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1.
Opt Lett ; 47(6): 1533-1536, 2022 Mar 15.
Artigo em Inglês | MEDLINE | ID: mdl-35290357

RESUMO

We report on the potential to perform image reconstruction in 3D k-space reflectance fluorescence tomography (FT) using deep learning (DL). Herein, we adopt a modified AUTOMAP architecture and develop a training methodology that leverages an open-source Monte-Carlo-based simulator to generate a large dataset. Using an enhanced EMNIST (EEMNIST) dataset as an embedded contrast function allows us to train the network efficiently. The optical strategy utilizes k-space illumination in a reflectance configuration to probe tissue in the mesoscopic regime with high sensitivity and resolution. The proposed DL model training and validation is performed with both in silico data and a phantom experiment. Overall, our results indicate that the approach can correctly reconstruct both single and multiple fluorescent embedding(s) in a 3D volume. Furthermore, the presented technique is shown to outperform the traditional approaches [least-squares (LSQ) and total-variation minimization (TVAL)], especially at higher depths. We, therefore, expect the proposed computational technique to have future implications in preclinical studies.


Assuntos
Aprendizado Profundo , Processamento de Imagem Assistida por Computador/métodos , Método de Monte Carlo , Imagens de Fantasmas , Tomografia/métodos
2.
Biomed Opt Express ; 14(3): 1041-1053, 2023 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-36950248

RESUMO

Widefield illumination and detection strategies leveraging structured light have enabled fast and robust probing of tissue properties over large surface areas and volumes. However, when applied to diffuse optical tomography (DOT) applications, they still require a time-consuming and expert-centric solving of an ill-posed inverse problem. Deep learning (DL) models have been recently proposed to facilitate this challenging step. Herein, we expand on a previously reported deep neural network (DNN) -based architecture (modified AUTOMAP - ModAM) for accurate and fast reconstructions of the absorption coefficient in 3D DOT based on a structured light illumination and detection scheme. Furthermore, we evaluate the improved performances when incorporating a micro-CT structural prior in the DNN-based workflow, named Z-AUTOMAP. This Z-AUTOMAP significantly improves the widefield imaging process's spatial resolution, especially in the transverse direction. The reported DL-based strategies are validated both in silico and in experimental phantom studies using spectral micro-CT priors. Overall, this is the first successful demonstration of micro-CT and DOT fusion using deep learning, greatly enhancing the prospect of rapid data-integration strategies, often demanded in challenging pre-clinical scenarios.

3.
J Biomed Opt ; 27(8)2022 04.
Artigo em Inglês | MEDLINE | ID: mdl-35484688

RESUMO

SIGNIFICANCE: Deep learning (DL) models are being increasingly developed to map sensor data to the image domain directly. However, DL methodologies are data-driven and require large and diverse data sets to provide robust and accurate image formation performances. For research modalities such as 2D/3D diffuse optical imaging, the lack of large publicly available data sets and the wide variety of instrumentation designs, data types, and applications leads to unique challenges in obtaining well-controlled data sets for training and validation. Meanwhile, great efforts over the last four decades have focused on developing accurate and computationally efficient light propagation models that are flexible enough to simulate a wide variety of experimental conditions. AIM: Recent developments in Monte Carlo (MC)-based modeling offer the unique advantage of simulating accurately light propagation spatially, temporally, and over an extensive range of optical parameters, including minimally to highly scattering tissue within a computationally efficient platform. Herein, we demonstrate how such MC platforms, namely "Monte Carlo eXtreme" and "Mesh-based Monte Carlo," can be leveraged to generate large and representative data sets for training the DL model efficiently. APPROACH: We propose data generator pipeline strategies using these platforms and demonstrate their potential in fluorescence optical topography, fluorescence optical tomography, and single-pixel diffuse optical tomography. These applications represent a large variety in instrumentation design, sample properties, and contrast function. RESULTS: DL models trained using the MC-based in silico datasets, validated further with experimental data not used during training, show accurate and promising results. CONCLUSION: Overall, these MC-based data generation pipelines are expected to support the development of DL models for rapid, robust, and user-friendly image formation in a wide variety of applications.


Assuntos
Aprendizado Profundo , Tomografia Óptica , Método de Monte Carlo , Tomografia Óptica/métodos
4.
NPJ Sci Learn ; 6(1): 5, 2021 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-33649355

RESUMO

Online education is important in the COVID-19 pandemic, but online exam at individual homes invites students to cheat in various ways, especially collusion. While physical proctoring is impossible during social distancing, online proctoring is costly, compromises privacy, and can lead to prevailing collusion. Here we develop an optimization-based anti-collusion approach for distanced online testing (DOT) by minimizing the collusion gain, which can be coupled with other techniques for cheating prevention. With prior knowledge of student competences, our DOT technology optimizes sequences of questions and assigns them to students in synchronized time slots, reducing the collusion gain by 2-3 orders of magnitude relative to the conventional exam in which students receive their common questions simultaneously. Our DOT theory allows control of the collusion gain to a sufficiently low level. Our recent final exam in the DOT format has been successful, as evidenced by statistical tests and a post-exam survey.

5.
Artigo em Inglês | MEDLINE | ID: mdl-28792892

RESUMO

We present a novel method for estimating the mean scatterer spacing (MSS) of breast tumors using ensemble empirical mode decomposition (EEMD) domain analysis of deconvolved backscattered radio frequency (RF) data. The autoregressive (AR) spectrum from which the MSS is estimated is obtained from the intrinsic mode functions (IMFs) due to regular scatterers embedded in RF data corrupted by the diffuse scatterers. The IMFs are chosen by giving priority to the presence of an enhanced fundamental harmonic and the presence of a greater number of higher harmonics in the AR spectrum estimated from the IMFs. The AR model order is chosen by minimizing the mean absolute percentage error (MAPE) criterion. In order to ensure that the backscattered data is indeed from a source of coherent scattering, we begin by performing a non-parametric Kolmogorov-Smirnov (K-S) classification test on the backscattered RF data. Deconvolution of the backscattered RF data, which have been classified by the K-S test as sources of significant coherent scattering, is done to reduce the system effect. EEMD domain analysis is then performed on the deconvolved data. The proposed method is able to recover the harmonics associated with the regular scatterers and overcomes many problems encountered while estimating the MSS from the AR spectrum of raw RF data. Using our technique, a mean absolute percentage error (MAPE) of 5.78% is obtained while estimating the MSS from simulated data, which is lower than that of the existing techniques. Our proposed method is shown to outperform the state of the art techniques, namely, singular spectrum analysis, generalized spectrum (GS), spectral autocorrelation (SAC), and modified SAC for different simulation conditions. The MSS for in vivo normal breast tissue is found to be 0.69 ± 0.04 mm; for benign and malignant tumors it is found to be 0.73 ± 0.03 and 0.79 ± 0.04 mm, respectively. The separation between the MSS values of normal and benign tissues for our proposed method is similar to the separations obtained for the conventional methods, but the separation between the MSS values for benign and malignant tissues for our proposed method is slightly higher than that for the conventional methods. When the MSS is used to classify breast tumors into benign and malignant, for a threshold-based classifier, the increase in specificity, accuracy, and area under curve are 18%, 19%, and 22%, respectively, and that for statistical classifiers are 9%, 13%, and 19%, respectively, from that of the next best existing technique.

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