Chuyang Ye

Wan Liu, Yuqian Chen, Chuyang Ye et al.

Neuroimaging measures of the brain's white matter connections can enable the prediction of non-imaging phenotypes, such as demographic and cognitive measures. Existing works have investigated traditional microstructure and connectivity measures from diffusion MRI tractography, without considering the shape of the connections reconstructed by tractography. In this paper, we investigate the potential of fiber tract shape features for predicting non-imaging phenotypes, both individually and in combination with traditional features. We focus on three basic shape features: length, diameter, and elongation. Two different prediction methods are used, including a traditional regression method and a deep-learning-based prediction method. Experiments use an efficient two-stage fusion strategy for prediction using microstructure, connectivity, and shape measures. To reduce predictive bias due to brain size, normalized shape features are also investigated. Experimental results on the Human Connectome Project (HCP) young adult dataset (n=1065) demonstrate that individual shape features are predictive of non-imaging phenotypes. When combined with microstructure and connectivity features, shape features significantly improve performance for predicting the cognitive score TPVT (NIH Toolbox picture vocabulary test). Overall, this study demonstrates that the shape of fiber tracts contains useful information for the description and study of the living human brain using machine learning.

Wan Liu, Qi Lu, ZhiZheng Zhuo et al.

Deep learning based methods have achieved state-of-the-art performance for automated white matter (WM) tract segmentation. In these methods, the segmentation model needs to be trained with a large number of manually annotated scans, which can be accumulated throughout time. When novel WM tracts, i.e., tracts not included in the existing annotated WM tracts, are to be segmented, additional annotations of these novel WM tracts need to be collected. Since tract annotation is time-consuming and costly, it is desirable to make only a few annotations of novel WM tracts for training the segmentation model, and previous work has addressed this problem by transferring the knowledge learned for segmenting existing WM tracts to the segmentation of novel WM tracts. However, accurate segmentation of novel WM tracts can still be challenging in the one-shot setting, where only one scan is annotated for the novel WM tracts. In this work, we explore the problem of one-shot segmentation of novel WM tracts. Since in the one-shot setting the annotated training data is extremely scarce, based on the existing knowledge transfer framework, we propose to further perform extensive data augmentation for the single annotated scan, where synthetic annotated training data is produced. We have designed several different strategies that mask out regions in the single annotated scan for data augmentation. Our method was evaluated on public and in-house datasets. The experimental results show that our method improves the accuracy of one-shot segmentation of novel WM tracts.

Tianshu Zheng, Cong Sun, Weihao Zheng et al.

Diffusion magnetic resonance imaging (dMRI) is an important tool in characterizing tissue microstructure based on biophysical models, which are complex and highly non-linear. Resolving microstructures with optimization techniques is prone to estimation errors and requires dense sampling in the q-space. Deep learning based approaches have been proposed to overcome these limitations. Motivated by the superior performance of the Transformer, in this work, we present a learning-based framework based on Transformer, namely, a Microstructure Estimation Transformer with Sparse Coding (METSC) for dMRI-based microstructure estimation with downsampled q-space data. To take advantage of the Transformer while addressing its limitation in large training data requirements, we explicitly introduce an inductive bias - model bias into the Transformer using a sparse coding technique to facilitate the training process. Thus, the METSC is composed with three stages, an embedding stage, a sparse representation stage, and a mapping stage. The embedding stage is a Transformer-based structure that encodes the signal to ensure the voxel is represented effectively. In the sparse representation stage, a dictionary is constructed by solving a sparse reconstruction problem that unfolds the Iterative Hard Thresholding (IHT) process. The mapping stage is essentially a decoder that computes the microstructural parameters from the output of the second stage, based on the weighted sum of normalized dictionary coefficients where the weights are also learned. We tested our framework on two dMRI models with downsampled q-space data, including the intravoxel incoherent motion (IVIM) model and the neurite orientation dispersion and density imaging (NODDI) model. The proposed method achieved up to 11.25 folds of acceleration in scan time and outperformed the other state-of-the-art learning-based methods.

