Udith Haputhanthri

Henry Arguello, Jorge Bacca, Hasindu Kariyawasam et al. · cmu

Computational optical imaging (COI) systems leverage optical coding elements (CE) in their setups to encode a high-dimensional scene in a single or multiple snapshots and decode it by using computational algorithms. The performance of COI systems highly depends on the design of its main components: the CE pattern and the computational method used to perform a given task. Conventional approaches rely on random patterns or analytical designs to set the distribution of the CE. However, the available data and algorithm capabilities of deep neural networks (DNNs) have opened a new horizon in CE data-driven designs that jointly consider the optical encoder and computational decoder. Specifically, by modeling the COI measurements through a fully differentiable image formation model that considers the physics-based propagation of light and its interaction with the CEs, the parameters that define the CE and the computational decoder can be optimized in an end-to-end (E2E) manner. Moreover, by optimizing just CEs in the same framework, inference tasks can be performed from pure optics. This work surveys the recent advances on CE data-driven design and provides guidelines on how to parametrize different optical elements to include them in the E2E framework. Since the E2E framework can handle different inference applications by changing the loss function and the DNN, we present low-level tasks such as spectral imaging reconstruction or high-level tasks such as pose estimation with privacy preserving enhanced by using optimal task-based optical architectures. Finally, we illustrate classification and 3D object recognition applications performed at the speed of the light using all-optics DNN.

Udith Haputhanthri, Kithmini Herath, Ramith Hettiarachchi et al. · cmu

With applications ranging from metabolomics to histopathology, quantitative phase microscopy (QPM) is a powerful label-free imaging modality. Despite significant advances in fast multiplexed imaging sensors and deep-learning-based inverse solvers, the throughput of QPM is currently limited by the speed of electronic hardware. Complementarily, to improve throughput further, here we propose to acquire images in a compressed form such that more information can be transferred beyond the existing electronic hardware bottleneck. To this end, we present a learnable optical compression-decompression framework that learns content-specific features. The proposed differentiable quantitative phase microscopy ($\partial μ$) first uses learnable optical feature extractors as image compressors. The intensity representation produced by these networks is then captured by the imaging sensor. Finally, a reconstruction network running on electronic hardware decompresses the QPM images. In numerical experiments, the proposed system achieves compression of $\times$ 64 while maintaining the SSIM of $\sim 0.90$ and PSNR of $\sim 30$ dB on cells. The results demonstrated by our experiments open up a new pathway for achieving end-to-end optimized (i.e., optics and electronic) compact QPM systems that may provide unprecedented throughput improvements.

Kithmini Herath, Udith Haputhanthri, Ramith Hettiarachchi et al. · cmu

Since the late 16th century, scientists have continuously innovated and developed new microscope types for various applications. Creating a new architecture from the ground up requires substantial scientific expertise and creativity, often spanning years or even decades. In this study, we propose an alternative approach called "Differentiable Microscopy," which introduces a top-down design paradigm for optical microscopes. Using all-optical phase retrieval as an illustrative example, we demonstrate the effectiveness of data-driven microscopy design through $\partialμ$. Furthermore, we conduct comprehensive comparisons with competing methods, showcasing the consistent superiority of our learned designs across multiple datasets, including biological samples. To substantiate our ideas, we experimentally validate the functionality of one of the learned designs, providing a proof of concept. The proposed differentiable microscopy framework supplements the creative process of designing new optical systems and would perhaps lead to unconventional but better optical designs.

Udith Haputhanthri, Declan Campbell, Rim Assouel et al.

