addition to its empirical impact as a practical clustering method for biological sequences, this article opens up new avenues for developing biological sequence clustering approaches from the viewpoint of interpretable machine learning.

bioinformatics↗

Three-dimensional Virtual Adult Cardiomyocyte Transcriptomics

Obtaining transcriptomes of adult cardiomyocytes at single-cell resolution remains challenging due to their large size, elongated morphology, and frequent multinucleation. Although spatial transcriptomics preserves tissue architecture and captures gene expression in situ, current analytical frameworks largely rely on nuclear-based segmentation and are therefore poorly suited to adult cardiomyocytes. Furthermore, individual tissue sections capture only a fraction of a cardiomyocyte, preventing reconstruction of complete cell-level transcriptomes. Here we present three-dimensional virtual cardiomyocyte (3D-VirtualCM), a membrane-guided framework that integrates cell-contour similarity and optimal transport to reconstruct volumetric cardiomyocyte transcriptomes from consecutive spatial transcriptomic sections. Applying 3D-VirtualCM to infarcted adult mouse hearts, we generated a panoramic transcriptomic atlas spanning 100 m thickness at single-cell resolution. 3D-VirtualCM identified spatially and transcriptionally distinct cardiomyocyte populations within the infarct border zone, enabled high-throughput quantification of cardiomyocytes re-entering the cell cycle together with their associated molecular signatures, and revealed heterogeneous RNA distribution along the longitudinal axis of individual cardiomyocytes. By integrating three-dimensional cellular morphology with in situ transcriptomic data, 3D-VirtualCM provides a scalable approach for resolving cardiomyocyte states and spatial organization in physiological and pathological cardiac remodeling.

bioinformatics↗

Retinoic acid resolves the conflict between X-chromosome inactivation and pluripotency program in female cleavage-stage embryos

The tight coupling of X-chromosome inactivation (XCI) and pluripotency is a paradigm of holistic developmental regulation, and their inverse correlation enables XCI establishment during implantation. In contrast, the co-establishment of imprinted XCI (iXCI) and pluripotency program in female preimplantation embryos challenges the holistic pattern, but how embryos coordinate the two remains unknown. Here, we find that Nanog during the cleavage stage strongly represses the co-upregulated Rnf12-Xist axis, the triggering signaling of iXCI, creating a conflict that threatens iXCI. We identify retinoic acid (RA) as the coordinator that resolves the conflict and safeguards iXCI. RA activates its receptor RARG to evict NANOG from Rnf12 5region, avoiding NANOGs threat. In vivo, either maternal vitamin A deficiency or embryonic RA synthesis defects results in impaired iXCI and female-biased embryonic lethality. Thus, we highlight RA as a master regulator to holistically balance iXCI and pluripotency during cleavage stages, thereby ensuring proper female embryogenesis.

developmental biology↗

Fruit trichome density outweighs cuticle thickness as the dominant barrier to postharvest water loss in tomato

Fruit cuticle thickness and biochemical composition have traditionally been regarded as the primary determinants of postharvest water loss in fleshy fruits. However, several reports indicate that some tomato mutants with thinner fruit cuticles or less cutin and waxes do not always show increased transpiration, suggesting that additional surface features influence postharvest water loss. Here, we s how that fruit trichome density is a previously underappreciated determinant of postharvest water loss in tomatoes. Using two independent mutants, cr-slhdziv7 and cr-slhdziv9, which exhibit reduced fruit trichome density, we found that both mutants displayed reduced water loss rates and extended shelf life during postharvest storage despite having thinner cuticles and reduced levels of key cutin monomers. Further molecular analyses, including RNA-seq, yeast one-hybrid (Y1H), and dual-luciferase reporter assays, revealed that these two HD-ZIP IV proteins not only regulate fruit trichome formation but also directly or indirectly modulate the expression of multiple cutin biosynthesis genes. Collectively, our results demonstrate that the benefit of reducing trichome-associated microchannels can outweigh the negative effects of cuticle thinning on postharvest water loss. This study establishes fruit trichome density as an important and previously underestimated target for improving postharvest fruit quality and shelf life. HighlightO_LIFruit trichome density controls tomato postharvest water loss and dominates over cuticle thickness barrier. C_LIO_LILess trichomes reduce microchannels, lowering transpiration despite thin cuticles and extending tomato fruit shelf life. C_LI

