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Related Concept Videos

Brain Imaging01:14

Brain Imaging

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Brain imaging technologies provide critical insights into both the structure and function of the human brain, enabling medical professionals and researchers to diagnose, study, and treat neurological disorders or psychiatric disorders more effectively.
These technologies include computerized axial tomography (CAT or CT scans), positron-emission tomography (PET scans),  magnetic resonance imaging (MRI),  functional magnetic resonance imaging (fMRI), and Transcranial Magnetic...
898

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Faster permutation inference in brain imaging.

Anderson M Winkler1, Gerard R Ridgway2, Gwenaëlle Douaud1

  • 1Oxford Centre for Functional MRI of the Brain, University of Oxford, Oxford, UK.

Neuroimage
|June 12, 2016
PubMed
Summary
This summary is machine-generated.

Permutation tests in neuroimaging are slow. This study accelerates them by exploiting statistical properties, finding method (iv) fastest for uncorrected p-values and method (iii) best for corrected p-values, with minimal resampling risk.

Keywords:
Gamma distributionGeneralised Pareto distributionLow rank matrix completionNegative binomial distributionPearson type III distributionPermutation testsTail approximation

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Area of Science:

  • Neuroimaging analysis
  • Statistical inference
  • Computational neuroscience

Background:

  • Permutation tests are crucial for reliable inference in neuroimaging but are computationally intensive.
  • The computational burden increases significantly with large, complex neuroimaging datasets, limiting their practical application.
  • Existing hardware and software improvements offer generic acceleration but do not address the core computational demands of permutation testing.

Purpose of the Study:

  • To develop and evaluate computationally efficient methods for permutation testing in neuroimaging.
  • To compare the performance of various acceleration techniques against traditional permutation approaches.
  • To identify the optimal method balancing speed, accuracy, and statistical validity for different neuroimaging analysis scenarios.

Main Methods:

  • Compared six acceleration approaches: limited permutations, negative binomial distribution, generalized Pareto distribution tail fitting, gamma distribution moment approximation, empirical gamma distribution fitting, and reduced voxel permutation with matrix theory.
  • Assessed methods using synthetic data for error rates, statistical power, agreement with reference results, and resampling risk.
  • Re-analyzed a voxel-based morphometry study using real neuroimaging data to validate findings.

Main Results:

  • All evaluated methods achieved exact error rates and similar statistical power.
  • Methods (i), (iii), and (v) exhibited higher resampling risks.
  • Method (iv) (no permutations, gamma distribution approximation) was the fastest for comparable resampling risks.
  • Methods (iii) and (v) detected stronger effects in family-wise error rate corrected maps for real data.
  • Method (iv) is recommended for uncorrected p-values assuming symmetric errors; method (iii) is recommended for corrected p-values and other settings.

Conclusions:

  • Several computationally efficient methods can accelerate permutation testing in neuroimaging without compromising error rates or power.
  • The choice of method depends on whether corrected or uncorrected p-values are required and assumptions about error distribution symmetry.
  • The recommended methods are available in the PALM (Permutation Analysis of Linear Models) tool.