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Data User Agreement
1. Dataset
The multimodal healthy control (multimodal-hc) dataset comprises comprehensive whole-body PET, CT, and MR images and statistical readouts from 100 healthy controls of the study: Healthy Digital Twin (HEDIT Study) — Towards a Synthetic Baseline PET for Precision Medicine (ref. number H-23065644, approved by the Danish Regional Ethics Committee). All healthy control participants were informed, verbally and in writing, of the data-sharing nature of the study prior to providing written consent to participate.
2. Definitions
In this Agreement, the following capitalised terms have the meanings set out below.
Agreement means this Data Use Agreement, including the signature page. Provider means Copenhagen University Hospital, Rigshospitalet.
Materials means the multimodal-hc dataset described in Section 1, including all imaging data, derived statistical readouts, accompanying metadata, and documentation made available under this Agreement.
User means the individual signing this Agreement as project coordinator or principal investigator and who is personally responsible for compliance with its terms.
Authorized Users means the User and the members of the User's research group who require access to the Materials for the Permitted Purpose, who act under the User's direction and responsibility, and who are bound by terms no less protective than those of this Agreement. The User remains responsible for any act or omission of an Authorized User as if it were the User's own.
3. Terms and Conditions
By accessing the Materials, the User agrees to be bound by the following terms.
3.1. Permitted Purpose
The User and Authorized Users may use the Materials for the purposes of research and analysis. This specifically includes both academic, non-commercial research and commercial Research and Development (R&D). For the avoidance of doubt, the Materials may not be used for the direct clinical diagnosis, treatment, or medical care of patients.
3.2. Prohibitions on Redistribution and Sale
Direct commercialisation or redistribution of the dataset itself is prohibited. The User shall not sell, license, lease, sub-license, distribute, publish, or otherwise make available the Materials (in whole or in part) to any third party, nor repackage the Materials as a commercial product.
3.3. Protection of Human Subjects
The Provider considers the Materials to be anonymized. The User's undertakings in this Section 3.3 are a condition of access and are intended to preserve that status. The User will not attempt to use the Materials, either alone or in combination with other information, to discover the identity of, or contact, any individual participant. If the User inadvertently discovers identifying information, they must immediately notify the Provider, isolate the data, and securely destroy it upon instruction. The User shall not attempt to identify, diagnose, classify, or otherwise infer the presence of any disease, lesion, or pathological condition in any individual participant in the Materials.
3.4. Data Security and Institutional Compliance
The User must implement appropriate technical, physical, and administrative safeguards to protect the Materials from unauthorized access. The User will comply with all relevant local, national, and international data protection regulations.
3.5. Citation and Attribution
In any publications, presentations, or outputs arising from the use of the Materials, the User shall appropriately cite the primary multimodal-hc dataset publication, including the DOI [DOI TO BE INSERTED].
3.6. Disclaimer of Warranties
The Materials are provided as a research tool on an 'as is' basis, without any express or implied warranties. The Provider offers no warranties regarding merchantability, fitness for a particular purpose, or non-infringement of third-party rights.
3.7. Liability and Indemnification
In no event shall the Provider be liable for damages (including loss of data or derivative losses) arising from the use of the Materials. The User agrees to indemnify and hold harmless the Provider against claims or damages arising directly or indirectly from the use of the Materials. This includes any direct and indirect damages from a force majeure or similar event.
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