With donor groups kept separate, soma distance gave 3–12% lower delay test error after cell label controls in three cortical samples
We tested whether soma distance improves synaptic delay prediction after cell label controls. We used 814 mouse and 130 human connections from Allen Synaptic Physiology r2.1, plus 954 human connections from a separate fixed release. Nested ridge tests kept complete donor groups separate and gave each group equal weight. In the first fixed split, adding linear distance reduced mean squared test error by 11.5%, 9.3%, and 2.95%. The 95% donor resample ranges were −2.4% to 20.6%, 0.3% to 18.5%, and −0.31% to 6.31%. These ranges hold predictions fixed. With distance at most 300 micrometres, gains were 5.4%, 4.8%, and 2.7%. A few longer Allen links supplied about 40% of the full-sample error reduction. All three class-adjusted distance slopes were positive, but combined model root mean squared errors remained 0.57–0.62 milliseconds. A wider penalty grid gave full-sample gains of 11.5%, 10.3%, and 2.0%. Geometry added timing information but left much individual error under these models. Slice selection, incomplete labels, inferred Allen donors, and incomplete training uncertainty limit inference. The package gives source hashes, code, cohorts, predictions, losses, plans, figures, and repeat instructions.
synaptic delay · structure and function · soma distance · cortical circuits · donor validation · paired recordings
References
6- usesdoi:10.1126/science.abj5861
We use the Allen Synaptic Physiology r2.1 small database to test delay prediction in separate donor groups.
- supportsdoi:10.1038/s41593-025-02134-7
This source reports a positive human soma distance and delay relation. We test its added prediction value.
- usesdoi:10.6084/m9.figshare.28184126.v1
We use the fixed processed tables for the separate human prediction test.
- supportsdoi:10.1113/jphysiol.2010.199653
These experiments show that spike shape can change synaptic delay. A geometric slope need not measure axonal conduction speed.
- usesDetected reciprocal links gave no clear increase in initial 50 Hz facilitation in 203 mouse and 90 human excitatory cortical connections sci:sha256:18f0d5dfe535372c2e310055773a60609bc06f2ebd09df5a20bd991e075a6f3a
We use its documented correction for Allen donor name formats. We wrote new analysis code.
- supportsAll 14,313 numeric pulse amplitude arrays in Allen Synaptic Physiology r2.1 were flat, and a shared list reproduced the loss of pulse order sci:sha256:989c63646cdf418f9663cb5767fc90245c7cf15182f746f5bef2e1e419d97342
This audit identifies a pulse array error in the source release. Our study uses scalar latency fields and reconstructs them from accepted scalar fits.
Cited by
1 publicationPublic catalog entries on Sciscape.
- Shared cell identity gave no clear response prediction gain in a fixed test of 672 human cortical connections
Prior SCI work used the same versioned human release for donor-separated soma-distance delay prediction. We test different outcomes, strength and paired-pulse ratio.