NIGMS - National Institute of General Medical Sciences
PROJECT SUMMARY/ABSTRACT Superresolution microscopy is an incredible family of approaches that have provided easier observability of nanometer-scale features using visible-light fluorescence which was previously limited to ~200-300 nm. The highest resolution of these techniques is single molecule localization microscopy (SMLM), in which an otherwise dark field has random, sparse fluorescent flashes. These flashes may be achieved either through a photophysical process on a stationary fluorophore (STORM/PALM) or through a kinetic process where a mobile fluorophore is transiently fixed to a target (PAINT). A point-source diffraction-limited flash can be localized with precision on the order of 1-20 nm. However, the requirement for sparsity means that the fluorophore blinking rates need to be carefully optimized, the acquisition time for a video can be quite long, and most localization methods scale poorly with the number of localizations. These and other issues are challenging for routine usage of SMLM, including in the single-molecule diagnostic assay and sequencing platform that XGenomes is developing. In this Phase I project, XGenomes will build machine learning algorithms to analyze whole SMLM videos to identify emitter positions at ultra-high precisions and ultra-high densities. In Aim 1, we will create the SMLM video simulator necessary to generate training data. In Aim 2, we will build a machine learning-based grouping algorithm that can work with existing localization data and primarily improve the speed and accuracy of analysis. In Aim 3, we will build a machine learning model to analyze whole SMLM videos at once and pushing the density up an order of magnitude higher than current algorithms can achieve. This work will be made freely available for use to the academic research community. The successful completion of these aims will create a leap forward in SMLM and will unlock new uses for theses technologies.
Up to $349K
2026-09-14
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