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Damon D. Pham

Publications and source records attributed to Damon D. Pham.

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Bayesian brain mapping: a population-informed framework for personalized functional network topography and connectivity

The spatial topography of functional brain organization is increasingly recognized to play an important role in cognition and disease. Accounting for individual differences in functional topography is also crucial for accurately distinguishing spatial and temporal aspects of functional brain connectivity. Yet, accurate estimation of personalized functional brain networks from functional magnetic resonance imaging (fMRI) without extensive scanning remains challenging due to high noise levels. Here, we describe Bayesian Brain Mapping (BBM), a technique for personalized functional topography and connectivity informed by population information. BBM relies on population-derived priors on both spatial topography of networks and between-network functional connectivity to guide subject-level estimation and combat noise. These priors are based on existing spatial templates, such as parcellations or continuous network maps, providing correspondence to those templates. Yet BBM is highly flexible, avoiding strong spatial or temporal constraints and allowing for overlap between networks and heterogeneous patterns of engagement. BBM is designed for single-subject analysis, making it computationally efficient and translatable to clinical settings. Here, we describe the BBM model and illustrate the use of the BayesBrainMap R package to construct population-derived priors, fit the model, and perform inference to identify engagements. A demo is provided in an accompanying Github repo. We also share priors derived from the Human Connectome Project and provide code to support the construction of priors from different data sources, lowering the barrier to adoption of BBM for studies of individual brain organization.

stat.AP

A robust multivariate, non-parametric outlier identification method for scrubbing in fMRI

Functional magnetic resonance imaging (fMRI) data contain high levels of noise and artifacts. To avoid contamination of downstream analyses, fMRI-based studies must identify and remove these noise sources prior to statistical analysis. One common approach is the "scrubbing" of fMRI volumes that are thought to contain high levels of noise. However, existing scrubbing techniques are based on ad hoc measures of signal change. We consider scrubbing via outlier detection, where volumes containing artifacts are considered multidimensional outliers. Robust multivariate outlier detection methods are proposed using robust distances (RDs), which are related to the Mahalanobis distance. These RDs have a known distribution when the data are i.i.d. normal, and that distribution can be used to determine a threshold for outliers where fMRI data violate these assumptions. Here, we develop a robust multivariate outlier detection method that is applicable to non-normal data. The objective is to obtain threshold values to flag outlying volumes based on their RDs. We propose two threshold candidates that embark on the same two steps, but the choice of which depends on a researcher's purpose. Our main steps are dimension reduction and selection, robust univariate outlier imputation to get rid of the effect of outliers on the distribution, and estimating an outlier threshold based on the upper quantile of the RD distribution without outliers. The first threshold candidate is an upper quantile of the empirical distribution of RDs obtained from the imputed data. The second threshold candidate calculates the upper quantile of the RD distribution that a nonparametric bootstrap uses to account for uncertainty in the empirical quantile. We compare our proposed fMRI scrubbing method to motion scrubbing, data-driven scrubbing, and restrictive parametric multivariate outlier detection methods.

stat.ME

Sources of residual autocorrelation in multiband task fMRI and strategies for effective mitigation

In task fMRI analysis, OLS is typically used to estimate task-induced activation in the brain. Since task fMRI residuals often exhibit temporal autocorrelation, it is common practice to perform prewhitening prior to OLS to satisfy the assumption of residual independence, equivalent to GLS. While theoretically straightforward, a major challenge in prewhitening in fMRI is accurately estimating the residual autocorrelation at each location of the brain. Assuming a global autocorrelation model, as in several fMRI software programs, may under- or over-whiten particular regions and fail to achieve nominal false positive control across the brain. Faster multiband acquisitions require more sophisticated models to capture autocorrelation, making prewhitening more difficult. These issues are becoming more critical now because of a trend towards subject-level analysis, where prewhitening has a greater impact than in group-average analyses. In this article, we first thoroughly examine the sources of residual autocorrelation in multiband task fMRI. We find that residual autocorrelation varies spatially throughout the cortex and is affected by the task, the acquisition method, modeling choices, and individual differences. Second, we evaluate the ability of different AR-based prewhitening strategies to effectively mitigate autocorrelation and control false positives. We find that allowing the prewhitening filter to vary spatially is the most important factor for successful prewhitening, even more so than increasing AR model order. To overcome the computational challenge associated with spatially variable prewhitening, we developed a computationally efficient R implementation based on parallelization and fast C++ backend code. This implementation is included in the open source R package BayesfMRI.

stat.ME