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Qin, H.

Publications and source records attributed to Qin, H..

At least 19 recordsLinked to original sources

Information contracts determine what inverse perturbation benchmarks measure

Inverse perturbation benchmarks rank interventions toward a desired cellular state, but high accuracy can answer a different question from biological prioritization. We present InverseBench, which makes candidate information and endpoint construction explicit, and FSTN, a linear pipeline evaluated under it. With identical inputs, candidates and validation, nested ridge reaches Spearman 0.959 for a transcriptional principal-component proxy but 0.445 for independently measured K562 growth fitness across 7,354 genes. Controlled response-entry availability across seven tasks gives heterogeneous gains, 0.442 for CD4 activation and 0.116 for external fitness. Yet predefined shortlist comparisons show no primary-cutoff penalty in K562 or a melanoma co-culture screen, and secondary cutoffs reverse the K562 ordering. FSTN's nonnegative set selector recovers 0.840 of measured two-gene constituents in three picks, against 0.771 for an unconstrained greedy. The framework separates proxy reconstruction, response-informed prioritization and unseen-intervention ranking: an endpoint-dependent accuracy gap does not by itself mean worse biological decisions.

bioinformatics↗

DCAF: Unifying Data Validity, Evaluation Validity and Predictive Modeling for Single-cell Perturbation Simulation

Single-cell perturbation profiling is limited by cost and throughput, while computational methods remain constrained by inconsistent evaluation and underperformance relative to simple baselines. Here we present DCAF, a unified framework for single-cell perturbation simulation that that jointly addresses data validity, evaluation validity and predictive modeling. Among its three components, DCAF-data addresses the single-measurement limitation by reconstructing pre- and post-perturbation status using entropy-regularized optimal transport, and is demonstrated on both cell line and multi-cell type datasets. DCAF-criterion evaluates log fold changes in non-silenced genes to improve sensitivity to model error and robustness to zero inflation noise, validated on synthetic datasets. DCAF-model combines JEPA with explicit modeling for regulatory-dynamics modeling for interpretable prediction. Across benchmarks, DCAF outperforms state-of-the-art deep-learning methods, as well as mean and linear baselines in cross-gene, cross-cell-type and cross-region generalization. In adult Mouse brain, DCAF recapitulates known cell-type-specific regulatory heterogeneity of Dgcr8 knockdown at both cell type and gene levels. DCAF thus provides a rigorous and biologically grounded foundation for reliable perturbation simulation across development, disease and therapeutic discovery.

bioinformatics↗

Beyond Equilibrium Ensembles: Time Rescaling in Coarse-Grained Simulations across Single-Molecule and Condensate Regimes

Residue-level coarse-grained simulations provide a powerful route for modeling biomolecular condensates over length and time scales that are difficult to access with atomistic molecular dynamics. Coarse-grained models have been shown to reproduce many aspects of equilibrium phase behavior. However, it remains unclear to what extent such models can reproduce the relative timescales of molecular dynamics. Here, we examine this question for complex coacervates with markedly different dynamics, formed by the highly acidic intrinsically disordered protein prothymosin with four cationic partners: linker histone H1, protamine, polylysine, and polyarginine. Coexistence simulations using a residue-level coarse-grained model reproduce key equilibrium observables from experiments, including dense-phase concentrations, ionic-strength-dependent phase behavior, and chain dimensions in the dense and dilute phases. Dynamics are accelerated in these simulations, but a composition-specific time-rescaling factor captures the ionic-strength dependence of chain reconfiguration times within a given complex coacervate. In contrast, time rescaling is not transferable between dense and dilute phases or across condensate compositions and can depend on the chosen observable. These results show that agreement with measured equilibrium observables does not imply a universally transferable timescale for conformational dynamics in residue-level coarse-grained simulations. However, we find that the required time rescaling strongly correlates with the interaction energy of the protein chains, suggesting that the missing frictional effects arise from protein-protein interactions rather than solely from protein-solvent interactions, reminiscent of internal friction. Our findings highlight the need to combine thermodynamic validation with kinetic calibration when interpreting chain relaxation, molecular diffusion, and material properties from residue-level coarse-grained simulations of biomolecular condensates.

biophysics↗

Intracranial Targeting of Cholesterol Processing Reveals a Therapeutic Vulnerability that Reprograms Glioblastoma and Promotes Antitumor Immunity

