Scene: Figure 8
WU-Minn HCP Consortium Open Access Data Use Terms
1. I will not attempt to establish the identity of or attempt to contact any of the included human subjects.
2. I understand that under no circumstances will the code that would link these data to Protected Health Information be given to me, nor will any additional information about individual human subjects be released to me under these Open Access Data Use Terms.
3. I will comply with all relevant rules and regulations imposed by my institution. This may mean that I need my research to be approved or declared exempt by a committee that oversees research on human subjects, e.g. my IRB or Ethics Committee. The released HCP data are not considered de-identified, insofar as certain combinations of HCP Restricted Data (available through a separate process) might allow identification of individuals. Different committees operate under different national, state and local laws and may interpret regulations differently, so it is important to ask about this. If needed and upon request, the HCP will provide a certificate stating that you have accepted the HCP Open Access Data Use Terms.
4. I may redistribute original WU-Minn HCP Open Access data and any derived data as long as the data are redistributed under these same Data Use Terms.
5. I will acknowledge the use of WU-Minn HCP data and data derived from WU-Minn HCP data when publicly presenting any results or algorithms that benefitted from their use.
1. Papers, book chapters, books, posters, oral presentations, and all other printed and digital presentations of results derived from HCP data should contain the following wording in the acknowledgments section: "Data were provided [in part] by the Human Connectome Project, WU-Minn Consortium (Principal Investigators: David Van Essen and Kamil Ugurbil; 1U54MH091657) funded by the 16 NIH Institutes and Centers that support the NIH Blueprint for Neuroscience Research; and by the McDonnell Center for Systems Neuroscience at Washington University."
2. Authors of publications or presentations using WU-Minn HCP data should cite relevant publications describing the methods used by the HCP to acquire and process the data. The specific publications that are appropriate to cite in any given study will depend on what HCP data were used and for what purposes. An annotated and appropriately up-to-date list of publications that may warrant consideration is available at http://www.humanconnectome.org/about/acknowledgehcp.html
3. The WU-Minn HCP Consortium as a whole should not be included as an author of publications or presentations if this authorship would be based solely on the use of WU-Minn HCP data.
6. Failure to abide by these guidelines will result in termination of my privileges to access WU-Minn HCP data.
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The HCP language task (story vs baseline) beta maps and their spatial gradients. Beta maps (rows 1 and 3) and gradient maps (rows 2 and 4) are from two independent groups of 210 HCP subjects, "210P" (rows 1 and 2) and "210V" (rows 3 and 4). Because of the large number of high quality HCP subjects, the beta maps are very similar across the two groups, and the strong gradients in the beta maps are also very similar. Also shown are white contours of a Bonferroni corrected significance threshold across all 91282 grayordinates (z+/- ~5). Two things are apparent: 1) Because of the large amount of high quality data, most of the brain is either significantly activated or deactivated. Thus the statistical threshold is not particularly biologically meaningful (a point about statistical thresholds that generally applies). At the same time, the statistical threshold is also not strongly reproducible, in spite of the large amount of high quality data (highlighted ellipses show large differences in the area of activation classified as "significant" that are not particularly impressive when viewing the unthresholded beta maps). In contrast, the strong gradients in the beta maps are much more reproducible, are likely also more biologically meaningful, and hence provide a better substrate for defining regions of activation or comparing across studies.
Surface Mesh:32k fs LR, Registration:MSMAll, Species:Human, Modality:Myelin Map, Modality:T2-weighted, Modality:T1-weighted