Evidence map›Paper›PMID 34505116›Full record

ArticleNeurons, behavior, data analysis, and theory2020

Sensitivity and specificity of a Bayesian single trial analysis for time varying neural signals.

Jeff T Mohl, Valeria C Caruso, Surya T Tokdar, Jennifer M Groh

Abstract read
In one paragraph

Article in Neurons, behavior, data analysis, and theory, 2020. 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
–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

7 citing papers in PubMed.

  1. Spike count analysis for multiplexing inference (SCAMPI).Journal of computational neuroscience · 2026
    Article
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  4. Review
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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

4 authors.

Jeff T MohlDuke Institute for Brain Sciences, Duke University, Durham, NC, 27708, USA.
Valeria C CarusoDuke Institute for Brain Sciences, Duke University, Durham, NC, 27708, USA.
Surya T TokdarDuke Institute for Brain Sciences, Duke University, Durham, NC, 27708, USA.
Jennifer M GrohDuke Institute for Brain Sciences, Duke University, Durham, NC, 27708, USA.

Funding

Information in Limited-Capacity Neural CodesR01DC013906 · NIDCD · DUKE UNIVERSITY · PI GROH, JENNIFER M · 2015 to 2019
$1.6M
Spatial Information CodesR01DC016363 · NIDCD · DUKE UNIVERSITY · PI GROH, JENNIFER M, TOKDAR, SURYA T · 2017 to 2021
$1.6M
NIDCD NIH HHS R01 DC013906NIDCD NIH HHS R01 DC016363
6 · The paper itself

Abstract

We recently reported the existence of fluctuations in neural signals that may permit neurons to code multiple simultaneous stimuli sequentially across time [1]. This required deploying a novel statistical approach to permit investigation of neural activity at the scale of individual trials. Here we present tests using synthetic data to assess the sensitivity and specificity of this analysis. We fabricated datasets to match each of several potential response patterns derived from single-stimulus response distributions. In particular, we simulated dual stimulus trial spike counts that reflected fluctuating mixtures of the single stimulus spike counts, stable intermediate averages, single stimulus winner-take-all, or response distributions that were outside the range defined by the single stimulus responses (such as summation or suppression). We then assessed how well the analysis recovered the correct response pattern as a function of the number of simulated trials and the difference between the simulated responses to each "stimulus" alone. We found excellent recovery of the mixture, intermediate, and outside categories (>97% correct), and good recovery of the single/winner-take-all category (>90% correct) when the number of trials was >20 and the single-stimulus response rates were 50Hz and 20Hz respectively. Both larger numbers of trials and greater separation between the single stimulus firing rates improved categorization accuracy. These results provide a benchmark, and guidelines for data collection, for use of this method to investigate coding of multiple items at the individual-trial time scale.

Indexed as

multiple stimulisingle trial analysisstatistical modelsvalidation

Identifiers

PMID34505116
PMCPMC8425354

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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.