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Biology subjects

Zeng, Y.

Publications and source records attributed to Zeng, Y..

At least 37 records · Page 2Linked to original sources

Instantaneous Beta Frequency Regulates Self-Generated Timing in Humans

Self-generated timing requires the brain to determine when to terminate an ongoing action without reference to external cues. Although beta-band oscillations have been implicated in temporal control, how their intrinsic dynamics shape moment-to-moment variability in internally generated time remains unclear. Here, combining scalp EEG with intracranial recordings in humans, we show that the instantaneous frequency of beta oscillations (13-30 Hz) provides a dynamic control signal for self-generated timing. During a self-paced time production task, higher instantaneous beta frequency reliably predicted longer produced durations, both within individuals on a trial-by-trial basis and across individuals. This relationship was beta-specific, frontoparietally distributed, robust to motor and spectral confounds, and validated by convergent intracranial recordings. These findings run counter to classical pacemaker-accumulator models and instead establish beta-frequency dynamics as a mechanism that delays action termination by increasing the density of intrinsic stabilizing control updates during self-generated timing.

neuroscience↗

Massive-scale single-nucleus multi-omics identifies novel rare noncoding drivers of Parkinson's disease

Most genetic variants contributing to complex diseases reside in the noncoding genome. While common variants uncovered by genome-wide association studies often fail to explain much of the observed heritability of these diseases, rare variants often have higher effect sizes and cumulatively explain a larger portion of heritability. However, rare variants, particularly rare noncoding variants, have remained under-characterized largely due to the difficulties of accurately predicting variant functionality at scale, given that each individual carries an average of [~]10,000 rare variants. Here, we generated multi-omic data from >3.3 million nuclei sampled from five brain regions across a cohort of 80 individuals with Parkinsons disease (PD) and 21 neurologically normal control individuals with matched 30x whole-genome sequencing. We use this data to identify cell type-specific features of PD, map cell type-specific chromatin accessibility and expression quantitative trait loci, and train machine learning models to predict the effect of variants on gene regulation. We identify rare noncoding variants statistically associated with sporadic PD and extend our approaches to predict drivers of familial PD of unknown genetic origin. Our results underscore the significance of rare noncoding variants in complex diseases and provide a roadmap for applying similar approaches in other disease systems.

genetics↗

Metformin Stabilizes the Abdominal Aorta in Aneurysm by Restoring VSMC Mitochondrial Homeostasis via the AMPK-SIRT1-PGC-1α Axis

BACKGROUNDAbdominal aortic aneurysm (AAA) is a life-threatening condition with >80% mortality upon rupture and no effective pharmacotherapy available. Despite epidemiological evidence linking metformin use to reduced AAA progression, its mechanism remains elusive. Notably, peroxisome proliferator-activated receptor {gamma} coactivator 1 (PGC-1, encoded by Ppargc1a) is downregulated in human AAA, yet its functional role in metformins protection is unknown. METHODSWe employed porcine pancreatic elastase (PPE)-induced murine AAA, VSMC-specific Ppargc1a knockout (Ppargc1aVSMC-KO), primary VSMC senescence models, and pharmacological inhibition (Compound C for AMPK; Ex-527 for SIRT1) to define the AMPK-SIRT1-PGC-1 axis. RESULTSMetformin significantly inhibited AAA expansion, suppressed VSMC senescence (p53/p21{downarrow}, SA-{beta}-gal{downarrow}), and preserved contractile phenotype (SMTN{uparrow}, IL-6/TNF-{downarrow}). Crucially, all benefits were abrogated in Ppargc1aVSMC-KO mice, which exhibited accelerated aneurysm growth, mitochondrial fragmentation, ATP depletion, and ROS accumulation. Mechanistically, metformin activated AMPK/SIRT1 to upregulate PGC-1; AMPK or SIRT1 inhibition blocked this cascade and reversed protection. CONCLUSIONMetformin restrains AAA by restoring VSMC mitochondrial homeostasis via the AMPK/SIRT1[->]PGC-1 axis, positioning PGC-1 as a non-redundant, cell-autonomous guardian against vascular degeneration. These findings provide a mechanistic foundation for repurposing metformin and developing PGC-1-targeted therapies in AAA.

cell biology↗

GRAVITY: Dynamic gene regulatory network-enhanced RNA velocity modeling for trajectory inference and biological discovery