plant biology↗

MTB-KB: A Curated Knowledgebase of Mycobacterium tuberculosis Related Studies

Tuberculosis (TB), caused by Mycobacterium tuberculosis (MTB), has regained its position as the worlds leading killer among infectious diseases. Despite extensive research progress across epidemiology, diagnosis, drug development, treatment regimens, vaccines, drug resistance, virulence factors, and immune mechanisms, MTB-related knowledge remains fragmented across thousands of publications, limiting its effective use. To address this gap, we present MTB-KB, a literature-curated knowledgebase that systematically integrates high-impact findings from eight major sections of TB research. The current release contains 75,170 associations from 1,246 publications, covering 18,439 entities standardized using authoritative databases and WHO-endorsed classifications. A central feature is the interactive knowledge graph, which links cross-section associations to reveal and infer MTB-host interactions, treatment strategies, and vaccine development opportunities. MTB-KB also provides a user-friendly interface with browsing, advanced search, and statistical visualization. Overall, by consolidating dispersed MTB knowledge into a structured and accessible platform, MTB-KB provides a valuable resource for researchers, clinicians, and policymakers, supporting both basic and clinical TB research, enabling evidence-based TB prevention, diagnosis, and treatment, and contributing to global elimination efforts. MTB-KB is accessible at https://ngdc.cncb.ac.cn/mtbkb/.

bioinformatics↗

UQ-PhysiCell: An extensible Python framework for uncertainty quantification and model analysis in PhysiCell

Agent-based models (ABMs) are widely used to study complex multiscale biological systems, particularly in cancer research. However, their high-dimensional parameter spaces, stochasticity, and computational costs pose significant challenges for uncertainty quantification, calibration, and systematic comparison of competing mechanistic hypotheses. PhysiCell has evolved into a growing ecosystem of open-source tools supporting physics-based multicellular modeling, including model construction, visualization, experimental data integration (e.g., spatial multiomics), and downstream output analysis. However, despite these advances, systematic support for uncertainty-aware model analysis, scalable parameter exploration, and formal calibration workflows remains limited. Here, we introduce UQ-PhysiCell, an open-source Python package that enables uncertainty quantification, calibration, and model selection for PhysiCell models using a modular and scalable workflow. UQ-PhysiCell acts as a manager of PhysiCell simulation inputs and outputs, including parameters, initial conditions, rules, and MultiCellDS-compliant objects, and provides automated orchestration of large ensembles of simulations. The framework supports multiple levels of parallelism to accelerate the analysis, including the parallel execution of independent simulations, stochastic replicates, and downstream analysis tasks. UQ-PhysiCell integrates directly with established Python libraries for sensitivity analysis, optimization, Bayesian inference, and surrogate modeling, allowing users to construct customized pipelines that match their modeling goals and computational resource requirements. UQ-PhysiCell decouples model execution from statistical analysis and emphasizes extensibility and reproducibility. This lowers the barrier to rigorous uncertainty-aware analysis and supports systematic evaluation of PhysiCell models in biological and biomedical research. Author summaryWe developed UQ-PhysiCell to address a key challenge in agent-based modeling: the systematic quantification of uncertainty in complex stochastic simulations. PhysiCell is widely used to model multicellular biological systems, particularly in cancer research; however, practical tools for uncertainty analysis, calibration, and model comparison are often developed in an ad hoc manner. This makes the results difficult to reproduce and limits the ability to rigorously evaluate competing biological hypotheses. UQ-PhysiCell provides a flexible Python framework that manages the inputs and outputs of PhysiCell simulations and enables large-scale computational analysis. We designed the software to be modular, allowing users to build their own analysis pipelines and combine different methodologies for sensitivity analysis, calibration, and model selection. Rather than enforcing a single workflow, UQ-PhysiCell supports customization to match specific scientific questions and computational requirements. To make uncertainty-aware analyses feasible for computationally intensive agent-based models, UQ-PhysiCell implements multiple parallelism strategies, enabling the concurrent execution of simulations, stochastic replicates, and downstream analyses. UQ-PhysiCell promotes reproducibility, scalability, and methodological flexibility. This helps researchers move beyond single best-fit simulations toward more reliable and interpretable computational modeling.

