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Raw temporal derivatives reduced maximum contrast error on a ±1 s grid in 431 AOMIC designs with equal responses and a 0.2 mm motion limit

We tested response timing error in 431 public AOMIC working memory designs. The change and nochange responses had equal unit size under a defined response kernel. We removed row zero and scans above 0.2 mm framewise displacement. We tested independent condition delays from minus one to plus one second on a 0.1 second grid. Adding raw temporal derivatives reduced maximum contrast error in all 431 primary designs. The mean maximum error fell from 0.071675 to 0.045709 contrast units. The mean contrast variance increased by 3.47% under independent white noise. Finite error remained in every design. We provide exact finite grid witnesses, an analytic bound between grid points, and a reusable contrast weight method. An exact repeat and an isolated numeric repeat passed. The results apply to the specified scan clock, response kernel, contrast, and masks. The package contains source files, pinned retrieval recipes, code, results, and reproduction instructions.

functional MRI · hemodynamic response · temporal derivatives · contrast error · design audit · least squares · motion regressors · response timing

Admitted 4 citing publications

References

7
  1. usesResponse-only removal of six motion terms reduced known unit contrasts in 431 fixed AOMIC v2.0.0 working memory designs after shared drift removal sci:sha256:061d9a1371b95e2dddc49d3124d269c10d26416b55b4f8728ff06b3f8fa82087

    This study used its 431 complete working memory event and motion records. It also used four unchanged source and design code files. The new analysis tested contrast error from condition timing changes with equal response size.

  2. usesdoi:10.18112/openneuro.ds002785.v2.0.0

    The analysis used 207 complete PIOP1 working memory event, motion, and scan metadata records from version 2.0.0.

  3. usesdoi:10.18112/openneuro.ds002790.v2.0.0

    The analysis used 224 complete PIOP2 working memory event, motion, and scan metadata records from version 2.0.0.

  4. doi:10.1038/s41597-021-00870-6
  5. doi:10.1016/j.neuroimage.2008.10.065
  6. doi:10.1016/j.neuroimage.2003.12.029
  7. doi:10.1371/journal.pone.0126255

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