Xinru Zhang, Ni Ou, Chenghao Liu et al.

Automated brain tumor segmentation based on deep learning (DL) has achieved promising performance. However, it generally relies on annotated images for model training, which is not always feasible in clinical settings. Therefore, the development of unsupervised DL-based brain tumor segmentation approaches without expert annotations is desired. Motivated by the success of prompt learning (PL) in natural language processing, we propose an approach to unsupervised brain tumor segmentation by designing image-based prompts that allow indication of brain tumors, and this approach is dubbed as PL-based Brain Tumor Segmentation (PL-BTS). Specifically, instead of directly training a model for brain tumor segmentation with a large amount of annotated data, we seek to train a model that can answer the question: is a voxel in the input image associated with tumor-like hyper-/hypo-intensity? Such a model can be trained by artificially generating tumor-like hyper-/hypo-intensity on images without tumors with hand-crafted designs. Since the hand-crafted designs may be too simplistic to represent all kinds of real tumors, the trained model may overfit the simplistic hand-crafted task rather than actually answer the question of abnormality. To address this problem, we propose the use of a validation task, where we generate a different hand-crafted task to monitor overfitting. In addition, we propose PL-BTS+ that further improves PL-BTS by exploiting unannotated images with brain tumors. Compared with competing unsupervised methods, the proposed method has achieved marked improvements on both public and in-house datasets, and we have also demonstrated its possible extension to other brain lesion segmentation tasks.

Zipei Zhao, Fengqian Pang, Yaou Liu et al.

Cell detection in histopathology images is of great interest to clinical practice and research, and convolutional neural networks (CNNs) have achieved remarkable cell detection results. Typically, to train CNN-based cell detection models, every positive instance in the training images needs to be annotated, and instances that are not labeled as positive are considered negative samples. However, manual cell annotation is complicated due to the large number and diversity of cells, and it can be difficult to ensure the annotation of every positive instance. In many cases, only incomplete annotations are available, where some of the positive instances are annotated and the others are not, and the classification loss term for negative samples in typical network training becomes incorrect. In this work, to address this problem of incomplete annotations, we propose to reformulate the training of the detection network as a positive-unlabeled learning problem. Since the instances in unannotated regions can be either positive or negative, they have unknown labels. Using the samples with unknown labels and the positively labeled samples, we first derive an approximation of the classification loss term corresponding to negative samples for binary cell detection, and based on this approximation we further extend the proposed framework to multi-class cell detection. For evaluation, experiments were performed on four publicly available datasets. The experimental results show that our method improves the performance of cell detection in histopathology images given incomplete annotations for network training.

Chuyang Ye, Dongyan Wei, Zhendong Liu et al.

Test-Time Adaptation (TTA) addresses domain shifts between training and testing. However, existing methods assume a homogeneous target domain (e.g., single domain) at any given time. They fail to handle the dynamic nature of real-world data, where single-domain and multiple-domain distributions change over time. We identify that performance drops in multiple-domain scenarios are caused by batch normalization errors and gradient conflicts, which hinder adaptation. To solve these challenges, we propose Domain Diversity Adaptive Test-Time Adaptation (DATTA), the first approach to handle TTA under dynamic domain shift data streams. It is guided by a novel domain-diversity score. DATTA has three key components: a domain-diversity discriminator to recognize single- and multiple-domain patterns, domain-diversity adaptive batch normalization to combine source and test-time statistics, and domain-diversity adaptive fine-tuning to resolve gradient conflicts. Extensive experiments show that DATTA significantly outperforms state-of-the-art methods by up to 13%. Code is available at https://github.com/DYW77/DATTA.

