Abstract
With the recent advances in genetic and computer technology, enormous databases containing genetic information have become available for research and other purposes. An example of such databases is the Icelandic Health Database containing health and genetic records about the total population of Iceland. This has raised many privacy and ethical questions, both among health professionals and the general public. Many agree that genetic information bears more ethical and privacy concerns than other health databases. In this paper we review the main privacy and ethical issues connected to genetic information and we pay special attention to disclosure of individual values through statistical analysis.
| Original language | English |
|---|---|
| Title of host publication | Proceedings of the 3rd Australian Institute of Computer Ethics Conference (AiCE2002) |
| Editors | Matthew Warren, John barlow |
| Place of Publication | Australia |
| Publisher | Australian Institute on Computer Ethics |
| Pages | 39-50 |
| ISBN (Print) | 0730025608 |
| Publication status | Published - 30 Sept 2002 |
| Event | AICE 2002: 3rd Australian Institute of Computer Ethics Conference (AiCE2002) - Sydney, Australia Duration: 30 Sept 2002 → 30 Sept 2002 |
Conference
| Conference | AICE 2002: 3rd Australian Institute of Computer Ethics Conference (AiCE2002) |
|---|---|
| City | Sydney, Australia |
| Period | 30/09/02 → 30/09/02 |
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