Resting variation gave no clear late voltage prediction gain after strength controls in ridge tests of 993 mouse cortical connections
Connection models need rules for signal size during repeated activity. We tested whether resting response variation adds late voltage prediction information. Baseline inputs included cell class, geometry, recording conditions and response strength. We used separate scalar summaries from Allen Synaptic Physiology r2.1. Ridge models used five outer donor folds and four inner donor folds. Each donor had equal weight. The primary sample had 993 connections from 433 inferred mice. Adding resting variation reduced error by 23.73% when strength features were omitted. With strength included, added variation increased error by 0.75%. The central 95% donor resample range for error reduction was -1.62% to +0.10%. These ranges keep predictions fixed and omit uncertainty from new model fits. Wider penalty choices gave an uncertain +0.51% gain, with a range of -2.20% to +3.38%. An added second-response control reduced error by 20.74% in 986 connections. Human results were uncertain. The large gain without strength controls did not persist clearly after those controls in the tested models. Summaries can share trials and fitting assumptions. This retrospective prediction test does not estimate release probability or release-site count. The package preserves code, provenance, predictions, all checks, figures and repeat instructions. The exact source database remains external under its original terms.
cortical connectivity · synaptic variability · short-term plasticity · response strength · donor validation · ridge regression
References
4- usesdoi:10.1126/science.abj5861
The study supplies the original cortical recordings and source database.
- Soma distance reduced delay error but gave no clear 50 Hz change gain in fixed tests of mouse cortical connections with separate donors sci:sha256:f2cc328292feac61c57b76d13be26c8d6d94544105805c165f927e30308ea32c
The earlier study tests added soma-distance information with separate donors on the same source. It informs the present study design and source-field distinctions.
- Adding the second 50 Hz response cut late voltage test error by 28% in 960 mouse cortical connections with separate donor folds and an asinh score sci:sha256:ef6636548bf1e251a22417d6efaeaea1035f5c8898048a9e850215e49d7e5242
[Legacy relation: reproduces] An added control repeats the direction of the second-response prediction gain on the same source with different selection, baseline features and donor weighting. This is not an independent biological replication.
- usesAll 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
The source audit distinguishes faulty exported pulse arrays from separate scalar summaries. We use only those scalar fields.
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