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Genome-wide array and mtDNA data Mercheros

This dataset includes genome-wide autosomal array data and whole mtDNA sequences for 24 Merchero individuals.

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Data Access Policy for genome-wide array data and whole mitochondrial sequences of Mercheros

DATA ACCESS AGREEMENT These terms and conditions govern access to the managed access datasets to which the User Institution has requested access. The User Institution agrees to be bound by these terms and conditions. Definitions Authorised Personnel: The individuals at the User Institution to whom Dr.David Comas grants access to the Data. This includes the User, the individuals listed in Appendix II and any other individuals for whom the User Institution subsequently requests access to the Data. Details of the initial Authorised Personnel are set out in Appendix II. Data: The managed access datasets to which the User Institution has requested access. Data Producers: Dr.David Comas and the collaborators listed in Appendix I responsible for the development, organisation, and oversight of these Data. External Collaborator: A collaborator of the User, working for an institution other than the User Institution. Project: The project for which the User Institution has requested access to these Data. A description of the Project is set out in Appendix II. Publications: Includes, without limitation, articles published in print journals, electronic journals, reviews, books, posters and other written and verbal presentations of research. Research Participant: An individual whose data form part of these Data. Research Purposes: Shall mean research that is seeking to advance the understanding of genetics and genomics, including the treatment of disorders, and work on statistical methods that may be applied to such research. User: The principal investigator for the Project. User Institution(s): The Institution that has requested access to the Data. David Comas 1. The User Institution agrees to only use these Data for the purpose of the Project (described in Appendix II) and only for Research Purposes. The User Institution further agrees that it will only use these Data for Research Purposes which are within the limitations (if any) set out in Appendix I. 2. The User Institution agrees to preserve, at all times, the confidentiality of these Data. In particular, it undertakes not to use, or attempt to use these Data to compromise or otherwise infringe the confidentiality of information on Research Participants. Without prejudice to the generality of the foregoing, the User Institution agrees to use at least the measures set out in Appendix I to protect these Data. 3. The User Institution agrees to protect the confidentiality of Research Participants in any research papers or publications that they prepare by taking all reasonable care to limit the possibility of identification. 4. The User Institution agrees not to link or combine these Data to other information or archived data available in a way that could re-identify the Research Participants, even if access to that data has been formally granted to the User Institution or is freely available without restriction. 5. The User Institution agrees only to transfer or disclose these Data, in whole or part, or any material derived from these Data, to the Authorised Personnel. Should the User Institution wish to share these Data with an External Collaborator, the External Collaborator must complete a separate application for access to these Data. 6. The User Institution agrees that the Data Producers, and all other parties involved in the creation, funding or protection of these Data: a) make no warranty or representation, express or implied as to the accuracy, quality or comprehensiveness of these Data; b) exclude to the fullest extent permitted by law all liability for actions, claims, proceedings, demands, losses (including but not limited to loss of profit), costs, awards damages and payments made by the Recipient that may arise (whether directly or indirectly) in any way whatsoever from the Recipient’s use of these Data or from the unavailability of, or break in access to, these Data for whatever reason and; c) bear no responsibility for the further analysis or interpretation of these Data. 7. The User Institution agrees to follow the Fort Lauderdale Guidelines (http://www.wellcome.ac.uk/stellent/groups/corporatesite/@policy_communications/documents/web_document/wtd003207.pdf) and the Toronto Statement (http://www.nature.com/nature/journal/v461/n7261/full/461168a.html). This includes but is not limited to recognising the contribution of the Data Producers and including a proper acknowledgement in all reports or publications resulting from the use of these Data. 8. The User Institution agrees to follow the Publication Policy in Appendix III. This includes respecting the moratorium period for the Data Producers to publish the first peer-reviewed report describing and analysing these Data. 9. The User Institution agrees not to make intellectual property claims on these Data and not to use intellectual property protection in ways that would prevent or block access to, or use of, any element of these Data, or conclusion drawn directly from these Data. 10. The User Institution can elect to perform further research that would add intellectual and resource capital to these data and decide to obtain intellectual property rights on these downstream discoveries. In this case, the User Institution agrees to implement licensing policies that will not obstruct further research and to follow the U.S. National Institutes of Health Best Practices for the Licensing of Genomic Inventions (2005) (https://www.icgc.org/files/daco/NIH_BestPracticesLicensingGenomicInventions_2005_en.pdf ) in conformity with the Organisation for Economic Co-operation and Development Guidelines for the Licensing of the Genetic Inventions (2006) (http://www.oecd.org/science/biotech/36198812.pdf ). 11. The User Institution agrees to destroy/discard the Data held, once it is no longer used for the Project, unless obliged to retain the data for archival purposes in conformity with audit or legal requirements. 12. The User Institution will notify Dr.David Comas within 30 days of any changes or departures of Authorised Personnel. 13. The User Institution will notify Dr.David Comas prior to any significant changes to the protocol for the Project. 14. The User Institution will notify Dr.David Comas as soon as it becomes aware of a breach of the terms or conditions of this agreement. 15. Dr.David Comas may terminate this agreement by written notice to the User Institution. If this agreement terminates for any reason, the User Institution will be required to destroy any Data held, including copies and backup copies. This clause does not prevent the User Institution from retaining these data for archival purpose in conformity with audit or legal requirements. 16. The User Institution accepts that it may be necessary for the Data Producers to alter the terms of this agreement from time to time. As an example, this may include specific provisions relating to the Data required by Data Producers other than Dr.David Comas. In the event that changes are required, the Data Producers or their appointed agent will contact the User Institution to inform it of the changes and the User Institution may elect to accept the changes or terminate the agreement. 17. If requested, the User Institution will allow data security and management documentation to be inspected to verify that it is complying with the terms of this agreement. 18. The User Institution agrees to distribute a copy of these terms to the Authorised Personnel. The User Institution will procure that the Authorised Personnel complies with the terms of this agreement. 19. This agreement (and any dispute, controversy, proceedings or claim of whatever nature arising out of this agreement or its formation) shall be construed, interpreted and governed by the laws of Spain.

