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Title: Penetrating radar combined with 3-D imaging for real-time augmented reality sensing and classification
This paper presents research on the use of penetrating radar combined with 3-D computer vision for real-time augmented reality enabled target sensing. Small scale radar systems face the issue that positioning systems are inaccurate, non-portable or challenged by poor GPS signals. The addition of modern computer vision to current cutting-edge penetrating radar technology expands the common 2-D imaging plane to 6 degrees of freedom. Applying the fact that the radar scan itself is a vector with length equivalent to depth from the transmitting and receiving antennae, these technologies used in conjunction can generate an accurate 3-D model of the internal structure of any material for which radar can penetrate. The same computer vision device that localizes the radar data can also be used as the basis for an augmented reality system. Augmented reality radar technology has applications in threat detection (human through-wall, IED, landmine) as well as civil (wall and door structure, buried item detection). For this project, the goal is to create a data registration pipeline and display the radar scan data visually in a 3-D environment using localization from a computer vision tracking device. Processed radar traces are overlayed in real time to an augmented reality screen where the user can view the radar signal intensity to identify and classify targets.  more » « less
Award ID(s):
1647095
NSF-PAR ID:
10311960
Author(s) / Creator(s):
; ; ;
Editor(s):
Dennison, Mark S.; Krum, David M.; Sanders-Reed, John ; Arthur, Jarvis 
Date Published:
Journal Name:
SPIE Defense + Commercial Sensing: Virtual, Augmented, and Mixed Reality (XR) Technology for Multi-Domain Operations II
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
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The breast corpus subset should be released by November 2021. By December 2021 we should also release the unannotated FCCC data. We are currently annotating urinary tract data as well. We expect to release about 5,600 processed TUH slides in this subset. We have an additional 53,000 unprocessed TUH slides digitized. Corpora of this size will stimulate the development of a new generation of deep learning technology. In clinical settings where resources are limited, an assistive diagnoses model could support pathologists’ workload and even help prioritize suspected cancerous cases. ACKNOWLEDGMENTS This material is supported by the National Science Foundation under grants nos. CNS-1726188 and 1925494. Any opinions, findings, and conclusions or recommendations expressed in this material are those of the author(s) and do not necessarily reflect the views of the National Science Foundation. REFERENCES [1] N. 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Wu et al., “Machine Learning at Facebook: Understanding Inference at the Edge,” in Proceedings of the IEEE International Symposium on High Performance Computer Architecture (HPCA), 2019, pp. 331–344. https://ieeexplore.ieee.org/document/8675201. [5] I. Caswell and B. Liang, “Recent Advances in Google Translate,” Google AI Blog: The latest from Google Research, 2020. [Online]. Available: https://ai.googleblog.com/2020/06/recent-advances-in-google-translate.html. [Accessed: 01-Aug-2021]. [6] V. Khalkhali, N. Shawki, V. Shah, M. Golmohammadi, I. Obeid, and J. Picone, “Low Latency Real-Time Seizure Detection Using Transfer Deep Learning,” in Proceedings of the IEEE Signal Processing in Medicine and Biology Symposium (SPMB), 2021, pp. 1 7. https://www.isip. piconepress.com/publications/conference_proceedings/2021/ieee_spmb/eeg_transfer_learning/. [7] J. Picone, T. Farkas, I. Obeid, and Y. Persidsky, “MRI: High Performance Digital Pathology Using Big Data and Machine Learning,” Philadelphia, Pennsylvania, USA, 2020. https://www.isip.piconepress.com/publications/reports/2020/nsf/mri_dpath/. [8] I. Hunt, S. Husain, J. Simons, I. Obeid, and J. Picone, “Recent Advances in the Temple University Digital Pathology Corpus,” in Proceedings of the IEEE Signal Processing in Medicine and Biology Symposium (SPMB), 2019, pp. 1–4. https://ieeexplore.ieee.org/document/9037859. [9] A. P. Martinez, C. Cohen, K. Z. Hanley, and X. (Bill) Li, “Estrogen Receptor and Cytokeratin 5 Are Reliable Markers to Separate Usual Ductal Hyperplasia From Atypical Ductal Hyperplasia and Low-Grade Ductal Carcinoma In Situ,” Arch. Pathol. Lab. Med., vol. 140, no. 7, pp. 686–689, Apr. 2016. https://doi.org/10.5858/arpa.2015-0238-OA. 
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