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Improving Patch-Based Convolutional Neural Networks for MRI Brain Tumor Segmentation by Leveraging Location Information.
The manual brain tumor annotation process is time consuming and resource consuming, therefore, an automated and accurate brain tumor segmentation tool is greatly in demand. In this paper, we introduce a novel method to integrate location information with the state-of-the-art patch-based neural networks for brain tumor segmentation. This is motivated by the observation that lesions are not uniformly distributed across different brain parcellation regions and that a locality-sensitive segmentation is likely to obtain better segmentation accuracy. Toward this, we use an existing brain parcellation atlas in the Montreal Neurological Institute (MNI) space and map this atlas to the individual subject data. This mapped atlas in the subject data space is integrated with structural Magnetic Resonance (MR) imaging data, and patch-based neural networks, including 3D U-Net and DeepMedic, are trained to classify the different brain lesions. Multiple state-of-the-art neural networks are trained and integrated with XGBoost fusion in the proposed two-level ensemble method. The first level reduces the uncertainty of the same type of models with different seed initializations, and the second level leverages the advantages of different types of neural network models. The proposed location information fusion method improves the segmentation performance of state-of-the-art networks including 3D U-Net and DeepMedic. Our proposed ensemble also achieves better segmentation performance compared to the state-of-the-art networks in BraTS 2017 and rivals state-of-the-art networks in BraTS 2018. Detailed results are provided on the public multimodal brain tumor segmentation (BraTS) benchmarks
Automatic Brain Tumor Segmentation using Convolutional Neural Networks with Test-Time Augmentation
Automatic brain tumor segmentation plays an important role for diagnosis,
surgical planning and treatment assessment of brain tumors. Deep convolutional
neural networks (CNNs) have been widely used for this task. Due to the
relatively small data set for training, data augmentation at training time has
been commonly used for better performance of CNNs. Recent works also
demonstrated the usefulness of using augmentation at test time, in addition to
training time, for achieving more robust predictions. We investigate how
test-time augmentation can improve CNNs' performance for brain tumor
segmentation. We used different underpinning network structures and augmented
the image by 3D rotation, flipping, scaling and adding random noise at both
training and test time. Experiments with BraTS 2018 training and validation set
show that test-time augmentation helps to improve the brain tumor segmentation
accuracy and obtain uncertainty estimation of the segmentation results.Comment: 12 pages, 3 figures, MICCAI BrainLes 201
Brain Tumor Segmentation with Deep Neural Networks
In this paper, we present a fully automatic brain tumor segmentation method
based on Deep Neural Networks (DNNs). The proposed networks are tailored to
glioblastomas (both low and high grade) pictured in MR images. By their very
nature, these tumors can appear anywhere in the brain and have almost any kind
of shape, size, and contrast. These reasons motivate our exploration of a
machine learning solution that exploits a flexible, high capacity DNN while
being extremely efficient. Here, we give a description of different model
choices that we've found to be necessary for obtaining competitive performance.
We explore in particular different architectures based on Convolutional Neural
Networks (CNN), i.e. DNNs specifically adapted to image data.
We present a novel CNN architecture which differs from those traditionally
used in computer vision. Our CNN exploits both local features as well as more
global contextual features simultaneously. Also, different from most
traditional uses of CNNs, our networks use a final layer that is a
convolutional implementation of a fully connected layer which allows a 40 fold
speed up. We also describe a 2-phase training procedure that allows us to
tackle difficulties related to the imbalance of tumor labels. Finally, we
explore a cascade architecture in which the output of a basic CNN is treated as
an additional source of information for a subsequent CNN. Results reported on
the 2013 BRATS test dataset reveal that our architecture improves over the
currently published state-of-the-art while being over 30 times faster
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