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
EGAS00001005360 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
EGAF00005310995 vcf 51.4 MB
EGAF00005316370 fastq.gz 14.1 MB
EGAF00005316371 fastq.gz 15.9 MB
EGAF00005316372 fastq.gz 16.9 MB
EGAF00005316373 fastq.gz 19.3 MB
EGAF00005316374 fastq.gz 9.7 MB
EGAF00005316375 fastq.gz 11.0 MB
EGAF00005316376 fastq.gz 5.7 MB
EGAF00005316377 fastq.gz 6.6 MB
EGAF00005316378 fastq.gz 8.2 MB
EGAF00005316379 fastq.gz 8.6 MB
EGAF00005316380 fastq.gz 8.9 MB
EGAF00005316381 fastq.gz 9.5 MB
EGAF00005316382 fastq.gz 8.5 MB
EGAF00005316383 fastq.gz 9.2 MB
EGAF00005316384 fastq.gz 9.7 MB
EGAF00005316385 fastq.gz 10.5 MB
EGAF00005316386 fastq.gz 9.9 MB
EGAF00005316387 fastq.gz 10.9 MB
EGAF00005316388 fastq.gz 6.9 MB
EGAF00005316389 fastq.gz 7.7 MB
EGAF00005316390 fastq.gz 11.7 MB
EGAF00005316391 fastq.gz 12.6 MB
EGAF00005316392 fastq.gz 7.9 MB
EGAF00005316393 fastq.gz 8.4 MB
EGAF00005316394 fastq.gz 5.7 MB
EGAF00005316395 fastq.gz 6.2 MB
EGAF00005316396 fastq.gz 10.4 MB
EGAF00005316397 fastq.gz 10.9 MB
EGAF00005316398 fastq.gz 9.5 MB
EGAF00005316399 fastq.gz 10.3 MB
EGAF00005316400 fastq.gz 3.3 MB
EGAF00005316401 fastq.gz 3.6 MB
EGAF00005316402 fastq.gz 8.6 MB
EGAF00005316403 fastq.gz 9.4 MB
EGAF00005316404 fastq.gz 9.8 MB
EGAF00005316405 fastq.gz 9.8 MB
EGAF00005316406 fastq.gz 3.7 MB
EGAF00005316407 fastq.gz 3.9 MB
EGAF00005316408 fastq.gz 5.7 MB
EGAF00005316409 fastq.gz 6.1 MB
EGAF00005316410 fastq.gz 9.8 MB
EGAF00005316411 fastq.gz 11.2 MB
EGAF00005316412 fastq.gz 6.9 MB
EGAF00005316413 fastq.gz 7.7 MB
EGAF00005316414 fastq.gz 8.8 MB
EGAF00005316415 fastq.gz 9.8 MB
47 Files (471.0 MB)