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ECoG

33 entries

Electrocorticography places electrode grids on the cortical surface, balancing signal resolution and invasiveness. This topic covers ECoG applications in speech decoding, motor control, and seizure monitoring, along with advances in high-density micro-ECoG arrays.

June 2026

Hybrid micro-ECoG for multi-scale neural recording

Published in Cell Reports Methods on June 12, 2026, the study presents high-density micro-electrocorticography arrays that integrate silicone elastomers (optical transparency, repeated penetration with intracortical arrays) and polyimide films (fine photolithographic feature definition) for multi-scale studies of brain activity. The combination facilitates high-throughput functional mapping to identify targets and insertion of intracortical arrays for dense local sampling. The authors demonstrated functional mapping in rats, cats and marmosets, guiding multi-area laminar recordings, and demonstrated local and feedforward optogenetic stimulation to investigate cortico-cortical interactions.

Utrecht Team Finds Well-Placed 32-Electrode ECoG Grid Matches Larger Arrays for Speech BCI

A team led by the UMC Utrecht Brain Center in the Netherlands analyzed 8 participants with high-density electrocorticography (ECoG) grids of 64 to 128 electrodes and found that a well-positioned 32-electrode grid classified 12 Dutch words with 76 ± 16% accuracy, comparable to 75 ± 17% for the larger grids. The best placement was vertical and centered on the central sulcus. Speech brain-computer interfaces aim to restore communication to people paralyzed and unable to speak, but larger grids carry higher surgical risk. The participants were not paralyzed and testing was limited to a fixed word set.
February 2026

Layer 7 Array Decodes Speech and Cursor Direction in Four Surgical Patients

A Neurosurgical Focus paper tested Precision Neuroscience's 1,024-channel Layer 7 micro-ECoG array in four awake-craniotomy patients. Four-word speech classification reached 77.5% accuracy and four-direction cursor classification reached 78% to 84%, with no device-related adverse events reported during the procedures. The small, short intraoperative study was a feasibility test rather than a pivotal motor-restoration trial.
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