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. 2022 Aug 30:11:e79277.
doi: 10.7554/eLife.79277.

Neuroscout, a unified platform for generalizable and reproducible fMRI research

Affiliations

Neuroscout, a unified platform for generalizable and reproducible fMRI research

Alejandro de la Vega et al. Elife. .

Abstract

Functional magnetic resonance imaging (fMRI) has revolutionized cognitive neuroscience, but methodological barriers limit the generalizability of findings from the lab to the real world. Here, we present Neuroscout, an end-to-end platform for analysis of naturalistic fMRI data designed to facilitate the adoption of robust and generalizable research practices. Neuroscout leverages state-of-the-art machine learning models to automatically annotate stimuli from dozens of fMRI studies using naturalistic stimuli-such as movies and narratives-allowing researchers to easily test neuroscientific hypotheses across multiple ecologically-valid datasets. In addition, Neuroscout builds on a robust ecosystem of open tools and standards to provide an easy-to-use analysis builder and a fully automated execution engine that reduce the burden of reproducible research. Through a series of meta-analytic case studies, we validate the automatic feature extraction approach and demonstrate its potential to support more robust fMRI research. Owing to its ease of use and a high degree of automation, Neuroscout makes it possible to overcome modeling challenges commonly arising in naturalistic analysis and to easily scale analyses within and across datasets, democratizing generalizable fMRI research.

Keywords: fMRI; generalizability; human; naturalistic; neuroinformatics; neuroscience; open source; reproducibility.

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Conflict of interest statement

Ad, RR, RB, CM, JM, JK, PH, SG, RP, TY No competing interests declared

Figures

Figure 1.
Figure 1.. Example of automated feature extraction on stimuli from the “Merlin” dataset.
Visual features were extracted from video stimuli at a frequency of 1 Hz. ‘Faces’: we applied a well-validated cascaded convolutional network trained to detect the presence of faces (Zhang et al., 2016). ‘Building’: We used Clarifai’s General Image Recognition model to compute the probability of the presence of buildings in each frame. ‘Spoken word frequency’ codes for the lexical frequency of words in the transcript, as determined by the SubtlexUS database (Brysbaert and New, 2009). Language features are extracted using speech transcripts with precise word-by-word timing determined through forced alignment.
Figure 2.
Figure 2.. Overview schematic of analysis creation and model execution.
(a) Interactive analysis creation is made possible through an easy-to-use web application, resulting in a fully specified reproducible analysis bundle. (b) Automated model execution is achieved with little-to-no configuration through a containerized model fitting workflow. Results are automatically made available in NeuroVault, a public repository for statistical maps.
Figure 3.
Figure 3.. Meta-analytic statistical maps for GLM models targeting a variety of effects with strong priors from fMRI research.
Individual GLM models were fit for each effect of interest, and dataset level estimates were combined using image-based meta-analysis. Images were thresholded at Z=3.29 (P<0.001) voxel-wise. Abbreviations: V1=primary visual cortex; FEF = frontal eye fields; AG = angular gyrus; PCUN = precuneus; A1=primary auditory cortex; PMC = premotor cortex; IFG = inferior frontal gyrus; STS = superior temporal sulcus; STG = superior temporal gyrus; PPA = parahippocampal place area; VWFA = visual word-form area; IPL = inferior parietal lobule; IPS = inferior parietal sulcus; LOTC = lateral occipito-temporal cortex.
Figure 4.
Figure 4.. Comparison of a sample of four single study results with meta-analysis (N=20) for three features: ‘building’ and ‘text’ extracted through Clarifai visual scene detection models, and sound ‘loudness’ (root mean squared of the auditory signal).
Images were thresholded at Z=3.29 (p<0.001) voxel-wise. Regions with a priori association with each predictor are highlighted: PPA, parahippocampal place area; VWFA, visual word form area; STS, superior temporal sulcus. Datasets: Budapest, Learning Temporal Structure (LTS), 500daysofsummer task from Naturalistic Neuroimaging Database, and Sherlock.
Figure 5.
Figure 5.. Meta-analysis of face perception with iterative addition of covariates.
Left; Only including binary predictors coding for the presence of faces on screen did not reveal activity in the right fusiform face area (rFFA). Middle; Controlling for speech removed spurious activations and revealed rFFA association with face presentation. Right; Controlling for temporal adaptation to face identity in addition to speech further strengthened the association between rFFA and face presentation. N=17 datasets; images were thresholded at Z=3.29 (p<0.001) voxel-wise.
Figure 6.
Figure 6.. Meta-analytic statistical maps for concreteness and frequency controlling for speech, text length, number of syllables and phonemes, and phone-level Levenshtein distance.
N=33 tasks; images were thresholded at Z=3.29 (p<0.001) voxel-wise. Visual word form area, VWFA.

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