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Telschow, F.

Publications and source records attributed to Telschow, F..

3 recordsLinked to original sources

Spatial Confidence Sets for Standardized Effect Size Images

Current statistical inference methods for task-fMRI suffer from two fundamental limitations. First, the focus is solely on detection of non-zero signal or signal change, a problem that is exasperated for large scale studies (e.g. UK Biobank, N = 40, 000+) where the null hypothesis fallacy causes even trivial effects to be determined as significant. Second, for any sample size, widely used cluster inference methods only indicate regions where a null hypothesis can be rejected, without providing any notion of spatial uncertainty about the activation. In this work, we address these issues by developing spatial Confidence Sets (CSs) on clusters found in thresholded Cohens d effect size images. We produce an upper and lower CS to make confidence statements about brain regions where Cohens d effect sizes have exceeded and fallen short of a non-zero threshold, respectively. The CSs convey information about the magnitude and reliability of effect sizes that is usually given separately in a t-statistic and effect estimate map. We expand the theory developed in our previous work on CSs for %BOLD change effect maps (Bowring et al., 2019) using recent results from the bootstrapping literature. By assessing the empirical coverage with 2D and 3D Monte Carlo simulations resembling fMRI data, we find our method is accurate in sample sizes as low as N = 60. We compute Cohens d CSs for the Human Connectome Project working memory taskfMRI data, illustrating the brain regions with a reliable Cohens d response for a given threshold. By comparing the CSs with results obtained from a traditional statistical voxelwise inference, we highlight the improvement in activation localization that can be gained with the Confidence Sets.

neuroscience↗

Spatial Confidence Sets for Raw Effect Size Images

The mass-univariate approach for functional magnetic resonance imagery (fMRI) analysis remains a widely used and fundamental statistical tool within neuroimaging. However, this method suffers from at least two fundamental limitations: First, with sample sizes growing to 4, 5 or even 6 digits, the entire approach is undermined by the null hypothesis fallacy, i.e. with sufficient sample size, there is high enough statistical power to reject the null hypothesis everywhere, making it difficult if not impossible to localize effects of interest. Second, with any sample size, when cluster-size inference is used a significant p-value only indicates that a cluster is larger than chance, and no notion of spatial uncertainty is provided. Therefore, no perception of confidence is available to express the size or location of a cluster that could be expected with repeated sampling from the population.\n\nIn this work, we address these issues by extending on a method proposed by Sommerfeld, Sain, and Schwartzman (2018) to develop spatial Confidence Sets (CSs) on clusters found in thresholded raw effect size maps. While hypothesis testing indicates where the null, i.e. a raw effect size of zero, can be rejected, the CSs give statements on the locations where raw effect sizes exceed, and fall short of, a non-zero threshold, providing both an upper and lower CS.\n\nWhile the method can be applied to any parameter in a mass-univariate General Linear Model, we motivate the method in the context of BOLD fMRI contrast maps for inference on percentage BOLD change raw effects. We propose several theoretical and practical implementation advancements to the original method in order to deliver an improved performance in small-sample settings. We validate the method with 3D Monte Carlo simulations that resemble fMRI data. Finally, we compute CSs for the Human Connectome Project working memory task contrast images, illustrating the brain regions that show a reliable %BOLD change for a given %BOLD threshold.

neuroscience↗

Peak p-values and false discovery rate inference in neuroimaging

Peaks are a mainstay of neuroimage analysis for reporting localization results. The current peak detection procedure in SPM12 requires a pre-threshold for approximating p-values and a false discovery rate (FDR) nominal level for inference. However, the pre-threshold is an undesirable feature, while the FDR level is meaningless if the signal is assumed to be nonzero everywhere. This article provides: 1) a peak height distribution for smooth Gaussian error fields that does not require a screening pre-threshold; 2) a signal-plus-noise model where FDR of peaks can be controlled and properly interpreted. Matlab code for calculation of p-values using the exact peak height distribution is available as an SPM extension.

neuroscience↗