RNA velocity techniques have emerged as efficient tools for unraveling the complex trajectories of cell development and differentiation. However, most of existing RNA velocity approaches are constrained by estimating transcriptional parameters for each gene in isolation and neglects the regulatory relationships among genes, which limits the ability to jointly resolve the dynamic rewiring of gene regulation and the underlying gene transcriptional kinetics across cell state transitions. To address these limitations, we present GRAVITY, a novel deep learning framework that explicitly integrates regulatory dynamics into transcriptional kinetics inference and utilizes a refined two-stage optimization strategy. Benchmarking across various simulated and real single-cell RNA sequencing datasets demonstrates that GRAVITY accurately infers both cellular and gene trajectories, along with their associated kinetic parameters. Most importantly, GRAVITY uncovers terminal cell states L5/L6 in embryonic brain development dataset. Furthermore, GRAVITY not only provides mechanistic insights by identifying the driver regulatory factors and modules governing cell fate, but also enables the systematic in silico simulation of cellular velocity changes induced by targeted regulatory perturbations.

bioinformatics↗

Single-Cell Multi-Omics Insights into BMI-Mediated Immune-Related Disease Risk

This study is based on the Chinese Immune Multi-Omics Atlas (CIMA) cohort and performs an integrated single-cell multi-omics analysis of peripheral blood mononuclear cells (PBMCs) from 210 individuals aged 20-29, comprising 3,311,699 scRNA-seq cells and 1,839,860 scATAC-seq cells, to decipher immune characteristics across different body mass index (BMI) categories. By integrating gene regulatory network (GRN) and cell type-level molecular quantitative trait loci (xQTL) data, and conducting summary-data-based Mendelian randomization (SMR) analysis in conjunction with genome-wide association studies (GWAS) of BMI-mediated immune-related diseases, we identified key disease-associated cell types and molecular features. Using rheumatoid arthritis (RA) as an example, multi-omics evidence revealed that in MAIT-SLC4A10 cells of underweight individuals, increased chromatin accessibility at the CCR6 locus (chr6:167119627-167120128) and enhanced transcriptional activity of RORC/RORA collectively drive elevated CCR6 expression, which may represent a potential molecular mechanism underlying the higher risk of RA in underweight populations. Our study leverages single-cell multi-omics data to systematically dissect the molecular mechanisms by which different BMI categories mediate susceptibility to immune-related diseases through coordinated regulation of immune cell chromatin accessibility, transcription factor activity, and downstream gene expression.

bioinformatics↗

Dual-mode ClfA-targeting DARPin biologics protect against diverse methicillin-resistant Staphylococcus aureus strains

Staphylococcus aureus uses the adhesin clumping factor A (ClfA) to bind fibrinogen and promote invasive infection through two distinct interfaces: an exposed, low-afinity site on the N3 head domain and a buried, high-afinity "dock, lock, and latch" (DLL) trench that is exposed only under shear. This dual-interface architecture allows limited antibody penetration, as antibodies typically block only the exposed site. Here, we establish a dual-mode inhibition strategy that overcomes this constraint by combining a high-afinity ClfA-binding designed ankyrin repeat protein (DARPin) with a fibrinogen {gamma}-chain peptide capable of occupying the DLL trench. Using cell-free click display and kinetics-guided afinity maturation, we engineer DARPin-{gamma}-peptide fusion biologics that simultaneously block both fibrinogen-binding interfaces. These molecules inhibit ClfA-fibrinogen interactions, prevent methicillin-resistant S. aureus agglutination in human plasma, neutralize major clinical ClfA variants, and confer Fc-independent protection in a lethal murine bacteremia model. This work provides a strategy for targeting antibody-intractable force-activated staphylococcal adhesins.

molecular biology↗

Parthenogenote-Derived Brain Unveils the Critical Role of Paternal Genome in Neural Development

Genomic imprinting, an epigenetic mechanism that governs parent-of-origin-specific gene expression, is essential for mammalian development, yet its role in late-stage development remains unclear due to the lethality of parthenogenetic (Pg) embryos. Here, we establish cell replacement with parthenogenote-derived cells (CReP), a blastocyst complementation strategy that enables survival and tissue-specific contribution of Pg-derived cells. Brain-targeted CReP showed that Pg-derived cells can participate in neural development but fail to maintain neuronal-glial balance due to aberrant activation of Notch signaling caused by the loss of the paternally expressed gene Dlk1. Restoration of Dlk1 normalized Notch activity and rescued neuronal differentiation. These findings reveal a critical role of the paternal genome, through Dlk1-mediated regulation of Notch signaling, in ensuring neural stem cell expansion and balanced cell fate decisions. The CReP model provides a powerful platform for investigating genomic imprinting and parental genome contributions in development and disease.

