arXiv subjects

Vince Calhoun

Publications and source records attributed to Vince Calhoun.

47 records · Page 3Linked to original sources

arXiv2018

Deep Learning for Quality Control of Subcortical Brain 3D Shape Models

We present several deep learning models for assessing the morphometric fidelity of deep grey matter region models extracted from brain MRI. We test three different convolutional neural net architectures (VGGNet, ResNet and Inception) over 2D maps of geometric features. Further, we present a novel geometry feature augmentation technique based on a parametric spherical mapping. Finally, we present an approach for model decision visualization, allowing human raters to see the areas of subcortical shapes most likely to be deemed of failing quality by the machine. Our training data is comprised of 5200 subjects from the ENIGMA Schizophrenia MRI cohorts, and our test dataset contains 1500 subjects from the ENIGMA Major Depressive Disorder cohorts. Our final models reduce human rater time by 46-70%. ResNet outperforms VGGNet and Inception for all of our predictive tasks.

q-bio.NC↗

arXiv2018

Spatio-temporal Dynamics of Intrinsic Networks in Functional Magnetic Imaging Data Using Recurrent Neural Networks

We introduce a novel recurrent neural network (RNN) approach to account for temporal dynamics and dependencies in brain networks observed via functional magnetic resonance imaging (fMRI). Our approach directly parameterizes temporal dynamics through recurrent connections, which can be used to formulate blind source separation with a conditional (rather than marginal) independence assumption, which we call RNN-ICA. This formulation enables us to visualize the temporal dynamics of both first order (activity) and second order (directed connectivity) information in brain networks that are widely studied in a static sense, but not well-characterized dynamically. RNN-ICA predicts dynamics directly from the recurrent states of the RNN in both task and resting state fMRI. Our results show both task-related and group-differentiating directed connectivity.

cs.NE↗

arXiv2018

FDR-Corrected Sparse Canonical Correlation Analysis with Applications to Imaging Genomics

Reducing the number of false discoveries is presently one of the most pressing issues in the life sciences. It is of especially great importance for many applications in neuroimaging and genomics, where datasets are typically high-dimensional, which means that the number of explanatory variables exceeds the sample size. The false discovery rate (FDR) is a criterion that can be employed to address that issue. Thus it has gained great popularity as a tool for testing multiple hypotheses. Canonical correlation analysis (CCA) is a statistical technique that is used to make sense of the cross-correlation of two sets of measurements collected on the same set of samples (e.g., brain imaging and genomic data for the same mental illness patients), and sparse CCA extends the classical method to high-dimensional settings. Here we propose a way of applying the FDR concept to sparse CCA, and a method to control the FDR. The proposed FDR correction directly influences the sparsity of the solution, adapting it to the unknown true sparsity level. Theoretical derivation as well as simulation studies show that our procedure indeed keeps the FDR of the canonical vectors below a user-specified target level. We apply the proposed method to an imaging genomics dataset from the Philadelphia Neurodevelopmental Cohort. Our results link the brain connectivity profiles derived from brain activity during an emotion identification task, as measured by functional magnetic resonance imaging (fMRI), to the corresponding subjects' genomic data.

stat.ME↗

arXiv2018

Improving Classification Rate of Schizophrenia Using a Multimodal Multi-Layer Perceptron Model with Structural and Functional MR

The wide variety of brain imaging technologies allows us to exploit information inherent to different data modalities. The richness of multimodal datasets may increase predictive power and reveal latent variables that otherwise would have not been found. However, the analysis of multimodal data is often conducted by assuming linear interactions which impact the accuracy of the results. We propose the use of a multimodal multi-layer perceptron model to enhance the predictive power of structural and functional magnetic resonance imaging (sMRI and fMRI) combined. We also use a synthetic data generator to pre-train each modality input layers, alleviating the effects of the small sample size that is often the case for brain imaging modalities. The proposed model improved the average and uncertainty of the area under the ROC curve to 0.850+-0.051 compared to the best results on individual modalities (0.741+-0.075 for sMRI, and 0.833+-0.050 for fMRI).

cs.CV↗

arXiv2018

Iterative Refinement of the Approximate Posterior for Directed Belief Networks

Variational methods that rely on a recognition network to approximate the posterior of directed graphical models offer better inference and learning than previous methods. Recent advances that exploit the capacity and flexibility in this approach have expanded what kinds of models can be trained. However, as a proposal for the posterior, the capacity of the recognition network is limited, which can constrain the representational power of the generative model and increase the variance of Monte Carlo estimates. To address these issues, we introduce an iterative refinement procedure for improving the approximate posterior of the recognition network and show that training with the refined posterior is competitive with state-of-the-art methods. The advantages of refinement are further evident in an increased effective sample size, which implies a lower variance of gradient estimates.

cs.LG↗

arXiv2017

Almost instant brain atlas segmentation for large-scale studies

Large scale studies of group differences in healthy controls and patients and screenings for early stage disease prevention programs require processing and analysis of extensive multisubject datasets. Complexity of the task increases even further when segmenting structural MRI of the brain into an atlas with more than 50 regions. Current automatic approaches are time-consuming and hardly scalable; they often involve many error prone intermediate steps and don't utilize other available modalities. To alleviate these problems, we propose a feedforward fully convolutional neural network trained on the output produced by the state of the art models. Incredible speed due to available powerful GPUs neural network makes this analysis much easier and faster (from $>10$ hours to a minute). The proposed model is more than two orders of magnitudes faster than the state of the art and yet as accurate. We have evaluated the network's performance by comparing it with the state of the art in the task of differentiating region volumes of healthy controls and patients with schizophrenia on a dataset with 311 subjects. This comparison provides a strong evidence that speed did not harm the accuracy. The overall quality may also be increased by utilizing multi-modal datasets (not an easy task for other models) by simple adding more modalities as an input. Our model will be useful in large-scale studies as well as in clinical care solutions, where it can significantly reduce delay between the patient screening and the result.

