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Biology subjects

Jiang, R.

Publications and source records attributed to Jiang, R..

At least 37 records · Page 2Linked to original sources

Hi-Cformer enables multi-scale chromatin contact map modeling for single-cell Hi-C data analysis

Single-cell Hi-C captures the three-dimensional organization of chromatin in individual cells and provides insights into fundamental genomic processes such as gene regulation and transcription. While analyses of bulk Hi-C data have revealed multi-scale chromatin structures like A/B compartments and topologically associating domains, single-cell Hi-C data remain challenging to analyze due to sparsity and uneven distribution of chromatin contacts across genomic distances. These characteristics lead to strong signals near the diagonal and complex multi-scale local patterns in single-cell contact maps. Here, we propose Hi-Cformer, a transformer-based method that simultaneously models multi-scale blocks of chromatin contact maps and incorporates a specially designed attention mechanism to capture the dependencies between chromatin interactions across genomic regions and scales, enabling the integration of both global and fine-grained chromatin interaction features. Building on this architecture, Hi-Cformer robustly derives low-dimensional representations of cells from single-cell Hi-C data, achieving clearer separation of cell types compared to existing methods. Hi-Cformer can also accurately impute chromatin interaction signals associated with cellular heterogeneity, including 3D genome features such as topologically associating domain-like boundaries and A/B compartments. Furthermore, by leveraging its learned embeddings, Hi-Cformer can be extended to cell type annotation, achieving high accuracy and robustness across both intra- and inter-dataset scenarios.

bioinformatics↗

Modeling Post-Gastrula Development via Bidirectional Pluripotent Stem Cells

The absence of stem cells capable of efficiently generating both trophoblast and epiblast lineages has hindered precise recapitulation of embryonic development. Through high-content chemical screening, we established an AL medium to generate mouse and human bidirectional pluripotent stem cells (BPSCs) characterized by concurrent OCT4/CDX2 expression. Mouse BPSCs demonstrated high plastic differentiation into trophoblast, epiblast and primitive endoderm lineages in vitro within 48 hours without exogenous induction factors and efficiently contributed to the embryo and extraembryonic tissues in vivo. Mechanistically, hyperactivation of the Wnt signaling pathway breaks the early lineage differentiation barrier by initiating a Lef1-dependent bypass. Remarkably, BPSCs can efficiently generated E8.5 embryoids that completed gastrulation and displayed advanced features such as brain development, a closed neural tube, a beating heart, somite formation, and primordial germ cells. These findings highlight BPSCs as a powerful tool for investigating early lineage specification and post-gastrulation embryonic development, with potential applications across multiple species.

developmental biology↗

A Geometrical Optics Model of Individual Ommatidia in Compound Eyes and a Hypothesis for Monocular Stereopsis

This study proposes a novel geometrical optics-based visual model suggesting that individual ommatidia in insect compound eyes may possess intrinsic three-dimensional imaging capabilities and enable monocular stereoscopic perception. Building upon the authors previous hypothesis that certain vertebrate retinal cell nuclei act as microlenses, the optical model is extended in this work to the arthropod compound eye system. By conceptualizing the cornea, crystalline cones, and layered rhabdomeric nuclei as components of a "multi-angle miniature real-image telescope," we construct a three-tiered imaging system composed of objectives, relay conjugate lenses, and microlenses. The model predicts that an ommatidium can actively perceive spatial depth and object distance by adjusting the focal length of crystalline cones and the distance between focused planes, thus achieving stereoscopic imaging with a single eye. Simulations based on representative species such as Drosophila melanogaster, Viggiani parasitic wasps, and fireflies (Lampyris) support the feasibility of this model in distance perception across scales ranging from microns to meters. The model breaks away from the "one ommatidium--one image point" paradigm and offers a new theoretical architecture for understanding insect stereopsis. It also presents a promising framework for bioinspired 3D imaging systems and optical designs with multi-focal capabilities.

biophysics↗

TWEAK Signaling Drives the Transition from Psoriasis to Atopic Dermatitis-like Inflammation in Paradoxical Skin Reactions

