Evidence map›Paper›PMID 34773436›Full record

ArticleHuman brain mapping2022

Isolating the sources of pipeline-variability in group-level task-fMRI results.

Alexander Bowring, Thomas E Nichols, Camille Maumet

Abstract read
In one paragraph

Article in Human brain mapping, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Processing, evaluating, and understanding FMRI data with afni_proc.py.Imaging neuroscience (Cambridge, Mass.) · 2024
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Alexander BowringLi Ka Shing Centre for Health Information and Discovery, Nuffield Department of Population Health, Big Data Institute, University of Oxford, Oxford, UK.ORCID 0000-0002-5553-7249
Thomas E NicholsLi Ka Shing Centre for Health Information and Discovery, Nuffield Department of Population Health, Big Data Institute, University of Oxford, Oxford, UK.ORCID 0000-0002-4516-5103
Camille MaumetInria, Univ Rennes, CNRS, Inserm, IRISA UMR 6074, Empenn ERL U 1228, Rennes, France.

Funding

Large-scale meta-analysis of functional MRI dataR01MH096906 · NIMH · UNIVERSITY OF TEXAS AT AUSTIN · PI Alejandro De La Vega · 2012 to 2026
$7.9M
NIH HHS NIH R01MH096906NIMH NIH HHS R01 MH096906Wellcome TrustWellcome Trust 100309/Z/12/ZWellcome Trust 20319/Z/16/Z
6 · The paper itself

Abstract

Task-fMRI researchers have great flexibility as to how they analyze their data, with multiple methodological options to choose from at each stage of the analysis workflow. While the development of tools and techniques has broadened our horizons for comprehending the complexities of the human brain, a growing body of research has highlighted the pitfalls of such methodological plurality. In a recent study, we found that the choice of software package used to run the analysis pipeline can have a considerable impact on the final group-level results of a task-fMRI investigation (Bowring et al., 2019, BMN). Here we revisit our work, seeking to identify the stages of the pipeline where the greatest variation between analysis software is induced. We carry out further analyses on the three datasets evaluated in BMN, employing a common processing strategy across parts of the analysis workflow and then utilizing procedures from three software packages (AFNI, FSL, and SPM) across the remaining steps of the pipeline. We use quantitative methods to compare the statistical maps and isolate the main stages of the workflow where the three packages diverge. Across all datasets, we find that variation between the packages' results is largely attributable to a handful of individual analysis stages, and that these sources of variability were heterogeneous across the datasets (e.g., choice of first-level signal model had the most impact for the balloon analog risk task dataset, while first-level noise model and group-level model were more influential for the false belief and antisaccade task datasets, respectively). We also observe areas of the analysis workflow where changing the software package causes minimal differences in the final results, finding that the group-level results were largely unaffected by which software package was used to model the low-frequency fMRI drifts.

Indexed as

Brain MappingImage Processing, Computer-AssistedMagnetic Resonance ImagingBrainHumansAFNIanalytic flexibilityanalytic variabilityfMRIFSLreproducibilitysoftware comparisonSPMtask-fMRI

Identifiers

PMID34773436
PMCPMC8764489

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.