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1. Using convolutional neural networks to develop starting models for near-surface 2-D full waveform inversion

   https://doi.org/10.1093/gji/ggac179  

   Vantassel, Joseph P. ; Kumar, Krishna ; Cox, Brady R. ( May 2022 , Geophysical Journal International)

   Non-invasive subsurface imaging using full waveform inversion (FWI) has the potential to fundamentally change near-surface (<30 m) site characterization by enabling the recovery of high-resolution (metre-scale) 2-D/3-D maps of subsurface elastic material properties. Yet, FWI results are quite sensitive to their starting model due to their dependence on local-search optimization techniques and inversion non-uniqueness. Starting model dependence is particularly problematic for near-surface FWI due to the complexity of the recorded seismic wavefield (e.g. dominant surface waves intermixed with body waves) and the potential for significant spatial variability over short distances. In response, convolutional neural networks (CNNs) are investigated as a potential tool for developing starting models for near-surface 2-D elastic FWI. Specifically, 100 000 subsurface models were generated to be representative of a classic near-surface geophysics problem; namely, imaging a two-layer, undulating, soil-over-bedrock interface. A CNN has been developed from these synthetic models that is capable of transforming an experimental wavefield acquired using a seismic source located at the centre of a linear array of 24 closely spaced surface sensors directly into a robust starting model for FWI. The CNN approach was able to produce 2-D starting models with seismic image misfits that were significantly less than the misfits from other common starting model approaches, and in many cases even less than the misfits obtained by FWI with inferior starting models. The ability of the CNN to generalize outside its two-layered training set was assessed using a more complex, three-layered, soil-over-bedrock formation. While the predictive ability of the CNN was slightly reduced for this more complex case, it was still able to achieve seismic image and waveform misfits that were comparable to other commonly used starting models, despite not being trained on any three-layered models. As such, CNNs show great potential as tools for rapidly developing robust, site-specific starting models for near-surface elastic FWI.

    

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2. Deep Convolutional Neural Network for Flood Extent Mapping Using Unmanned Aerial Vehicles Data

   https://doi.org/10.3390/s19071486  

   Gebrehiwot, Asmamaw ; Hashemi-Beni, Leila ; Thompson, Gary ; Kordjamshidi, Parisa ; Langan, Thomas ( April 2019 , Sensors)

   Flooding is one of the leading threats of natural disasters to human life and property, especially in densely populated urban areas. Rapid and precise extraction of the flooded areas is key to supporting emergency-response planning and providing damage assessment in both spatial and temporal measurements. Unmanned Aerial Vehicles (UAV) technology has recently been recognized as an efficient photogrammetry data acquisition platform to quickly deliver high-resolution imagery because of its cost-effectiveness, ability to fly at lower altitudes, and ability to enter a hazardous area. Different image classification methods including SVM (Support Vector Machine) have been used for flood extent mapping. In recent years, there has been a significant improvement in remote sensing image classification using Convolutional Neural Networks (CNNs). CNNs have demonstrated excellent performance on various tasks including image classification, feature extraction, and segmentation. CNNs can learn features automatically from large datasets through the organization of multi-layers of neurons and have the ability to implement nonlinear decision functions. This study investigates the potential of CNN approaches to extract flooded areas from UAV imagery. A VGG-based fully convolutional network (FCN-16s) was used in this research. The model was fine-tuned and a k-fold cross-validation was applied to estimate the performance of the model on the new UAV imagery dataset. This approach allowed FCN-16s to be trained on the datasets that contained only one hundred training samples, and resulted in a highly accurate classification. Confusion matrix was calculated to estimate the accuracy of the proposed method. The image segmentation results obtained from FCN-16s were compared from the results obtained from FCN-8s, FCN-32s and SVMs. Experimental results showed that the FCNs could extract flooded areas precisely from UAV images compared to the traditional classifiers such as SVMs. The classification accuracy achieved by FCN-16s, FCN-8s, FCN-32s, and SVM for the water class was 97.52%, 97.8%, 94.20% and 89%, respectively. 

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3. Robust and simplified machine learning identification of pitfall trap‐collected ground beetles at the continental scale

   https://doi.org/10.1002/ece3.6905  

   Blair, Jarrett ; Weiser, Michael D. ; Kaspari, Michael ; Miller, Matthew ; Siler, Cameron ; Marshall, Katie E. ( November 2020 , Ecology and Evolution)

   Insect populations are changing rapidly, and monitoring these changes is essential for understanding the causes and consequences of such shifts. However, large‐scale insect identification projects are time‐consuming and expensive when done solely by human identifiers. Machine learning offers a possible solution to help collect insect data quickly and efficiently.

   Here, we outline a methodology for training classification models to identify pitfall trap‐collected insects from image data and then apply the method to identify ground beetles (Carabidae). All beetles were collected by the National Ecological Observatory Network (NEON), a continental scale ecological monitoring project with sites across the United States. We describe the procedures for image collection, image data extraction, data preparation, and model training, and compare the performance of five machine learning algorithms and two classification methods (hierarchical vs. single‐level) identifying ground beetles from the species to subfamily level. All models were trained using pre‐extracted feature vectors, not raw image data. Our methodology allows for data to be extracted from multiple individuals within the same image thus enhancing time efficiency, utilizes relatively simple models that allow for direct assessment of model performance, and can be performed on relatively small datasets.

   The best performing algorithm, linear discriminant analysis (LDA), reached an accuracy of 84.6% at the species level when naively identifying species, which was further increased to >95% when classifications were limited by known local species pools. Model performance was negatively correlated with taxonomic specificity, with the LDA model reaching an accuracy of ~99% at the subfamily level. When classifying carabid species not included in the training dataset at higher taxonomic levels species, the models performed significantly better than if classifications were made randomly. We also observed greater performance when classifications were made using the hierarchical classification method compared to the single‐level classification method at higher taxonomic levels.

   The general methodology outlined here serves as a proof‐of‐concept for classifying pitfall trap‐collected organisms using machine learning algorithms, and the image data extraction methodology may be used for nonmachine learning uses. We propose that integration of machine learning in large‐scale identification pipelines will increase efficiency and lead to a greater flow of insect macroecological data, with the potential to be expanded for use with other noninsect taxa.

    

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4. The Temple University Digital Pathology Corpus: The Breast Tissue Subset

   https://doi.org/10.1109/SPMB52430.2021.9672275  

   Wevodau, Z. ; Doshna, B. ; Jhala, N. ; Akhtar, I. ; Obeid, I. ; Picone, J. ( December 2021 , Proceedings of the IEEE Signal Processing in Medicine and Biology Symposium (SPMB))

   Obeid, I. (Ed.)

   The Neural Engineering Data Consortium (NEDC) is developing the Temple University Digital Pathology Corpus (TUDP), an open source database of high-resolution images from scanned pathology samples [1], as part of its National Science Foundation-funded Major Research Instrumentation grant titled “MRI: High Performance Digital Pathology Using Big Data and Machine Learning” [2]. The long-term goal of this project is to release one million images. We have currently scanned over 100,000 images and are in the process of annotating breast tissue data for our first official corpus release, v1.0.0. This release contains 3,505 annotated images of breast tissue including 74 patients with cancerous diagnoses (out of a total of 296 patients). In this poster, we will present an analysis of this corpus and discuss the challenges we have faced in efficiently producing high quality annotations of breast tissue. It is well known that state of the art algorithms in machine learning require vast amounts of data. Fields such as speech recognition [3], image recognition [4] and text processing [5] are able to deliver impressive performance with complex deep learning models because they have developed large corpora to support training of extremely high-dimensional models (e.g., billions of parameters). Other fields that do not have access to such data resources must rely on techniques in which existing models can be adapted to new datasets [6]. A preliminary version of this breast corpus release was tested in a pilot study using a baseline machine learning system, ResNet18 [7], that leverages several open-source Python tools. The pilot corpus was divided into three sets: train, development, and evaluation. Portions of these slides were manually annotated [1] using the nine labels in Table 1 [8] to identify five to ten examples of pathological features on each slide. Not every pathological feature is annotated, meaning excluded areas can include focuses particular to these labels that are not used for training. A summary of the number of patches within each label is given in Table 2. To maintain a balanced training set, 1,000 patches of each label were used to train the machine learning model. Throughout all sets, only annotated patches were involved in model development. The performance of this model in identifying all the patches in the evaluation set can be seen in the confusion matrix of classification accuracy in Table 3. The highest performing labels were background, 97% correct identification, and artifact, 76% correct identification. A correlation exists between labels with more than 6,000 development patches and accurate performance on the evaluation set. Additionally, these results indicated a need to further refine the annotation of invasive ductal carcinoma (“indc”), inflammation (“infl”), nonneoplastic features (“nneo”), normal (“norm”) and suspicious (“susp”). This pilot experiment motivated changes to the corpus that will be discussed in detail in this poster presentation. To increase the accuracy of the machine learning model, we modified how we addressed underperforming labels. One common source of error arose with how non-background labels were converted into patches. Large areas of background within other labels were isolated within a patch resulting in connective tissue misrepresenting a non-background label. In response, the annotation overlay margins were revised to exclude benign connective tissue in non-background labels. Corresponding patient reports and supporting immunohistochemical stains further guided annotation reviews. The microscopic diagnoses given by the primary pathologist in these reports detail the pathological findings within each tissue site, but not within each specific slide. The microscopic diagnoses informed revisions specifically targeting annotated regions classified as cancerous, ensuring that the labels “indc” and “dcis” were used only in situations where a micropathologist diagnosed it as such. Further differentiation of cancerous and precancerous labels, as well as the location of their focus on a slide, could be accomplished with supplemental immunohistochemically (IHC) stained slides. When distinguishing whether a focus is a nonneoplastic feature versus a cancerous growth, pathologists employ antigen targeting stains to the tissue in question to confirm the diagnosis. For example, a nonneoplastic feature of usual ductal hyperplasia will display diffuse staining for cytokeratin 5 (CK5) and no diffuse staining for estrogen receptor (ER), while a cancerous growth of ductal carcinoma in situ will have negative or focally positive staining for CK5 and diffuse staining for ER [9]. Many tissue samples contain cancerous and non-cancerous features with morphological overlaps that cause variability between annotators. The informative fields IHC slides provide could play an integral role in machine model pathology diagnostics. Following the revisions made on all the annotations, a second experiment was run using ResNet18. Compared to the pilot study, an increase of model prediction accuracy was seen for the labels indc, infl, nneo, norm, and null. This increase is correlated with an increase in annotated area and annotation accuracy. Model performance in identifying the suspicious label decreased by 25% due to the decrease of 57% in the total annotated area described by this label. A summary of the model performance is given in Table 4, which shows the new prediction accuracy and the absolute change in error rate compared to Table 3. The breast tissue subset we are developing includes 3,505 annotated breast pathology slides from 296 patients. The average size of a scanned SVS file is 363 MB. The annotations are stored in an XML format. A CSV version of the annotation file is also available which provides a flat, or simple, annotation that is easy for machine learning researchers to access and interface to their systems. Each patient is identified by an anonymized medical reference number. Within each patient’s directory, one or more sessions are identified, also anonymized to the first of the month in which the sample was taken. These sessions are broken into groupings of tissue taken on that date (in this case, breast tissue). A deidentified patient report stored as a flat text file is also available. Within these slides there are a total of 16,971 total annotated regions with an average of 4.84 annotations per slide. Among those annotations, 8,035 are non-cancerous (normal, background, null, and artifact,) 6,222 are carcinogenic signs (inflammation, nonneoplastic and suspicious,) and 2,714 are cancerous labels (ductal carcinoma in situ and invasive ductal carcinoma in situ.) The individual patients are split up into three sets: train, development, and evaluation. Of the 74 cancerous patients, 20 were allotted for both the development and evaluation sets, while the remain 34 were allotted for train. The remaining 222 patients were split up to preserve the overall distribution of labels within the corpus. This was done in hope of creating control sets for comparable studies. Overall, the development and evaluation sets each have 80 patients, while the training set has 136 patients. In a related component of this project, slides from the Fox Chase Cancer Center (FCCC) Biosample Repository (https://www.foxchase.org/research/facilities/genetic-research-facilities/biosample-repository -facility) are being digitized in addition to slides provided by Temple University Hospital. This data includes 18 different types of tissue including approximately 38.5% urinary tissue and 16.5% gynecological tissue. These slides and the metadata provided with them are already anonymized and include diagnoses in a spreadsheet with sample and patient ID. We plan to release over 13,000 unannotated slides from the FCCC Corpus simultaneously with v1.0.0 of TUDP. Details of this release will also be discussed in this poster. Few digitally annotated databases of pathology samples like TUDP exist due to the extensive data collection and processing required. 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. Shawki et al., “The Temple University Digital Pathology Corpus,” in Signal Processing in Medicine and Biology: Emerging Trends in Research and Applications, 1st ed., I. Obeid, I. Selesnick, and J. Picone, Eds. New York City, New York, USA: Springer, 2020, pp. 67 104. https://www.springer.com/gp/book/9783030368432. [2] J. Picone, T. Farkas, I. Obeid, and Y. Persidsky, “MRI: High Performance Digital Pathology Using Big Data and Machine Learning.” Major Research Instrumentation (MRI), Division of Computer and Network Systems, Award No. 1726188, January 1, 2018 – December 31, 2021. https://www. isip.piconepress.com/projects/nsf_dpath/. [3] A. Gulati et al., “Conformer: Convolution-augmented Transformer for Speech Recognition,” in Proceedings of the Annual Conference of the International Speech Communication Association (INTERSPEECH), 2020, pp. 5036-5040. https://doi.org/10.21437/interspeech.2020-3015. [4] C.-J. 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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5. MAGIC: Multitask Automated Generation of Inter-modal CT Perfusion Maps via Generative Adversarial Network