developmental biology↗

PPARgene 2.0: leveraging large language models and multi-omics data for enhanced identification and prediction of PPAR target genes

Peroxisome proliferator-activated receptors (PPARs) are ligand-activated transcription factors of the nuclear receptor superfamily. Upon ligand binding, PPARs activate target gene transcription and regulate a variety of important physiological processes such as lipid metabolism, inflammation, wound healing and immune responses. PPARgene is a database that integrates literature-curated and computationally predicted PPAR target genes. It provides gene-level annotations including tissue specificity, species, and supporting PubMed IDs. Computational predictions are generated using a machine learning method that combines PPRE motif analysis with microarray expression data. Here, we introduce PPARgene 2.0, a 10-year update to the original PPARgene database. This update adds 35 newly reported PPAR target genes, 20 PPAR{beta}/{delta} target genes, and 72 PPAR{gamma} target genes, bringing the total number of curated target genes in the database to 337. To retrieve newly reported PPAR target genes from the literature, we used two language models to screen publications after 2016. Candidate papers were then manually reviewed, and verified target genes were added to the updated database. This update also improved the predictive method by expanding the volume of high-throughput gene expression data and incorporating PPAR-related ChIP-seq datasets alongside in silico PPRE analysis. Fivefold cross-validation demonstrated that the new predictive method outperforms the original one. The updated prediction tool is available as part of the PPARgene 2.0 platform. The database is openly accessible at https://www.ppargene.org.

bioinformatics↗

Dynamic brain states during encoding and their post-encoding reinstatement predicts episodic memory in children

Episodic memory, the ability to rapidly learn and explicitly remember past events and experiences, plays a critical role in childrens academic learning and knowledge acquisition. The formation of lasting memories relies on the brains ability to dynamically organize its activity. How these neural configurations unfold moment-by-moment across encoding and offline phases remains poorly understood. To probe these dynamics, we applied a novel Bayesian Switching Dynamic Systems approach, a hidden Markov model with automatic state detection, to fMRI data from children performing scene encoding followed by an offline post-encoding rest. We identified four distinct brain states during encoding with unique activation modes between visual, medial temporal lobe, and frontoparietal and default mode network nodes. An "active-encoding" state with integrated visual-hippocampal and frontoparietal activity dominated encoding and predicted individual memory performance, while an inactive state negatively predicted performance. State transition dynamics revealed that flexible shifts into the active-encoding state enhanced memory formation, whereas transitions toward inactive states impaired it, demonstrating that memory success depends on dynamic neural flexibility. Critically, encoding states spontaneously reemerged during post-encoding rest. A "default-mode" state characterized by enhanced default mode network activity showed sustained maintenance during rest and robustly predicted memory outcomes, an effect specific to post-encoding, not pre-encoding rest. These findings establish that episodic memory emerges from coordinated brain state sequences bridging online encoding with offline consolidation, providing a computational framework for how moment-to-moment neural dynamics support memory formation in children. This work has broad implications for optimizing educational interventions and understanding developmental disorders affecting learning and memory.

neuroscience↗

High-throughput discovery of a dearomative cycloaddition enables dual photochemical-photophysical perturbative probing of protein function

