(Photo by A. Ciarlo.)Jiacheng Huang started his PhD at the Physics Department of the University of Gothenburg on 1st July 2025.
Jiacheng has a Master degree in Material and Chemical Engineering from the Department of Chemical and Biochemical Engineering, Xiamen University, China.
In his PhD, which is part of the MSCA-DN SPM4.0, he will focus on machine learning and smart microscopy.
Electromagnetic light scattering underpins a wide range of phenomena in both fundamental and applied research, from characterizing complex materials to tracking particles and cells in microfluidic devices. Video microscopy, in particular, has become a powerful method for studying scattering processes and extracting quantitative information. Yet, conventional algorithmic approaches for analyzing scattering data often prove cumbersome, computationally expensive, and highly specialized.
Recent advances in deep learning offer a compelling alternative. By leveraging data-driven models, we can automate the extraction of scattering characteristics with unprecedented speed and accuracy—uncovering insights that classical techniques might miss or require substantial computation to achieve. Despite these advantages, deep-learning-based tools remain underutilized in light-scattering research, largely because of the steep learning curve required to design and train such models.
To address these challenges, we have developed a user-friendly software platform (DeepTrack, now in version 2.2) that simplifies the entire workflow of deep-learning applications in digital microscopy. DeepTrack enables straightforward creation of custom datasets, network architectures, and training pipelines specifically tailored for quantitative scattering analyses. In this talk, I will discuss how emerging deep-learning methods can be combined with advanced imaging technologies to push the boundaries of electromagnetic light scattering research—reducing computational overhead, improving accuracy, and ultimately broadening access to powerful, data-driven solutions.
(Photo by A. Ciarlo.)John Tember joined the Soft Matter Lab on 15 June 2025.
John is a PhD student in Physics at the University of Gothenburg.
He holds a Master’s degree in Media Technology and Engineering from Linköping University.
During his time at the Soft Matter Lab, he will work on data-driven life science, with a focus on developing and analyzing 3D models derived from lightsheet microscopy.
Linde Viaene presenting at the PhD conference. (Image by S. Kilde Westberg.)Studying heat adaptation in yeast one-molecule at a time: The use of single-molecule microscopy for aggregate identification and tracking.
Linde Viaene Date: 25th of April Time: 13:00 Place: Veras Gräsmatta, Gothenburg
The importance of protein folding and misfolding is indicated by the broad range of clinical manifestations that have protein aggregation at the base, such as neurodegenerative diseases, cancer and type II diabetes. A key factor in (energy) homeostasis is the DNA configuration of chromatin which allows for essential gene expression and adaptation to environmental factors. The Rpd3 deacetylase histone complex (DHAC) plays a crucial role in gene regulation and its disruption impairs stress-induced gene activation, highlighting its importance in cellular adaptation.
Using Saccharomyces cerevisiae as a model system, we aim to investigate the role of chromatin remodelling components in protein aggregation and cellular rejuvenation, which may influence aggregate retention and recovery speed. We will expose yeast cells to stressors such as heat shock, metabolic shifts, and oxidative stress to assess their effects on protein homeostasis and chromatin regulation. Growth assays will evaluate survival rates, while Western blotting will measure Hsp104 expression, a key heat shock protein involved in aggregate clearance. By employing our bespoke single-molecule fluorescence microscope, we will track aggregate formation, clearance, and spatial localization in live cells at molecular precision.
Our preliminary results indicate that some components of the Rpd3L complex, respectively alter the recovery rate after heat stress exposure. Hence, the goal is to explore further candidate genes and to determine their role in the stress-induced response. By elucidating the role of chromatin remodelers in stress adaptation, our findings may inform novel therapeutic strategies for age-related diseases.