Wan Liu, Chuyang Ye

White matter (WM) tract segmentation is a crucial step for brain connectivity studies. It is performed on diffusion magnetic resonance imaging (dMRI), and deep neural networks (DNNs) have achieved promising segmentation accuracy. Existing DNN-based methods use an annotated dataset for model training. However, the performance of the trained model on a different test dataset may not be optimal due to distribution shift, and it is desirable to design WM tract segmentation approaches that allow better generalization of the segmentation model to arbitrary test datasets. In this work, we propose a WM tract segmentation approach that improves the generalization with scaled residual bootstrap. The difference between dMRI scans in training and test datasets is most noticeably caused by the different numbers of diffusion gradients and noise levels. Since both of them lead to different signal-to-noise ratios (SNRs) between the training and test data, we propose to augment the training scans by adjusting the noise magnitude and develop an adapted residual bootstrap strategy for the augmentation. To validate the proposed approach, two dMRI datasets were used, and the experimental results show that our method consistently improved the generalization of WM tract segmentation under various settings.

Xinru Zhang, Ni Ou, Berke Doga Basaran et al.

Brain lesion segmentation plays an essential role in neurological research and diagnosis. As brain lesions can be caused by various pathological alterations, different types of brain lesions tend to manifest with different characteristics on different imaging modalities. Due to this complexity, brain lesion segmentation methods are often developed in a task-specific manner. A specific segmentation model is developed for a particular lesion type and imaging modality. However, the use of task-specific models requires predetermination of the lesion type and imaging modality, which complicates their deployment in real-world scenarios. In this work, we propose a universal foundation model for 3D brain lesion segmentation, which can automatically segment different types of brain lesions for input data of various imaging modalities. We formulate a novel Mixture of Modality Experts (MoME) framework with multiple expert networks attending to different imaging modalities. A hierarchical gating network combines the expert predictions and fosters expertise collaboration. Furthermore, we introduce a curriculum learning strategy during training to avoid the degeneration of each expert network and preserve their specialization. We evaluated the proposed method on nine brain lesion datasets, encompassing five imaging modalities and eight lesion types. The results show that our model outperforms state-of-the-art universal models and provides promising generalization to unseen datasets.

Ruizhi Zhu, Xinru Zhang, Haowen Pang et al.

Synthesizing healthy brain scans from diseased brain scans offers a potential solution to address the limitations of general-purpose algorithms, such as tissue segmentation and brain extraction algorithms, which may not effectively handle diseased images. We consider this a 3D inpainting task and investigate the adaptation of 2D inpainting methods to meet the requirements of 3D magnetic resonance imaging(MRI) data. Our contributions encompass potential modifications tailored to MRI-specific needs, and we conducted evaluations of multiple inpainting techniques using the BraTS2023 Inpainting datasets to assess their efficacy and limitations.

Haowen Pang, Weiyan Guo, Chuyang Ye

Multi-modal brain magnetic resonance imaging (MRI) plays a crucial role in clinical diagnostics by providing complementary information across different imaging modalities. However, a common challenge in clinical practice is missing MRI modalities. In this paper, we apply SwinUNETR to the synthesize of missing modalities in brain MRI. SwinUNETR is a novel neural network architecture designed for medical image analysis, integrating the strengths of Swin Transformer and convolutional neural networks (CNNs). The Swin Transformer, a variant of the Vision Transformer (ViT), incorporates hierarchical feature extraction and window-based self-attention mechanisms, enabling it to capture both local and global contextual information effectively. By combining the Swin Transformer with CNNs, SwinUNETR merges global context awareness with detailed spatial resolution. This hybrid approach addresses the challenges posed by the varying modality characteristics and complex brain structures, facilitating the generation of accurate and realistic synthetic images. We evaluate the performance of SwinUNETR on brain MRI datasets and demonstrate its superior capability in generating clinically valuable images. Our results show significant improvements in image quality, anatomical consistency, and diagnostic value.

Fengqian Pang, Chunyue Lei, Hongfei Zhao et al.

Drug Mechanism of Action (MoA) mainly investigates how drug molecules interact with cells, which is crucial for drug discovery and clinical application. Recently, deep learning models have been used to recognize MoA by relying on high-content and fluorescence images of cells exposed to various drugs. However, these methods focus on spatial characteristics while overlooking the temporal dynamics of live cells. Time-lapse imaging is more suitable for observing the cell response to drugs. Additionally, drug molecules can trigger cellular dynamic variations related to specific MoA. This indicates that the drug molecule modality may complement the image counterpart. This paper proposes MolCLIP, the first visual language model to combine microscopic cell video- and molecule-modalities. MolCLIP designs a molecule-auxiliary CLIP framework to guide video features in learning the distribution of the molecular latent space. Furthermore, we integrate a metric learning strategy with MolCLIP to optimize the aggregation of video features. Experimental results on the MitoDataset demonstrate that MolCLIP achieves improvements of 51.2% and 20.5% in mAP for drug identification and MoA recognition, respectively.