systems biology↗

Ramping-up hippocampal ripples and their neocortical coupling support human visual short-term memory

Emerging evidence suggests that the hippocampus contributes to visual short-term memory (VSTM). However, the neural mechanisms through which hippocampal activity supports the maintenance of VSTM representations remain largely unknown. Here, using intracranial EEG recordings from human participants performing a delayed match-to-sample task for naturalistic objects, we investigated the role of hippocampal ripple activity--brief high-frequency oscillations associated with memory replay--in VSTM maintenance and hippocampal-neocortical communication. We found that hippocampal ripple rates progressively ramped up during the maintenance period and supported successful VSTM. More critically, hippocampal ripples were temporally coupled with the ripples in the lateral temporal lobe (LTL), and these coupled ripples were associated with memory reactivation in the LTL. These findings provide direct evidence that hippocampal-neocortical interaction via coupled ripples supports VSTM, extending the role of hippocampal ripples from long-term consolidation to short-term mnemonic processes and offering new insights into the dynamic coding mechanisms of working memory. Impact StatementHippocampal ripple ramping-up and neocortical coupling support a dynamic coding mechanism for visual short-term memory maintenance

neuroscience↗

Nucleoid-associated proteins sense phage-induced genome damage to elicit abortive infection

Bacteria have evolved diverse immune strategies to detect and neutralize bacteriophage infection. Here, we describe an unprecedented paradigm in which a chromosome-architecting nucleoid-associated protein (NAP) is repurposed as a viral infection sensor. When phage attack leads to genome degradation, the NAP sensor is released from the nucleoid to the cytoplasm, where it binds and activates diverse immune effectors. One such effector is a nucleotide-modifying toxin normally existing as an inactive homotetramer. NAP binding converts it into a catalytically active heterotrimer that halts both transcription and translation. Phylogenetic analyses unveiled the high modularity, polyphyletic origin, and wide distribution of NAP-mediated defenses. Collectively, we define a distinct class of defense systems in which bacteria sense phage-induced genome damage through NAP relocation, highlighting an unexpected but essential role for these proteins as sentinels of genome integrity.

microbiology↗

Harnessing Diacylglycerol-Terminated Cationic Oligomers for Next-Generation Antibacterial Therapeutics

Cationic polymers, which mimic the structure of antimicrobial peptides (AMPs), are increasingly recognized as promising antimicrobial materials. Here, we report the synthesis and evaluation of a new class of cationic lipid-terminated oligomers (CLOs), comprised of 2C18-hydrophobic lipid tails, and short oligomeric cationic chains synthesised via Cu(0)-mediated reversible-deactivation radical polymerization (RDRP). Two 2-vinyl-4,4-dimethyl-5-oxazolone (VDM) oligomers with degrees of polymerization (DP) of 20 or 50 were synthesized using the lipid functional initiator (R)-3-((2-bromo-2-methylpropanoyl) oxy)propane-1,2-diyl dioctadecanoate (2C18-Br). Post-polymerization modification of the pendant oxazolone moieties was carried out using reactive amines, including N-Boc-ethylenediamine (BEDA) and N,N-dimethylethylenediamine (DMEN). Subsequent deprotection of the BEDA groups and quaternization of DMEN groups enabled the synthesis of six functional CLOs exhibiting distinct cationic functionalities. Antimicrobial assays against a panel of WHO bacterial and fungal priority pathogens (methicillin-resistant Staphylococcus aureus [MRSA], Escherichia coli, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, Candida albicans, and Cryptococcus neoformans) revealed that these CLOs exhibited potent and selective structure-dependent antibacterial activity, particularly against MRSA, with minimum inhibitory concentrations (MICs) in the clinically relevant range, below 4 {micro}g mL-1, comparable to antibiotics vancomycin and colistin. Among these, BEDA-functionalized CLOs demonstrated the strongest antimicrobial profile, which was significantly increased by increasing DP, as evidenced by a reduction in MIC values from 64 {micro}g mL-1 (for DP20) to [≤] 4 {micro}g mL-1 (for DP50) against A. baumannii. Biocompatibility assays against red blood cells and HEK293 cells indicated negligible toxicity, with haemolytic (HC50) and cytotoxic (CC50) values exceeding 512 {micro}g mL-1 across all CLOs. All CLOs displayed minimal activity against C. albicans (MIC [≥] 512 {micro}g mL-1). In contrast, activity against C. neoformans was influenced by both cationic functionality and DP, with DMEN-based CLOs exhibited superior antifungal activity at higher DP relative to their BEDA-based counterparts. Most CLOs displayed high selectivity (SI) toward MRSA (SI >128), while 2C18-O(BEDA)50 exhibited the broadest spectrum, showing potent antimicrobial activity and high selectivity against E. coli (MIC [≤] 4 {micro}g mL-1, SI [≥] 128), A. baumannii (MIC [≤] 4 {micro}g mL-1, SI [≥] 128), and MRSA (MIC [≤] 4 {micro}g mL-1, SI [≥] 128), along with moderate activity against P. aeruginosa (MIC = 32 {micro}g mL-1, SI > 16). Taken together, these findings elucidate the combined influence of end-group lipidation, cationic functionality, and polymer length in modulating antimicrobial activity, thereby establishing 2C18-terminated CLOs as a rationally tunable and biocompatible platform for antimicrobial material development.

