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Kumar, S.

Publications and source records attributed to Kumar, S..

At least 19 recordsLinked to original sources

A statistical framework for system-level synthesis

Simultaneous profiling of thousands of biological features is now routine. Yet transforming the data into interpretable models of system behavior remains a fundamental bottleneck as current analyses generally identify feature-wise associations or extract latent structure without anchoring it to the variables that define the scientific question. Here we propose a framework for system-level synthesis that learns and predicts overarching processes, and reliably identifies participating features without data reuse. We develop Smoothing Spline Analysis of Variance-Singular Value Decomposition to learn overarching processes as smooth, flexible functions of nominal, ordinal and continuous covariates and their interactions. This unlocks prediction from covariates alone, while reserving measurements for conditional inference of feature participation. In applications, the framework recovered established biology while generating predictions and testable hypotheses. By linking high-dimensional variation to covariates, the framework advances analysis beyond feature-wise associations and unsupervised patterns, toward interpretable system-level models that vary with biological and experimental context.

systems biology↗

PGC-1α Links Estrogen Receptor Signaling to Japanese Encephalitis Virus Replication in Neuronal cell

Acute encephalitis due to the viral causative agents, such as Japanese Encephalitis Virus (JEV), remains a leading cause of viral encephalitis in Asia, contributing to high mortality and long-term neurological sequelae. The host factors that modulate JEV replication are not well understood. In this study, we investigated the modulation of JEV infection by estrogen in vitro and in vivo. The results demonstrated that estrogen enhances JEV replication in neuronal cells via estrogen receptor alpha (ER) by modulating peroxisome proliferator-activated receptor gamma coactivator-1 alpha (PGC-1). Since JEV pathogenesis increases cellular production demands, it results in dysregulation of cellular homeostasis, whereas estrogen treatment helps keep cellular health in check. Also, the mouse model exhibited an increased viral burden with protective antibody titers in response to estrogen. Conclusively, this work highlights the mechanistic link of estrogen-driven mechanisms and identifies the ER-PGC-1-axis as a potential target for sex-specific therapeutic interventions.

microbiology↗

Prenatal immune priming to Plasmodium falciparum is characterized by multi-lineage T-cell responses that are influenced by maternal microchimerism and predict malaria outcomes

In malaria endemic settings, the fetus may be exposed to Plasmodium falciparum (Pf) antigens leading to prenatal immune primming (PIP). The fetus also acquires a graft of maternal cells in utero, a phenomenon known as maternal microchimerism (MMc). We have previously identified that MMc at birth predicts altered malaria susceptibility in early childhood, and we hypothesized that this association may be mediated via two potential mechanisms. First, the fetus may acquire Pf-specific MMc T-cells that directly respond to postnatal parasitemia. Alternatively, MMc may indirectly influence the quantity or quality of PIP. To investigate this hypothesis, infant cord bloods from 97 Malian primigravidae were screened for MMc using qPCR. A subset of ten cord blood mononuclear cells with variable MMc levels were stimulated with purified Pf merozoite extract and activated T-cells were sorted by flow cytometry for scRNAseq analysis. Transcriptional profile was used to differentiate Pf-responsive versus bystander activated T-cells, and MMc cells were identified using the Cellector algorithm. Among Pf-responsive cells, we identified four key populations: activated CD4 T-cells, ZBTB16+ CD4 T-cells, activated V{delta}1+ {gamma}{delta} T-cells, and cytotoxic V{gamma}9V{delta}2+ {gamma}{delta} T-cells. The minority of sorted cells were of MMc origin; however, there was a strong association between the presence of MMc and the quantity and quality of PIP. MMc+ infants had significantly fewer Pf-responsive T-cells, as well as a shifted distribution of these cells with fewer ZBTB16+ CD4 and cytotoxic V{gamma}9V{delta}2+ {gamma}{delta} T-cells. Clinically, MMc was protective from incident parasitemia and febrile malaria, whereas the frequencies of ZBTB16+ CD4 and activated CD4 T-cells were associated with increased risk. Together, these data demonstrate that MMc influences malaria outcomes through regulation of offspring inflammatory responses to Pf.

