Abstract:Traditional fluorescence microscopy is constrained by inherent trade-offs among resolution, field-of-view, and system complexity. To navigate these challenges, we introduce a simple and low-cost computational multi-aperture miniature microscope, utilizing a microlens array for single-shot wide-field, high-resolution imaging. Addressing the challenges posed by extensive view multiplexing and non-local, shift-variant aberrations in this device, we present SV-FourierNet, a novel multi-channel Fourier neural network. SV-FourierNet facilitates high-resolution image reconstruction across the entire imaging field through its learned global receptive field. We establish a close relationship between the physical spatially-varying point-spread functions and the network's learned effective receptive field. This ensures that SV-FourierNet has effectively encapsulated the spatially-varying aberrations in our system, and learned a physically meaningful function for image reconstruction. Training of SV-FourierNet is conducted entirely on a physics-based simulator. We showcase wide-field, high-resolution video reconstructions on colonies of freely moving C. elegans and imaging of a mouse brain section. Our computational multi-aperture miniature microscope, augmented with SV-FourierNet, represents a major advancement in computational microscopy and may find broad applications in biomedical research and other fields requiring compact microscopy solutions.
Abstract:Ultrafast 3D imaging is indispensable for visualizing complex and dynamic biological processes. Conventional scanning-based techniques necessitate an inherent tradeoff between the acquisition speed and space-bandwidth product (SBP). While single-shot 3D wide-field techniques have emerged as an attractive solution, they are still bottlenecked by the synchronous readout constraints of conventional CMOS architectures, thereby limiting the data throughput by frame rate to maintain a high SBP. Here, we present EventLFM, a straightforward and cost-effective system that circumnavigates these challenges by integrating an event camera with Fourier light field microscopy (LFM), a single-shot 3D wide-field imaging technique. The event camera operates on a novel asynchronous readout architecture, thereby bypassing the frame rate limitations intrinsic to conventional CMOS systems. We further develop a simple and robust event-driven LFM reconstruction algorithm that can reliably reconstruct 3D dynamics from the unique spatiotemporal measurements from EventLFM. We experimentally demonstrate that EventLFM can robustly image fast-moving and rapidly blinking 3D samples at KHz frame rates and furthermore, showcase EventLFM's ability to achieve 3D tracking of GFP-labeled neurons in freely moving C. elegans. We believe that the combined ultrafast speed and large 3D SBP offered by EventLFM may open up new possibilities across many biomedical applications.
Abstract:We experimentally demonstrate a camera whose primary optic is a cannula (diameter=0.22mm and length=12.5mm) that acts a lightpipe transporting light intensity from an object plane (35cm away) to its opposite end. Deep neural networks (DNNs) are used to reconstruct color and grayscale images with field of view of 180 and angular resolution of ~0.40. When trained on images with depth information, the DNN can create depth maps. Finally, we show DNN-based classification of the EMNIST dataset without and with image reconstructions. The former could be useful for imaging with enhanced privacy.