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Chang, S.-C.

Publications and source records attributed to Chang, S.-C..

2 recordsLinked to original sources

Latent-centric Isotropic Resolution Enhancement for Expansion Microscopy Imaging via Neural Compression and Self-supervised Learning

Expansion microscopy (ExM) enables nanoscale imaging for disease characterization. However, whole-organ analyses remain limited by several challenges. Current super-resolution methods either require high-resolution ground-truth data or assume spatially uniform point spread functions--assumptions that rarely hold in whole-organ imaging with depth-varying aberrations and illumination drift. Existing methods also worsen storage demands by inflating already multi-terabyte datasets without using neural compression. We propose a single-stage, self-supervised framework that addresses both resolution anisotropy and storage constraints through compression-aware isotropic super-resolution. Our approach combines a 2D lateral encoder that operates directly on raw slices to avoid memory limits with a lightweight volumetric decoder that preserves cross-slice continuity. A vector-quantized variational autoencoder (VQ-VAE) provides an information-sufficient bottleneck, achieving up to 128x slice compression and up to 8x axial resolution enhancement. This latent-centric design yields approximately 1000x reduction in storage compared with storing fully isotropic volumes. The framework achieves higher GPU throughput, lower memory usage, and stronger multi-GPU scalability than prior methods. By designating compressed latent space as the native storage format, it enables efficient on-demand isotropic reconstruction directly from compact representations. This combination of isotropic enhancement and neural compression framework therefore makes large-scale, whole-organ ExM analysis practical while maintaining analysis-ready accessibility, addressing a bottleneck in translating ExM to clinical biomarker discovery.

bioinformatics↗

Relationship between maximal incremental and high-intensity interval exercise performance in elite athletes

It remains unclear whether the number of total bouts to limitation (Blim) in high-intensity interval testing (HIIT) differs among individuals, no matter if performed at the same relative intensity. This study aimed to explore the physiologic factors determining tolerance to effort during a HIIT. Forty-seven female participants (15-28 years old) were included: 23 athletes from Taiwan national or national reserve teams, and 24 moderately-active female. Each participant underwent maximal incremental (INC; modified-Bruce protocol) cardiopulmonary exercise testing and HIIT on treadmill, on separate days. HIIT protocol alternated a 1-min effort at 120% of the maximal speed and the same slope reached at the end of INC, with a 1-min rest, until volitional exhaustion. Gas-exchanges, and muscle oxygenation at right vastus lateralis by near-infrared spectroscopy, were continuously recorded. Additionally, bioelectrical impedance was utilized for body composition analysis. The result showed that Blim differed greatly (range: 2.6 to 12) among participants. Stepwise regression revealed that Blim was determined primarily by oxygen consumption (VO2) and heart rate (HR) at second-minute recovery; and, muscle tissue saturation index at peak of INC (R=0.644). Also, age and percent body fat were linearly correlated with Blim (adjusted R=-0.475, -0.371, p<0.05). Therefore, HIIT performance is determined by fast recovery of VO2 and HR, rather than maximal VO2 or muscle oxygenation recovery. Moreover, capacity to sustain a HIIT declines with age since as early as late adolescent. Further investigations on which factors should be manipulated to further improve athletes performance are warrant.

physiology↗