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A 10 micrometre path test found no clear movie-response grouping of distinct inputs on 237 dendritic trees from one MICrONS mouse

We tested local input grouping in one mouse visual cortex map. We joined measured mean movie responses to a preserved MICrONS path-distance dataset. Exact nucleus and optical recording matches retained 3,131 of 3,437 selected sources. The primary test used 237 target cells, 718 sources, 529 near pairs, and 1,269 reference pairs. Near paths were at most 10 micrometres. Reference paths were greater than 20 and at most 50 micrometres. Each distinct source pair entered once per target. Targets had equal weight. Source response labels were exchanged within area, cell type, and 100 micrometre soma cubes across the full graph. The excess near-input Pearson correlation was 0.00972. Its upper-tail probability was 0.1946 from 4,999 draws. The central 95% target resample range was -0.01291 to 0.03268. A planned reviewed-axon check gave excess 0.05393 and probability 0.017 on 58 targets. Exploratory finer spatial and optical-scan controls reduced that excess and weakened its evidence. Including contacts from one source raised the raw contact-pair contrast from 0.0110 to 0.1677. Those contacts share one response label by construction. Independent formulas, official pair values, source checks, and a clean repeat passed. All 72 numerical output files matched exactly. The package preserves code, measured response extracts, anatomical distances, provenance, all results, figures, and repeat steps. The study has one mouse, selected sources, sparse input coverage, finite response reliability, and approximate contact attachment. It does not measure spine responses or establish absence of functional input groups.

MICrONS · dendritic input · functional connectomics · measured movie responses · signal correlation · source identity · skeleton path distance · spatial controls · recording controls

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References

8
  1. usesWith 100 micrometre source blocks, a 10 micrometre path test on 274 MICrONS dendrites gave model orientation excess 0.068 with a target resample range of -0.032 to 0.170 sci:sha256:59ad886466a6b8872a332964f3ea9beec32b9df44da3041b7791ee85faa766d4

    We use its unchanged source and target tables, synapse projections, path distances, and source provenance. We test a new measured movie response outcome and exact recording joins.

  2. usesIncluding contacts from the same source changed the sign of an orientation similarity score on 354 MICrONS targets with tuning assigned by source sci:sha256:654a755c6faae91d1012ecce9bd0a43f1d24b0e9c107407f47511950cfdd0408

    The anatomical source extract and its full synapse-table audit are preserved in this upstream SCI dependency.

  3. usesdoi:10.1038/s41586-025-08790-w

    MICrONS anatomical and functional observations and public skeleton resource from one mouse.

  4. usesdoi:10.1038/s41586-025-08840-3

    The v1 measured response vectors and official signal correlations. This study also provides context for spatial source controls.

  5. usesdoi:10.60533/BOSS-2021-T0SY

    MICrONS data resource. Exact source versions and SHA-256 hashes are given in the supporting provenance.

  6. usesdoi:10.1038/s41586-025-08829-y

    The parent source selection used this released visual response model. The new outcome is measured mean movie response.

  7. usesdoi:10.1038/s41586-024-07765-7

    Released cortical cell labels used in the anatomical source selection and conditional reference.

  8. doi:10.1038/nature23019

    Direct spine imaging provides prior evidence for local groups with shared visual response properties. The present source soma response test has a different scope.

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