Evidence map›Paper›PMID 36602951›Full record

ArticlePLoS computational biology2023

Mapping of morpho-electric features to molecular identity of cortical inhibitory neurons.

Yann Roussel, Csaba Verasztó, Dimitri Rodarie, Tanguy Damart, Michael Reimann, Srikanth Ramaswamy, Henry Markram, Daniel Keller

Open access · goldAbstract read
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In one paragraph

Article in PLoS computational biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.6field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 11 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Yann RousselBlue Brain Project, École polytechnique fédérale de Lausanne (EPFL), Geneva, Switzerland.ORCID 0000-0002-2847-4502
Csaba VerasztóBlue Brain Project, École polytechnique fédérale de Lausanne (EPFL), Geneva, Switzerland.ORCID 0000-0001-6295-7148
Dimitri RodarieBlue Brain Project, École polytechnique fédérale de Lausanne (EPFL), Geneva, Switzerland.ORCID 0000-0003-2496-2311
Tanguy DamartBlue Brain Project, École polytechnique fédérale de Lausanne (EPFL), Geneva, Switzerland.
Michael ReimannBlue Brain Project, École polytechnique fédérale de Lausanne (EPFL), Geneva, Switzerland.ORCID 0000-0003-3455-2367
Srikanth RamaswamyBlue Brain Project, École polytechnique fédérale de Lausanne (EPFL), Geneva, Switzerland.ORCID 0000-0001-6642-7136
Henry MarkramBlue Brain Project, École polytechnique fédérale de Lausanne (EPFL), Geneva, Switzerland.
Daniel KellerBlue Brain Project, École polytechnique fédérale de Lausanne (EPFL), Geneva, Switzerland.
École Polytechnique Fédérale de Lausanne · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Knowledge of the cell-type-specific composition of the brain is useful in order to understand the role of each cell type as part of the network. Here, we estimated the composition of the whole cortex in terms of well characterized morphological and electrophysiological inhibitory neuron types (me-types). We derived probabilistic me-type densities from an existing atlas of molecularly defined cell-type densities in the mouse cortex. We used a well-established me-type classification from rat somatosensory cortex to populate the cortex. These me-types were well characterized morphologically and electrophysiologically but they lacked molecular marker identity labels. To extrapolate this missing information, we employed an additional dataset from the Allen Institute for Brain Science containing molecular identity as well as morphological and electrophysiological data for mouse cortical neurons. We first built a latent space based on a number of comparable morphological and electrical features common to both data sources. We then identified 19 morpho-electrical clusters that merged neurons from both datasets while being molecularly homogeneous. The resulting clusters best mirror the molecular identity classification solely using available morpho-electrical features. Finally, we stochastically assigned a molecular identity to a me-type neuron based on the latent space cluster it was assigned to. The resulting mapping was used to derive inhibitory me-types densities in the cortex.

Indexed as

Electrophysiological PhenomenaNeuronsAnimalsCell CountMiceRatsSomatosensory Cortex

Identifiers

PMID36602951
OpenAlexW4313544536

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.