immunology↗

Adaptive co-transmission shapes sensory encoding and behavior

Co-transmission expands the chemical repertoire of neurons, but whether coexisting neurotransmitters can be independently organized and remodeled by experience to control distinct aspects of behavior remains unclear. Here, we address this question in the AFD thermosensory neuron of Caenorhabditis elegans, which directs navigation toward a learned temperature preference. We find that glutamatergic and cholinergic vesicular transporters coexist within individual presynaptic boutons but differ in axonal trafficking, subsynaptic organization, and dependence on presynaptic machinery. Sensory experience differentially regulates the two systems: animals trained to prefer higher temperatures exhibit increased VGLUT/EAT-4 abundance, whereas those trained to prefer lower temperatures exhibit increased VAChT/UNC-17 abundance. The two transmitters also make distinct, context-dependent contributions to goal-directed navigation. Glutamatergic transmission promotes movement toward the learned thermal preference, whereas cholinergic transmission restrains continued migration beyond it. Analysis of locomotor trajectories further reveals that the two transmitters differentially regulate reorientation decisions across regions of the thermal gradient. Together, these findings identify adaptive co-transmission, a form of synaptic plasticity in which coexisting neurotransmitter systems are differentially organized and regulated by experience, and make distinct, context-dependent contributions to behavior.

neuroscience↗

High-yield expression and purification of the non-phosphorylated form of Human CaMKIIα Kinase

Human Ca2+/calmodulin (CaM)-dependent protein kinase II alpha (CaMKII) is a highly abundant and conserved protein in the brain. It is a multifunctional serine/threonine kinase that phosphorylates cellular substrates across subcellular compartments, activating signaling pathways essential for long-term memory storage. However, a detailed understanding of protein structure and enzyme-substrate interaction mechanisms require a method to produce active, stable, and pure proteins at scale. Since phosphorylation can alter catalytic activity and substrate affinity, examining the non-phosphorylated state enables an unbiased characterization of basal enzymatic function. Therefore, producing the non-phosphorylated form of the kinase is important for biochemical and structural studies aimed at understanding kinase activation mechanisms. We describe a detailed protocol for the expression and high-yield purification of full-length, non-phosphorylated human CaMKII in bacterial cells. CaMKII was co-expressed with {lambda}-phosphatase to maintain it in a non-phosphorylated state. Protein expression was induced by autoinduction at low temperature to enhance the stability and solubility of CaMKII. Recombinant CaMKII was purified by Ni-NTA affinity chromatography, followed by gel filtration chromatography. Although CaMKII has been considered difficult to purify in its non-phosphorylated form, we obtained it in high yield, and the protein was predominantly non-phosphorylated. Our results show that combining co-expression with autoinduction improves both the solubility and yield of the homogeneous non-phosphorylated form of CaMKII, which could be suitable for subsequent biochemical and structural studies.

biochemistry↗

Distinct sequence grammars of nucleosomal and linker DNA shape mutational and methylation landscapes in cancer

Nucleosomes regulate DNA accessibility and thereby influence gene expression, DNA repair, and mutagenesis. Although DNA sequence strongly determines nucleosome positioning, the higher-order sequence grammar underlying nucleosome organization and its relationship to cancer-associated mutational and epigenetic processes remain poorly understood. We developed DeepND, an interpretable deep learning framework that distinguishes nucleosomal from inter-nucleosomal DNA and identifies sequence features associated with nucleosome architecture. Our interpretable framework enabled analysis of sequence patterns and identified 210 sequence motifs of 2-16 bp length that were significantly enriched or depleted in nucleosomal DNA, substantially extending the previously characterized nucleosomal motifs. These motifs revealed distinct sequence grammars within nucleosomal footprints and linker regions, including patterns associated with inward- and outward-facing minor grooves. Forty-four of these motifs showed cancer-type-specific enrichment or depletion of somatic mutations, and six motifs were associated with differential DNA methylation levels. In lung and endometrial cancers, mutations exhibited a significant ~10-bp periodic enrichment pattern across distinct minor-groove orientations, consistent with differential sensitivity of mutational and DNA repair processes to nucleosomal rotational positioning. We further identified sequence-specific methylation patterns consistent with reduced accessibility of nucleosomal DNA to DNA methyltransferases, including differential methylation at inward- and outward-facing CpG motifs. Together, these findings provide a sequence-resolved characterization of nucleosome-level organization and its link to cancer-specific mutational processes and epigenetic landscapes.

