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The HCP 7T Retinotopy Dataset: Description and pRF Analysis

Noah C. Benson, Keith W. Jamison, Michael J. Arcaro, An Vu, Matthew F. Glasser, Timothy S. Coalson, David C. Van Essen, Essa Yacoub, Kamil Ugurbil, Jonathan Winawer, Kendrick Kay
doi: https://doi.org/10.1101/308247
Noah C. Benson
1Department of Psychology and Center for Neural Science, New York University
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Keith W. Jamison
2Center for Magnetic Resonance Research (CMRR), Department of Radiology, University of Minnesota
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Michael J. Arcaro
3Department of Neurobiology, Harvard Medical School
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An Vu
2Center for Magnetic Resonance Research (CMRR), Department of Radiology, University of Minnesota
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Matthew F. Glasser
4Department of Neuroscience, Washington University in St. Louis
5Department of Radiology, Washington University in St. Louis
6St. Luke’s Hospital, St. Louis
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Timothy S. Coalson
4Department of Neuroscience, Washington University in St. Louis
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David C. Van Essen
4Department of Neuroscience, Washington University in St. Louis
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Essa Yacoub
2Center for Magnetic Resonance Research (CMRR), Department of Radiology, University of Minnesota
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Kamil Ugurbil
2Center for Magnetic Resonance Research (CMRR), Department of Radiology, University of Minnesota
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Jonathan Winawer
1Department of Psychology and Center for Neural Science, New York University
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Kendrick Kay
2Center for Magnetic Resonance Research (CMRR), Department of Radiology, University of Minnesota
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Abstract

About a quarter of human cerebral cortex is dedicated mainly to visual processing. The large-scale organization of visual cortex can be measured with functional magnetic resonance imaging (fMRI) while subjects view spatially modulated visual stimuli, also known as ‘retinotopic mapping’. One of the datasets collected by the Human Connectome Project (HCP) involved ultra-high-field (7 Tesla) fMRI retinotopic mapping in 181 healthy young adults (1.6-mm resolution), yielding the largest freely available collection of retinotopy data. Here, we describe the experimental paradigm and the results of model-based analysis of the fMRI data. These results provide estimates of population receptive field position and size. Our analyses include both results from individual subjects as well as results obtained by averaging fMRI time-series across subjects at each cortical and subcortical location and then fitting models. Both the group-average and individual-subject results reveal robust signals across much of the brain, including occipital, temporal, parietal, and frontal cortex as well as subcortical areas. The group-average results agree well with previously published parcellations of visual areas. In addition, split-half analyses show strong within-subject reliability, further demonstrating the high quality of the data. We make publicly available the analysis results for individual subjects and the group average, as well as associated stimuli and analysis code. These resources provide an opportunity for studying fine-scale individual variability in cortical and subcortical organization and the properties of high-resolution fMRI. In addition, they provide a set of observations that can be compared with other HCP measures acquired in these same participants.

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Posted August 30, 2018.
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The HCP 7T Retinotopy Dataset: Description and pRF Analysis
Noah C. Benson, Keith W. Jamison, Michael J. Arcaro, An Vu, Matthew F. Glasser, Timothy S. Coalson, David C. Van Essen, Essa Yacoub, Kamil Ugurbil, Jonathan Winawer, Kendrick Kay
bioRxiv 308247; doi: https://doi.org/10.1101/308247
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The HCP 7T Retinotopy Dataset: Description and pRF Analysis
Noah C. Benson, Keith W. Jamison, Michael J. Arcaro, An Vu, Matthew F. Glasser, Timothy S. Coalson, David C. Van Essen, Essa Yacoub, Kamil Ugurbil, Jonathan Winawer, Kendrick Kay
bioRxiv 308247; doi: https://doi.org/10.1101/308247

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