Evidence map›Paper›PMID 37986854›Full record

ArticlebioRxiv : the preprint server for biology2024

Using Multivariate Pattern Analysis to Increase Effect Sizes for Event-Related Potential Analyses.

Carlos Daniel Carrasco, Brett Bahle, Aaron Matthew Simmons, Steven J Luck

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Carlos Daniel CarrascoCenter for Mind & Brain, University of California, Davis.
Brett BahleCenter for Mind & Brain, University of California, Davis.ORCID 0000-0002-8965-7003
Aaron Matthew SimmonsCenter for Mind & Brain, University of California, Davis.
Steven J LuckCenter for Mind & Brain, University of California, Davis.

Funding

ERPLAB: Extensible, open source software for analysis of event-related potentialsR01MH087450 · NIMH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LUCK, STEVEN J · 2010 to 2025
$2.7M
Learning, Memory, and Plasticity (LaMP) Training ProgramT32MH112507 · NIMH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Karen Zito · 2017 to 2026
$2.4M
Using Population Vectors to Understand Visual Working Memory for Natural StimuliR01EY033329 · NEI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LUCK, STEVEN J · 2022 to 2025
$1.8M
NEI NIH HHS R01 EY033329NIMH NIH HHS R01 MH087450NIMH NIH HHS T32 MH112507
6 · The paper itself

Abstract

Multivariate pattern analysis approaches can be applied to the topographic distribution of event-related potential (ERP) signals to 'decode' subtly different stimulus classes, such as different faces or different orientations. These approaches are extremely sensitive, and it seems possible that they could also be used to increase effect sizes and statistical power in traditional paradigms that ask whether an ERP component differs in amplitude across conditions. To assess this possibility, we leveraged the open-source ERP CORE dataset and compared the effect sizes resulting from conventional univariate analyses of mean amplitude with two multivariate pattern analysis approaches (support vector machine decoding and the cross-validated Mahalanobis distance, both of which are easy to compute using open-source software). We assessed these approaches across seven widely studied ERP components (N170, N400, N2pc, P3b, lateral readiness potential, error related negativity, and mismatch negativity). Across all components, we found that multivariate approaches yielded effect sizes that were as large or larger than the effect sizes produced by univariate approaches. These results indicate that researchers could obtain larger effect sizes, and therefore greater statistical power, by using multivariate analysis of topographic voltage patterns instead of traditional univariate analyses in many ERP studies.

Indexed as

ClassificationCross-Validated Mahalanobis DistanceDecodingEEGERPsSupport Vector Machine

Identifiers

PMID37986854
PMCPMC10659264

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.