Targeted biologics have significantly advanced the treatment of inflammatory skin diseases such as psoriasis; however, some patients paradoxically develop eczematous skin reactions during or after anti-TNF, IL-17, or IL-23 therapy. Although these paradoxical reactions resemble atopic dermatitis clinically and histologically, the molecular mechanisms that drive their development are not fully understood. Here, we generated high-resolution cellular and spatial maps of healthy skin, psoriasis, atopic dermatitis, and paradoxical reactions using single-cell RNA sequencing, spatial transcriptomics, immunohistochemistry, and in vitro assays. In paradoxical reactions, we identified a distinct transcriptional landscape characterized by myeloid and T-cell expansion and an altered keratinocyte phenotype shaped by TWEAK signaling. Mechanistically, we showed that TWEAK synergizes with IL-13 to drive the Th2/type I interferon-polarized epithelial program. Notably, anti-TNF therapy induced TWEAK gene expression in myeloid cells, suggesting a compensatory inflammatory circuit. Together, these findings identify the TWEAK-IL-13 axis as a central driver of paradoxical skin reactions and provide a mechanistic framework for how cytokine blockade may rewire cutaneous immune responses. One Sentence Summary The TWEAK-IL-13 signaling axis is a key driver of immune reprogramming underlying paradoxical skin reactions.

immunology↗

Physical Activity and Depressive Mood Shared the Structural Connectivity between Motor and Reward Network: a population-based study from the UK Biobank

BackgroundExercise has been revealed to leave a positive effect on alleviating depressive symptoms by various existing studies. However, the neural basis behind this phenomenon remains unknown, as well as its underlying biological mechanism.AimsUsing a large neuroimaging cohort from UK Biobank, this study aimed to identify structural connectivity (SC) patterns simultaneously linked with physical activity and depression, as well as its biological interpretation.Method492 participants with major depression disorder (MDD) and 535 healthy controls (HC) were extracted from the UK Biobank dataset. Partial least squares regression was first utilized to explore a replicable SC pattern simultaneously associated with physical activity and depressive mood. The neuromaps toolbox was applied to interpret the biological ontologies of the identified SC pattern. Neuroimaging-transcriptome association and enrichment analyses were conducted to explore its underlying genetic basis, pathways and cell types. The reproducibility and generalizability were tested on another independent MDD dataset (N=3,496) and bipolar disorder (BD) dataset (N=81).ResultsA SC pattern linked with exercise was identified to be both significantly correlated with depressive mood and group discriminative between MDDs and HCs, which primarily located between the motor-related regions and reward-related regions. This pattern was associated with multiple neurotransmitter receptors, such as serotonin and GABA receptors, and enriched in pathways like synaptic signaling and astrocytes cell type. The SC pattern and genetic results were also replicated in another independent MDD dataset and present commonalities with BD.ConclusionsThis study not only initially identified a reproducible shared SC pattern between physical activity and depressive mood, but also elucidated the underlying biological mechanisms, which enhanced our understanding of how exercise helps alleviate depression and may inform the development of novel neuromodulation targets.

neuroscience↗

C12ORF57: a novel principal regulator of synaptic AMPA currents and excitatory neuronal homeostasis

ObjectiveExcitatory neuronal homeostasis is crucial for neuronal survival, circuit function, and plasticity. Disruptions in this form of homeostasis are believed to underpin a variety of neuronal conditions including intellectual disability, epilepsy, and autism. However, the underlying genetic and molecular mechanisms maintaining this homeostasis remain poorly understood. Biallelic recurrent loss of function mutations in C12ORF57, an evolutionarily conserved X amino acid novel open reading frame, underlie Temtamy syndrome (TS)--a neurodevelopmental disorder characterized by epilepsy, dysgenesis of the corpus callosum, and severe intellectual disability. MethodsThrough multiple lines of inquiry, we establish that C12ORF57/GRCC10 plays an unexpected central role in synaptic homeostatic downscaling in response to elevated activity, uncovering a novel mechanism for neuronal excitatory homeostasis. To probe these mechanisms, we developed a new knockout (KO) mouse model of the genes murine ortholog, Grcc10 as well as cellular and in vitro assays. ResultsGrcc10 KO mice exhibit the characteristic phenotypic features seen in human TS patients, including increased epileptiform activity. Corresponding with the enhanced seizure susceptibility, hippocampal neurons in these mice exhibited significantly increased AMPA receptor expression levels and higher amplitude of miniature excitatory postsynaptic currents (mEPSCs). We further found that GRCC10/C12ORF57 modulates the activity of calcium/calmodulin dependent kinase 4 (CAMK4) and thereby regulates the expression of CREB and ARC. InterpretationOur study suggests through this novel mechanism, deletion of Grcc10 disrupts the characteristic synaptic AMPA receptor downscaling that accompanies increased activity in glutamatergic neurons.