Lujun Gui, Chuyang Ye, Tianyi Yan

Contrast-enhanced magnetic resonance imaging (MRI) is pivotal in the pipeline of brain tumor segmentation and analysis. Gadolinium-based contrast agents, as the most commonly used contrast agents, are expensive and may have potential side effects, and it is desired to obtain contrast-enhanced brain tumor MRI scans without the actual use of contrast agents. Deep learning methods have been applied to synthesize virtual contrast-enhanced MRI scans from non-contrast images. However, as this synthesis problem is inherently ill-posed, these methods fall short in producing high-quality results. In this work, we propose Conditional Autoregressive Vision Model (CAVM) for improving the synthesis of contrast-enhanced brain tumor MRI. As the enhancement of image intensity grows with a higher dose of contrast agents, we assume that it is less challenging to synthesize a virtual image with a lower dose, where the difference between the contrast-enhanced and non-contrast images is smaller. Thus, CAVM gradually increases the contrast agent dosage and produces higher-dose images based on previous lower-dose ones until the final desired dose is achieved. Inspired by the resemblance between the gradual dose increase and the Chain-of-Thought approach in natural language processing, CAVM uses an autoregressive strategy with a decomposition tokenizer and a decoder. Specifically, the tokenizer is applied to obtain a more compact image representation for computational efficiency, and it decomposes the image into dose-variant and dose-invariant tokens. Then, a masked self-attention mechanism is developed for autoregression that gradually increases the dose of the virtual image based on the dose-variant tokens. Finally, the updated dose-variant tokens corresponding to the desired dose are decoded together with dose-invariant tokens to produce the final contrast-enhanced MRI.

Qinting Jiang, Chuyang Ye, Dongyan Wei et al.

Despite progress, deep neural networks still suffer performance declines under distribution shifts between training and test domains, leading to a substantial decrease in Quality of Experience (QoE) for multimedia applications. Existing test-time adaptation (TTA) methods are challenged by dynamic, multiple test distributions within batches. This work provides a new perspective on analyzing batch normalization techniques through class-related and class-irrelevant features, our observations reveal combining source and test batch normalization statistics robustly characterizes target distributions. However, test statistics must have high similarity. We thus propose Discover Your Neighbours (DYN), the first backward-free approach specialized for dynamic TTA. The core innovation is identifying similar samples via instance normalization statistics and clustering into groups which provides consistent class-irrelevant representations. Specifically, Our DYN consists of layer-wise instance statistics clustering (LISC) and cluster-aware batch normalization (CABN). In LISC, we perform layer-wise clustering of approximate feature samples at each BN layer by calculating the cosine similarity of instance normalization statistics across the batch. CABN then aggregates SBN and TCN statistics to collaboratively characterize the target distribution, enabling more robust representations. Experimental results validate DYN's robustness and effectiveness, demonstrating maintained performance under dynamic data stream patterns.

Xinru Zhang, Chenghao Liu, Ni Ou et al.

Brain lesion segmentation provides a valuable tool for clinical diagnosis, and convolutional neural networks (CNNs) have achieved unprecedented success in the task. Data augmentation is a widely used strategy that improves the training of CNNs, and the design of the augmentation method for brain lesion segmentation is still an open problem. In this work, we propose a simple data augmentation approach, dubbed as CarveMix, for CNN-based brain lesion segmentation. Like other "mix"-based methods, such as Mixup and CutMix, CarveMix stochastically combines two existing labeled images to generate new labeled samples. Yet, unlike these augmentation strategies based on image combination, CarveMix is lesion-aware, where the combination is performed with an attention on the lesions and a proper annotation is created for the generated image. Specifically, from one labeled image we carve a region of interest (ROI) according to the lesion location and geometry, and the size of the ROI is sampled from a probability distribution. The carved ROI then replaces the corresponding voxels in a second labeled image, and the annotation of the second image is replaced accordingly as well. In this way, we generate new labeled images for network training and the lesion information is preserved. To evaluate the proposed method, experiments were performed on two brain lesion datasets. The results show that our method improves the segmentation accuracy compared with other simple data augmentation approaches.

