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This project publishes the code used in the following publication: Bron et al., Cross-Cohort Generalizability of Deep and Conventional Machine Learning for MRI-based diagnosis and prediction of Alzheimer’s disease, NeuroImage: Clinical, 2021 Link: https://doi.org/10.1016/j.nicl.2021.102712, arxiv.org/2012.08769 Starting point: Overview.ipynb {"references": ["Bron et al., Cross-Cohort Generalizability of Deep and Conventional Machine Learning for MRI-based diagnosis and prediction of Alzheimer's disease, NeuroImage: Clinical, 2021"]} https://gitlab.com/radiology/neuro/bron-cross-cohort/-/tree/v1.0

Snakemake pipeline for imputation of mitochondrial genetic variants using Impute2 Chromosome X protocol.

Linking interindividual differences in psychological phenotype to variations in brain structure is an old dream for psychology and a crucial question for cognitive neurosciences. Yet, replicability of the previously-reported “structural brain behavior” (SBB)-associations has been questioned, recently. Here, we conducted an empirical investigation, assessing replicability of SBB among heathy adults. For a wide range of psychological measures, the replicability of associations with gray matter volume was assessed. Our results revealed that among healthy individuals 1) finding an association between performance at standard psychological tests and brain morphology is relatively unlikely 2) significant associations, found using an exploratory approach, have overestimated effect sizes and 3) can hardly be replicated in an independent sample. After considering factors such as sample size and comparing our findings with more replicable SBB-associations in a clinical cohort and replicable associations between brain structure and non-psychological phenotype, we discuss the potential causes and consequences of these findings.

Functional brain image synthesis using the KDE or MVN distribution. Currently in beta. Python code. Find the documentation at http://brainsimulator.readthedocs.io/ brainSimulator is a brain image synthesis procedure intended to generate a new image set that share characteristics with an original one. The system focuses on nuclear imaging modalities such as PET or SPECT brain images. It analyses the dataset by applying PCA to the original dataset, and then model the distribution of samples in the projected eigenbrain space using a Probability Density Function (PDF) estimator. Once the model has been built, anyone can generate new coordinates on the eigenbrain space belonging to the same class, which can be then projected back to the image space.

Recent advances in multi-atlas based algorithms address many of the previous limitations in model-based and probabilistic segmentation methods. However, at the label fusion stage, a majority of algorithms focus primarily on optimizing weight-maps associated with the atlas library based on a theoretical objective function that approximates the segmentation error. In contrast, we propose a novel method—Autocorrecting Walks over Localized Markov Random Fields (AWoL-MRF)—that aims at mimicking the sequential process of manual segmentation, which is the gold-standard for virtually all the segmentation methods. AWoL-MRF begins with a set of candidate labels generated by a multi-atlas segmentation pipeline as an initial label distribution and refines low confidence regions based on a localized Markov random field (L-MRF) model using a novel sequential inference process (walks). We show that AWoL-MRF produces state-of-the-art results with superior accuracy and robustness with a small atlas library compared to existing methods. We validate the proposed approach by performing hippocampal segmentations on three independent datasets: (1) Alzheimer's Disease Neuroimaging Database (ADNI); (2) First Episode Psychosis patient cohort; and (3) A cohort of preterm neonates scanned early in life and at term-equivalent age. We assess the improvement in the performance qualitatively as well as quantitatively by comparing AWoL-MRF with majority vote, STAPLE, and Joint Label Fusion methods. AWoL-MRF reaches a maximum accuracy of 0.881 (dataset 1), 0.897 (dataset 2), and 0.807 (dataset 3) based on Dice similarity coefficient metric, offering significant performance improvements with a smaller atlas library (< 10) over compared methods. We also evaluate the diagnostic utility of AWoL-MRF by analyzing the volume differences per disease category in the ADNI1: Complete Screening dataset. We have made the source code for AWoL-MRF public at: https://github.com/CobraLab/AWoL-MRF.