Glioblastoma (GBM) remains the most lethal primary brain cancer due to its remarkable metabolic plasticity and therapeutic resistance. Here, we identify cholesterol dependency as a therapeutically exploitable vulnerability in GBM using two FDA approved drugs: the H1 histamine antagonist clemastine and the retinoid X receptor agonist bexarotene. Combined treatment induces potent synergistic anti tumor activity across patient-derived glioma models, suppressing proliferation, stemness, and survival at sub IC50 concentrations. Mechanistically, this therapy disrupts cholesterol biosynthesis, transport, and homeostasis, triggering endoplasmic reticulum stress and activation of the unfolded protein response, ultimately leading to autophagy and apoptotic cell death. Orthotopic patient derived glioma models recapitulate these mechanisms in vivo, where local intracranial administration significantly reduces tumor progression and prolongs survival using fourfold lower doses than systemic intraperitoneal delivery. Single cell RNA sequencing revealed activation of regeneration and plasticity programs, accompanied by immune microenvironment remodeling and enhanced inflammatory signaling. Importantly, syngeneic models preserved immune cell composition, supporting future integration with immunotherapeutic strategies. Together, these findings establish cholesterol dysregulation induced metabolic collapse as a promising therapeutic approach for GBM.

cancer biology↗

Single-cell foundation models identify shared and divergent transcriptomic signatures of aging across invertebrates and mammals

Cross-species aging clocks have so far stayed within mammals. We asked whether a single model can predict age from single cells of fly, worm, mouse, and human, species separated by roughly 800 million years of evolution. We fine-tuned scGPT and Geneformer on 1.3 million such cells, using one parameter set per architecture. Both models classified cells as young, middle, or old, reaching 78.6% and 80.5% accuracy. SHAP attribution then showed where the two architectures agreed and where they diverged. scGPT ranked ribosomal proteins highest in every species, with RPL12 first throughout. Geneformer did the same in mouse and human but favored signaling, chromatin, and ubiquitin-ligase genes in fly and worm. Hiding all 51 ribosomal-protein genes at inference cost 22-28 percentage points of accuracy, against 0.3 points for size-matched random gene sets. Bootstrap resampling, five-fold cross-validation, and comparison with six published aging studies left the rankings largely unchanged. Age-associated signal is therefore accessible to a pooled cross-species model, but which genes carry it depends on how the model encodes expression.

genomics↗

Noncanonical Circular RNAs and Potential Functions

Circular RNAs (circRNAs) are ubiquitous in eukaryotes; dysregulated circRNA expression is linked to diseases, including lung cancer. In contrast to canonical circRNAs arising from exon-intron boundaries, noncanonical circRNAs originating within exonic, intronic, and intergenic regions have typically been dismissed as transcriptional noise or technical artifacts. To explore circRNA diversity and appreciate their functions, we developed an algorithm to identify both canonical and noncanonical circRNAs without relying on genome annotation, enabling the identification of circRNAs of all types and in newly sequenced or poorly annotated species. Results from lung cancer cells revealed that noncanonical circRNAs constituted over two-thirds of the circRNA population and were expressed more abundantly than canonical circRNAs, and genes with fewer and shorter exons were hotspots for noncanonical circRNA and circRNA isoform production. Further analyses showed that many noncanonical circRNAs were indeed endogenous circRNAs transcribed within cells rather than experimental artifacts, were potentially translated into proteins or peptides, and were conserved across species. Moreover, we validated 65 noncanonical circRNAs in NCI-H23 cells using multiple bioassays and demonstrated that both exonic and intergenic noncanonical circRNAs influenced cell viability. CircRNA profiles in tumor and tumor-adjacent tissues of lung cancer patients revealed tissue-specific expression and differentially expressed canonical and noncanonical circRNAs from cognate genes involved in cancer-related pathways, indicating their potential clinical relevance. This study confirmed the authenticity of noncanonical circRNAs and provided the first experimental evidence that noncanonical circRNAs influence cancer cell phenotypes. These findings broaden our understanding of circRNA biology, highlighting their widespread genomic distribution, diverse functions, and potential clinical relevance.

molecular biology↗

Benchmarking cell type annotation in spatial transcriptomics: resolving cellular hierarchies, biological fidelity, and dynamic cell states

