Evidence map›Paper›PMID 30686967›Full record

ArticleFrontiers in neuroscience2018

Optimizing Data for Modeling Neuronal Responses.

Peter Zeidman, Samira M Kazan, Nick Todd, Nikolaus Weiskopf, Karl J Friston, Martina F Callaghan

Abstract read
In one paragraph

Article in Frontiers in neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

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  7. An information-theoretic analysis of resting-state versus task fMRI.Network neuroscience (Cambridge, Mass.) · 2023
    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.

Peter ZeidmanWellcome Centre for Human Neuroimaging, UCL Institute of Neurology, University College London, London, United Kingdom.
Samira M KazanWellcome Centre for Human Neuroimaging, UCL Institute of Neurology, University College London, London, United Kingdom.
Nick ToddDepartment of Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States.
Nikolaus WeiskopfWellcome Centre for Human Neuroimaging, UCL Institute of Neurology, University College London, London, United Kingdom.
Karl J FristonWellcome Centre for Human Neuroimaging, UCL Institute of Neurology, University College London, London, United Kingdom.
Martina F CallaghanWellcome Centre for Human Neuroimaging, UCL Institute of Neurology, University College London, London, United Kingdom.

Funding

European Research Council 616905Wellcome Trust
6 · The paper itself

Abstract

In this technical note, we address an unresolved challenge in neuroimaging statistics: how to determine which of several datasets is the best for inferring neuronal responses. Comparisons of this kind are important for experimenters when choosing an imaging protocol-and for developers of new acquisition methods. However, the hypothesis that one dataset is better than another cannot be tested using conventional statistics (based on likelihood ratios), as these require the data to be the same under each hypothesis. Here we present Bayesian data comparison (BDC), a principled framework for evaluating the quality of functional imaging data, in terms of the precision with which neuronal connectivity parameters can be estimated and competing models can be disambiguated. For each of several candidate datasets, neuronal responses are modeled using Bayesian (probabilistic) forward models, such as General Linear Models (GLMs) or Dynamic Casual Models (DCMs). Next, the parameters from subject-specific models are summarized at the group level using a Bayesian GLM. A series of measures, which we introduce here, are then used to evaluate each dataset in terms of the precision of (group-level) parameter estimates and the ability of the data to distinguish similar models. To exemplify the approach, we compared four datasets that were acquired in a study evaluating multiband fMRI acquisition schemes, and we used simulations to establish the face validity of the comparison measures. To enable people to reproduce these analyses using their own data and experimental paradigms, we provide general-purpose Matlab code via the SPM software.

Indexed as

DCMdynamic causal modelingfMRImultibandPEB

Identifiers

PMID30686967
PMCPMC6335328

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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.