Exact path selection increased SEEG calibration scores with an uncertain later yield increase under a rounded 50 percent contact limit in eight patients
This study tested a fixed recording contact limit in public SEEG data from eight patients with epilepsy. An exact path method used five early pulses to select contacts. Five separate later pulses measured response repeatability. At the rounded 50% contact limit, mean retained yield was 23.65% for the exact method and 22.97% for pair rank. The paired gain was 0.67 percentage points. The descriptive 95% patient bootstrap interval was -0.59 to 2.48 points. The exact method increased the calibration score. These data did not establish a later yield advantage. The package contains the contact selector, compact trial data, figures, source hashes, and reproduction instructions. This was a test of stored stimulation responses. It was not a live brain-computer interface test.
stereoelectroencephalography · contact selection · dynamic programming · electrical stimulation · waveform repeatability
References
5- usesA five-pulse check selected more repeatable bipolar SEEG pairs within eight epilepsy patient sessions sci:sha256:b5b7963746f5c6d2a2a8f7844ec590732a4eb152bc7a70979b3bc95c3e27820f
This study used the exact trial Gram representation and extraction method that originated in this publication. A later cited publication supplied the corrected archive. The new outcome used five later pulses separate from the calibration pulses.
- usesThe nearest half of bipolar SEEG pairs outside the stimulated shaft had a higher mean rate of repeatable responses than the random expectation in eight epilepsy sessions sci:sha256:1a26d36b188a95ead0d43f052fc29b919849315f46a2562310a4fc08e2efdae2
This study used its corrected ten-pulse Gram archives, source edge tables, source metadata, and GPL retrieval program. They supplied the chronological pulse inputs for the contact selection test.
- usesdoi:10.18112/openneuro.ds004696.v1.0.1
This study analyzed author-derived trial waveforms from OpenNeuro ds004696, version 1.0.1.
- doi:10.1523/JNEUROSCI.2201-22.2023
- doi:10.1371/journal.pcbi.1011105
Cited by
0 publicationsPublic catalog entries on Sciscape.
No incoming citations on Sciscape.