Proteins exist in multiple conformations or states, often associated with different functional capacities. The ability to selectively identify and study these states is crucial for understanding the dynamic nature of proteins and their roles in cellular processes, yet can be currently limited by the artefacts of existing molecular labels and the lack of strategies to exploit them in diverse ways. Whilst i) methods for the photochemical perturbation of proteins and ii) photophysical protein probes and sensors are both known powerful tools, simultaneous methods for site- and context-specific photochemical modification of a protein side chain with concomitant modulation of photophysical properties would allow interrogation of protein function via diverse modes (potentially reporting simultaneously on structure and dynamics of ground- and reactive-state properties). Due to their mechanistic complexity, rational approaches for the design of suitable photochemical strategies can be difficult and non-intuitive. Here, we describe a high-throughput experimentation (HTE) strategy designed to allow the photochemical modification of a genetically-encoded, minimally disruptive ( zero-size), photophysically-active - yet typically unreactive and biologically-inert - unnatural amino acid (uAA) residue in proteins. The discovery of a novel dearomative, formal [4+3] photocycloaddition of imidazopyrimidine reagents which proceeds via photochemically generated C* intermediates with polyaromatic substrates enabled chemoselective application to the normally unreactive Trp-mimetic residue, 2-naphthylalanine (Npa). Npas site-selective installation allows dual photochemical and photophysical dearomative perturbation benignly and efficiently in proteins. Replacement of Trp in the archetypal apoptotic biosensor protein Annexin A5 (AnxV) enabled dual photochemical-photophysical determination of switched, conformationally-determined reactive states induced by Ca2+-binding, without any apparent functional perturbation of its in vitro or cellular recognition of phospholipids, indicating an ordered annexin mechanism. This ready and benign unification of photochemistry and photophysics suggests a general approach for using high-throughput light-mediated experimentation in artefact-free chemical biology to capture different functional states of proteins and to interrogate those states using combined photochemical-photophysical methods. HighlightsO_LIDevelopment of a general, high-throughput experimentation (HTE) approach enabled identification of an unprecedented photochemical reaction with potential for editing amino acid side chains within proteins. C_LIO_LIGenetic incorporation of 2-naphthylalanine, a minimally-disruptive ( zero-size) Trp mimic, enabled photochemical side chain editing with concomitant modulation of its distinctive photophysical properties in proteins. C_LIO_LIA naphthalene-tagged variant of the apoptotic biomarker protein AnxV enabled dual photochemical-photophysical exploration of its dynamic conformational states induced by Ca2+-binding whilst fully maintaining its functional capacity for in vitro or cellular recognition of phospholipids. C_LI

biochemistry↗

Transplantation of active mitochondria condensed in liquid-liquid phase-separated hydrogels ameliorates myocardial ischemia-reperfusion injury

Mitochondrial dysfunction is a key driver of myocardial ischemia-reperfusion injury (MIRI), which exacerbates cardiac damage following the restoration of blood flow. Although single-phase hydrogel-based mitochondria transplantation therapy (MTT) holds promise for restoring cellular energy metabolism, its effectiveness is limited by extracellular calcium-induced mitochondrial degradation. In this study, we design a thermo-sensitive hydrogel utilizing liquid-liquid phase separation (LLPS), composed of gelatin and polyethylene glycol (PEG), to condense freshly isolated mitochondria. Compared to conventional single-phase hydrogels, the LLPS hydrogel significantly increases the sol-gel transition temperature above physiological levels, allowing it to remain injectable at body temperature while enabling rapid mitochondrial release following transplantation. More importantly, the LLPS structure enhances mitochondrial packing density and protects the activity of condensed mitochondria against calcium toxicity through spatial confinement and gelatin-mediated calcium chelation. In vitro, LLPS hydrogel-condensed mitochondria exhibit improved mitochondrial membrane potential and ATP production ability compared to those delivered via single-phase gelatin hydrogel. In vivo, mitochondria released from the LLPS hydrogel are effectively internalized by cardiomyocytes, resulting in improved cardiac function and reduced tissue damage after MIRI. These findings suggest that LLPS-based hydrogels offer a promising strategy to enhance MTT efficacy for MIRI and other mitochondria-related disorders.

bioengineering↗

Single-cell transcriptomic profiling of bam mutant tumor reveals germline heterogeneity and gcrf1 as a modulator in Drosophila germ cells

The bam mutant ovary of Drosophila represents a classic tumor model caused by germline stem cell (GSC) differentiation defects. To date, its molecular and genetic features have rarely been characterized in detail at the single-cell resolution. Here, we performed single-cell RNA sequencing (scRNA-seq) to comprehensively delineate the transcriptomic landscape and identify distinct germline cell types in bam mutant ovaries by using in situ hybridization. Differentially expressed gene analysis and PAGA plots reveal different transcriptional profiles and developmental relationships in ovarian cells. Based on the expression pattern of eggpl, a useful marker for undifferentiated germ cell identity, and morphological differences in bam mutant ovarioles, two potentially distinct germ cell states are distinguished. Comparative single-cell analysis reveals the potential regulatory network and cellular communication in subclusters of undifferentiated germ cells, and contributes to the identification of gcrf1 as a novel marker gene for female GSC, which involves in the regulation of early germ cell proliferation and Drosophila fertility. Collectively, our study not only provides insights into tumorigenesis caused by GSC differentiation defects but also offers a valuable transcriptomic resource that can be mined for the reproductive features of bam mutant tumors by community.