neuroscience↗

A Geometric Optical Analysis of Human Retinal Cells and the Hypothesis of Monocular Stereoscopic Vision

We propose a geometric optical model that describes real-image formation via monocular vision in three dimensions. We only assume that the ganglion cell nuclei, bipolar cell nuclei, and photoreceptor cell nuclei in the human retina can be treated as microlenses and actively participate in imaging. In particular, we suggest that monocular vision operates via an array of high-magnification micro-real-image telescopes oriented in various azimuthal directions. The main elements of each telescope are the following. The first is the cornea and crystalline lens, which serve as objective lenses with tunable focal lengths. The second is a paired array of ganglion cell nuclei and bipolar cell nuclei, which act as a conjugate mirror. The third is an individual photoreceptor cell nuclei (cone or rod nuclei), which function as a micro-eyepiece. The fourth is the outer segment of each photoreceptor cell, which serves as a micro-object-distance sensor. We also hypothesize that six combinations of conjugate mirrors and micro-eyepiece arrays work within the human eye. Each combination is responsible for perceiving different ranges of object distances. We further hypothesize that the process by which one human eye perceives object distances involves two stages: from near to finite distances, and from finite distances to infinite distances. In different stages, the distance between different optical elements is tuned so that the object distance can be computed a specific formula when the photocurrent at the retina photoreceptors outer segment layer vanishes. Lastly, we conduct computational simulations. We find that there are two possible processes. By tuning the distances between the elements of our optical model, the eye can perceive object distances as close as 25 cm to dozens of meters in one process and dozens of meters to kilometers in the other process, depending on the sensitivity of the eye to small changes in focal plane spacing.

physiology↗

EpiAgent: Foundation model for single-cell epigenomic data

Large-scale foundation models have recently opened new avenues for artificial general intelligence. Such a research paradigm has recently shown considerable promise in the analysis of single-cell sequencing data, while to date, efforts have centered on transcriptome. In contrast to gene expression, chromatin accessibility provides more decisive insights into cell states, shaping the chromatin regulatory landscapes that control transcription in distinct cell types. Yet, challenges also persist due to the abundance of features, high data sparsity, and the quasi-binary nature of these data. Here, we introduce EpiAgent, the first foundation model for single-cell epigenomic data, pretrained on a large-scale Human-scATAC-Corpus comprising approximately 5 million cells and 35 billion tokens. EpiAgent encodes chromatin accessibility patterns of cells as concise "cell sentences," and employs bidirectional attention to capture cellular heterogeneity behind regulatory networks. With comprehensive benchmarks, we demonstrate that EpiAgent excels in typical downstream tasks, including unsupervised feature extraction, supervised cell annotation, and data imputation. By incorporating external embeddings, EpiAgent facilitates the prediction of cellular responses to both out-of-sample stimulated and unseen genetic perturbations, as well as reference data integration and query data mapping. By simulating the knockout of key cis-regulatory elements, EpiAgent enables in-silico treatment for cancer analysis. We further extended zero-shot capabilities of EpiAgent, allowing direct cell type annotation on newly sequenced datasets without additional training.

bioinformatics↗

DNA tensiometer reveals catch-bond detachment kinetics of kinesin-1, -2 and -3

Bidirectional cargo transport by kinesin and dynein is essential for cell viability, and defects are linked to neurodegenerative disease. Computational models predict that load-dependent motor detachment strongly determines the outcome of kinesin-dynein tug-of-war, with kinesin-3 and kinesin-2 more load-sensitive than kinesin-1. Yet reconstituted assays show that all three kinesin families compete similarly well against dynein. Previous work demonstrated that vertical forces from optical trapping assays can enhance kinesin-1 dissociation, suggesting that motor behavior may depend strongly on cargo geometry. To measure kinesin detachment and reattachment kinetics under forces applied parallel to the microtubule, we developed a DNA-based tensiometer using an entropic DNA spring linking motors to microtubules. For kinesin-1, -2, and -3, dissociation rates at stall were slower than during unloaded motion, and reattachment kinetics were consistent with a weakly bound slip state preceding detachment. Kinesin-3 behavior further suggested that long KIF1A run lengths arise from multiple short runs connected by diffusive episodes. Stochastic simulations reproduced the measured load-dependent kinetics and enabled direct comparison of transition rates among kinesin families. These results provide insight into how kinesin-1, -2 and -3 transport cargo in complex cellular geometries and compete against dynein during bidirectional transport. Impact StatementAll three kinesin transport families exhibit unexpectedly slow dissociation under load, explaining robust competition with dynein during bidirectional cargo transport.

