# Deep Learning-Assisted Localisation of Nanoparticles in synthetically generated two-photon microscopy images

arXiv: https://arxiv.org/abs/2303.16903 · HTML: https://mlsanity.com/paper/2303.16903/

## Key facts

- No citing papers in the map yet (data through 14 Oct 2026).
- Builds on 6 of its 24 references that are in the map.
- First posted on arXiv 17 Mar 2023.

## Builds on (most cited first, 6 of 6)

- [Deep Residual Learning for Image Recognition](https://mlsanity.com/paper/1512.03385/) (2015)
- [PyTorch: An Imperative Style, High-Performance Deep Learning Library](https://mlsanity.com/paper/1912.01703/) (2019)
- [Faster R-CNN: Towards Real-Time Object Detection with Region Proposal Networks](https://mlsanity.com/paper/1506.01497/) (2015)
- [Mask R-CNN](https://mlsanity.com/paper/1703.06870/) (2017)
- [You Only Look Once: Unified, Real-Time Object Detection](https://mlsanity.com/paper/1506.02640/) (2015)
- [Deep Learning for Generic Object Detection: A Survey](https://mlsanity.com/paper/1809.02165/) (2018)

## Abstract (arXiv)

Tracking single molecules is instrumental for quantifying the transport of molecules and nanoparticles in biological samples, e.g., in brain drug delivery studies. Existing intensity-based localisation methods are not developed for imaging with a scanning microscope, typically used for in vivo imaging. Low signal-to-noise ratios, movement of molecules out-of-focus, and high motion blur on images recorded with scanning two-photon microscopy (2PM) in vivo pose a challenge to the accurate localisation of molecules. Using data-driven models is challenging due to low data volumes, typical for in vivo experiments. We developed a 2PM image simulator to supplement scarce training data. The simulator mimics realistic motion blur, background fluorescence, and shot noise observed in vivo imaging. Training a data-driven model with simulated data improves localisation quality in simulated images and shows why intensity-based methods fail.