genomics↗

Association between breeding-habitat bacterial communities and oviposition behavior of Aedes aegypti: Insights from arboviral outbreak-affected areas of Pune, Western India

Aedes aegypti, an important vector of several arboviral diseases, is highly adapted to human-associated environments and commonly exploits anthropogenic water-holding containers for breeding. Understanding the ecological factors governing oviposition-site selection is essential for developing sustainable vector control strategies. Previous studies have established that microbial communities in breeding waters influence mosquito oviposition-site selection through the production of volatile organic compounds. Importantly, rapid urbanization in India has increased the availability of artificial breeding habitats for Ae. aegypti, potentially facilitating the transmission and persistence of arboviral diseases. However, the composition of bacterial communities in these larval habitats and their potential role in shaping the oviposition behavior of Ae. aegypti remain poorly characterized in the Indian context. Here, we investigated the bacterial diversity and community composition of Aedes larval habitats during the 2024 Zika and chikungunya outbreaks in Pune, India. Water samples, collected from artificial urban containers and natural freshwater habitats, were subjected to 16S rRNA amplicon sequencing. Artificial breeding habitats exhibited significantly higher bacterial diversity and were enriched with Enterobacter spp. compared with natural habitats. Oviposition bioassays further demonstrated a strong preference of gravid Ae. aegypti females for Enterobacter-conditioned water. GCMS analysis of bacterial suspension identified indole as a prominent volatile metabolite associated with Enterobacter, suggesting its possible role in mediating oviposition site selection. Together, these findings provide insights into the microbial and chemical ecology of Ae. aegypti breeding habitats and establish a basis for investigating microbial volatile cues as potential targets for vector surveillance and environmentally sustainable attract-and-kill strategies.

genomics↗

Rewiring systemic nodulation control to engineer heat-tolerant nitrogen fixation in Medicago truncatula and chickpea

Root nodule symbiosis allows legumes to meet their nitrogen requirements. However, the causes of symbiosis failure at high temperatures remain unknown. We demonstrated that elevated temperatures affect both the host and the microbial partner in Medicago truncatula and chickpea. Rhizobial viability and nod gene expression persisted under heat stress, but plant transcriptome analysis revealed a strong downregulation of the nodule organogenesis machinery. Nodule organogenesis was restored by constitutive overexpression of NIN-LBD16-NFYA1-NFYB16, miR2111, and CLE5 knockdown but failed to restore nitrogen fixation. In contrast, the genetic manipulation of the competence pathway involving CEP peptides significantly improved both nodulation and nitrogen fixation. Constitutive loss of the autoregulation of nodulation (AON) pathway in the SUNN alleles also rescued root nodulation and nitrogen fixation. Therefore, heat stress perturbs the balance between AON and the competence pathway, and genetic manipulation of these pathways is a promising approach to engineer thermotolerant nitrogen fixation in crop legumes.

plant biology↗

Distinct Longitudinal Antibody Responses Following Primary Influenza Infection or Vaccination in Infants: A Prospective Birth Cohort Study

