New open-source software for subcellular segmentation and analysis of spatiotemporal fluorescence signals using deep learning
Sharif Amit Kamran,
Khondker Fariha Hossain,
Hussein Moghnieh,
Sarah Riar,
Allison Bartlett,
Alireza Tavakkoli,
Kenton M. Sanders,
Salah A. Baker
Affiliations
Sharif Amit Kamran
Department of Physiology and Cell Biology, University of Nevada, Reno School of Medicine, Anderson Medical Building MS352, Reno, NV 89557, USA; Department of Computer Science and Engineering, University of Nevada, Reno, NV 89557, USA
Khondker Fariha Hossain
Department of Computer Science and Engineering, University of Nevada, Reno, NV 89557, USA
Hussein Moghnieh
Department of Electrical and Computer Engineering], McGill University, Montréal, QC H3A 0E9, Canada
Sarah Riar
Department of Physiology and Cell Biology, University of Nevada, Reno School of Medicine, Anderson Medical Building MS352, Reno, NV 89557, USA
Allison Bartlett
Department of Physiology and Cell Biology, University of Nevada, Reno School of Medicine, Anderson Medical Building MS352, Reno, NV 89557, USA
Alireza Tavakkoli
Department of Computer Science and Engineering, University of Nevada, Reno, NV 89557, USA
Kenton M. Sanders
Department of Physiology and Cell Biology, University of Nevada, Reno School of Medicine, Anderson Medical Building MS352, Reno, NV 89557, USA
Salah A. Baker
Department of Physiology and Cell Biology, University of Nevada, Reno School of Medicine, Anderson Medical Building MS352, Reno, NV 89557, USA; Corresponding author
Summary: Cellular imaging instrumentation advancements as well as readily available optogenetic and fluorescence sensors have yielded a profound need for fast, accurate, and standardized analysis. Deep-learning architectures have revolutionized the field of biomedical image analysis and have achieved state-of-the-art accuracy. Despite these advancements, deep learning architectures for the segmentation of subcellular fluorescence signals is lacking. Cellular dynamic fluorescence signals can be plotted and visualized using spatiotemporal maps (STMaps), and currently their segmentation and quantification are hindered by slow workflow speed and lack of accuracy, especially for large datasets. In this study, we provide a software tool that utilizes a deep-learning methodology to fundamentally overcome signal segmentation challenges. The software framework demonstrates highly optimized and accurate calcium signal segmentation and provides a fast analysis pipeline that can accommodate different patterns of signals across multiple cell types. The software allows seamless data accessibility, quantification, and graphical visualization and enables large dataset analysis throughput.