James R. Hopgood

Isabel Schlangen, André Brandenburger, Mengwei Sun et al.

The performance of tracking algorithms strongly depends on the chosen model assumptions regarding the target dynamics. If there is a strong mismatch between the chosen model and the true object motion, the track quality may be poor or the track is easily lost. Still, the true dynamics might not be known a priori or it is too complex to be expressed in a tractable mathematical formulation. This paper provides a comparative study between three different methods that use machine learning to describe the underlying object motion based on training data. The first method builds on Gaussian Processes (GPs) for predicting the object motion, the second learns the parameters of an Interacting Multiple Model (IMM) filter and the third uses a Long Short-Term Memory (LSTM) network as a motion model. All methods are compared against an Extended Kalman Filter (EKF) with an analytic motion model as a benchmark and their respective strengths are highlighted in one simulated and two real-world scenarios.

Qiang Wang, Susan Fernandes, Gareth O. S. Williams et al.

Autofluorescence lifetime images reveal unique characteristics of endogenous fluorescence in biological samples. Comprehensive understanding and clinical diagnosis rely on co-registration with the gold standard, histology images, which is extremely challenging due to the difference of both images. Here, we show an unsupervised image-to-image translation network that significantly improves the success of the co-registration using a conventional optimisation-based regression network, applicable to autofluorescence lifetime images at different emission wavelengths. A preliminary blind comparison by experienced researchers shows the superiority of our method on co-registration. The results also indicate that the approach is applicable to various image formats, like fluorescence intensity images. With the registration, stitching outcomes illustrate the distinct differences of the spectral lifetime across an unstained tissue, enabling macro-level rapid visual identification of lung cancer and cellular-level characterisation of cell variants and common types. The approach could be effortlessly extended to lifetime images beyond this range and other staining technologies.