Despite success on standard benchmarks, vision language models display persistent failures on tasks involving processing of multi-object scenes, including many tasks that are relatively easy for humans. Recent work has found that these failures may stem from a basic inability to accurately bind object features in-context, a challenge that is referred to as the "binding problem" in cognitive science and neuroscience. The human visual system is thought to solve this binding problem via serial processing, attending to individual objects one at a time so as to avoid interference from other objects. Recent work has proposed "pointing" -- the use of explicit spatial coordinates to refer to objects -- as an analogous solution for vision language models, and found that it improves performance on challenging multi-object tasks. However, it is unclear $\textit{why}$ (i.e., on a mechanistic or representational level) this approach improves performance, and how directly this relates to serial processing in human vision. Here, we investigate this question. We find that learning to point-via-text induces an internal visual search routine, and we characterize the mechanisms that support this procedure. We also find that pointing behavior can be generalized to new tasks via fine-tuning, and that doing so eliminates binding errors and enables compositional generalization. These results provide a proof-of-principle that serial processing can solve the binding problem for vision language models just as it does for biological vision.

Udith Haputhanthri, Andrew Seeber, Dushan Wadduwage

The trade-off between throughput and image quality is an inherent challenge in microscopy. To improve throughput, compressive imaging under-samples image signals; the images are then computationally reconstructed by solving a regularized inverse problem. Compared to traditional regularizers, Deep Learning based methods have achieved greater success in compression and image quality. However, the information loss in the acquisition process sets the compression bounds. Further improvement in compression, without compromising the reconstruction quality is thus a challenge. In this work, we propose differentiable compressive fluorescence microscopy ($\partial μ$) which includes a realistic generalizable forward model with learnable-physical parameters (e.g. illumination patterns), and a novel physics-inspired inverse model. The cascaded model is end-to-end differentiable and can learn optimal compressive sampling schemes through training data. With our model, we performed thousands of numerical experiments on various compressive microscope configurations. We show that learned sampling encodes important information about the specimens in the illumination field of the microscope allowing higher compression up to $\times 1024$. We further utilize our framework for Task Aware Compression. The experimental results show superior performance on the cell segmentation task.

Mohamed Afham, Udith Haputhanthri, Jathurshan Pradeepkumar et al.

Human behavioral monitoring during sleep is essential for various medical applications. Majority of the contactless human pose estimation algorithms are based on RGB modality, causing ineffectiveness in in-bed pose estimation due to occlusions by blankets and varying illumination conditions. Long-wavelength infrared (LWIR) modality based pose estimation algorithms overcome the aforementioned challenges; however, ground truth pose generations by a human annotator under such conditions are not feasible. A feasible solution to address this issue is to transfer the knowledge learned from images with pose labels and no occlusions, and adapt it towards real world conditions (occlusions due to blankets). In this paper, we propose a novel learning strategy comprises of two-fold data augmentation to reduce the cross-domain discrepancy and knowledge distillation to learn the distribution of unlabeled images in real world conditions. Our experiments and analysis show the effectiveness of our approach over multiple standard human pose estimation baselines.

Ramith Hettiarachchi, Udith Haputhanthri, Kithmini Herath et al.

Diagnosing pre-existing heart diseases early in life is important as it helps prevent complications such as pulmonary hypertension, heart rhythm problems, blood clots, heart failure and sudden cardiac arrest. To identify such diseases, phonocardiogram (PCG) and electrocardiogram (ECG) waveforms convey important information. Therefore, effectively using these two modalities of data has the potential to improve the disease screening process. We evaluate this hypothesis on a subset of the PhysioNet Challenge 2016 Dataset which contains simultaneously acquired PCG and ECG recordings. Our novel Dual-Convolutional Neural Network based approach uses transfer learning to tackle the problem of having limited amounts of simultaneous PCG and ECG data that is publicly available, while having the potential to adapt to larger datasets. In addition, we introduce two main evaluation frameworks named record-wise and sample-wise evaluation which leads to a rich performance evaluation for the transfer learning approach. Comparisons with methods which used single or dual modality data show that our method can lead to better performance. Furthermore, our results show that individually collected ECG or PCG waveforms are able to provide transferable features which could effectively help to make use of a limited number of synchronized PCG and ECG waveforms and still achieve significant classification performance.