Spatial transcriptomics enables the quantification of gene expression within its native tissue context, providing unprecedented insight into tissue architecture, cellular ecosystems, and local cell-cell interactions at regional and single-cell resolution. Accurate cell type annotation is a critical prerequisite for interpreting these data and is often the first and most essential step in downstream analysis. Despite rapid advances in computational methods, cell type annotation remains challenging and frequently requires extensive expert-driven manual curation based on marker-gene expression, spatial context, and prior biological knowledge. While early approaches relied primarily on transcriptional similarity, newer methods increasingly incorporate spatial information, histological features, and multimodal data to improve annotation accuracy. Nevertheless, reliable annotation remains difficult when biological interpretation requires fine-grained subtype resolution, particularly for platforms with limited gene panels, tissues undergoing dynamic cellular state transitions, and studies in which reference and query datasets differ substantially in biological context or technical modality. Here, we present a systematic benchmark of 20 state-of-the-art cell type annotation methods across four spatial transcriptomics datasets spanning diverse technologies, experimental conditions, cell numbers, and gene panel sizes. Importantly, all benchmark datasets contain expert-curated cell type labels, including wellresolved cell populations and subtype annotations, providing high-quality biological ground truth for evaluation. The benchmark encompasses both reference-based and reference-free methods representing a broad range of computational frameworks. Performance was assessed using conventional classification metrics, including accuracy and F1-based measures, together with structure-aware metrics that evaluate both cell-level annotation accuracy and preservation of higher-order biological organization. Across datasets, annotation performance varied substantially according to tissue context, reference-query similarity, and annotation granularity. Fine-grained subtype annotation and recovery of rare cell populations remained challenging for many methods, particularly in datasets capturing injury, repair, developmental, and regenerative processes characterized by continuous cellular state transitions. Notably, high classification accuracy did not necessarily correspond to preservation of global cellular relationships or biologically coherent downstream pathway and gene-set enrichment analyses. Overall, scANVI, Seurat, and TACCO consistently ranked among the top-performing methods, although their relative advantages were context dependent. Together, our results provide a comprehensive assessment of current annotation strategies for spatial transcriptomics and offer practical guidance for selecting methods that best align with specific biological questions, dataset characteristics, and analytical priorities.

bioinformatics↗

RepGene: Toward a Unified Gene Representation Space Robust to Missing Biological Views

This study evaluates how multi-view gene representations should be compared under a matched contract. Each of 18,460 genes is described by five aligned views: DNA sequence-derived features (D), RNA sequence-derived features (R), protein language-model embeddings (P), curated text knowledge (K), and single-cell expression (X). The contract fixes the gene universe, the 256-D output, label-free outer-training-only fitting, one random-forest probe, and task-equal Macro-F1 over nine registered binary tasks, and varies only the fusion operator across four protocol-defined input states: Core (DNA+RNA+protein), Core+K, Core+X, and Core+K+X. Under these states, the top-scoring operator changes with the available view combination and all task-bootstrap intervals overlap, establishing a condition-dependent rather than universal ranking pattern. An independently configured external RF track provides a separate check of the numerical range, while a gene-to-cell boundary diagnostic shows that gene-level differences attenuate toward a dimension-matched random control under expression-weighted aggregation, as predicted by a dilution identity. Historical log-derived multiplicative-interaction screening is retained only as magnitude-only supplementary evidence because fold-level records are unavailable. The contribution is therefore the matched contract and its audit trail: an evidence-graded protocol for turning fusion claims into comparable, condition-bounded measurements.

bioinformatics↗

Donor Age and Oligosaccharide Structure Jointly Shape the Gut Microbiome Function

