Deep speckle correlation: a deep learning approach toward scalable imaging through scattering media

Imaging through scattering is an important yet challenging problem. Tremendous progress has been made by exploiting the deterministic input–output “transmission matrix” for a fixed medium. However, this “one-to-one” mapping is highly susceptible to speckle decorrelations – small perturbations to the scattering medium lead to model errors and severe degradation of the imaging performance. Our goal here is to develop a new framework that is highly scalable to both medium perturbations and measurement requirement. To do so, we propose a statistical “one-to-all” deep learning (DL) technique that encapsulates a wide range of statistical variations for the model to be resilient to speckle decorrelations. Specifically, we develop a convolutional neural network (CNN) that is able to learn the statistical information contained in the speckle intensity patterns captured on a set of diffusers having the same macroscopic parameter. We then show for the first time, to the best of our knowledge, that the trained CNN is able to generalize and make high-quality object predictions through an entirely different set of diffusers of the same class. Our work paves the way to a highly scalable DL approach for imaging through scattering media.National Science Foundation (NSF) (1711156); Directorate for Engineering (ENG). (1711156 - National Science Foundation (NSF); Directorate for Engineering (ENG))First author draf

Deep learning approach to scalable imaging through scattering media

We propose a deep learning technique to exploit “deep speckle correlations”. Our work paves the way to a highly scalable deep learning approach for imaging through scattering media.Published versio

Illumination coding meets uncertainty learning: toward reliable AI-augmented phase imaging

We propose a physics-assisted deep learning (DL) framework for large space-bandwidth product (SBP) phase imaging. We design an asymmetric coded illumination scheme to encode high-resolution phase information across a wide field-of-view. We then develop a matching DL algorithm to provide large-SBP phase estimation. We show that this illumination coding scheme is highly scalable in achieving flexible resolution, and robust to experimental variations. We demonstrate this technique on both static and dynamic biological samples, and show that it can reliably achieve 5X resolution enhancement across 4X FOVs using only five multiplexed measurements -- more than 10X data reduction over the state-of-the-art. Typical DL algorithms tend to provide over-confident predictions, whose errors are only discovered in hindsight. We develop an uncertainty learning framework to overcome this limitation and provide predictive assessment to the reliability of the DL prediction. We show that the predicted uncertainty maps can be used as a surrogate to the true error. We validate the robustness of our technique by analyzing the model uncertainty. We quantify the effect of noise, model errors, incomplete training data, and "out-of-distribution" testing data by assessing the data uncertainty. We further demonstrate that the predicted credibility maps allow identifying spatially and temporally rare biological events. Our technique enables scalable AI-augmented large-SBP phase imaging with dependable predictions.Published versio

Deep learning approach to Fourier ptychographic microscopy

Convolutional neural networks (CNNs) have gained tremendous success in solving complex inverse problems. The aim of this work is to develop a novel CNN framework to reconstruct video sequences of dynamic live cells captured using a computational microscopy technique, Fourier ptychographic microscopy (FPM). The unique feature of the FPM is its capability to reconstruct images with both wide field-of-view (FOV) and high resolution, i.e. a large space-bandwidth-product (SBP), by taking a series of low resolution intensity images. For live cell imaging, a single FPM frame contains thousands of cell samples with different morphological features. Our idea is to fully exploit the statistical information provided by these large spatial ensembles so as to make predictions in a sequential measurement, without using any additional temporal dataset. Specifically, we show that it is possible to reconstruct high-SBP dynamic cell videos by a CNN trained only on the first FPM dataset captured at the beginning of a time-series experiment. Our CNN approach reconstructs a 12800×10800 pixel phase image using only ∼25 seconds, a 50× speedup compared to the model-based FPM algorithm. In addition, the CNN further reduces the required number of images in each time frame by ∼ 6×. Overall, this significantly improves the imaging throughput by reducing both the acquisition and computational times. The proposed CNN is based on the conditional generative adversarial network (cGAN) framework. We further propose a mixed loss function that combines the standard image domain loss and a weighted Fourier domain loss, which leads to improved reconstruction of the high frequency information. Additionally, we also exploit transfer learning so that our pre-trained CNN can be further optimized to image other cell types. Our technique demonstrates a promising deep learning approach to continuously monitor large live-cell populations over an extended time and gather useful spatial and temporal information with sub-cellular resolution.We would like to thank NVIDIA Corporation for supporting us with the GeForce Titan Xp through the GPU Grant Program. (NVIDIA Corporation; GeForce Titan Xp through the GPU Grant Program)First author draf

