Abstract
Over nearly two decades, Differential Dynamic Microscopy (DDM) has become a standard technique for extracting dynamic correlation functions from time-lapse microscopy data, with applications spanning colloidal suspensions, polymer solutions, active fluids, and biological systems. In its most common implementation, DDM analyzes image sequences acquired with a conventional microscope equipped with a digital camera, yielding time- and wavevector-resolved information analogous to that obtained in multi-angle Dynamic Light Scattering (DLS). With a widening array of applications and a growing, heterogeneous user base, lowering the technical barrier to performing DDM has become a central objective. In this tutorial article, we provide a step-by-step guide to conducting DDM experiments – from planning and acquisition to data analysis – and introduce the open-source software package fastDDM, designed to efficiently process large image datasets. fastDDM employs optimized, parallel algorithms that reduce analysis times by up to four orders of magnitude on typical datasets (e.g., 10,000 frames), thereby enabling high-throughput workflows and making DDM more broadly accessible across disciplines.
Enrico Lattuada
Postdoctoral Researcher
My research interests include Advanced optical techniques, High-performance computing and soft matter.
Fabian Krautgasser
MSc Student
My research interests include structure & dynamics of cellular monolayers, data analysis & visualisation in Python.
Maxime Lavaud
Postdoctoral Researcher
My research interests include Interferometry, Langevian simulations and Soft Matter Physics.
Roberto Cerbino
Professor of Experimental Soft Matter Physics
My research interests include Soft matter physics, living matter, cell biophysics and quantitative microscopy.