biophysics↗

PlantRing: A high-throughput wearable sensor system for decoding plant growth, water relations and innovating irrigation

The combination of flexible electronics and plant science has generated various plant-wearable sensors, yet challenges persist in their applications in real-world agriculture, particularly in high-throughput settings. Overcoming the trade-off between sensing sensitivity and range, adapting them to a wide range of crop types, and bridging the gap between sensor measurements and biological understandings remain the primary obstacles. Here we introduce PlantRing, an innovative, nano-flexible sensing system designed to address the aforementioned challenges. PlantRing employs bio-sourced carbonized silk georgette as the strain sensing material, offering exceptional resolution (tensile deformation: < 100 m), stretchability (tensile strain up to 100 %), and remarkable durability (season long), exceeding existing plant strain sensors. PlantRing effectively monitors plant growth and water status, by measuring organ circumference dynamics, performing reliably under harsh conditions and being adaptable to a wide range of plants. Applying PlantRing to study fruit cracking in tomato and watermelon reveals novel hydraulic mechanism, characterized by genotype-specific excess sap flow within the plant to fruiting branches. Its high-throughput application enabled large-scale quantification of stomatal sensitivity to soil drought, a traditionally difficult-to-phenotype trait, facilitating drought tolerant germplasm selection. Combing PlantRing with soybean mutant led to the discovery of a potential novel function of the GmLNK2 circadian clock gene in stomatal regulation. More practically, integrating PlantRing into feedback irrigation achieves simultaneous water conservation and quality improvement, signifying a paradigm shift from experience- or environment-based to plant-based feedback control. Collectively, PlantRing represents a groundbreaking tool ready to revolutionize botanical studies, agriculture, and forestry.

plant biology↗

Motor Clustering Enhances Kinesin-driven Vesicle Transport

Intracellular vesicles are typically transported by a small number of kinesin and dynein motors. However, the slow microtubule binding rate of kinesin-1 observed in in vitro biophysical studies suggests that long-range transport may require a high number of motors. To address the discrepancy in motor requirements between in vivo and in vitro studies, we reconstituted motility of 120-nm-diameter liposomes driven by multiple GFP-labeled kinesin-1 motors. Consistent with predictions based on previous binding rate measurements, we found that long-distance transport requires a high number of kinesin-1 motors. We hypothesized that this discrepancy from in vivo observations may arise from differences in motor organization and tested whether motor clustering can enhance transport efficiency using a DNA scaffold. Clustering just three motors improved liposome travel distances across a wide range of motor numbers. Our findings demonstrate that, independent of motor number, the arrangement of motors on a vesicle regulates transport distance, suggesting that differences in motor organization may explain the disparity between in vivo and in vitro motor requirements for long-range transport. Significance StatementIntracellular vesicles frequently travel long distances, despite having few kinesin and dynein motors. By reconstituting liposome motility with kinesin-1 motors, we demonstrate the need for high motor copy numbers for long-range transport when motors are randomly distributed on the liposome surface. We further show that motor clustering reduces the required motor number, emphasizing its potential role in enhancing transport efficiency. Our findings highlight the significance of motor organization in regulating intracellular transport and suggest that motor clustering, such as by scaffolding proteins or lipid domains, influences bidirectional transport outcomes.

biophysics↗

CREATE: cell-type-specific cis-regulatory elements identification via discrete embedding

