The shows a probably incomplete following list of presentations (posters, talks, abstracts) from group members. Usually, PDF versions of the slides or posters are linked from the details pages.
The understanding of the impact of individual inherited and somatic genome variants on phenotypes and diseases requires a thorough understanding of the occurrence of such variants amongst populations in general and carriers of the phenotypes and diseases in particular. This information can only be provided through the inclusion of data from a multitude of genome resources in variant evaluation efforts, including such from outside (international) jurisdictions. However, opening such resources carries the inherent risk of breaching privacy, particularly through re-identification of individuals or their relatives and potentially through the exposure of individual genome-related personal information including phenotypic and “performance” prediction and relative disease risk.
2020-12-07: more ...
2020-10-30: more ...
2020-09-30: more ...
2020-09-30: more ...
2020-09-02: more ...
2020-06-30: more ...
2020-04-20: more ...
2020-03-19: more ...
2020-02-06: more ...
2020-01-28: more ...
2019-11-08: more ...
2019-10-08: more ...
2019-09-10: more ...
2019-09-10: more ...
2019-09-03: more ...
2019-06-14: more ...
2019-01-25: more ...
2018-09-17: more ...
2018-09-08: more ...
Qingyao 2018-06-29: more ...
2018-06-06: more ...
2018-06-04: more ...
2018-06-04: more ...
2018-06-04: more ...
2018-06-04: more ...
2018-06-04: more ...
2018-02-15: more ...
2017-12-07: more ...
2017-12-01: more ...
2017-10-15: more ...
2017-09-19: more ...
2017-09-13: more ...
2017-08-29: more ...
2017-08-29: more ...
2017-02-21: more ...
2017-02-01: more ...
2017-01-26: more ...
2016-12-19: more ...
2016-12-02: more ...
2016-03-17: more ...
2001-10-20: more ...