   Fullerton, Garrett ; Kato, Simon ; Fang, Ruogu ( October 2021 , Biomedical Engineering Society Annual Meeting)

   Introduction: Computed tomography perfusion (CTP) imaging requires injection of an intravenous contrast agent and increased exposure to ionizing radiation. This process can be lengthy, costly, and potentially dangerous to patients, especially in emergency settings. We propose MAGIC, a multitask, generative adversarial network-based deep learning model to synthesize an entire CTP series from only a non-contrasted CT (NCCT) input. Materials and Methods: NCCT and CTP series were retrospectively retrieved from 493 patients at UF Health with IRB approval. The data were deidentified and all images were resized to 256x256 pixels. The collected perfusion data were analyzed using the RapidAI CT Perfusion analysis software (iSchemaView, Inc. CA) to generate each CTP map. For each subject, 10 CTP slices were selected. Each slice was paired with one NCCT slice at the same location and two NCCT slices at a predefined vertical offset, resulting in 4.3K CTP images and 12.9K NCCT images used for training. The incorporation of a spatial offset into the NCCT input allows MAGIC to more accurately synthesize cerebral perfusive structures, increasing the quality of the generated images. The studies included a variety of indications, including healthy tissue, mild infarction, and severe infarction. The proposed MAGIC model incorporates a novel multitask architecture, allowing for the simultaneous synthesis of four CTP modalities: mean transit time (MTT), cerebral blood flow (CBF), cerebral blood volume (CBV), and time to peak (TTP). We propose a novel Physicians-in-the-loop module in the model's architecture, acting as a tunable layer that allows physicians to manually adjust the amount of anatomic detail present in the synthesized CTP series. Additionally, we propose two novel loss terms: multi-modal connectivity loss and extrema loss. The multi-modal connectivity loss leverages the multi-task nature to assert that the mathematical relationship between MTT, CBF, and CBV is satisfied. The extrema loss aids in learning regions of elevated and decreased activity in each modality, allowing for MAGIC to accurately learn the characteristics of diagnostic regions of interest. Corresponding NCCT and CTP slices were paired along the vertical axis. The model was trained for 100 epochs on a NVIDIA TITAN X GPU. Results and Discussion: The MAGIC model’s performance was evaluated on a sample of 40 patients from the UF Health dataset. Across all CTP modalities, MAGIC was able to accurately produce images with high structural agreement between the entire synthesized and clinical perfusion images (SSIMmean=0.801 , UQImean=0.926). MAGIC was able to synthesize CTP images to accurately characterize cerebral circulatory structures and identify regions of infarct tissue, as shown in Figure 1. A blind binary evaluation was conducted to assess the presence of cerebral infarction in both the synthesized and clinical perfusion images, resulting in the synthesized images correctly predicting the presence of cerebral infarction with 87.5% accuracy. Conclusions: We proposed a MAGIC model whose novel deep learning structures and loss terms enable high-quality synthesis of CTP maps and characterization of circulatory structures solely from NCCT images, potentially eliminating the requirement for the injection of an intravenous contrast agent and elevated radiation exposure during perfusion imaging. This makes MAGIC a beneficial tool in a clinical scenario increasing the overall safety, accessibility, and efficiency of cerebral perfusion and facilitating better patient outcomes. Acknowledgements: This work was partially supported by the National Science Foundation, IIS-1908299 III: Small: Modeling Multi-Level Connectivity of Brain Dynamics + REU Supplement, to the University of Florida. 

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