The longitudinal effects of initial influenza exposure on the magnitude, persistence, and antigen specificity of antibody responses during infancy remain incompletely understood. We investigated humoral antibody responses following primary influenza infection or seasonal vaccination in a prospective US birth cohort with weekly respiratory surveillance for influenza infection. Influenza-specific serum IgG binding to H1 and H3 haemagglutinin (HA) antigens, HA inhibition (HAI), and live-virus neutralizing antibody responses were assessed longitudinally. To minimize influence of maternally derived antibodies, analyses of primary exposure responses were restricted to infants for whom influenza-specific maternal antibodies had declined below the assay detection limit before exposure. Antibody responses were compared following primary infection and vaccination and examined after subsequent annual vaccination. We found that maternal influenza-specific IgG declined rapidly during early infancy. Among infants without detectable pre-exposure influenza-specific antibodies, primary influenza infection was associated with greater post-exposure antibody responses and less measurable decline over follow-up than primary vaccination. These groups differed in age, calendar season, and exposure characteristics, limiting direct attribution of these differences to route of exposure. In infants with previous influenza infection followed by vaccination, responses after subsequent vaccination initially showed greater binding to the previously infecting subtype among the tested HA antigens. With repeated vaccination, responses became more distributed across the tested antigens. Our findings reveal differences in the magnitude, persistence, and antigen specificity of antibody responses according to the nature and sequence of influenza exposure. By prospectively capturing early-life exposures, this study provides longitudinal evidence linking exposure history to subsequent humoral antibody responses.

immunology↗

Sensing the heart, seeing the world: Neural mechanisms of attentional allocation between interoception and exteroception

Adaptive behaviour requires the flexible allocation of attention between sensory information arising from the external environment (exteroception) and signals originating within the body (interoception). While the neural mechanisms supporting exteroceptive attention have been extensively characterised, considerably less is known about how attention is allocated between competing interoceptive and exteroceptive sources of information. To address this question, we used functional magnetic resonance imaging (fMRI) to compare cardiac interoceptive attention during heartbeat counting with a carefully matched visual target counting task. Importantly, external visual input was held constant during both tasks, and behavioural accuracy and subjective confidence ratings for task difficulty did not differ significantly between conditions. This provided a controlled comparison in which attention was selectively allocated between internal bodily signals and external sensory information. Cardiac interoceptive and visual exteroceptive attention engaged largely distinct cortical networks. Cardiac interoceptive attention recruited a distributed insula-centred network supporting interoceptive processing and cognitive control. In contrast, visual target counting engaged a dorsal frontoparietal attention network and selectively shaped activity within visual cortex, enhancing regions representing task-relevant central visual information while suppressing regions representing task-irrelevant peripheral visual information. Despite this functional segregation, activity within these systems was not independent of where attention was directed. Exteroceptive attention suppressed activity within the posterior insula, suggesting down-regulation of interoceptive processing. Conversely, peripheral visual regions remained suppressed during interoceptive attention, suggesting that externally directed sensory processing is also down-regulated when attention is directed towards the body. More accurate heartbeat counting was additionally associated with less engagement of the right inferior parietal lobule, consistent with reduced bottom-up attentional capture by external sensory information. Together, these findings are consistent with competitive allocation of attentional resources between neural systems supporting internal bodily signals and external sensory information. More broadly, they provide a system-level account of how the human brain flexibly balances internal and external information during goal-directed behaviour.

neuroscience↗

Plasma Extracellular Vesicle Lipidomics Reveals an SMPD1-Driven Sphingomyelin Salvage Pathway Collapse in Parkinson's Disease

While lysosomal lipid dysregulation is implicated in Parkinsons disease (PD), identifying the precise enzymatic drivers remains limited by the lack of subcellularly resolved metabolic mapping. Leveraging endosome-origin plasma extracellular vesicle (PsEV) lipidomics, we identified a profound bidirectional disruption of the ceramide-sphingomyelin (SM) axis in PD, driven by asymmetric upregulation of sphingomyelin phosphodiesterase 1 (SMPD1) and sphingomyelin synthase 1 (SGMS1). BODIPY-C5 SM tracking revealed that SMPD1 perturbation severely impairs lysosomal SM turnover. Crucially, this SMPD1-driven hydrolysis forces a salvage pathway collapse, bottlenecked by SPHK1/SGPL1 downregulation, which precipitates oxidative membrane damage and PINK1/Parkin-dependent mitophagy failure. We robustly validated this multi-pathway dysfunction across orthogonal in vitro, in vivo mouse, and postmortem human brain models. Furthermore, SMPD1/SGMS1 expression distinctly stratifies clinical phenotypes, marking the aggressive Postural Instability/Gait Difficulty (PIGD) subtype. Our findings establish SMPD1-mediated lysosomal impairment and ceramide-SM imbalance as a core biochemical axis in PD pathophysiology.