microbiology↗

Hierarchical Assembly of Native Cytoplasmic Lattices Revealed by Cryo-EM

Oocytes depend on maternal factors for maturation and early embryogenesis. Cytoplasmic lattices (CPLs) are distinctive fibrillar structures in mammalian oocyte cytoplasm implicated in maternal factor storage and developmental competence, yet their molecular composition and architecture remain elusive. Here, we use cryo-electron microscopy to resolve the high-resolution structure of native mouse oocyte CPLs. We identify 14 intrinsic components of multiple copies that assemble into filaments in which PADI6-mediated self-assembly and two subtypes of subcortical maternal complexes (SCMCs) form the core scaffold. Unexpectedly, we discover that /{beta}-tubulin dimers and two autoinhibited ubiquitination modules (UHRF1-UBE2D3, SKP1-FBXW18) are internal components of CPLs. We also uncover multivalent interactions that organize adjacent CPL filaments into higher-order helical bundles. By integrating CPL structure with biochemical and proteomic data, we propose a hierarchical assembly mechanism of CPLs, from subcomplexes to filaments to supramolecular lattices. Our study offers mechanistic insights into how maternal proteins are spatially organized to ensure successful early embryonic development and provides a structural foundation for understanding female infertility related to CPL-associated gene mutations.

developmental biology↗

A Non-Canonical Role of SMAD4 in Regulating 3D Genome Architecture to Inhibit Lung Squamous Cell Carcinoma Development

Lung squamous cell carcinoma (LUSC) lacks clearly defined key drivers and effective targeted therapies, reflecting an incomplete understanding of its molecular pathogenesis. Here, we identify SMAD4 as a critical regulator of three-dimensional (3D) genome organization in LUSC and uncover a mechanistic link between tumor suppressor loss and oncogenic transcriptional activation. By integrating clinical datasets, genetically engineered mouse models, human and murine LUSC cell lines, and multi-omics analyses, we demonstrate that SMAD4 deficiency promotes LUSC progression by unleashing EP300-mediated enhancer-promoter looping at the SOX2 locus. Mechanistically, SMAD4 does not directly bind SOX2 regulatory elements but instead constrains chromatin looping by sequestering EP300 away from loop anchor regions. Loss of SMAD4 leads to enhanced H3K27ac deposition, aberrant SOX2 activation, and increased LUSC tumor cell proliferation. Together, these findings reveal a non-canonical role for a transcription factor (e.g., SMAD4) in regulating dysregulated 3D genome architecture to inhibit tumor development.

