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Title: Identifying non-thrive trees and predicting wood density from resistograph using temporal convolution network
Deep learning approaches have been adopted in Forestry research including tree classification and inventory prediction. In this study, we proposed an application of a deep learning approach, Temporal Convolution Network, on sequences of radial resistograph profiles to identify non-thrive trees and to predict wood density. Non-destructive resistance drilling measurements on South and West orientations of 274 trees in a 41-year-old Douglas-fir stand in Marion County, Oregon, USA were used as input series. Non-thrive trees were defined based on their changes in social status since establishment. Wood density was derived by X-ray densitometry from cores obtained by increment borers. Data was split for cross validation. Optimal models were fine-tuned with training and validation datasets, then run with test datasets for model evaluation metrics. Results confirmed that the application of the Temporal Convolution Network on resistograph profiles enables non-thrive tree identification with the probability, represented by the area under the Receiver Operator Characteristic curve, equal to 0.823. Temporal Convolution Network for wood density prediction showed a slight improvement in accuracy (RMSE = 18.22) compared to the traditional linear (RMSE = 20.15) and non-linear (RMSE = 20.33) regression methods. We suggest that the use of machine learning algorithms can be a promising methodology for the analysis of sequential data from non-destructive devices.  more » « less
Award ID(s):
1916155
NSF-PAR ID:
10398317
Author(s) / Creator(s):
;
Date Published:
Journal Name:
Forest Science and Technology
Volume:
18
Issue:
22
ISSN:
2158-0103
Page Range / eLocation ID:
144-149
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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