cs.CV↗

arXiv2017

Machine Learning for Large-Scale Quality Control of 3D Shape Models in Neuroimaging

As very large studies of complex neuroimaging phenotypes become more common, human quality assessment of MRI-derived data remains one of the last major bottlenecks. Few attempts have so far been made to address this issue with machine learning. In this work, we optimize predictive models of quality for meshes representing deep brain structure shapes. We use standard vertex-wise and global shape features computed homologously across 19 cohorts and over 7500 human-rated subjects, training kernelized Support Vector Machine and Gradient Boosted Decision Trees classifiers to detect meshes of failing quality. Our models generalize across datasets and diseases, reducing human workload by 30-70\%, or equivalently hundreds of human rater hours for datasets of comparable size, with recall rates approaching inter-rater reliability.

q-bio.QM↗

arXiv2017

Kernel Method for Detecting Higher Order Interactions in multi-view Data: An Application to Imaging, Genetics, and Epigenetics

In this study, we tested the interaction effect of multimodal datasets using a novel method called the kernel method for detecting higher order interactions among biologically relevant mulit-view data. Using a semiparametric method on a reproducing kernel Hilbert space (RKHS), we used a standard mixed-effects linear model and derived a score-based variance component statistic that tests for higher order interactions between multi-view data. The proposed method offers an intangible framework for the identification of higher order interaction effects (e.g., three way interaction) between genetics, brain imaging, and epigenetic data. Extensive numerical simulation studies were first conducted to evaluate the performance of this method. Finally, this method was evaluated using data from the Mind Clinical Imaging Consortium (MCIC) including single nucleotide polymorphism (SNP) data, functional magnetic resonance imaging (fMRI) scans, and deoxyribonucleic acid (DNA) methylation data, respectfully, in schizophrenia patients and healthy controls. We treated each gene-derived SNPs, region of interest (ROI) and gene-derived DNA methylation as a single testing unit, which are combined into triplets for evaluation. In addition, cardiovascular disease risk factors such as age, gender, and body mass index were assessed as covariates on hippocampal volume and compared between triplets. Our method identified $13$-triplets ($p$-values $\leq 0.001$) that included $6$ gene-derived SNPs, $10$ ROIs, and $6$ gene-derived DNA methylations that correlated with changes in hippocampal volume, suggesting that these triplets may be important in explaining schizophrenia-related neurodegeneration. With strong evidence ($p$-values $\leq 0.000001$), the triplet ({\bf MAGI2, CRBLCrus1.L, FBXO28}) has the potential to distinguish schizophrenia patients from the healthy control variations.

stat.ML↗

arXiv2017

End-to-end learning of brain tissue segmentation from imperfect labeling

Segmenting a structural magnetic resonance imaging (MRI) scan is an important pre-processing step for analytic procedures and subsequent inferences about longitudinal tissue changes. Manual segmentation defines the current gold standard in quality but is prohibitively expensive. Automatic approaches are computationally intensive, incredibly slow at scale, and error prone due to usually involving many potentially faulty intermediate steps. In order to streamline the segmentation, we introduce a deep learning model that is based on volumetric dilated convolutions, subsequently reducing both processing time and errors. Compared to its competitors, the model has a reduced set of parameters and thus is easier to train and much faster to execute. The contrast in performance between the dilated network and its competitors becomes obvious when both are tested on a large dataset of unprocessed human brain volumes. The dilated network consistently outperforms not only another state-of-the-art deep learning approach, the up convolutional network, but also the ground truth on which it was trained. Not only can the incredible speed of our model make large scale analyses much easier but we also believe it has great potential in a clinical setting where, with little to no substantial delay, a patient and provider can go over test results.

cs.CV↗

arXiv2016

Learning Schizophrenia Imaging Genetics Data Via Multiple Kernel Canonical Correlation Analysis

Kernel and Multiple Kernel Canonical Correlation Analysis (CCA) are employed to classify schizophrenic and healthy patients based on their SNPs, DNA Methylation and fMRI data. Kernel and Multiple Kernel CCA are popular methods for finding nonlinear correlations between high-dimensional datasets. Data was gathered from 183 patients, 79 with schizophrenia and 104 healthy controls. Kernel and Multiple Kernel CCA represent new avenues for studying schizophrenia, because, to our knowledge, these methods have not been used on these data before. Classification is performed via k-means clustering on the kernel matrix outputs of the Kernel and Multiple Kernel CCA algorithm. Accuracies of the Kernel and Multiple Kernel CCA classification are compared to that of the regularized linear CCA algorithm classification, and are found to be significantly more accurate. Both algorithms demonstrate maximal accuracies when the combination of DNA methylation and fMRI data are used, and experience lower accuracies when the SNP data are incorporated.

q-bio.QM↗

arXiv2013

MIGRAINE: MRI Graph Reliability Analysis and Inference for Connectomics

Currently, connectomes (e.g., functional or structural brain graphs) can be estimated in humans at $\approx 1~mm^3$ scale using a combination of diffusion weighted magnetic resonance imaging, functional magnetic resonance imaging and structural magnetic resonance imaging scans. This manuscript summarizes a novel, scalable implementation of open-source algorithms to rapidly estimate magnetic resonance connectomes, using both anatomical regions of interest (ROIs) and voxel-size vertices. To assess the reliability of our pipeline, we develop a novel nonparametric non-Euclidean reliability metric. Here we provide an overview of the methods used, demonstrate our implementation, and discuss available user extensions. We conclude with results showing the efficacy and reliability of the pipeline over previous state-of-the-art.

q-bio.QM↗