neuroscience↗

Scalable Computational Phenomics of Nuclear Morphology

Interpretable computational pathology is constrained by a trade-off between scalable learned representations and biologically explicit phenotypes. Here we present NucXplore, a nuclear phenomics framework that converts each hematoxylin-and-eosin (H&E)-stained nucleus into 129 explicitly defined features spanning morphology, chromatin, intensity, texture, color, and spatial context. A Rust-based implementation accelerates extraction 17.6-fold over the Python reference implementation. Across three histopathology cohorts, NucXplore outperformed classical descriptors and larger deep-learning embeddings while retaining feature attribution. Applied to human skin, hierarchical multiple-instance models resolved eight cellular compartments and decoded age and sun-exposure states, revealing a largely shared aging program with age and cell-specific exposure-dependent recalibration. Conditional flow matching and neural ODE integration transformed cross-sectional phenotypes into model-implied trajectories, uncovering a midlife velocity minimum, late-life re-acceleration, and cell-specific changes in trajectory magnitude and direction. Source-free domain adaptation enabled preliminary transfer of age-associated predictions to an independent hospital cohort. NucXplore thus unifies interpretable representation, high-performance computing, and dynamical modeling for cellular phenotyping from routine histology.

pathology↗

A Turing-Style Test for In-Silico Antibodies: How Sampling Mode Makes WGAN-GP Beat VAE in the Wet Lab

Recently, it has become feasible to generate antibodies in silico using AI-based approaches such as deep learning, natural language processing, and diffusion models. This opens the door to computational antibody design as a complement to laboratory-based methods (animal immunization, hybridoma technology, and molecular display) for biologic drug discovery. However, when proposing human antibody sequences, or libraries thereof, it remains essential to determine whether they can be expressed, purified, and biophysically characterized using standardized laboratory assays typically applied early in discovery campaigns. In this work, we devised a Turing imitation game inspired experiment to compare two deep learning methods, Generative Adversarial Networks (GANs) and Variational Autoencoders (VAEs), for generating experimentally viable de novo antibody sequences. Under the sampling protocols tested here, a Wasserstein GAN with gradient penalty produced sequences that were experimentally validated at a markedly higher rate (92/93; 99%) than those from a VAE (2/40; 5%). Importantly, the two sets of experimental candidates were not sampled identically: GAN sequences were drawn unconditionally from the trained generator, whereas VAE sequences were generated from latent seeds corresponding to marketed antibodies not seen during training. This methodological asymmetry, rather than model architecture alone, largely accounts for the contrasting outcomes, and when the VAE was instead seeded from its training distribution its in-silico developability profiles were comparable to the GAN's. Our findings highlight both the promise of computationally driven discovery of antibody-based biotherapeutics and the decisive role of sampling strategy in determining experimental success.

bioinformatics↗

Brain-resident myeloid cells promote rapid leukocyte adhesion in leptomeningeal vessels after anti-Aβ immunotherapy

