Scene: Figure 12
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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Effects of averaging surface coordinates and folding maps after areal feature-based registration (MSMAll). The first row shows the group average midthickness surface (left), and the group average curvature map also displayed on inflated and flat surfaces (center and right). The group consisted of 210 subjects. The second row shows an individual subject's midthickness surface (left), and the individual's curvature map displayed also on inflated and flat surfaces (center and right). Note how much less detailed the group average surfaces and curvature maps are in most regions of cortex. However, in regions with consistent folding patterns across subjects and consistent relationships between cortical areas and folds, the group average patterns remain sharp (e.g. the central and calcarine sulci and the insula). The third row shows the group average T1w volume (after FNIRT nonlinear volume registration to MNI152 space of each subject in the group) together with the group average white (green) and pial (blue) surface contours. The fourth row shows the same individual subject's T1w volume together with the individual's white and pial surfaces (after aligning both the T1w volume and the surfaces to the group average in MNI space using FNIRT nonlinear volume registration). Despite the high precision of the white and pial surfaces in following the grey matter ribbon in the individual, the group average surfaces do not follow the group average volume particularly well, except in the regions where there are consistent folding patterns across subjects and consistent relationships between cortical areas and folds (as mentioned above). These issues also occur with folding-based surface registration (not shown), though they are less severe, because for folding-based registration the dominant factor is inconsistency in folding patterns across subjects (as no attempt is made to directly align cortical areas). The midthickness surfaces are the average of the white and pial surfaces (this average is performed on each individual, and the group midthickness surface is the average of the individual midthickness surfaces).
Surface Mesh:32k fs LR, Registration:MSMAll, Species:Human, Modality:Myelin Map, Modality:T1-weighted, Modality:T2-weighted