A comparison of automatic multi-tissue segmentation methods of the human fetal brain using the FeTA Dataset

It is critical to quantitatively analyse the developing human fetal brain in order to fully understand neurodevelopment in both normal fetuses and those with congenital disorders. To facilitate this analysis, automatic multi-tissue fetal brain segmentation algorithms are needed, which in turn requires open databases of segmented fetal brains. Here we introduce a publicly available database of 50 manually segmented pathological and non-pathological fetal magnetic resonance brain volume reconstructions across a range of gestational ages (20 to 33 weeks) into 7 different tissue categories (external cerebrospinal fluid, grey matter, white matter, ventricles, cerebellum, deep grey matter, brainstem/spinal cord). In addition, we quantitatively evaluate the accuracy of several automatic multi-tissue segmentation algorithms of the developing human fetal brain. Four research groups participated, submitting a total of 10 algorithms, demonstrating the benefits the database for the development of automatic algorithms.

Developing Brain Atlas through Deep Learning

To uncover the organizational principles governing the human brain, neuroscientists are in need of developing high-throughput methods that can explore the structure and function of distinct brain regions using animal models. The first step towards this goal is to accurately register the regions of interest in a mouse brain, against a standard reference atlas, with minimum human supervision. The second step is to scale this approach to different animal ages, so as to also allow insights into normal and pathological brain development and aging. We introduce here a fully automated convolutional neural network-based method (SeBRe) for registration through Segmenting Brain Regions of interest in mice at different ages. We demonstrate the validity of our method on different mouse brain post-natal (P) developmental time points, across a range of neuronal markers. Our method outperforms the existing brain registration methods, and provides the minimum mean squared error (MSE) score on a mouse brain dataset. We propose that our deep learning-based registration method can (i) accelerate brain-wide exploration of region-specific changes in brain development and (ii) replace the existing complex brain registration methodology, by simply segmenting brain regions of interest for high-throughput brain-wide analysis.