Identifying cis-regulatory elements (CREs) within non-coding genomic regions--such as enhancers, silencers, promoters, and insulators--is pivotal for elucidating the intricate gene regulatory mechanisms underlying complex biological traits. The current prevalent sequence-based methods often focus on singular CRE types, limiting insights into cell-type-specific biological implications. Here, we introduce CREATE, a multimodal deep learning model based on the Vector Quantized Variational AutoEncoder framework, designed to extract discrete CRE embeddings and classify multiple CRE classes using genomic sequences, chromatin accessibility, and chromatin interaction data. CREATE excels in accurate CRE identification and exhibits strong effectiveness and robustness. We showcase CREATEs capability in generating comprehensive CRE-specific feature spectrum, offering quantitative and interpretable insights into CRE specificity. By enabling large-scale prediction of CREs in specific cell types, CREATE facilitates the recognition of disease- or phenotype-related biological variabilities of CREs, thereby expanding our understanding of gene regulation landscapes.

bioinformatics↗

Astrocyte ezrin defines resilience to stress-induced depressive behaviours in mice

Astrocyte atrophy is the main histopathological hallmark of major depressive disorder (MDD) in humans and in animal models of depression. Here we demonstrated that manipulating with ezrin expression specifically in astrocytes significantly increases the resilience of mice to chronic unpredictable mild stress (CUMS). Overexpression of ezrin in astrocytes from prefrontal cortex (PFC) rescued depressive-like behaviours induced by CUMS, whereas down-regulation of ezrin in astrocytes from PFC increased mice susceptibility to CUMS and promoted depressive-like behaviours. These behavioural changes correlated with astrocytic morphology. Astrocytes from PFC of mice sensitive to CUMS demonstrated significant atrophy; similar atrophy was found in astrocytes from animals with down-regulated ezrin expression. To the contrary morphology remains unchanged astrocytes in animals resistant to CUMS and in animals with astrocytic overexpression of ezrin. Morphological changes also correlated with ezrin immunoreactivity which was low in mice with depressive-like behaviours and high in mice resistant to stress. We conclude that Ezrin-dependent morphological remodelling of astrocytes defines the sensitivity of mice to stress: high ezrin expression renders them stress resilient, whereas low ezrin expression promotes depressive-like behaviour in response to chronic stress.

neuroscience↗

Cross-modality representation and multi-sample integration of spatially resolved omics data

Spatially resolved sequencing technologies have revolutionized our understanding of biological regulatory processes within the microenvironment by accessing the states of genomic regions, genes and proteins as well as spatial coordinates of cells. However, discrepancies between different modalities and samples hinder the analysis of spatial omics data, necessitating the development of advanced computational methods. In this article, we propose PRESENT, an effective and scalable contrastive learning framework, for the cross-modality representation and multi-sample integration of spatial multi-omics, epigenomics and transcriptomics data. Through comprehensive experiments on spatial datasets, PRESENT demonstrates superior performance across various species, tissues, and technologies. Specifically, PRESENT effectively integrates spatial dependency and omics information simultaneously, facilitating the detection of spatially functional domains and the exploration of biological regulatory mechanisms. Furthermore, PRESENT can be extended for the integrative analysis of tissue samples across different dissected regions or developmental stages, promoting the identification of hierarchical structures from systematic and spatiotemporal perspectives.

bioinformatics↗

INSTINCT: Multi-sample integration of spatial chromatin accessibility sequencing data via stochastic domain translation

Recent advances in spatial epigenomic techniques have given rise to spatial assay for transposase-accessible chromatin using sequencing (spATAC-seq) data, enabling the characterization of epigenomic heterogeneity and spatial information simultaneously. Integrative analysis of multiple spATAC-seq samples, for which no method has been developed, allows for effective identification and elimination of unwanted non-biological factors within the data, enabling comprehensive exploration of tissue structures and providing a holistic epigenomic landscape, thereby facilitating the discovery of biological implications and the study of regulatory processes. In this article, we present INSTINCT, a method for multi-sample INtegration of Spatial chromaTIN accessibility sequencing data via stochastiC domain Translation. INSTINCT can efficiently handle the high dimensionality of spATAC-seq data and eliminate the complex noise and batch effects of samples from different conditions through a stochastic domain translation procedure. We demonstrate the superiority and robustness of INSTINCT in integrating spATAC-seq data across multiple simulated scenarios and real datasets. Additionally, we highlight the advantages of INSTINCT in spatial domain identification, visualization, spot-type annotation, and various downstream analyses, including motif enrichment analysis, expression enrichment analysis, and partitioned heritability analysis.

bioinformatics↗

Modulation of endogenous opioid signaling by inhibitors of puromycin sensitive aminopeptidase