cancer biology↗

Polyclonal-Monoclonal Transition in Lung Squamous Cell Carcinoma Evolution

The evolutionary trajectory of lung squamous cell carcinoma (LUSC) remains poorly defined, hindering the development of effective therapies. By integrating genomic and transcriptomic sequencing from human LUSC specimens, we delineated a polyclonal-to-monoclonal evolutionary trajectory during LUSC progression. This evolutionary pattern was corroborated by single-cell RNA sequencing, which revealed consistent tumor cell heterogeneity. Specifically, the SBS5 mutational signature was enriched and correlated with poor prognosis independent of tumor stage. By further utilizing the spontaneous LUSC mouse model to identify key genomic and genetic events in LUSC progression, we observed that the JNK pathway was inhibited and that cytoskeleton-related pathways were dysregulated during LUSC development, and identified the mutations in the JNK pathway (e.g., DACT1) and cytoskeletal regulators (e.g., KIF26A). Collectively, these findings established a polyclonal-monoclonal evolution paradigm for LUSC, potentially regulated by JNK pathways, which could benefit LUSC precision therapeutics.

genomics↗

Metagenomic strain-resolved DNA modification patterns link extrachromosomal genetic elements to host strains

DNA modification is central to microbial defense against extrachromosomal genetic elements (ECEs), consequently ECEs tend to adopt their hosts modification patterns. Shared ECE-host modification patterns enable linking ECEs to their hosts, but modification detection tools are designed for single genomes and are ineffective at metagenome scale. Here, we present MODIFI, software for detecting DNA modifications in metagenomes. MODIFI assumes that each k-mer in a metagenome is mostly unmodified and calculates background signal levels for that k-mer from PacBio HiFi reads, eliminating the need for matched control experiments. MODIFI ECE-host linkages were validated using >1,000 isolate and mock microbiome datasets. Illustrating the approach, we identified 315 strain-resolved, non-redundant ECE-host linkages in environmental and human metagenomes. In infant gut microbiomes, a chromosomal inversion in Enterococcus faecalis alters host and associated plasmid methylation motifs simultaneously. Overall, MODIFI solves a major bottleneck in DNA modification analysis and provides a foundational tool for understanding microbial epigenomics.

microbiology↗

Modeling the dynamics of social exchange in groups with reinforcement learning and Theory of Mind

Accurately attributing belief to others is a milestone of social cognition and serves as an indicator of intact cognitive functioning. However, tracking all others beliefs in complex social interactions is often inefficient or even impossible. We propose that in such cases, attributing ones own belief to others (i.e., egocentric belief attribution) may serve as a functional approximation, enabling individuals to interact with others successfully. In this study, we employed computational modeling with behavioral measures to investigate this approach in social exchange in a novel group decision-making task across three experiments. We found that, beyond the well-documented reciprocity, participants exhibited consistent alternating behavior, characterized by the switching between potential recipients. This alternation was not driven by fairness concerns but reflected a strategic balance between maintaining stable partnerships and exploring alternatives. Crucially, a reinforcement learning model incorporating egocentric belief attribution (eToM) consistently outperformed all alternative models. These findings highlight that egocentric belief attribution is not a cognitive deficit, but a core mechanism supporting adaptive decision-making in complex social environments.

animal behavior and cognition↗

Collective microfibril sliding underlies plant cell wall creep

Plant cell growth depends on slow, irreversible creep of the fibrous cell wall stretched by turgor, yet the mechanics of creep--and how it differs from elasto-plastic deformation--remains uncertain1-3. Using multiscale modeling, we show how wall creep emerges from elementary sliding of cellulose microfibrils along their contact interfaces. A dominant sliding mode involves localized dislocation-like defects that stochastically nucleate at laterally bonded microfibril contacts and then glide along the interface by surmounting discrete energy barriers. Embedding these sliding events into Monte Carlo simulations of stretched cellulose networks recapitulates whole-wall creep kinetics. Elevated stress lowers sliding energy barriers and triggers rapid irreversible deformation characteristic of plastic flow. Compared with elasto-plastic stretching, creep induces less microfibril reorientation but promotes bundling, thereby reducing subsequent yielding. These results clarify the microfibril rearrangements underlying cell wall creep and show how they redistribute stress to permit sustained wall expansion at steady turgor without compromising structural integrity.

