Universal evaluation and design of imaging systems using information estimation

Information theory, which describes the transmission of signals in the presence of noise, has enabled the development of reliable communication systems that underlie the modern world. Imaging systems can also be viewed as a form of communication, in which information about the object is "transmitted" through images. However, the application of information theory to imaging systems has been limited by the challenges of accounting for their physical constraints. Here, we introduce a framework that addresses these limitations by modeling the probabilistic relationship between objects and their measurements. Using this framework, we develop a method to estimate information using only a dataset of noisy measurements, without making any assumptions about the image formation process. We demonstrate that these estimates comprehensively quantify measurement quality across a diverse range of imaging systems and applications. Furthermore, we introduce Information-Driven Encoder Analysis Learning (IDEAL), a technique to optimize the design of imaging hardware for maximum information capture. This work provides new insights into the fundamental performance limits of imaging systems and offers powerful new tools for their analysis and design.

The Berkeley Single Cell Computational Microscopy (BSCCM) Dataset

Computational microscopy, in which hardware and algorithms of an imaging system are jointly designed, shows promise for making imaging systems that cost less, perform more robustly, and collect new types of information. Often, the performance of computational imaging systems, especially those that incorporate machine learning, is sample-dependent. Thus, standardized datasets are an essential tool for comparing the performance of different approaches. Here, we introduce the Berkeley Single Cell Computational Microscopy (BSCCM) dataset, which contains over ~12,000,000 images of 400,000 of individual white blood cells. The dataset contains images captured with multiple illumination patterns on an LED array microscope and fluorescent measurements of the abundance of surface proteins that mark different cell types. We hope this dataset will provide a valuable resource for the development and testing of new algorithms in computational microscopy and computer vision with practical biomedical applications.