The endogenous opioid system regulates pain through local release of neuropeptides and modulation of their action on opioid receptors. However, the effect of opioid peptides, the enkephalins, is short-lived due to their rapid hydrolysis by enkephalin-degrading enzymes. In turn, an innovative approach to the management of pain would be to increase the local concentration and prolong the stability of enkephalins by preventing their inactivation by neural enkephalinases such as puromycin sensitive aminopeptidase (PSA). Our previous structure-activity relationship studies offered the S-diphenylmethyl cysteinyl derivative of puromycin (20) as a nanomolar inhibitor of PSA. This chemical class, however, suffered from undesirable metabolism to nephrotoxic puromycin aminonucleoside (PAN). To prevent such toxicity, we designed and synthesized 5'-chloro substituted derivatives. The compounds retained the PSA inhibitory potency of the corresponding 5'-hydroxy analogs and had improved selectivity toward PSA. In vivo treatment with the lead compound 19 caused significantly reduced pain response in antinociception assays, alone and in combination with Met-enkephalin. The analgesic effect was reversed by the opioid antagonist naloxone, suggesting the involvement of opioid receptors. Further, PSA inhibition by compound 19 in brain slices caused local increase in endogenous enkephalin levels, corroborating our rationale. Pharmacokinetic assessment of compound 19 showed desirable plasma stability and identified the cysteinyl sulfur as the principal site of metabolic liability. We gained additional insight into inhibitor-PSA interactions by molecular modeling, which underscored the importance of bulky aromatic amino acid in puromycin scaffold. The results of this study strongly support our rationale for the development of PSA inhibitors for effective pain management.

pharmacology and toxicology↗

collectNET: a web server for integrated inference of cell-cell communication network

SummaryCell-cell communication through ligand-receptor pairs forms the cornerstone for complex functionalities in multicellular organisms. Deciphering such intercellular signaling can contribute to un-raveling disease mechanisms and enables targeted therapy. Nonetheless, notable biases and inconsistencies are evident among the inferential outcomes generated by current methods for inferring cell-cell communication network. To fill this gap, we developed collectNET (http://health.tsing-hua.edu.cn/collectnet) as the first web server for efficiently inferring the cell-cell communication network, with efficient calculation, hierarchical browsing, comprehensive statistics, advanced searching, and intuitive visualization. collectNET provides a reliable online inference service with prior knowledge of three public ligand-receptor databases and systematic integration of three mainstream inference methods. Additionally, collectNET has assembled a human cell-cell communication atlas, including 126,785 significant communication pairs based on 343,023 single cells. We anticipate that collectNET will benefit researchers in gaining a more holistic understanding of cell development and differentiation mechanisms. Availability and ImplementationcollectNET is freely available at http://health.tsinghua.edu.cn/collectnet. Contactruijiang@tsinghua.edu.cn Supplementary informationSupplementary data are available at Bioinformatics online.

genomics↗

ERNIE-RNA: An RNA Language Model with Structure-enhanced Representations

With large amounts of unlabeled RNA sequences data produced by high-throughput sequencing technologies, pre-trained RNA language models have been developed to estimate semantic space of RNA molecules, which facilities the understanding of grammar of RNA language. However, existing RNA language models overlook the impact of structure when modeling the RNA semantic space, resulting in incomplete feature extraction and suboptimal performance across various downstream tasks. In this study, we developed a RNA pre-trained language model named ERNIE-RNA (Enhanced Representations with base-pairing restriction for RNA modeling) based on a modified BERT (Bidirectional Encoder Representations from Transformers) by incorporating base-pairing restriction with no MSA (Multiple Sequence Alignment) information. We found that the attention maps from ERNIE-RNA with no fine-tuning are able to capture RNA structure in the zero-shot experiment more precisely than conventional methods such as fine-tuned RNAfold and RNAstructure, suggesting that the ERNIE-RNA can provide comprehensive RNA structural representations. Furthermore, ERNIE-RNA achieved SOTA (state-of-the-art) performance after fine-tuning for various downstream tasks, including RNA structural and functional predictions. In summary, our ERNIE-RNA model provides general features which can be widely and effectively applied in various subsequent research tasks. Our results indicate that introducing key knowledge-based prior information in the BERT framework may be a useful strategy to enhance the performance of other language models.

bioinformatics↗