Non-digestible oligosaccharides are widely used as prebiotics, yet structurally related glycans can elicit distinct gut microbiome responses. Here, we combined controlled ex vivo fermentation, deep DIA metaproteomics, and targeted metabolomics to determine how oligosaccharide structure and donor age shape microbiome function. Stool microbiomes from 18 healthy donors across three age groups were cultured with seven structurally related oligosaccharides from two glycan families, fructo-oligosaccharides (FOS) and galactosyl-sucrose derivatives (GSD). We found that oligosaccharide structure organized a functional response landscape rather than simply separating substrates into broad prebiotic classes. Structurally related glycans produced more similar response profiles overall, yet closely related FOS substrates remained functionally distinguishable, indicating that subtle structural differences were resolved by the microbiome as graded functional changes. These structure-responsive functions were further associated with producer-level reorganization relative to baseline, while targeted enzyme-level analyses indicated that substrate-specific CAZyme responses could also reflect altered functional investment within shared producer backgrounds. Despite these substrate-specific entry processes, network analysis revealed convergence onto shared downstream physiological states enriched for translation, amino-acid biosynthesis, secretion/export, and chemotaxis-related pathways. Across treatments, major short-chain fatty acids increased while mucin glycan degradation-associated markers decreased, suggesting coordinated shifts toward saccharolytic metabolism and reduced host-glycan foraging. Tryptophan-associated metabolism was also consistently linked to primary fructan processing, accompanied by higher extracellular tryptophan availability. Donor age modified selected microbial functional axes and enzyme-metabolite coupling relationships rather than the overall direction of core fermentation outputs. In particular, oligosaccharides attenuated an Methanobrevibacter smithii (M. smithii) and M00567 methanogenesis-related signature in microbiomes from older adults and altered age-dependent relationships between butyrate-pathway enzymes and extracellular butyrate levels. Together, these findings show that oligosaccharide structure determines how gut microbial communities organize carbohydrate processing and downstream functional states, while donor age reshapes the taxonomic and metabolic context of these responses. This work provides a mechanistic framework for structure-aware and age-aware precision prebiotic design.

microbiology↗

DOC Release and Physiological Response of Zostera marina Under Light and Nutrient Gradients

The seagrass bed, known as an important blue carbon ecosystem, not only has robust carbon sequestration capacity, but also releases the fixed organic carbon into the water column in the form of dissolved organic carbon (DOC). Zostera marina is the main constructive species of the seagrass meadows of northern China, but the regulatory mechanism of its DOC release in response to environmental changes still remains unclear. Adult Z. marina was used as the experimental material in this research to investigate the effects of light intensity and nutrient concentration on its DOC release, and to observe its physiological responses. By using a total organic carbon (TOC) analyzer, dissolved oxygen monitoring, transmission electron microscopy (TEM), and transcriptome analysis, we explored how light and nutrients affect DOC release and the underlying physiological mechanisms in Z. marina. The results showed that both elevated light intensity and short-term nutrient enrichment promoted organic carbon release from Z. marina to the environment. Increased light enhanced the net primary productivity (NPP) of Z. marina, while the magnitude of DOC release increased more than NPP itself. Nutrient enrichment reduced NPP while raising the proportion of DOC released by Z. marina. Transcriptome analysis showed that nutrient enrichment significantly affected pathways, including flavonoid biosynthesis and fatty acid degradation. This study demonstrated that changes in light and nutrients can significantly influence DOC release and carbon allocation patterns in Z. marina, providing a theoretical basis for blue carbon accounting and ecological restoration evaluation in seagrass beds.

plant biology↗

Large-scale quantum computing framework enhances drug discovery in multiple stages

Coherent Ising machines (CIMs) excel at solving large-scale combinational optimization problems (COPs), but their insufficient long-term stability has hindered their applications in compute-intensive tasks like computer-aided drug discovery (CADD). By improving fiber vibration isolation and temperature control system, we have implemented a 2000-node CIM named QBoson-CPQC-3Gen achieving stable solutions over one hour on large-scale COPs. Graph-based encoding schemes were further introduced to realize a CIM-based CADD workflow including allosteric site detection, protein-peptide docking and intermolecular similarity calculation. CIM-based methods demonstrated superior speed and accuracy than heuristic algorithms. Especially, QBoson-CPQC-3Gen identified 2 novel druggable sites and bioactive compounds for 6 targets, which were further validated in vitro, in-cell and by crystal structures. Our contributions established a quantum-computing framework for multi-stage drug discovery, representing a significant advancement in both quantum computing applications and pharmaceutical research.

bioinformatics↗

Multimodal Behavior Scoring quantifies depression-like severity across chronic stress models and identifies stress-resilient mice

