Terms of Use
All data here are released openly and publicly for the benefit of the wider biomedical community. You can freely download and search the data, and we encourage the use and publication of results generated from these data. We note that this research has been conducted using the UK Biobank Resource (project IDs 26041 and 48511), and use of this data is bound by all terms of usage of the UK Biobank: more information can be found here. These data are summary statistics only. Whilst considerable effort has been taken to prevent the possibility of re-identification of participants, all users of these data agree to these terms of use and are bound by obligations agree to not attempt to re-identify participants. From the perspective of the genebass team, there are no additional restrictions or embargoes on the publication of results derived from this data.
These data are provided on an "AS-IS" basis, without warranty of any type, expressed or implied, including but not limited to any warranty as to their performance, merchantability, or fitness for any particular purpose; and without warranty as to the accuracy, completeness, currency or reliability of any content available through this website. Use of this website and the content available on this website is at investigators’ sole risk. Investigators are responsible for taking all necessary precautions to ensure that any content you may obtain from the website is free of viruses. This dataset has been subjected to quality control, but variant calling and statistical methods to associate variants and phenotypes is an imperfect and probabilistic process, so many errors no doubt remain. If you find any glaring errors, feel free to contact us. Users of the dataset certify that they are in compliance with all applicable local, state, and federal laws and/or regulations and institutional policies regarding use of this data (e.g., including regarding human subjects and genetics research).
The association results data produced by genebass are available under the Creative Commons Attribution 4.0 International (CC BY 4.0) license. We request that you acknowledge and give attribution to both the manuscript below and the UK Biobank, and link back to the relevant page, wherever possible.
Citation in publications
We request that any use of data obtained from genebass browser cite the following manuscript and any online resources that include the data set provide a link to the browser.
Karczewski, K. J., Solomonson, M., Chao, K. R., Goodrich, J. K., Tiao, G., Lu, W., Riley-Gillis, B. M., Tsai, E. A., Kim, H. I., Zheng, X., Rahimov, F., Esmaeeli, S., Jason Grundstad, A., Reppell, M., Waring, J., Jacob, H., Sexton, D., Bronson, P. G., Chen, X., Hu, X., Goldstein, J. I., King, D., Vittal, C., Poterba, T., Palmer, D. S., Churchhouse, C., Howrigan, D. P., Zhou, W., Watts, N. A., Nguyen, K., Nguyen, H., Mason, C., Farnham, C., Tolonen, C., Gauthier, L. D., Gupta, N., MacArthur, D. G., Rehm, H. L., Seed, C., Philippakis, A. A., Daly, M. J., Wade Davis, J., Runz, H., Miller, M. R. & Neale, B. M. Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes. Cell Genomics, (2022). https://doi.org/10.1016/j.xgen.2022.100168
There is no need to include us as authors on your manuscript, unless we contributed additional specific effort to your work.
The acknowledgement of UK Biobank should reference this research has been conducted using summary statistics generated from the UK Biobank resource (under application 26041 and 48511).