developmental biology↗

From Home to Transcriptome: Comparing the transcriptomic profile of induced immune response via lipopolysaccharide stimulation in homeRNA and venous blood

Remote blood sampling offers multiple advantages over traditional clinic-based blood sampling studies, including greater patient inclusion, more frequent sampling, and broader geographical reach. Combining remote blood sampling with transcriptomic analysis opens potential in translational applications for capturing acute and dynamic immune responses to various exposures. In this study, we establish the feasibility of homeRNA, a capillary blood collection and RNAlater-based stabilization kit, for use in downstream bulk RNA-sequencing applications via capturing a lipopolysaccharide (LPS)-induced inflammatory response. We also compared the baseline gene expression profiles and induced inflammatory response following LPS stimulation between homeRNA-stabilized samples and venous blood stabilized with RNAlater or PAXgene. We found that homeRNA was successfully able to capture an inflammatory response to LPS, specifically targeting various cytokines (e.g., IL6, IL12B, IL1B), chemokines (e.g., CCL3, CXCL10, CCL4), and other transcriptional factors in the toll-like receptor pathway, the primary pathway activated during LPS stimulation. Importantly, we also found that homeRNA captured a LPS-induced inflammatory response comparable to that of venous blood samples stabilized with either RNAlater or PAXgene. Overall, this work demonstrates that the homeRNA platform is compatible with downstream bulk RNA-sequencing analysis and can capture transcriptomic immune responses to a known stimulus which are analogous to results in traditional stabilized venous blood samples.

bioengineering↗

An Implementation Intention Combining Reappraisal and Anger Counteraction Reduces Fear Reinstatement

Fear extinction requires exposure to the conditioned stimulus (CS), yet patients with fear- and anxiety-related disorders often avoid the CS, thereby undermining extinction learning. Implementation intention (II) is a self-regulation strategy that automates goal-directed behavior through "if-then" planning. Building on the approach motivation elicited by anger and the principle of emotion-action incompatibility, we designed a novel II: "If I feel afraid when seeing fish/bird images (the CSs), then I will remind myself that it is foolish to fear a mere picture, and I will clench my fists and feel angry with myself." This strategy aims to transform fear-driven avoidance into self-directed anger, thereby promoting reappraisal and approach behavior. In a three-day differential fear conditioning paradigm, participants who practiced this II during extinction exhibited shorter avoidance distances to the CS+ than the standard-extinction control group. On Day 3, reinstatement testing revealed significantly lower subjective fear, anger, threat expectancy, and avoidance in the II group. These findings suggest that the combined reappraisal-plus-anger II requires practice during extinction to effectively reduce fear return without inducing overt aggression, offering a promising direction for optimizing exposure-based therapies.

animal behavior and cognition↗

TE-like DNA methylation of highly expressed endosperm genes in maize

Unlike the stable transcription of plant genes with CG gene body methylation alone, genes with methylation in TE-like CHG and CG contexts are poorly transcribed and often missanotated. In contrast, here we describe a set of TE-like methylated genes that are maternally demethylated and expressed toward the extreme high end of the spectrum in endosperm. They are enriched for short, secreted proteins, and about a third encode zeins, the major seed storage proteins of maize. Consistent with their dynamic expression in endosperm, they acquire either activating or repressive gene regulatory modifications when demethylated but are heterochromatic when methylated in other tissues. The majority are expressed both maternally and paternally, but a subset whose methylation/demethylation extends upstream of gene bodies into promoters are strongly imprinted. These and other data indicate that TE-like methylation and associated heterochromatin can be a signature of broad silencing but exceptionally high and specific gene expression in either pollen or endosperm.

molecular biology↗

Water body size shapes body size evolution via subgenomic selection in allopolyploid fish

