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Xuejun Sun

Publications and source records attributed to Xuejun Sun.

4 recordsLinked to original sources

LoopPerm-CPD: A Robust Loop Permutation Framework for Automatic Multiple Change-Point Detection in Longitudinal Data

Human viral challenge studies, in which participants are deliberately inoculated with influenza strains such as H1N1 or H3N2 and monitored through longitudinal transcriptomic profiling before and after inoculation, are critical for characterizing dynamic biological immune responses to viral infection. A key analytical goal in such settings is to detect critical transition times, or change points, at which an underlying trajectory shifts direction or rate, indicating events such as the onset of an immune response or recovery. However, change-point detection in these longitudinal data is fundamentally challenging because observations are often sparse and irregularly spaced, sample sizes are small, outliers are common, and the number of change points is unknown in advance. To address these challenges, we propose LoopPerm-CPD, a robust change-point detection approach with a built-in loop permutation procedure for automatic multiple change-point detection. The method evaluates candidate slope change points and assesses their significance using within-subject circular permutation combined with binary segmentation, jointly estimating both the number and locations of change points. The accompanying R package, LoopPerm-CPD, implements this framework and flexibly accommodates generalized least squares, quantile regression, and quantile rank-score statistics for different types of longitudinal outcomes. The proposed approach is evaluated through simulations, demonstrating Type I error control and improved power compared with competing methods. Applied to real data, the framework identifies interpretable transition points in multiple human respiratory viral inoculation studies. Together, these results establish LoopPerm-CPD and its companion software as a robust and user-friendly tool for change-point detection in complex human longitudinal cohort data.

stat.ME

HR-VILAGE-3K3M: A Human Respiratory Viral Immunization Longitudinal Gene Expression Dataset for Systems Immunity

Respiratory viral infections pose a global health burden, yet the cellular immune mechanisms underlying protection and pathology remain unclear. Natural infection cohorts often lack pre-exposure baselines and time-controlled sampling, whereas inoculation and vaccination trials generate well-structured longitudinal transcriptomic data. However, these datasets are scattered across repositories and processed inconsistently, hindering integrative and AI-driven analyses. To address these challenges, we developed the Human Respiratory Viral Immunization LongitudinAl Gene Expression (HR-VILAGE-3K3M) repository: an AI-ready resource integrating bulk and single-cell transcriptomic profiles from 3,178 subjects across 66 studies. The dataset spans vaccination, inoculation, and mixed exposures, with samples from blood and nasal swabs collected from public repositories including GEO, ImmPort, and ArrayExpress. We curated and harmonized subject-level metadata, standardized outcome measures, and applied unified preprocessing with rigorous quality control. We further provide benchmark analyses illustrating its utility. This resource supports discovery of biomarkers, immune mechanisms, and methodological development. As one of the largest longitudinal transcriptomic resources for human respiratory viral immunization, HR-VILAGE-3K3M enables reproducible and scalable analyses to accelerate vaccine and antiviral research.

q-bio.GN

Mitochondria in higher plants possess H2 evolving activity which is closely related to complex I

Hydrogenase occupy a central place in the energy metabolism of anaerobic bacteria. Although the structure of mitochondrial complex I is similar to that of hydrogenase, whether it has hydrogen metabolic activity remain unclear. Here, we show that a H2 evolving activity exists in higher plants mitochondria and is closely related to complex I, especially around ubiquinone binding site. The H2 production could be inhibited by rotenone and ubiquinone. Hypoxia could simultaneously promote H2 evolution and succinate accumulation. Redox properties of quinone pool, adjusted by NADH or succinate according to oxygen concentration, acts as a valve to control the flow of protons and electrons and the production of H2. The coupling of H2 evolving activity of mitochondrial complex I with metabolic regulation reveals a more effective redox homeostasis regulation mechanism. Considering the ubiquity of mitochondria in eukaryotes, H2 metabolism might be the innate function of higher organisms. This may serve to explain, at least in part, the broad physiological effects of H2.

q-bio.BM

Three-Layered Atmospheric Structure in Accretion Disks Around Stellar-Mass Black Holes

Modeling of the x-ray spectra of the Galactic superluminal jet sources GRS 1915+105 and GRO J1655-40 reveal a three-layered atmospheric structure in the inner region of their accretion disks. Above the cold and optically thick disk of a temperature 0.2-0.5 keV, there is a warm layer with a temperature of 1.0-1.5 keV and an optical depth around 10. Sometimes there is also a much hotter, optically thin corona above the warm layer, with a temperature of 100 keV or higher and an optical depth around unity. The structural similarity between the accretion disks and the solar atmosphere suggest that similar physical processes may be operating in these different systems.

astro-ph