Providers grant you a non-exclusive, non-transferable, non-sublicensable, limited right, to: (1) access and use the Site for internal non-commercial research purposes only, (2) download sequence data and related information through the Site, and (3) use such data and related information for internal non-commercial research purposes only.
You agree to use the Site in compliance with all applicable laws and regulations, including but not limited to any applicable state health information confidentiality laws.
You acknowledge that this agreement does not give you the right to use the Site to provide genetic counseling, healthcare, or other clinical services to a third party or for any commercial purposes. If you use the Site for any purpose other than internal, non-commercial research use (“Unauthorized Use”), then, in addition to any other rights and remedies available to Providers at law or in equity, you shall provide each Provider with all data, information and/or inventions generated or arising from such Unauthorized Use (“Unauthorized Data and Inventions”). You agree that Providers shall own all rights, title, and interest in and to Unauthorized Data and Inventions. Accordingly, you agree to assign and hereby do assign to Providers all right, title and interest in and to any and all of your right, title and interests in and to Unauthorized Data and Inventions without any compensation, and all patents or patent applications claiming or covering any Unauthorized Data and Inventions. If such assignment is not legally possible, you hereby grant to Providers a royalty-free, fully paid-up, perpetual, worldwide license, with the right to sublicense, to Unauthorized Data and Inventions. You agree to execute any and all forms of assignments and other instruments or documents, and to take such further actions as either Provider may reasonably request, in order to execute the assignment or license, for Unauthorized Data and Inventions. For clarity, Providers shall have the sole right to prepare, file and prosecute patents and patent applications claiming or covering Unauthorized Data and Inventions.
You acknowledge that the Site contains de-identified genomic and other data originating from (or derived from materials originating from) individual subjects (“Subjects”). You shall not attempt in any manner, directly or indirectly, to identify the Subjects (or their family members), or to enable any third party to do so, and shall not contact any Subject (or any such family member) if identified for any reason. You shall notify both Providers immediately if it identifies a Subject (or its family member). You will not, and will not permit any third party to: (1) translate, modify, adapt, enhance, decompile, disassemble or reverse engineer the Site or otherwise determine or attempt to determine source code or protocols from the executable code of the Site or create any derivative works based upon the Site; or (2) extract ideas, algorithms, procedures, workflows or hierarchies from the Site or otherwise use the Site or Data for the purpose of creating another product or service. You will use commercially reasonable efforts to prevent unauthorized access to, or use of, the Site or Data.
USE OF THE PENN MEDICINE BIOBANK ALLELE FREQUENCY BROWSER WEBSITE IS ENTIRELY AT YOUR OWN RISK, AND YOU ASSUME FULL RESPONSIBILITY FOR ALL ASSOCIATED RISKS. ALL DATA PROVIDED WITHIN THIS WEBSITE IS PROVIDED "AS IS". PROVIDERS MAKE NO REPRESENTATIONS AND EXTEND NO WARRANTIES OF ANY KIND, EITHER EXPRESSED OR IMPLIED. THERE ARE NO EXPRESS OR IMPLIED WARRANTIES OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE, FREEDOM FROM COMPUTER VIRUSES OR ERRORS, OR THAT THE USE OF THE SITE OR DATA WILL NOT INFRINGE ANY PATENT, COPYRIGHT, TRADEMARK, OR OTHER PROPRIETARY RIGHTS. IN NO EVENT SHALL PROVIDERS OR THEIR INDEMNITEES BE LIABLE TO YOU FOR ANY SPECIAL, CONSEQUENTIAL, EXEMPLARY, OR INCIDENTAL DAMAGES (INCLUDING LOST OR ANTICIPATED REVENUES OR PROFITS RELATING TO THE SAME), ARISING FROM OR RELATING TO YOUR USE OF THIS SITE. THE SITE IS PROVIDED FOR RESEARCH PURPOSES ONLY AND THE DATA AND INFORMATION CONTAINED IN THE SITE HAS NOT BEEN GENERATED IN A LABORATORY QUALIFIED UNDER THE CLINICAL LABORATORY IMPROVEMENT AMENDMENTS PROMULGATED BY THE CENTERS FOR MEDICARE & MEDICAID SERVICES. YOU ARE SOLELY RESPONSIBLE FOR (AND WE ASSUME NO RESPONSIBILITY AND WILL HAVE NO LIABILITY OF ANY KIND FOR) THE DECISIONS MADE BASED ON USE OF THIS SITE OR DATA, OR ANY EFFECTS THAT MAY RESULT FROM SUCH USE.
The disclaimers, indemnification provisions, and provisions regarding limitation of liability set forth above are for the benefit of the Providers. Each Provider shall have the right to assert and enforce those provisions directly against you on its own behalf.
We request that Penn Medicine and Regeneron Genetics Center be acknowledged as follows for publications:
“The authors would like to thank the Penn Medicine Biobank and Regeneron Genetics Center for providing genetic variant data for comparison. Great thanks also goes to the patient-participants of Penn Medicine who consented to participate in this research program."
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