IntroductionRodent chronic-stress models are central to preclinical depression research, yet behavioral phenotypes are often assessed assay-by-assay, which can reduce cross-cohort comparability and mask heterogeneity across symptom domains (e.g., anhedonia, anxiety-like behavior, and behavioral despair). An integrative behavioral index may provide a more robust and interpretable measure of overall stress-induced severity and facilitate stratification of susceptible versus resilient individuals. MethodsWe developed the Multimodal Behavior Scoring (MBS) algorithm to integrate outcomes from standard assays--sucrose preference test (SPT), open field test (OFT), and forced swim test (FST)--into a unified severity score. MBS was evaluated in two independent paradigms, chronic unpredictable mild stress (CUMS) and chronic social defeat stress (CSDS), quantifying group discrimination, reproducibility (intraclass correlation coefficient, ICC), and phenotypic stratification. ResultsMBS robustly separated stressed from control mice (CUMS: +39.8%, p<0.0001; CSDS: +121.8%, p<0.0001) and showed high cross-cohort reproducibility (ICC>0.88). MBS further identified stress-resilient subpopulations and uncovered paradigm-specific behavioral signatures, with despair-dominant patterns in CUMS (FST-MBS, r=0.61) and anxiety-centric patterns in CSDS (OFT-MBS, r=-0.74). Excluding TST did not reduce discrimination performance. ConclusionMBS provides an integrative framework for quantifying depression-like behavioral severity and heterogeneity, enabling streamlined protocols and improving the translational utility of preclinical cohorts for biomarker discovery and antidepressant screening.

animal behavior and cognition↗

BiOmics: A Foundational Agent for Grounded and Autonomous Multi-omics Interpretation

While AI has automated bioinformatic workflows, biological interpretation remains fragmented and often disconnected from mechanistic insights. Existing AI is bifurcated between statistical "black-box" models that lack logical grounding and simple agents restricted to shallow knowledge retrieval. To bridge this divide, we introduce BiOmics, a foundational agent that synthesizes multi-omics data with adaptive knowledge for biological interpretation. BiOmics introduces a novel dual-track architecture comprising a harmonized explicit reasoning space for grounded logic and a unified latent embedding space for high-dimensional association mapping. This architecture enables a transformative "Retrieving-Reasoning-Predicting" paradigm for purposeful, cross-scale inference traversing the biological hierarchy, from molecular variants to disease phenotypes. Empirical evaluations demonstrate that BiOmics surpasses state-of-the-art AI agents and specialized algorithms, markedly augmenting the granularity and depth of biological insights. Specifically, BiOmics exhibits unique superiority in uncovering indirect pathogenic variants, achieving reference-free cell annotation, and prioritizing drug repurposing candidates tailored to specific datasets. BiOmics further enriches the interpretive landscape of biological entities, leveraging its reasoning-grounded knowledge graph to uncover deep functional contexts. Ultimately, BiOmics provides a versatile engineering foundation to transition AI for Science from descriptive "data fitting" to autonomous, knowledge-driven interpretation.

bioinformatics↗

Asymmetric partition of the O-GlcNAcome in mitosis ensures binary cell fate decision

Many cellular components undergo biased segregation during stem cell division, but whether such order extends to the proteome has remained unknown. Using our real-time O-GlycoTracer, we find that O-GlcNAcylated proteins (the O-GlcNAcome) segregate asymmetrically during Drosophila neuroblast mitosis, predisposing the two daughters to distinct fates. The daughter that preserves stem cell identity inherits most of the O-GlcNAcome. This asymmetric partition requires putative O-GlcNAc readers, notably 14-3-3 proteins. We further identify the nuclear pore complex (NPC) as a major O-GlcNAc substrate in neuroblasts; Nup153, located in the nuclear basket, shows O-GlcNAc-dependent biased inheritance. Perturbing multiple steps in this segregation pathway disrupts neuroblast differentiation, reduces brain size, and causes adult learning deficits. These findings reveal a coordinated O-GlcNAc-driven mechanism for proteome-level asymmetric inheritance during neural stem cell division, with implications for neurodevelopmental disorders linked to OGT or 14-3-3 mutations.

cell biology↗

A hypothalamo-septo-hippocampal circuit for REM sleep-dependent consolidation of social memory

REM sleep constitutes a critical window for memory consolidation, yet the brain circuits orchestrating this process remain incompletely defined. Here, we identify a lateral supramammillary nucleus (SuM)-medial septum (MS) projection as a REM sleep-specialized pathway essential for hippocampal memory consolidation. Fiber photometry and optrode recordings revealed that lateral SuM-MS projecting neurons were selectively active during REM sleep. REM-specific optogenetic silencing of this projection impaired consolidation of both social and contextual fear memories. Crucially, silencing of its downstream target, the MS-CA2 pathway, during REM sleep selectively disrupted social memory while sparing contextual fear memory. This functional dissection establishes a hypothalamo-septo-hippocampal circuit (lateral SuM-MS-CA2) dedicated to social memory processing, in parallel to the recently-described direct SuM-CA2 pathway. These results also position the SuM as a REM sleep-hub that routes information via parallel septal pathways to consolidate distinct memory modalities.