Zipei Zhao, Fengqian Pang, Zhiwen Liu et al.

Cell detection in histopathology images is of great value in clinical practice. \textit{Convolutional neural networks} (CNNs) have been applied to cell detection to improve the detection accuracy, where cell annotations are required for network training. However, due to the variety and large number of cells, complete annotations that include every cell of interest in the training images can be challenging. Usually, incomplete annotations can be achieved, where positive labeling results are carefully examined to ensure their reliability but there can be other positive instances, i.e., cells of interest, that are not included in the annotations. This annotation strategy leads to a lack of knowledge about true negative samples. Most existing methods simply treat instances that are not labeled as positive as truly negative during network training, which can adversely affect the network performance. In this work, to address the problem of incomplete annotations, we formulate the training of detection networks as a positive-unlabeled learning problem. Specifically, the classification loss in network training is revised to take into account incomplete annotations, where the terms corresponding to negative samples are approximated with the true positive samples and the other samples of which the labels are unknown. To evaluate the proposed method, experiments were performed on a publicly available dataset for mitosis detection in breast cancer cells, and the experimental results show that our method improves the performance of cell detection given incomplete annotations for training.

Qi Lu, Chuyang Ye

Convolutional neural networks (CNNs) have achieved stateof-the-art performance for white matter (WM) tract segmentation based on diffusion magnetic resonance imaging (dMRI). These CNNs require a large number of manual delineations of the WM tracts of interest for training, which are generally labor-intensive and costly. The expensive manual delineation can be a particular disadvantage when novel WM tracts, i.e., tracts that have not been included in existing manual delineations, are to be analyzed. To accurately segment novel WM tracts, it is desirable to transfer the knowledge learned about existing WM tracts, so that even with only a few delineations of the novel WM tracts, CNNs can learn adequately for the segmentation. In this paper, we explore the transfer of such knowledge to the segmentation of novel WM tracts in the few-shot setting. Although a classic fine-tuning strategy can be used for the purpose, the information in the last task-specific layer for segmenting existing WM tracts is completely discarded. We hypothesize that the weights of this last layer can bear valuable information for segmenting the novel WM tracts and thus completely discarding the information is not optimal. In particular, we assume that the novel WM tracts can correlate with existing WM tracts and the segmentation of novel WM tracts can be predicted with the logits of existing WM tracts. In this way, better initialization of the last layer than random initialization can be achieved for fine-tuning. Further, we show that a more adaptive use of the knowledge in the last layer for segmenting existing WM tracts can be conveniently achieved by simply inserting a warmup stage before classic fine-tuning. The proposed method was evaluated on a publicly available dMRI dataset, where we demonstrate the benefit of our method for few-shot segmentation of novel WM tracts.

Shen Wang, Kongming Liang, Chengwei Pan et al.

The midline related pathological image features are crucial for evaluating the severity of brain compression caused by stroke or traumatic brain injury (TBI). The automated midline delineation not only improves the assessment and clinical decision making for patients with stroke symptoms or head trauma but also reduces the time of diagnosis. Nevertheless, most of the previous methods model the midline by localizing the anatomical points, which are hard to detect or even missing in severe cases. In this paper, we formulate the brain midline delineation as a segmentation task and propose a three-stage framework. The proposed framework firstly aligns an input CT image into the standard space. Then, the aligned image is processed by a midline detection network (MD-Net) integrated with the CoordConv Layer and Cascade AtrousCconv Module to obtain the probability map. Finally, we formulate the optimal midline selection as a pathfinding problem to solve the problem of the discontinuity of midline delineation. Experimental results show that our proposed framework can achieve superior performance on one in-house dataset and one public dataset.

