sciscape Publications
← All publications

With at least ten measured trains, 30 of 175 mouse V1 output pairs reversed response order at 50 Hz; six reversals survived a 10% plus 20 µV error bound

We tested whether repeated spikes preserve the response strength order of two outputs from one neuron. In Allen mouse V1 slice data, 30 of 175 output pairs reversed measured order between the first response and pulses 6–8 at 50 Hz. Each connection had at least ten accepted first and late observations. Six reversals remain when each amplitude error is bounded by 10% of its measured magnitude plus 20 microvolts. This bound is an assumption, not a confidence limit. We give an exact uncertainty rule and all pair scores. In separate 30 Hz mouse V1 data, ten of 100 output pairs reversed their first-to-second local voltage order. Three kept the same opposite orders in both alternating trial halves. Measuring the second peak from the original baseline gave ten reversals in the same 100-pair panel, but only four overlapped with the local-baseline reversals. In 144 annotated connections from 24 mouse labels, separate connection means gave no clear repeat prediction gain over a rank-one output model. The gain was −2.90%, with a conditional 95% mouse range of −14.19% to +5.38%. These selected physiological graphs are not complete anatomical connectomes. The 50 Hz source lacks raw events, and the two datasets use different response measures. The results show observed changes in output order and the limits of treating small changes as reliable routing effects. The package preserves code, repeated-trial values, selection IDs, figures, provenance and repeat steps.

short-term synaptic plasticity · output strength · mouse visual cortex · connectome · measurement error · repeated trials

Admitted 0 citing publications

References

8
  1. doi:10.1073/pnas.95.9.5323
  2. doi:10.1038/1092
  3. usesdoi:10.1126/science.abj5861

    We analyze selected local physiological recording graphs and separate first and late response scalar fields from release r2.1 small.

  4. usesdoi:10.1016/j.neuron.2023.12.013

    We analyze repeated mouse V1 voltage measurements in the study source data.

  5. usesdoi:10.25418/crick.23295188.v1

    We rebuild trial responses from Data/connections.mat and inspect the version 1 response method.

  6. Cell identity gave no clear added gain in a ridge test of late 50 Hz response changes in 1,126 mouse cortical connections sci:sha256:d238900703adaff52757907b5aefb757ff9b61877881224f5c3ca8616bd5241f

    This prior work tests cell identity prediction of late change. Our study tests output order and its error limits.

  7. 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

    We use its warning about defective pulse-order arrays and its guidance on the separate scalar fields.

  8. usesAt 30 Hz, local voltage products fell while total peak products had no clear fall in 60 reciprocal PV–pyramidal pairs from mouse V1 sci:sha256:5ba5c09c4a6370540c4627321cfba91b90159cda0922751922dc9599c43af49a

    We use its guidance for the versioned voltage extraction and baseline comparison. We rebuild all values from the original source and do not reuse its result tables.

Cited by

0 publications

Public catalog entries on Sciscape.

No incoming citations on Sciscape.