neuroscience↗

Predicting TCR-pMHC Binding by Reinforcement Learning

The binding between T cell receptors (TCRs) and peptide-major histocompat-ibility complexes (pMHCs) is fundamental to the immune systems ability to recognize and eliminate pathogens. Accurate prediction of TCR-pMHC inter-actions holds significant promise for advancing cancer immunotherapy, vaccine design, and autoimmune disease research. However, existing approaches often treat the sequences, structures, and functions of TCRs, peptides, and MHC molecules in isolation, neglecting their interdependencies and hence limiting the prediction accuracy. In this study, we present ProTCR, a novel approach that integrates sequence, structural, and functional information within a reinforce-ment learning framework, offering a new paradigm for predicting TCR-pMHC binding. The reinforcement learning optimization enables ProTCR to generate TCR-pMHC sequences with enhanced binding propensity, thereby improving prediction accuracy. On benchmark datasets such as IEDB and VDJdb, ProTCR achieves an AUROC of 0.75, outperforming state-of-the-art methods by 32.7%, while offering interpretable insights into the structural and sequence determi-nants of binding. We further validate ProTCR using TCRs and neoantigens derived from a cervical cancer patient via proteogenomic profiling. Our analysis reveals a strong correlation between T cell clonal expansion and ProTCR-predicted TCR-peptide binding scores, supporting the biological relevance of the model. Additionally, ProTCR demonstrates robust performance in predict-ing SARS-CoV-2 TCR-pMHC complexes and generating MHC-specific peptides with potential applications in peptide-based immunotherapies. Collectively, these findings establish ProTCR as a powerful and interpretable tool for TCR-pMHC binding prediction, with broad utility across immunology research and translational applications.

bioinformatics↗

BioLACE: unifying spatial geometry and marker priors for cohesive cell-type clustering in spatial transcriptomics

Spatial transcriptomics (ST) provides high-dimensional gene expression profiles together with spatial coordinates, enabling the reconstruction of tissue architecture at cellular resolution. While recent graph-based deep learning methods have advanced spatial clustering in ST, many rely on complex architectures that obscure interpretability and rarely integrate biological priors such as marker gene information. We introduce BioLACE, a scalable framework that unifies spatial structure, transcriptomic variation, and curated marker gene profiles within a shared Variational Autoencoder (VAE) latent space. BioLACEjointly optimizes three complementary objectives: (1) a VAE reconstruction loss to preserve transcriptional structure, (2) a graph Laplacian regularizer to enforce spatial smoothness, and (3) a temperature-scaled InfoNCE contrastive loss guided by marker-informed similarities. Applied to MERFISH hypothalamus, mouse spinal cord, and Slide-seq mouse cerebellum datasets, BioLACE achieves superior cell type clustering accuracy, well-defined biologically consistent boundaries, and interpretable latent representations, highlighting its generality and scalability for modern ST analysis. The source code and tutorials for BioLACE are publicly available at https://github.com/maiziezhoulab/BioLACE.

genomics↗

Flexible Skull-Conformal Phased Array for Aberration-Corrected Transcranial Focused Ultrasound Therapy

Transcranial focused ultrasound (tFUS) is a promising non-invasive tool for precise deep-brain interventions, including neuromodulation, blood-brain barrier opening, and drug delivery. However, conventional rigid tFUS arrays suffer from poor skull conformity, compromising patient comfort and targeting precision, while skull-induced aberrations degrade focal accuracy and efficiency. To address these challenges, we present the first flexible, skull-conformal aberration-corrected phased array (F-SCAPA), a transformative solution integrating mechanical adaptability with advanced acoustic correction. The 0.5-MHz array--comprising 8x8 elements--features an optimized fabrication process that enhances material efficiency, ensures flexibility and stretchability, and maintains uniform electrical performance. Coupled with CT-based skull modeling and time-reversal aberration correction, F-SCAPA dynamically conforms to cranial anatomy while compensating for phase distortions. Transcranial validation in a human skull demonstrates precise focusing at 36 mm depth, achieving an axial full width at half maximum (FWHM) of 8.9 mm. This breakthrough overcomes existing limitations by combining mechanical adaptability with high-resolution transcranial focusing, establishing F-SCAPA as a robust, patient-compatible platform for next-generation non-invasive brain therapies.

bioengineering↗