Anti-amyloid {beta} (A{beta}) immunotherapy improves cognitive outcomes in Alzheimer's disease (AD) but is associated with amyloid-related imaging abnormalities (ARIA), through poorly understood mechanisms. To define how anti-A{beta} antibodies acutely engage brain immune and vascular compartments, we developed a longitudinal in vivo two-photon imaging platform to track microglial dynamics, peripheral immune cell recruitment, and vascular responses in APP/PS1 mice. Anti-A{beta} antibodies, including aducanumab and lecanemab, rapidly initiated microglial activation and spatial reorganization within 24 hours of dosing, with recruitment to plaque-associated regions, stabilizing plaque growth. Aducanumab and lecanemab also triggered a rapid and transient cerebrovascular immune response characterized by rolling and adhesion of peripheral immune cells along leptomeningeal vessels, accompanied by endothelial activation. Immune cell characterization revealed recruitment of innate immune cells (Iba1Ki67 monocytes and Ly6G neutrophils) and proliferative CD3 T cells into the vascular compartment following treatment. Prophylactic treatment with high-dose dexamethasone reduced the number of adherent cells without affecting microglial activation. Depletion of brain-resident immune cells similarly reduced peripheral immune cell recruitment, supporting their contribution to leukocyte recruitment. Postmortem brain tissue from an AD patient treated with lecanemab showed higher proliferation-associated monocyte signature scores, suggesting translational relevance to the proliferative myeloid response observed in our mouse models. These findings demonstrate that anti-A{beta} immunotherapy rapidly initiates a coordinated central and peripheral immune response at the leptomeningeal interface. These early immune-vascular interactions represent a plausible initiating mechanism for ARIA and provide a mechanistic framework to guide strategies for mitigating ARIA risk

neuroscience↗

MUC5B and MUC5AC function in combination to regulate mucociliary transport on human airway epithelium

Muco-obstructive lung diseases are characterized by impaired airway clearance and altered mucin composition. MUC5B and MUC5AC are the primary gel-forming mucins in airway mucus, yet how their relative abundance influences the physical and functional properties of mucus remains poorly understood. Here, we investigated how compositional variations in MUC5B and MUC5AC within mucus impact mucociliary transport. Mucus enriched in either MUC5B or MUC5AC was generated using human airway epithelial models depleted for each mucin via CRISPR/Cas9-targeted knockout. Defined mixtures of these mucins were generated at physiologically relevant ratios, for assessment of their microrheological properties and mucociliary transport behavior in differentiated primary human airway epithelial tissue cultures. We found that increasing MUC5AC content reduced network pore size and increased microviscosity, concomitant with reduced mucociliary transport, demonstrating that mucin composition alters the biophysical and functional properties of the mucus barrier. In normal airway tissue cultures with MUC5B-predominant mucus, overlay of MUC5AC on the apical surface impaired mucociliary transport, whereas MUC5B had minimal effect. Conversely, MUC5B supplementation uniquely improved mucociliary transport in IL-13 stimulated cultures exhibiting mucostasis, whereas additional MUC5AC did not alter transport. Together, these findings demonstrate that the ratio of MUC5B to MUC5AC can shape mucus organization at the microscale, which in turn governs mucociliary transport at the tissue scale.

cell biology↗

Social-Cognitive Dysregulation Model of Misophonia: Perspective from a Behavioural Study

Misophonia is increasingly conceptualized as more than a disorder of sound tolerance, with trigger over-reactivity shaped by the social meaning of sounds, inferred intentions, and representations of others actions. We tested a social-cognitive dysregulation model of misophonia in (N = 341) adults using behavioural measures of Theory of Mind and emotion recognition, alongside measures of reflective functioning, empathy, alexithymia, and mimicry. Dimensional associations with misophonia severity and its five different dimensions were examined while accounting for age, sex, sound sensitivity, and anxiety/depressive symptoms. Increased misophonia severity was associated with less accurate and slower mental-state inference and emotion recognition. ToM accuracy effects were evident for more complex, cognitive, and affective mentalizing, but not for simpler mentalizing or physical control judgments, while emotion-recognition accuracy differences emerged for positive but not negative stimuli. Greater severity was also characterized by reduced certainty and greater uncertainty about mental states, greater difficulty identifying one s own feelings, and elevated alexithymia, whereas global self-reported empathy was largely preserved. Misophonia severity further predicted a greater propensity to mimic trigger-producing actions or sounds; 41% of participants exceeding the S-Five clinical cutoff (> 87) endorsed mimicry, which was particularly associated with a subjective restoration of control. Findings remained robust following influential-case sensitivity analyses. These results reveal a selective disturbance in self-other representation spanning mentalizing, emotion decoding, emotional self-representation, and embodied regulatory processes. They position misophonia within a broader social-cognitive framework in which auditory-affective reactivity may intersect with altered inferential and sensorimotor processing, while stopping short of causal inference.

