Data from N = 31 participants were used for the examples shown in this paper participating in a movie watching study (N = 12), in a visual study (N = 12) and in a sequence development study (N = 5). All experiments were conducted in accordance with the Belmont Report after participants granted informed consent. Data were acquired in FMRIF/NIMH/NIMH in Bethesda, USA and at Scannexus in Maastricht, The Netherlands. Experiments at NIH were conducted according to the US Federal Regulations that protect human subjects and approved by the Combined Neuroscience Institutional Review Board protocol 93-M-0170 (ClinicalTrials.gov identifier: NCT00001360). All experiments of this study were conducted on SIEMENS 7T scanners (Siemens Healthineers, Erlangen, Germany) using the vendor-provided IDEA environment (VB17A/VE11U/VE12K-UHF). The scanners were equipped with the standard body gradient coils (maximum effective gradient strength used here: 48 mT/m; maximum slew rate used: 198 T/m/s). For RF transmission and reception, volume-transmit and 32-channel receive head coils (Nova Medical, Wilmington, MA, USA) were used.