Allopolyploidization is a major force in species evolution, and studying allopolyploids in diverse environments provides insights into their genetic mechanisms. Here, we investigated how water body size variation influences body size in allopolyploid fish. We used a nascent allopolyploid lineage derived from goldfish (Carassius auratus) and common carp (Cyprinus carpio) and established two populations in small and large water bodies for two generations. Genomic, transcriptomic, and epigenomic analyses revealed that the larger population had higher genetic diversity in subgenome R, while the smaller population had higher diversity in subgenome C. Potential selection regions were associated with growth regulatory genes, suggesting a role for gene regulation in body size adaptation. Dynamic gene expression patterns in various tissues indicated potential mechanisms underlying muscle development and adaptation to smaller water bodies. Furthermore, selection regions were linked to changes in chromatin accessibility, with subgenome R being more susceptible to these changes during genetic divergence. Our findings demonstrate that water body size variation drives body size in allopolyploid fish through subgenomic selection, impacting genetic variation, gene regulation, and epigenetic mechanisms.

genomics↗

Restricted Retrieval Enhances Extinction Memory Generalization across Time and Context

During traditional extinction, the conditioned stimulus (CS) activates both the original fear memory and the newly formed extinction memory. Because fear memory is typically more robust, it interferes with the encoding, consolidation, and retrieval of extinction memory, resulting in a fragile and transient safety trace. Consequently, fear often returns after extinction. This pilot study examined whether repeated retrieval practice of the most recent nonreinforced CS during extinction could strengthen extinction memory and reduce fear relapse. Thirty-nine participants completed a four-day paradigm comprising fear acquisition (60% reinforcement rate), two extinction sessions, and a fear renewal test. The two groups (experimental vs. control) differed only during the extinction phase. Specifically, the experimental group received training identical to that of the Ctrl group during the first two and last two trials of the first extinction session, and the first and last two trials of the second session (for each CS type). During the intermediate trials, the experimental group recalled whether the preceding CS+/CS- trial was safe and then predicted the outcome of the current trial accordingly. Conditioned responses were assessed using skin conductance responses and subjective assessments (US expectancy, valence, and arousal). Both behavioral and physiological indices consistently suggested that restricted retrieval practice during extinction improved extinction memory retention and attenuated fear renewal. These findings suggest the potential benefits of incorporating restricted retrieval practice into extinction-based interventions to improve their long-term efficacy.

animal behavior and cognition↗

A Benchmark of Evo2 Genomic AI Models for Efficient and Practical Deployment

The rapid advancement of DNA foundation language models has brought about a transformative shift in genomics, allowing for the deciphering of intricate patterns and regulatory mechanisms embedded within DNA sequences. The genomic foundation model Evo2 demonstrates remarkable capabilities in decoding DNA functional patterns through cross-species pretraining. However, despite the great potential of Evo2 in basic genomics research, there is currently no clear and systematic guidance on its specific application scenarios, performance, and optimization directions in the field of tumor genomics, and its performance dependency on specialized hardware (such as FP8 precision on H800 GPUs) has not been empirically benchmarked. Here, we present a focused validation of Evo2 using two independent cancer genomic datasets (Bladder Urothelial Carcinoma and Ovarian Cancer), we tested the downstream tasks of Evo2, including the prediction of tumor pathogenic variants and the prediction of mutational effects, and compared its performance on A100 and H800 GPUs. The results show that critical importance of FP8 precision, enabling the H800 to achieve a 4x faster inference speed than the A100 with stable accuracy (AUC 0.88-0.95). The 7B-parameter model emerged as the top performer, whereas the 40B model experienced a severe performance drop (AUC to 0.48) on non-FP8 hardware like the A100. These findings empirically validated Evo2s hardware specifications and provided practical insights for researchers implementing the model with similar computational resources. Futhermore, our findings provide a framework for the application and optimization of downstream tasks of the DNA language model Evo2 in cancer, and can guide researchers in effectively applying it in genomic studies. Key PointsO_LIHardware Precision Impact: FP8 precision on H800 GPUs is critical for Evo 2s performance, enabling 4x faster inference than A100 (without FP8 support) while maintaining high accuracy (AUC 0.88-0.95). C_LIO_LIModel Scale Optimization: The 7B-parameter model outperformed larger variants (e.g., 40B), which suffered severe accuracy drops (AUC as low as 0.48) on non-FP8 hardware, highlighting a balance between efficiency and performance. C_LIO_LIPractical Guidelines: We provide a framework for deploying Evo 2 in cancer genomics, including hardware recommendations, dataset curation, and downstream task optimization--valuable for researchers with varied computational resources. C_LI

genomics↗