Anthony T. Fuller

Daniel G. Kyrollos, Anthony Fuller, Kim Greenwood et al.

Infant pose monitoring during sleep has multiple applications in both healthcare and home settings. In a healthcare setting, pose detection can be used for region of interest detection and movement detection for noncontact based monitoring systems. In a home setting, pose detection can be used to detect sleep positions which has shown to have a strong influence on multiple health factors. However, pose monitoring during sleep is challenging due to heavy occlusions from blanket coverings and low lighting. To address this, we present a novel dataset, Simultaneously-collected multimodal Mannequin Lying pose (SMaL) dataset, for under the cover infant pose estimation. We collect depth and pressure imagery of an infant mannequin in different poses under various cover conditions. We successfully infer full body pose under the cover by training state-of-art pose estimation methods and leveraging existing multimodal adult pose datasets for transfer learning. We demonstrate a hierarchical pretraining strategy for transformer-based models to significantly improve performance on our dataset. Our best performing model was able to detect joints under the cover within 25mm 86% of the time with an overall mean error of 16.9mm. Data, code and models publicly available at https://github.com/DanielKyr/SMaL

Anthony Fuller, Koreen Millard, James R. Green

Although the remote sensing (RS) community has begun to pretrain transformers (intended to be fine-tuned on RS tasks), it is unclear how these models perform under distribution shifts. Here, we pretrain a new RS transformer--called SatViT-V2--on 1.3 million satellite-derived RS images, then fine-tune it (along with five other models) to investigate how it performs on distributions not seen during training. We split an expertly labeled land cover dataset into 14 datasets based on source biome. We train each model on each biome separately and test them on all other biomes. In all, this amounts to 1638 biome transfer experiments. After fine-tuning, we find that SatViT-V2 outperforms SatViT-V1 by 3.1% on in-distribution (matching biomes) and 2.8% on out-of-distribution (mismatching biomes) data. Additionally, we find that initializing fine-tuning from the linear probed solution (i.e., leveraging LPFT [1]) improves SatViT-V2's performance by another 1.2% on in-distribution and 2.4% on out-of-distribution data. Next, we find that pretrained RS transformers are better calibrated under distribution shifts than non-pretrained models and leveraging LPFT results in further improvements in model calibration. Lastly, we find that five measures of distribution shift are moderately correlated with biome transfer performance. We share code and pretrained model weights. (https://github.com/antofuller/SatViT)

Anthony Fuller, Koreen Millard, James R. Green

A vital and rapidly growing application, remote sensing offers vast yet sparsely labeled, spatially aligned multimodal data; this makes self-supervised learning algorithms invaluable. We present CROMA: a framework that combines contrastive and reconstruction self-supervised objectives to learn rich unimodal and multimodal representations. Our method separately encodes masked-out multispectral optical and synthetic aperture radar samples -- aligned in space and time -- and performs cross-modal contrastive learning. Another encoder fuses these sensors, producing joint multimodal encodings that are used to predict the masked patches via a lightweight decoder. We show that these objectives are complementary when leveraged on spatially aligned multimodal data. We also introduce X- and 2D-ALiBi, which spatially biases our cross- and self-attention matrices. These strategies improve representations and allow our models to effectively extrapolate to images up to 17.6x larger at test-time. CROMA outperforms the current SoTA multispectral model, evaluated on: four classification benchmarks -- finetuning (avg. 1.8%), linear (avg. 2.4%) and nonlinear (avg. 1.4%) probing, kNN classification (avg. 3.5%), and K-means clustering (avg. 8.4%); and three segmentation benchmarks (avg. 6.4%). CROMA's rich, optionally multimodal representations can be widely leveraged across remote sensing applications.

Gabriel Tseng, Anthony Fuller, Marlena Reil et al.

We introduce a highly multimodal transformer to represent many remote sensing modalities - multispectral optical, synthetic aperture radar, elevation, weather, pseudo-labels, and more - across space and time. These inputs are useful for diverse remote sensing tasks, such as crop mapping and flood detection. However, learning shared representations of remote sensing data is challenging, given the diversity of relevant data modalities, and because objects of interest vary massively in scale, from small boats (1-2 pixels and fast) to glaciers (thousands of pixels and slow). We present a novel self-supervised learning algorithm that extracts multi-scale features across a flexible set of input modalities through masked modeling. Our dual global and local contrastive losses differ in their targets (deep representations vs. shallow input projections) and masking strategies (structured vs. not). Our Galileo is a single generalist model that outperforms SoTA specialist models for satellite images and pixel time series across eleven benchmarks and multiple tasks.

Youssef Megahed, Anthony Fuller, Saleh Abou-Alwan et al.

Hirschsprung's disease (HD) is a congenital birth defect diagnosed by identifying the lack of ganglion cells within the colon's muscularis propria, specifically within the myenteric plexus regions. There may be advantages for quantitative assessments of histopathology images of the colon, such as counting the ganglion and assessing their spatial distribution; however, this would be time-intensive for pathologists, costly, and subject to inter- and intra-rater variability. Previous research has demonstrated the potential for deep learning approaches to automate histopathology image analysis, including segmentation of the muscularis propria using convolutional neural networks (CNNs). Recently, Vision Transformers (ViTs) have emerged as a powerful deep learning approach due to their self-attention. This study explores the application of ViTs for muscularis propria segmentation in calretinin-stained histopathology images and compares their performance to CNNs and shallow learning methods. The ViT model achieved a DICE score of 89.9% and Plexus Inclusion Rate (PIR) of 100%, surpassing the CNN (DICE score of 89.2%; PIR of 96.0%) and k-means clustering method (DICE score of 80.7%; PIR 77.4%). Results assert that ViTs are a promising tool for advancing HD-related image analysis.

Youssef Megahed, Saleh Abou-Alwan, Anthony Fuller et al.

Hirschsprung Disease is characterized by the absence of ganglion cells in the myenteric plexus. Therefore, the correct identification of ganglion cells is crucial for diagnosing Hirschsprung disease. We introduce a three-stage analysis framework that mimics the pathologist's diagnostic approach. The framework, based on a Vision Transformer model (ViT-B/16), sequentially segments the muscularis propria, segments the myenteric plexus, and detects ganglion cells within anatomically valid regions. 30 whole-slide images of colon tissue were used, each containing manual annotations of muscularis, plexus, and ganglion cells. A 5-fold cross-validation scheme was applied to each stage, along with resolution-specific tiling strategies and tailored postprocessing to ensure anatomical consistency. The proposed method achieved a Dice coefficient of 89.9% and a Plexus Inclusion Rate of 100% for muscularis segmentation. Plexus segmentation reached a recall of 94.8%, a precision of 84.2% and a Ganglia Inclusion Rate of 99.7%. For ganglion cells annotated with high certainty, the model achieved 62.1\% precision and 89.1% recall. When considering all annotated ganglion cells, regardless of certainty level, the overall precision was 67.0%. These results indicate that ViT-based models are effective at leveraging global tissue context and capturing cellular morphology at small scales, even within complex histological tissue structures. This multi-stage methodology has great potential to support digital pathology workflows by reducing inter-observer variability and assisting in the evaluation of Hirschsprung disease. The clinical impact will be evaluated in future work with larger multi-center datasets and additional expert annotations.