Improving timing resolution of BGO for TOF-PET: a comparative analysis with and without deep learning.

EJNMMI Phys

Sherbrooke Molecular Imaging Center and Department of Nuclear Medicine and Radiobiology, Université de Sherbrooke, 12th Avenue N, Sherbrooke, J1H 5N4, Québec, Canada.

Published: January 2025

Background: The renewed interest in BGO scintillators for TOF-PET is driven by the improved Cherenkov photon detection with new blue-sensitive SiPMs. However, the slower scintillation light from BGO causes significant time walk with leading edge discrimination (LED), which degrades the coincidence time resolution (CTR). To address this, a time walk correction (TWC) can be done by using the rise time measured with a second threshold. Deep learning, particularly convolutional neural networks (CNNs), can also enhance CTR by training with digitized waveforms. It remains to be explored how timing estimation methods utilizing one (LED), two (TWC), or multiple (CNN) waveform data points compare in CTR performance of BGO scintillators.

Results: In this work, we compare classical experimental timing estimation methods (LED, TWC) with a CNN-based method using the signals from BGO crystals read out by NUV-HD-MT SiPMs and high-frequency electronics. For crystals, implementing TWC results in a CTR of 129 ± 2 ps FWHM, while employing the CNN yields 115 ± 2 ps FWHM, marking improvements of 18 % and 26 %, respectively, relative to the standard LED estimator. For crystals, both methods yield similar CTR (around 240 ps FWHM), offering a 15 % gain over LED. The CNN, however, exhibits better tail suppression in the coincidence time distribution.

Conclusions: The higher complexity of waveform digitization needed for CNNs could potentially be mitigated by adopting a simpler two-threshold approach, which appears to currently capture most of the essential information for improving CTR in longer BGO crystals. Other innovative deep learning models and training strategies may nonetheless contribute further in a near future to harnessing increasingly discernible timing features in TOF-PET detector signals.

Download full-text PDF

Source
http://dx.doi.org/10.1186/s40658-024-00711-6DOI Listing

Publication Analysis

Top Keywords

deep learning
12
time walk
8
coincidence time
8
timing estimation
8
estimation methods
8
led twc
8
bgo crystals
8
bgo
6
ctr
6
time
5

Similar Publications

Deep Equilibrium Unfolding Learning for Noise Estimation and Removal in Optical Molecular Imaging.

Comput Med Imaging Graph

January 2025

CAS Key Laboratory of Molecular Imaging, Institute of Automation, Chinese Academy of Sciences, Beijing 100190, China; School of Artificial Intelligence, University of Chinese Academy of Sciences, Beijing 100049, China; National Key Laboratory of Kidney Diseases, Beijing 100853, China. Electronic address:

In clinical optical molecular imaging, the need for real-time high frame rates and low excitation doses to ensure patient safety inherently increases susceptibility to detection noise. Faced with the challenge of image degradation caused by severe noise, image denoising is essential for mitigating the trade-off between acquisition cost and image quality. However, prevailing deep learning methods exhibit uncontrollable and suboptimal performance with limited interpretability, primarily due to neglecting underlying physical model and frequency information.

View Article and Find Full Text PDF

Objective: The extent of resection (EOR) and postoperative residual tumor (RT) volume are prognostic factors in glioblastoma. Calculations of EOR and RT rely on accurate tumor segmentations. Raidionics is an open-access software that enables automatic segmentation of preoperative and early postoperative glioblastoma using pretrained deep learning models.

View Article and Find Full Text PDF

Computational Methods for Predicting Chemical Reactivity of Covalent Compounds.

J Chem Inf Model

January 2025

Department of Medicinal Chemistry, School of Pharmacy, Fudan University, 826 Zhangheng Road, Shanghai 201203, People's Republic of China.

In recent decades, covalent inhibitors have emerged as a promising strategy for therapeutic development, leveraging their unique mechanism of forming covalent bonds with target proteins. This approach offers advantages such as prolonged drug efficacy, precise targeting, and the potential to overcome resistance. However, the inherent reactivity of covalent compounds presents significant challenges, leading to off-target effects and toxicities.

View Article and Find Full Text PDF

While single-cell experiments provide deep cellular resolution within a single sample, some single-cell experiments are inherently more challenging than bulk experiments due to dissociation difficulties, cost, or limited tissue availability. This creates a situation where we have deep cellular profiles of one sample or condition, and bulk profiles across multiple samples and conditions. To bridge this gap, we propose BuDDI (BUlk Deconvolution with Domain Invariance).

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!