Yu Qin, Yuxing Li, Zhiwen Liu et al.

Learning-based approaches, especially those based on deep networks, have enabled high-quality estimation of tissue microstructure from low-quality diffusion magnetic resonance imaging (dMRI) scans, which are acquired with a limited number of diffusion gradients and a relatively poor spatial resolution. These learning-based approaches to tissue microstructure estimation require acquisitions of training dMRI scans with high-quality diffusion signals, which are densely sampled in the q-space and have a high spatial resolution. However, the acquisition of training scans may not be available for all datasets. Therefore, we explore knowledge transfer between different dMRI datasets so that learning-based tissue microstructure estimation can be applied for datasets where training scans are not acquired. Specifically, for a target dataset of interest, where only low-quality diffusion signals are acquired without training scans, we exploit the information in a source dMRI dataset acquired with high-quality diffusion signals. We interpolate the diffusion signals in the source dataset in the q-space using a dictionary-based signal representation, so that the interpolated signals match the acquisition scheme of the target dataset. Then, the interpolated signals are used together with the high-quality tissue microstructure computed from the source dataset to train deep networks that perform tissue microstructure estimation for the target dataset. Experiments were performed on brain dMRI scans with low-quality diffusion signals, where the benefit of the proposed strategy is demonstrated.

Wenhui Cui, Yanlin Liu, Yuxing Li et al.

Automated brain lesion segmentation provides valuable information for the analysis and intervention of patients. In particular, methods based on convolutional neural networks (CNNs) have achieved state-of-the-art segmentation performance. However, CNNs usually require a decent amount of annotated data, which may be costly and time-consuming to obtain. Since unannotated data is generally abundant, it is desirable to use unannotated data to improve the segmentation performance for CNNs when limited annotated data is available. In this work, we propose a semi-supervised learning (SSL) approach to brain lesion segmentation, where unannotated data is incorporated into the training of CNNs. We adapt the mean teacher model, which is originally developed for SSL-based image classification, for brain lesion segmentation. Assuming that the network should produce consistent outputs for similar inputs, a loss of segmentation consistency is designed and integrated into a self-ensembling framework. Specifically, we build a student model and a teacher model, which share the same CNN architecture for segmentation. The student and teacher models are updated alternately. At each step, the student model learns from the teacher model by minimizing the weighted sum of the segmentation loss computed from annotated data and the segmentation consistency loss between the teacher and student models computed from unannotated data. Then, the teacher model is updated by combining the updated student model with the historical information of teacher models using an exponential moving average strategy. For demonstration, the proposed approach was evaluated on ischemic stroke lesion segmentation, where it improves stroke lesion segmentation with the incorporation of unannotated data.

Chuyang Ye

By capturing the anisotropic water diffusion in tissue, diffusion magnetic resonance imaging (dMRI) provides a unique tool for noninvasively probing the tissue microstructure and orientation in the human brain. The diffusion profile can be described by the ensemble average propagator (EAP), which is inferred from observed diffusion signals. However, accurate EAP estimation using the number of diffusion gradients that is clinically practical can be challenging. In this work, we propose a deep learning algorithm for EAP estimation, which is named learning-based ensemble average propagator estimation (LEAPE). The EAP is commonly represented by a basis and its associated coefficients, and here we choose the SHORE basis and design a deep network to estimate the coefficients. The network comprises two cascaded components. The first component is a multiple layer perceptron (MLP) that simultaneously predicts the unknown coefficients. However, typical training loss functions, such as mean squared errors, may not properly represent the geometry of the possibly non-Euclidean space of the coefficients, which in particular causes problems for the extraction of directional information from the EAP. Therefore, to regularize the training, in the second component we compute an auxiliary output of approximated fiber orientation (FO) errors with the aid of a second MLP that is trained separately. We performed experiments using dMRI data that resemble clinically achievable $q$-space sampling, and observed promising results compared with the conventional EAP estimation method.