High-speed in vitro intensity diffraction tomography

We demonstrate a label-free, scan-free intensity diffraction tomography technique utilizing annular illumination (aIDT) to rapidly characterize large-volume three-dimensional (3-D) refractive index distributions in vitro. By optimally matching the illumination geometry to the microscope pupil, our technique reduces the data requirement by 60 times to achieve high-speed 10-Hz volume rates. Using eight intensity images, we recover volumes of ∼350 μm  ×  100 μm  ×  20  μm, with near diffraction-limited lateral resolution of   ∼  487  nm and axial resolution of   ∼  3.4  μm. The attained large volume rate and high-resolution enable 3-D quantitative phase imaging of complex living biological samples across multiple length scales. We demonstrate aIDT’s capabilities on unicellular diatom microalgae, epithelial buccal cell clusters with native bacteria, and live Caenorhabditis elegans specimens. Within these samples, we recover macroscale cellular structures, subcellular organelles, and dynamic micro-organism tissues with minimal motion artifacts. Quantifying such features has significant utility in oncology, immunology, and cellular pathophysiology, where these morphological features are evaluated for changes in the presence of disease, parasites, and new drug treatments. Finally, we simulate the aIDT system to highlight the accuracy and sensitivity of the proposed technique. aIDT shows promise as a powerful high-speed, label-free computational microscopy approach for applications where natural imaging is required to evaluate environmental effects on a sample in real time.https://arxiv.org/abs/1904.06004Accepted manuscrip

Deep learning approach to Fourier ptychographic microscopy

Convolutional neural networks (CNNs) have gained tremendous success in solving complex inverse problems. The aim of this work is to develop a novel CNN framework to reconstruct video sequence of dynamic live cells captured using a computational microscopy technique, Fourier ptychographic microscopy (FPM). The unique feature of the FPM is its capability to reconstruct images with both wide field-of-view (FOV) and high resolution, i.e. a large space-bandwidth-product (SBP), by taking a series of low resolution intensity images. For live cell imaging, a single FPM frame contains thousands of cell samples with different morphological features. Our idea is to fully exploit the statistical information provided by this large spatial ensemble so as to make predictions in a sequential measurement, without using any additional temporal dataset. Specifically, we show that it is possible to reconstruct high-SBP dynamic cell videos by a CNN trained only on the first FPM dataset captured at the beginning of a time-series experiment. Our CNN approach reconstructs a 12800X10800 pixels phase image using only ~25 seconds, a 50X speedup compared to the model-based FPM algorithm. In addition, the CNN further reduces the required number of images in each time frame by ~6X. Overall, this significantly improves the imaging throughput by reducing both the acquisition and computational times. The proposed CNN is based on the conditional generative adversarial network (cGAN) framework. Additionally, we also exploit transfer learning so that our pre-trained CNN can be further optimized to image other cell types. Our technique demonstrates a promising deep learning approach to continuously monitor large live-cell populations over an extended time and gather useful spatial and temporal information with sub-cellular resolution

Regularized Fourier ptychography using an online plug-and-play algorithm

The plug-and-play priors (PnP) framework has been recently shown to achieve state-of-the-art results in regularized image reconstruction by leveraging a sophisticated denoiser within an iterative algorithm. In this paper, we propose a new online PnP algorithm for Fourier ptychographic microscopy (FPM) based on the accelerated proximal gradient method (APGM). Specifically, the proposed algorithm uses only a subset of measurements, which makes it scalable to a large set of measurements. We validate the algorithm by showing that it can lead to significant performance gains on both simulated and experimental data.https://arxiv.org/abs/1811.00120Published versio

