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RNA sequencing of human ILC3 from lymphoid organs and blood

Rna sequencing of purified human group 3 innate lymphoid cells from non-reactive lymph nodes and spleen, inflamed tonsils and peripheral blood.

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THE EMC-ILC3 consortium data access committee

THE EMC-ILC3 consortium data access committee DATA ACCESS AGREEMENT This agreement governs the terms on which access will be granted to the next generation sequencing data generated by the EMC-ILC3 consortium of the Erasmus university Rotterdam department of Hematology. In signing this agreement, You are agreeing to be bound by the terms and conditions of access set out in this agreement. For the sake of clarity, the terms of access set out in this agreement apply both to the User and the User’s Institution (as defined below). User Institution and User are referred to within the agreement as “You” and “Your” shall be construed accordingly. Definitions: The EMC-ILC3 consortium, part of the Erasmus university Rotterdam department of Hematology is represented by the following members: Dr. Tom Cupedo, Dr. Mathijs A. Sanders and Remco Hoogenboezem. Data means all human genetic data obtained from the EMC-ILC3 consortium. Data Subject means a person, who has been informed of the purpose for which the Data is held and has given his/her informed consent thereto. User means a researcher whose User Institution has previously completed this Data Access Agreement and has received acknowledgement of its acceptance. Publications means, without limitation, articles published in print journals, electronic journals, reviews, books, posters and other written and verbal presentations of research. User Institution means the organization at which the User is employed, affiliated or enrolled. Terms and Conditions: In signing this Agreement: 1. You agree to use the Data only for the advancement of medical scientific research, according to the consent obtained from sample donors. 2. You agree not to use the data or any part thereof for the creation of products for sale or for any commercial purpose. 3. You agree to preserve, at all times, the confidentiality of information and Data pertaining to Data Subjects. In particular, You undertake not to use, or attempt to use the Data to compromise or otherwise infringe the confidentiality of information on Data Subjects and their right to privacy. 4. You agree not to attempt to link the data provided under this agreement to other information or archive data available for the data sets provided, even if access to that data has been formally granted to you, or it is freely available without restriction, without specific permission being sought from the relevant access committees. 5. You agree not to transfer or disclose the Data, in whole or part, or any identifiable material derived from the Data, to others, except as necessary for data/safety monitoring or programme management. Should You wish to share the Data with a collaborator outside the same Institution, the third party must make a separate application for access to the Data. 6. You agree to use the data for the approved purpose and project described in your application; use of the data for a new purpose or project will require a new application and approval. The relevant access committees will see to it that the Data is not used in publications outside the project described in the original application. 7. You accept that Data will be reissued from time to time, with suitable versioning. If the reissue is at the request of sample donors and/or other ethical scrutiny, You will destroy earlier versions of the Data. 8. You agree to acknowledge in any work based in whole or part on the Data the published paper from which the Data derives. 9. You accept that the Consortium, the original data creators, depositors or copyright holders, or the funders of the Data or any part of the Data supplied: a) bear no legal responsibility for the accuracy or comprehensiveness of the Data; and b) accept no liability for indirect, consequential, or incidental, damages or losses arising from use of the Data, or from the unavailability of, or break in access to, the Data for whatever reason. 10. You understand and acknowledge that the Data is protected by copyright and other intellectual property rights, and that duplication, except as reasonably required to carry out Your research with the Data, or sale of all or part of the Data on any media is not permitted. 11. You recognize that nothing in this agreement shall operate to transfer to the User Institution any intellectual property rights relating to the Data. The User Institution has the right to develop intellectual property based on comparisons with their own data. 12. You accept that this agreement will terminate immediately upon any breach of this agreement by You and You will be required to destroy any Data held. 13. You accept that it may be necessary for the Consortium or its appointed agent to alter the terms of this agreement from time to time in order to address new concerns. In this event, the Consortium or its appointed agent will contact You to inform You of any changes and You agree that Your continued use of the Data shall be dependent on the parties entering into a new version of the Agreement. 14. You agree that you will submit a report to the Consortium Data Access Committee, if requested, on completion of the agreed purpose. The Consortium Data Access Committee agrees to treat the report and all information, data, results, and conclusions contained within such report as confidential information belonging to the User Institution. 15. You accept that the Data is protected by and subject to international laws, and that You are responsible for ensuring compliance with any such applicable law. The Consortium Data Access Committee reserves the right to request and inspect data security and management documentation to ensure the adequacy of data protection measures in countries that have no national laws comparable to that which pertain in the EAA. 16. This agreement shall be construed, interpreted and governed by the laws of the Netherlands and shall be subject to the non-exclusive jurisdiction of the Dutch courts.

Studies are experimental investigations of a particular phenomenon, e.g., case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients.

Study ID Study Title Study Type
EGAS00001002636 Other

This table displays only public information pertaining to the files in the dataset. If you wish to access this dataset, please submit a request. If you already have access to these data files, please consult the download documentation.

ID File Type Size Located in
EGAF00001748681 fastq.gz 1.3 GB
EGAF00001748682 fastq.gz 1.3 GB
EGAF00001748683 fastq.gz 1.6 GB
EGAF00001748684 fastq.gz 1.6 GB
EGAF00001748685 fastq.gz 1.3 GB
EGAF00001748686 fastq.gz 1.3 GB
EGAF00001748687 fastq.gz 1.4 GB
EGAF00001748688 fastq.gz 1.4 GB
EGAF00001748689 fastq.gz 2.4 GB
EGAF00001748690 fastq.gz 2.7 GB
EGAF00001748691 fastq.gz 1.7 GB
EGAF00001748692 fastq.gz 1.9 GB
EGAF00001748693 fastq.gz 1.5 GB
EGAF00001748694 fastq.gz 1.5 GB
EGAF00001748695 fastq.gz 1.9 GB
EGAF00001748696 fastq.gz 1.9 GB
EGAF00001748697 fastq.gz 1.6 GB
EGAF00001748698 fastq.gz 1.6 GB
EGAF00001748699 fastq.gz 1.7 GB
EGAF00001748700 fastq.gz 1.7 GB
EGAF00001748701 fastq.gz 2.3 GB
EGAF00001748702 fastq.gz 2.3 GB
EGAF00001748703 fastq.gz 2.0 GB
EGAF00001748704 fastq.gz 2.0 GB
EGAF00001748705 fastq.gz 1.5 GB
EGAF00001748706 fastq.gz 1.5 GB
EGAF00001748707 fastq.gz 1.6 GB
EGAF00001748708 fastq.gz 1.6 GB
EGAF00001748709 fastq.gz 1.1 GB
EGAF00001748710 fastq.gz 1.1 GB
EGAF00001748711 fastq.gz 1.2 GB
EGAF00001748712 fastq.gz 1.2 GB
EGAF00001748713 fastq.gz 1.5 GB
EGAF00001748714 fastq.gz 1.5 GB
EGAF00001748715 fastq.gz 1.6 GB
EGAF00001748716 fastq.gz 1.7 GB
EGAF00001748717 fastq.gz 1.3 GB
EGAF00001748718 fastq.gz 1.4 GB
EGAF00001748719 fastq.gz 1.7 GB
EGAF00001748720 fastq.gz 1.7 GB
40 Files (64.5 GB)