Evidence map›Paper›PMID 38709828›Full record

ArticlePLoS computational biology2024

Removing direct photocurrent artifacts in optogenetic connectivity mapping data via constrained matrix factorization.

Benjamin Antin, Masato Sadahiro, Marta Gajowa, Marcus A Triplett, Hillel Adesnik, Liam Paninski

Abstract read
In one paragraph

Article in PLoS computational biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
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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

6 authors.

Benjamin AntinMortimer B. Zuckerman Mind Brain Behavior Institute, Grossman Center for the Statistics of Mind, and Center for Theoretical Neuroscience, Columbia University, New York, New York, United States of America.ORCID 0000-0002-3361-985X
Masato SadahiroDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, California, United States of America.
Marta GajowaDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, California, United States of America.
Marcus A TriplettMortimer B. Zuckerman Mind Brain Behavior Institute, Grossman Center for the Statistics of Mind, and Center for Theoretical Neuroscience, Columbia University, New York, New York, United States of America.
Hillel AdesnikDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, California, United States of America.
Liam PaninskiMortimer B. Zuckerman Mind Brain Behavior Institute, Grossman Center for the Statistics of Mind, and Center for Theoretical Neuroscience, Columbia University, New York, New York, United States of America.

Funding

Validating Theoretical Models with Neurophysiology and OptogeneticsU19NS107613 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI JI, NA · 2018 to 2022
$16.7M
High-throughput Physiological Micro-connectivity Mapping in VivoRF1MH120680 · NIMH · UNIVERSITY OF CALIFORNIA BERKELEY · PI ADESNIK, HILLEL · 2019 to 2021
$2.2M
Computational Methods for Precise Holographic Control and Mapping of Neural CircuitsK99NS135649 · NINDS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI TRIPLETT, MARCUS · 2024 to 2025
$272k
Cell-Type-Specific Mechanisms of Contextual Modulation in the Visual CortexF32EY034022 · NEI · UNIVERSITY OF CALIFORNIA BERKELEY · PI SADAHIRO, MASATO · 2022 to 2024
$218k
NEI NIH HHS F32 EY034022NIMH NIH HHS RF1 MH120680NINDS NIH HHS K99 NS135649NINDS NIH HHS U19 NS107613
6 · The paper itself

Abstract

Monosynaptic connectivity mapping is crucial for building circuit-level models of neural computation. Two-photon optogenetic stimulation, when combined with whole-cell recording, enables large-scale mapping of physiological circuit parameters. In this experimental setup, recorded postsynaptic currents are used to infer the presence and strength of connections. For many cell types, nearby connections are those we expect to be strongest. However, when the postsynaptic cell expresses opsin, optical excitation of nearby cells can induce direct photocurrents in the postsynaptic cell. These photocurrent artifacts contaminate synaptic currents, making it difficult or impossible to probe connectivity for nearby cells. To overcome this problem, we developed a computational tool, Photocurrent Removal with Constraints (PhoRC). Our method is based on a constrained matrix factorization model which leverages the fact that photocurrent kinetics are less variable than those of synaptic currents. We demonstrate on real and simulated data that PhoRC consistently removes photocurrents while preserving synaptic currents, despite variations in photocurrent kinetics across datasets. Our method allows the discovery of synaptic connections which would have been otherwise obscured by photocurrent artifacts, and may thus reveal a more complete picture of synaptic connectivity. PhoRC runs faster than real time and is available as open source software.

Indexed as

ArtifactsComputational BiologyModels, NeurologicalOptogeneticsAlgorithmsAnimalsComputer SimulationHumansMiceNeuronsPatch-Clamp TechniquesSoftwareSynapses

Identifiers

PMID38709828
PMCPMC11098512

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.