Hybrid Amorphous-Selenium/CMOS Low-Light Imager

This thesis aims to demonstrate a low-light imager capable of moonlight-level imag- ing by combining a custom-designed complementary-metal-oxide-semiconductor (CMOS) pixel array with amorphous selenium (a-Se) as its photosensor. Because of the low dark current of a-Se compared to standard silicon photodiodes, this hybrid structure could enable imagers fabricated in standard mixed-signal CMOS processes to achieve low- light imaging. Such hybrid imagers could have low-light performances comparable to other low-light imagers fabricated in specialized CMOS image-sensor processes. The 320 (H) x 240 (V) imager contains four different pixel designs arranged in four quadrants, with pixel pitches of 7.76 μm x 7.76 μm in quadrants 1 to 3 and 7.76 μm x 8.66 μm in quadrant 4 (Q4). The different quadrants are built to examine various performance-enhancing circuit designs and techniques, including series-stacked devices for leakage suppression, charge-injection suppression that uses dummy transistors, and a programmable dual-capacity design for extended pixel dynamic range. The imager- performance parameters, such as noise, dynamic range, conversion gain, linearity, and full-well capacity were simulated and experimentally verified. This work will also de- scribe the external hardware and software designs used to operate the imager. This thesis summarizes and reports the overall electrical and optical performance of pixels in quadrant 1. The observed signal-to-noise ratio (SNR) of above 20 dB at an illuminance of 0.267 lux demonstrates that the imager can produce excellent images under moonlight-imaging conditions. This was achieved mainly through utilization of the long integration time enabled by circuit techniques implemented at the pixel level, as well as the low dark current of a-Se

A deep-learning approach for high-speed Fourier ptychographic microscopy

We demonstrate a new convolutional neural network architecture to perform Fourier ptychographic Microscopy (FPM) reconstruction, which achieves high-resolution phase recovery with considerably less data than standard FPM.https://www.researchgate.net/profile/Thanh_Nguyen68/publication/325829575_A_deep-learning_approach_for_high-speed_Fourier_ptychographic_microscopy/links/5b2beec20f7e9b0df5ba4872/A-deep-learning-approach-for-high-speed-Fourier-ptychographic-microscopy.pdfhttps://www.researchgate.net/profile/Thanh_Nguyen68/publication/325829575_A_deep-learning_approach_for_high-speed_Fourier_ptychographic_microscopy/links/5b2beec20f7e9b0df5ba4872/A-deep-learning-approach-for-high-speed-Fourier-ptychographic-microscopy.pdfhttps://www.researchgate.net/profile/Thanh_Nguyen68/publication/325829575_A_deep-learning_approach_for_high-speed_Fourier_ptychographic_microscopy/links/5b2beec20f7e9b0df5ba4872/A-deep-learning-approach-for-high-speed-Fourier-ptychographic-microscopy.pdfhttps://www.researchgate.net/profile/Thanh_Nguyen68/publication/325829575_A_deep-learning_approach_for_high-speed_Fourier_ptychographic_microscopy/links/5b2beec20f7e9b0df5ba4872/A-deep-learning-approach-for-high-speed-Fourier-ptychographic-microscopy.pdfhttps://www.researchgate.net/profile/Thanh_Nguyen68/publication/325829575_A_deep-learning_approach_for_high-speed_Fourier_ptychographic_microscopy/links/5b2beec20f7e9b0df5ba4872/A-deep-learning-approach-for-high-speed-Fourier-ptychographic-microscopy.pdfhttps://www.researchgate.net/profile/Thanh_Nguyen68/publication/325829575_A_deep-learning_approach_for_high-speed_Fourier_ptychographic_microscopy/links/5b2beec20f7e9b0df5ba4872/A-deep-learning-approach-for-high-speed-Fourier-ptychographic-microscopy.pdfPublished versio