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BAM files of evolution T-ALL adults project

WGS BAMs of 19 adult patients with T-acute lymphoblastic leukemia with primary, remission and relapse sample per patient. Total = 58 samples sequenced with HiSeq 4000 or NovaSeq 6000 (Illumina).

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Policy for accessing the raw data associated to the project "The evolution of adult T-cell acute lymphoblastic leukemia"

DATA ACCESS AGREEMENT Between Fundació Institut de Recerca Biomèdica (IRB BARCELONA), a non-fo-profit Spanish research institution with VAT number ES-G63971451 and registered offices at Baldiri Reixac 10, 08028 Barcelona, SPAIN, and [USER INSTITUTION] Agree as follows: These terms and conditions govern access to the managed access datasets (details of which are set out in Appendix I) 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 Fundació Institut de Recerca Biomèdica (IRB BARCELONA) 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: Fundació Institut de Recerca Biomèdica (IRB BARCELONA) 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. Fundació Institut de Recerca Biomèdica (IRB BARCELONA): Your Institution details here 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 Fundació Institut de Recerca Biomèdica (IRB BARCELONA) within 30 days of any changes or departures of Authorised Personnel. 13. The User Institution will notify Fundació Institut de Recerca Biomèdica (IRB BARCELONA) prior to any significant changes to the protocol for the Project. 14. The User Institution will notify Fundació Institut de Recerca Biomèdica (IRB BARCELONA) as soon as it becomes aware of a breach of the terms or conditions of this agreement. 15. Fundació Institut de Recerca Biomèdica (IRB BARCELONA) 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 Fundació Institut de Recerca Biomèdica (IRB BARCELONA). 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 comply 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 and shall be subject to the exclusive jurisdiction of the courts of Barcelona, SPAIN. APPENDIX III – PUBLICATION POLICY Fundació Institut de Recerca Biomèdica (IRB BARCELONA) intend to publish the results of their analysis of this dataset and do not consider its deposition into public databases to be the equivalent of such publications. Fundació Institut de Recerca Biomèdica (IRB BARCELONA) anticipate that the dataset could be useful to other qualified researchers for a variety of purposes. However, some areas of work are subject to a publication moratorium. The publication moratorium covers any publications (including oral communications) that describe the use of the dataset. For research papers, submission for publication should not occur until XX months after these data were first made available on the relevant hosting database, unless Fundació Institut de Recerca Biomèdica (IRB BARCELONA) has provided written consent to earlier submission. In any publications based on these data, please describe how the data can be accessed, including the name of the hosting database (e.g., The European Genome-phenome Archive at the European Bioinformatics Institute) and its accession numbers (e.g., EGAS00000000029), and acknowledge its use in a form agreed by the User Institution with Fundació Institut de Recerca Biomèdica (IRB BARCELONA).

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
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
EGAF00004724359 bam 454.1 GB
EGAF00004724360 bam 144.3 GB
EGAF00004724361 bam 397.1 GB
EGAF00004724362 bam 346.5 GB
EGAF00004724363 bam 141.8 GB
EGAF00004724364 bam 410.3 GB
EGAF00004724365 bam 440.3 GB
EGAF00004724366 bam 141.3 GB
EGAF00004724367 bam 363.6 GB
EGAF00004724368 bam 491.3 GB
EGAF00004724369 bam 167.9 GB
EGAF00004724370 bam 182.8 GB
EGAF00004724371 bam 371.5 GB
EGAF00004724372 bam 140.3 GB
EGAF00004724373 bam 375.3 GB
EGAF00004724374 bam 459.6 GB
EGAF00004724375 bam 188.6 GB
EGAF00004724376 bam 432.3 GB
EGAF00004724377 bam 392.1 GB
EGAF00004724378 bam 148.8 GB
EGAF00004724379 bam 506.8 GB
EGAF00004724380 bam 482.0 GB
EGAF00004724381 bam 162.4 GB
EGAF00004724382 bam 495.3 GB
EGAF00004724383 bam 476.4 GB
EGAF00004724384 bam 154.6 GB
EGAF00004724385 bam 259.1 GB
EGAF00004724386 bam 491.3 GB
EGAF00004724387 bam 184.9 GB
EGAF00004724388 bam 487.8 GB
EGAF00004724389 bam 432.5 GB
EGAF00004724390 bam 174.2 GB
EGAF00004724391 bam 348.5 GB
EGAF00004724392 bam 174.1 GB
EGAF00004724393 bam 58.7 GB
EGAF00004724394 bam 175.8 GB
EGAF00004724395 bam 148.9 GB
EGAF00004724396 bam 56.3 GB
EGAF00004724397 bam 146.0 GB
EGAF00004724398 bam 189.5 GB
EGAF00004724399 bam 57.1 GB
EGAF00004724400 bam 153.3 GB
EGAF00004724401 bam 144.8 GB
EGAF00004724402 bam 55.7 GB
EGAF00004724403 bam 158.9 GB
EGAF00004724404 bam 395.8 GB
EGAF00004824569 bam 403.4 GB
EGAF00004824572 bam 423.0 GB
EGAF00004824573 bam 402.3 GB
EGAF00004824574 bam 357.5 GB
EGAF00004824575 bam 418.0 GB
EGAF00004824578 bam 138.6 GB
EGAF00004824579 bam 147.1 GB
EGAF00004824580 bam 141.7 GB
EGAF00004824581 bam 395.8 GB
EGAF00004824582 bam 405.0 GB
EGAF00004833936 bam 500.8 GB
57 Files (16.5 TB)