biophysics↗

MiCBuS: Marker Gene Mining for Unknown Cell Types Using Bulk and Single Cell RNA-Seq Data

Identifying cell type-specific expressed genes (marker genes) is essential for understanding the roles and interactions of cell populations within tissues. To achieve this, the traditional differential analysis approaches are often applied to individual cell-type bulk RNA-seq and single-cell RNA-seq data. However, real-world datasets often pose challenges, such as heterogeneous bulk RNA-seq and incomplete scRNA-seq. Heterogeneous bulk RNA-seq amalgamates gene expression profiles from multiple cell types and results in low resolution, while incomplete scRNA-seq does not capture some cell types from the tissue, leading to unknown cell types. Traditional methods fail to identify marker genes for such unknown cell types. MiCBuS addresses this limitation by generating Dirichlet-pseudo-bulk RNA-seq based on bulk and incomplete single-cell RNA-seq data. By performing differential analysis of gene expressions on bulk and Dirichlet-pseudo-bulk RNA-seq samples, MiCBuS can identify the marker genes of unknown cell types, enabling the identification and characterization of these elusive cellular components. Simulation studies and real data analyses demonstrate that MiCBuS reliably and robustly identifies marker genes specific to unknown cell types, a capability that traditional differential analysis methods cannot achieve. Availability and implementationMiCBuS is implemented in the R language and freely available at https://github.com/Shanshan-Zhang/MiCBuS.

bioinformatics↗

Dynamic optimization of extrachromosomal DNA copy number drives tumour evolution

Extrachromosomal DNA (ecDNA) is common in human cancers and is associated with poor clinical outcomes, yet how ecDNA-driven genetic heterogeneity is translated into functional heterogeneity remains unclear. Using single-cell multiomics sequencing and multiplexed IF-FISH, we show that asymmetric inheritance of ecDNA generates copy number heterogeneity that propagates to gene expression programs, including oncogenic signaling and cellular stress responses. Transgenerational live-cell lineage tracking directly shows that ecDNA heterogeneity arises within only a few cell divisions and modulates daughter cell division timing in a copy number-dependent manner, a property not observed for evenly inherited chromosomal amplicons. We identify an optimal middle ecDNA copy number range that maximizes proliferative fitness at baseline, while drug selection pressure induced by low-dose CHK1 inhibition selects for cells with a new optimal range at low ecDNA copy numbers. These low ecDNA copy number cells pre-exist in the population and can be generated de novo, driving copy number shifts promoting drug resistance. In vivo experiments further demonstrate that shifts toward ecDNA copy numbers that are optimal under the tumour microenvironment enhance tumourigenicity. Together, these findings establish ecDNA copy number plasticity as a central driver of tumour evolution.

cancer biology↗

SCALE: Scalable Conditional Atlas-Level Endpoint transport for virtual cell perturbation prediction

Virtual cell models aim to enable in silico experimentation by predicting how cells respond to genetic, chemical, or cytokine perturbations from single-cell measurements. In practice, however, large-scale perturbation prediction remains constrained by three coupled bottlenecks: inefficient training and inference pipelines, unstable modeling in high-dimensional sparse expression space, and evaluation protocols that overemphasize reconstruction-like accuracy while underestimating biological fidelity. In this work we present a specialized large-scale foundation model SCALE for virtual cell perturbation prediction that addresses the above limitations jointly. First, we build a BioNeMo-based training and inference framework that substantially improves data throughput, distributed scalability, and deployment efficiency, yielding 12.51* speedup on pretrain and 1.29* on inference over the prior SOTA pipeline under matched system settings. Second, we formulate perturbation prediction as conditional transport and implement it with a set-aware flow architecture that couples LLaMA-based cellular encoding with endpoint-oriented supervision. This design yields more stable training and stronger recovery of perturbation effects. Third, we evaluate the model on Tahoe-100M using a rigorous cell-level protocol centered on biologically meaningful metrics rather than reconstruction alone. On this benchmark, our model improves PDCorr by 12.02% and DE Overlap by 10.66% over STATE. Together, these results suggest that advancing virtual cells requires not only better generative objectives, but also the co-design of scalable infrastructure, stable transport modeling, and biologically faithful evaluation.

cell biology↗