Chuyang Ye, Jerry L. Prince

Diffusion magnetic resonance imaging (dMRI) is currently the only tool for noninvasively imaging the brain's white matter tracts. The fiber orientation (FO) is a key feature computed from dMRI for fiber tract reconstruction. Because the number of FOs in a voxel is usually small, dictionary-based sparse reconstruction has been used to estimate FOs with a relatively small number of diffusion gradients. However, accurate FO estimation in regions with complex FO configurations in the presence of noise can still be challenging. In this work we explore the use of a deep network for FO estimation in a dictionary-based framework and propose an algorithm named Fiber Orientation Reconstruction guided by a Deep Network (FORDN). FORDN consists of two steps. First, we use a smaller dictionary encoding coarse basis FOs to represent the diffusion signals. To estimate the mixture fractions of the dictionary atoms (and thus coarse FOs), a deep network is designed specifically for solving the sparse reconstruction problem. Here, the smaller dictionary is used to reduce the computational cost of training. Second, the coarse FOs inform the final FO estimation, where a larger dictionary encoding dense basis FOs is used and a weighted l1-norm regularized least squares problem is solved to encourage FOs that are consistent with the network output. FORDN was evaluated and compared with state-of-the-art algorithms that estimate FOs using sparse reconstruction on simulated and real dMRI data, and the results demonstrate the benefit of using a deep network for FO estimation.

Chuyang Ye

Diffusion magnetic resonance imaging (dMRI) provides a unique tool for noninvasively probing the microstructure of the neuronal tissue. The NODDI model has been a popular approach to the estimation of tissue microstructure in many neuroscience studies. It represents the diffusion signals with three types of diffusion in tissue: intra-cellular, extra-cellular, and cerebrospinal fluid compartments. However, the original NODDI method uses a computationally expensive procedure to fit the model and could require a large number of diffusion gradients for accurate microstructure estimation, which may be impractical for clinical use. Therefore, efforts have been devoted to efficient and accurate NODDI microstructure estimation with a reduced number of diffusion gradients. In this work, we propose a deep network based approach to the NODDI microstructure estimation, which is named Microstructure Estimation using a Deep Network (MEDN). Motivated by the AMICO algorithm which accelerates the computation of NODDI parameters, we formulate the microstructure estimation problem in a dictionary-based framework. The proposed network comprises two cascaded stages. The first stage resembles the solution to a dictionary-based sparse reconstruction problem and the second stage computes the final microstructure using the output of the first stage. The weights in the two stages are jointly learned from training data, which is obtained from training dMRI scans with diffusion gradients that densely sample the q-space. The proposed method was applied to brain dMRI scans, where two shells each with 30 gradient directions (60 diffusion gradients in total) were used. Estimation accuracy with respect to the gold standard was measured and the results demonstrate that MEDN outperforms the competing algorithms.

Chuyang Ye, Jiachen Zhuo, Rao P. Gullapalli et al.

Data from diffusion magnetic resonance imaging (dMRI) can be used to reconstruct fiber tracts, for example, in muscle and white matter. Estimation of fiber orientations (FOs) is a crucial step in the reconstruction process and these estimates can be corrupted by noise. In this paper, a new method called Fiber Orientation Reconstruction using Neighborhood Information (FORNI) is described and shown to reduce the effects of noise and improve FO estimation performance by incorporating spatial consistency. FORNI uses a fixed tensor basis to model the diffusion weighted signals, which has the advantage of providing an explicit relationship between the basis vectors and the FOs. FO spatial coherence is encouraged using weighted l1-norm regularization terms, which contain the interaction of directional information between neighbor voxels. Data fidelity is encouraged using a squared error between the observed and reconstructed diffusion weighted signals. After appropriate weighting of these competing objectives, the resulting objective function is minimized using a block coordinate descent algorithm, and a straightforward parallelization strategy is used to speed up processing. Experiments were performed on a digital crossing phantom, ex vivo tongue dMRI data, and in vivo brain dMRI data for both qualitative and quantitative evaluation. The results demonstrate that FORNI improves the quality of FO estimation over other state of the art algorithms.