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Personal Genomes: Mainstream In Five Years, But Who Should Have Access?

Date:
September 21, 2007
Source:
University of Alberta
Summary:
Imagine this: you visit your clinician, undergo genetic testing and then you are handed a miniature hard drive containing your personal genome sequence, which is subsequently uploaded onto publicly accessible databases. This may sound like science fiction, but it is scientific fact, and it is already happening. It may not be long before companies are able to offer Facebook-like social networking services centred around our genomes. In an article published in the journal Science, University of Alberta researcher Tim Caulfield and co-authors highlight the need to proceed cautiously when it comes to personal genomics.

Within five years, DNA sequencing technologies will be affordable enough that personal genomics will be integrated into routine clinical care, scientists predict.
Credit: iStockphoto

Imagine this: you visit your clinician, undergo genetic testing, and then you are handed a miniature hard drive containing your personal genome sequence, which is subsequently uploaded onto publicly accessible databases. This may sound like science fiction, but it is scientific fact, and it is already happening.

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In an article published in the upcoming issue of Science, University of Alberta researcher Tim Caulfield and co-authors highlight the need to proceed with caution when it comes to personal genomics projects that represent research milestones but are also fraught with ethical, social and clinical implications. Caulfield, who is the Canada Research Chair in Health Law at the U of A and professor and research director in public health sciences, is recognized as one of the foremost experts in health law research in Canada.

Scientists predict that within five years DNA sequencing technologies will be affordable enough that personal genomics will be integrated into routine clinical care. Companies are responding by offering their services for ancestry tracing, forensics, nutritional advice and reproductive assistance. It won't be long before companies are able to offer Facebook-like social networking services centred around our genomes.

Once we have our personal genomic information, what will we do with it and how might this information be used outside the medical context? How will physicians educate patients about the significance of genetic risk information? Will already-strained health-care systems be able to cope with the inevitable influx of "worried well" patients seeking follow-up investigations for genetic risks that are not clinically meaningful?

Caulfield and his colleagues pose these questions and warn that the routine generation of individual genome sequences will pose challenges to our health-care system.

They argue that only clinically meaningful genomic test results should be integrated into medical decision-making--however, this will require clear standards, multidisciplinary collaboration and careful consideration of the ethical, social and clinical implications.


Story Source:

The above story is based on materials provided by University of Alberta. Note: Materials may be edited for content and length.


Cite This Page:

University of Alberta. "Personal Genomes: Mainstream In Five Years, But Who Should Have Access?." ScienceDaily. ScienceDaily, 21 September 2007. <www.sciencedaily.com/releases/2007/09/070920145356.htm>.
University of Alberta. (2007, September 21). Personal Genomes: Mainstream In Five Years, But Who Should Have Access?. ScienceDaily. Retrieved March 28, 2015 from www.sciencedaily.com/releases/2007/09/070920145356.htm
University of Alberta. "Personal Genomes: Mainstream In Five Years, But Who Should Have Access?." ScienceDaily. www.sciencedaily.com/releases/2007/09/070920145356.htm (accessed March 28, 2015).

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