Partial Volume Segmentation of Brain MRI Scans of any Resolution and Contrast

Bibliographic Details
Title: Partial Volume Segmentation of Brain MRI Scans of any Resolution and Contrast
Authors: Billot, Benjamin, Robinson, Eleanor D., Dalca, Adrian V., Iglesias, Juan Eugenio
Source: International Conference on Medical Image Computing and Computer-Assisted Intervention (MICCAI) 2020, pp. 177-187
Publication Year: 2020
Collection: Computer Science
Quantitative Biology
Subject Terms: Computer Science - Computer Vision and Pattern Recognition, Computer Science - Machine Learning, Electrical Engineering and Systems Science - Image and Video Processing, Quantitative Biology - Quantitative Methods
More Details: Partial voluming (PV) is arguably the last crucial unsolved problem in Bayesian segmentation of brain MRI with probabilistic atlases. PV occurs when voxels contain multiple tissue classes, giving rise to image intensities that may not be representative of any one of the underlying classes. PV is particularly problematic for segmentation when there is a large resolution gap between the atlas and the test scan, e.g., when segmenting clinical scans with thick slices, or when using a high-resolution atlas. In this work, we present PV-SynthSeg, a convolutional neural network (CNN) that tackles this problem by directly learning a mapping between (possibly multi-modal) low resolution (LR) scans and underlying high resolution (HR) segmentations. PV-SynthSeg simulates LR images from HR label maps with a generative model of PV, and can be trained to segment scans of any desired target contrast and resolution, even for previously unseen modalities where neither images nor segmentations are available at training. PV-SynthSeg does not require any preprocessing, and runs in seconds. We demonstrate the accuracy and flexibility of the method with extensive experiments on three datasets and 2,680 scans. The code is available at https://github.com/BBillot/SynthSeg.
Comment: 12 pages, 7 figures
Document Type: Working Paper
DOI: 10.1007/978-3-030-59728-3_18
Access URL: http://arxiv.org/abs/2004.10221
Accession Number: edsarx.2004.10221
Database: arXiv
More Details
DOI:10.1007/978-3-030-59728-3_18