pathology↗

Protein Design Viz (PDV): lightweight protein structure visualization studio with validated quantitative analytics and antibody-specific toolkit

Motivation: Molecular visualization is dominated by two families of software. Desktop programs such as PyMOL, VMD and UCSF ChimeraX are powerful but heavy to install and operate. Web viewers such as Jmol, 3Dmol.js, NGL, Mol* and iCn3D are light and installation-free, but typically stop at rendering, lacking deeper functionality needed for even basic protein sequence, structural analyses and design tasks. Tools building upon these often lack comprehensive sequence/structure manipulation, surface, interface and antibody-specific analytics functionality or require an external backend. There is a need for a tool that is as frictionless as a web viewer yet carries the analytical depth normally reserved for the desktop or the command line software. Results: We present Protein Design Viz (PDV), a self-contained molecular visualization studio delivered as a single offline HTML file that runs entirely in the browser. Built as an extensive modification of 3Dmol.js, PDV combines a full visualization workflow: multi-object scenes, representations, coloring palette, linked sequence track, publication-quality outline rendering and portable sessions. Additionally we re-implemented four commonly used macromolecular analyses measures from scratch in client-side JavaScript: a Shrake-Rupley solvent-accessible surface area (SASA) engine, an antibody numbering and germline-assignment engine, a non-covalent interaction detector, and a developability-liability scanner. Each engine is validated against its established reference. PDV's SASA reproduces FreeSASA at Pearson r {approx} 0.997-0.998 across 2,582 structures spanning proteins, nucleic acids and ligands; its numbering reproduces RIOT for over 99.88% of 1.3 million residue positions across 16,996 sequences and four schemes; its interaction detector reproduces PLIP at macro-F1 0.82, matching Arpeggio as closely as PLIP itself does. PDV brings validated, quantitative structural analysis into a no-install, simple to use tool. Availability and implementation: PDV is a single HTML file, free for noncommercial use under the PolyForm Noncommercial License 1.0.0, available from pdv.naturalantibody.com. It requires only a WebGL-capable browser and runs fully offline.

bioinformatics↗

Genuinely Blind Identification of Sleep Spindles through Trispectral Modulation Analysis

Sleep spindles, transient 11-16 Hz oscillatory bursts, are a defining electrographic feature of non-rem (NREM) sleep and a key biomarker of sleep physiology. A need for efficient and reliable identification of spindles motivates a large literature on automated detection algorithms. In this literature, annotation by trained sleep specialists remains the gold standard against which automated methods are trained, tuned and evaluated. However, inter-scorer agreement among experts is modest, which leaves a significant role for subjective judgment in the definition of a spindle. Finding objective, scorer-independent, criteria for identifying spindles remains an unresolved challenge. We report here a robust, highly specific, and previously unrecognized signature of spindle activity in the fourth-order spectrum (trispectrum), from which we identify the presence of spindles, characterize their waveforms, and obtain an optimal detection filter through a decomposition of the trispectrum (HOSD). Although it is a strictly blind, data-driven method, HOSD-based spindle identification and detection agrees well with expert annotation (median AUROC ~0.9), yet identifies many more events at the native threshold than both human scorers and comparison detectors. Many of these additional detections are confirmed as meeting AASM spindle criteria by four blinded specialists, demonstrating that spindle-like oscillatory bursting is prevalent below conventional human and automated detection thresholds. We observe that N2 sleep is distinguished principally by high-amplitude bursts, while low-amplitude bursting persists throughout NREM sleep, being globally suppressed only in REM sleep. We also describe robust identification of recording-specific spindle waveform properties such as frequency deceleration.

neuroscience↗