Data Use Certification AgreementUse Certification Agreement • January 16th, 2024
datasets maintained in NIH-designated data repositories under the NIH Genomic Data Sharing Policy (e.g., the NIH database of Genotypes and Phenotypes (dbGaP)). The Addendum to this Agreement outlines additional terms and information which are specific to each requested dataset such as:
Data Use Certification AgreementUse Certification Agreement • March 27th, 2024
The National Institutes of Health (NIH) has established NIH-designated data repositories (e.g., database of Genotypes and Phenotypes (dbGaP), Sequence Read Archive (SRA), NIH Established Trusted Partnerships) for securely storing and sharing controlled-access human data submitted to NIH under the NIH Genomic Data Sharing (GDS) Policy. Because the volume of human genomic and phenotypic data contained in these repositories is substantial and, in some instances, potentially sensitive (e.g., data related to the presence or risk of developing particular diseases or conditions and information regarding family relationships or ancestry), data must be shared in a manner consistent with the research participants’ informed consent, and the confidentiality of the data and the privacy of participants must be protected.
Model Data Use Certification Agreement Pediatric Cardiac Genomics Consortium (PCGC) (April 21, 2010, version)Use Certification Agreement • March 7th, 2022
The National Institutes of Health (NIH) has developed central data repositories to archive and distribute the results of studies provided by Contributing Investigators examining the relationship between genomic data (e.g., genotype, sequence, or epigenetic information) and phenotype. Such studies include genome-wide association studies, medical sequencing, and molecular diagnostic assays. Implicit in the establishment of the NIH data repositories, for example the database of Genotypes and Phenotypes (dbGaP), is the view that scientific progress in this area will be greatly enhanced if the data produced by these studies are readily available to all investigators in the research community.
Model Data Use Certification AgreementUse Certification Agreement • December 25th, 2023
The National Institutes of Health (NIH) has established NIH-designated data repositories (e.g., database of Genotypes and Phenotypes (dbGaP), Sequence Read Archive (SRA), NIH Established Trusted Partnerships) for securely storing and sharing controlled-access human data submitted to NIH under the NIH Genomic Data Sharing (GDS) Policy. Because the volume of human genomic and phenotypic data contained in these repositories is substantial and, in some instances, potentially sensitive (e.g., data related to the presence or risk of developing particular diseases or conditions and information regarding family relationships or ancestry), data must be shared in a manner consistent with the research participants’ informed consent, and the confidentiality of the data and the privacy of participants must be protected.
Data Use Certification AgreementUse Certification Agreement • September 26th, 2022
The Genetic Association Information Network (GAIN) is a public-private partnership formed with the goal of identifying genetic variants that contribute to diseases of major public health importance by catalyzing genome-wide association analyses on samples from existing studies that include large numbers of affected and unaffected individuals. GAIN is founded on the principle that scientific progress will be most efficient and innovative if data are readily available to all investigators in the research community. Contributing Investigators who provide phenotype data and DNA samples from participants to a GAIN Project have committed to this principle and their professional investments and intellectual contributions will be fundamental to the ultimate success of GAIN.
Data Use Certification AgreementUse Certification Agreement • May 12th, 2024
The National Institutes of Health (NIH) has established NIH-designated data repositories (e.g., database of Genotypes and Phenotypes (dbGaP), Sequence Read Archive (SRA), NIH Established Trusted Partnerships) for securely storing and sharing controlled-access human data submitted to NIH under the NIH Genomic Data Sharing (GDS) Policy. Because the volume of human genomic and phenotypic data contained in these repositories is substantial and, in some instances, potentially sensitive (e.g., data related to the presence or risk of developing particular diseases or conditions and information regarding family relationships or ancestry), data must be shared in a manner consistent with the research participants’ informed consent, and the confidentiality of the data and the privacy of participants must be protected.
FaceBase Data Use Certification AgreementUse Certification Agreement • March 15th, 2022
FaceBase is a central repository for data generated by the FaceBase Consortium as well as data offered for inclusion by other investigators working on similar projects. Both the FaceBase database and the Consortium are funded by the National Institute of Dental and Craniofacial Research (NIDCR) of the National Institutes of Health (NIH). Implicit in the establishment of the FaceBase data repository is the idea that scientific progress in understanding craniofacial development and disorders of that process will be greatly
Data Use Certification AgreementUse Certification Agreement • August 21st, 2014
Implicit in the establishment of these data management systems is that scientific progress in genomic research will be greatly enhanced if the data are readily available to all scientific investigators and shared in a manner consistent with the human subjects protocols under which participant’s data and samples were donated to TCGA.
Data Use Certification AgreementUse Certification Agreement • January 28th, 2022
The National Institutes of Health (NIH) has developed central data repositories to archive and distribute the results of studies provided by Contributing Investigators examining the relationship between genomic data (e.g., genotype, sequence, or epigenetic information) and phenotype.
Data Use Certification AgreementUse Certification Agreement • August 5th, 2020
The National Institutes of Health (NIH) has developed central data repositories to archive and distribute the results of studies provided by Contributing Investigators examining the relationship between genomic data (e.g., genotype, sequence, or epigenetic information) and phenotype. Such studies include genome-wide association studies, medical sequencing, and molecular diagnostic assays. Implicit in the establishment of the NIH data repositories, for example the database of Genotypes and Phenotypes (dbGaP), is the view that scientific progress in this area will be greatly enhanced if the data produced by these studies are readily available to all investigators in the research community.
Data Use Certification AgreementUse Certification Agreement • April 7th, 2022
This Data Use Certification Agreement outlines the terms of use for requested controlled-access datasets maintained in NIH-designated data repositories under the NIH Genomic Data Sharing Policy (e.g., the NIH database of Genotypes and Phenotypes (dbGaP)). The Addendum to this Agreement outlines additional terms and information which are specific to each requested dataset such as:
Data Use Certification AgreementUse Certification Agreement • September 26th, 2022
This Data Use Certification Agreement outlines the terms of use for requested controlled-access datasets maintained in NIH-designated data repositories under the NIH Genomic Data Sharing Policy (e.g., the NIH database of Genotypes and Phenotypes (dbGaP)). The Addendum to this Agreement outlines additional terms and information which are specific to each requested dataset such as:
Data Use Certification AgreementUse Certification Agreement • November 22nd, 2013
The National Institutes of Health (NIH) has developed central data repositories to archive and distribute the results of studies provided by Contributing Investigators examining the relationship between genomic data (e.g., genotype, sequence, or epigenetic information) and phenotype. Such studies include genome-wide association studies, medical sequencing, and molecular diagnostic assays. Implicit in the establishment of the NIH data repositories, for example the database of Genotypes and Phenotypes (dbGaP), is the view that scientific progress in this area will be greatly enhanced if the data produced by these studies are readily available to all investigators in the research community.
Data Use Certification AgreementUse Certification Agreement • September 26th, 2022
This Data Use Certification Agreement outlines the terms of use for requested controlled-access datasets maintained in NIH-designated data repositories under the NIH Genomic Data Sharing Policy (e.g., the NIH database of Genotypes and Phenotypes (dbGaP)). The Addendum to this Agreement outlines additional terms and information which are specific to each requested dataset such as:
