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Ethical and privacy issues in genetic databases

Research output: Chapter in Book/Report/Conference proceedingConference contributionpeer-review

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 languageEnglish
Title of host publicationProceedings of the 3rd Australian Institute of Computer Ethics Conference (AiCE2002)
EditorsMatthew Warren, John barlow
Place of PublicationAustralia
PublisherAustralian Institute on Computer Ethics
Pages39-50
ISBN (Print)0730025608
Publication statusPublished - 30 Sept 2002
EventAICE 2002: 3rd Australian Institute of Computer Ethics Conference (AiCE2002) - Sydney, Australia
Duration: 30 Sept 200230 Sept 2002

Conference

ConferenceAICE 2002: 3rd Australian Institute of Computer Ethics Conference (AiCE2002)
CitySydney, Australia
Period30/09/0230/09/02

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