PET PET
  • My Account
  • Subscribe
Become a Friend Donate
  • About Us
    • People
    • Press Office
    • Our History
  • Get Involved
    • Become a Friend of PET
    • Volunteer
    • Campaigns
    • Writing Scheme
    • Partnership and Sponsorship
    • Advertise with Us
  • Donate
    • Become a Friend of PET
  • BioNews
    • News
    • Comment
    • Reviews
    • Elsewhere
    • Topics
    • Glossary
    • Newsletters
  • Events
    • Upcoming Events
    • Previous Events
  • Engagement
    • Policy and Projects
      • Resources
    • Education
  • Jobs & Opportunities
  • Contact Us
  • About Us
    • People
    • Press Office
    • Our History
  • Get Involved
    • Become a Friend of PET
    • Volunteer
    • Campaigns
    • Writing Scheme
    • Partnership and Sponsorship
    • Advertise with Us
  • Donate
    • Become a Friend of PET
  • BioNews
    • News
    • Comment
    • Reviews
    • Elsewhere
    • Topics
    • Glossary
    • Newsletters
  • Events
    • Upcoming Events
    • Previous Events
  • Engagement
    • Policy and Projects
      • Resources
    • Education
  • Jobs & Opportunities
  • Contact Us
  • My Account
  • Subscribe
  • Privacy Statement
  • Advertising Policy
  • Thanks and Acknowledgements
PETBioNewsNewsResearch bodies remove personal genetic data from web

BioNews

Research bodies remove personal genetic data from web

Published 9 June 2009 posted in News and appears in BioNews 474

Author

Alison Cranage

Image by Peter Artymiuk via the Wellcome Collection. Depicts the shadow of a DNA double helix, on a background that shows the fluorescent banding of the output from a DNA sequencing machine.
CC BY 4.0
Image by Peter Artymiuk via the Wellcome Collection. Depicts the shadow of a DNA double helix, on a background that shows the fluorescent banding of the sequencing output from an automated DNA sequencing machine.

Scientists in the US have developed a new way of identifying an individual's DNA from a mixed sample. An individual can be picked out in a sample that contains up to 1000 people's DNA and where it makes up just 0.1 per cent of the total. The...

Scientists in the US have developed a new way of identifying an individual's DNA from a mixed sample. An individual can be picked out in a sample that contains up to 1000 people's DNA and where it makes up just 0.1 per cent of the total. The new method will assist forensic scientists, but has also raised concerns over the privacy of volunteers who have previously taken part in other genetic studies.


The research was led by Dr David W Craig, from the Translational Genomics Research Institute in Phoenix, Arizona, and was published in the August issue of the journal PloS Genetics. The team developed a statisitical method to identify an individual's DNA in a mixed sample by analysing up to 50,000 genetic variations, called SNPs (single nucleotide polymorphism). 'This is a potentially revolutionary advance in the field of forensics,' said Dr Craig. At present, it is difficult for forensic investigators to detect an individual's DNA if it is less than 10 per cent of a mixture, or if many other people's DNA is present.


SNPs are commonly used in genome-wide association studies, to identify genes that play a role in a particular disease. Summary statistics from such studies were published on the Internet, and list thousands of SNPs from groups of patients. There are concerns that with this new statistical method, and an individual's SNP profile, it may be possible to find out if that person took part in a study (i.e. they are among the summary statistics), and if they were in the group diagnosed as having the disease.


As a precautionary measure, the National Institutes of Health (NIH), the Broad Institute in Cambridge, Massachusetts (both in the US), and the Wellcome Trust in the UK have removed summary statistics from genome-wide association studies from the web. There is a strong demand for summary statistics from genome-wide association studies as they are a useful way for scientists to quickly find out if a genetic association they find has been borne out in other studies. Researchers will now have to apply directly to the NIH and adhere to strict confidentiality rules to see the data.


Some argue that the threat to the privacy of research volunteers would have been small, as no information about individuals could be discovered unless someone already had access to their SNP profile. Several researchers have criticised the move, saying that it could impede science, and hold back the sharing of information that facilitates many discoveries. Others disagree, arguing that it is vital to ensure absolute anonymity of study participants and the withdrawal of data from the public domain will not be restrictive.

Related Articles

Image by Peter Artymiuk via the Wellcome Collection. Depicts the shadow of a DNA double helix, on a background that shows the fluorescent banding of the output from a DNA sequencing machine.
CC BY 4.0
Image by Peter Artymiuk via the Wellcome Collection. Depicts the shadow of a DNA double helix, on a background that shows the fluorescent banding of the sequencing output from an automated DNA sequencing machine.
Comment
18 June 2009 • 3 minutes read

From principles to practice: implementing genetic database governance

by Sue Gibbons

Biobanking is flourishing. Techniques and technologies are evolving rapidly. Demand for harmonised standards, especially to facilitate cross-border data and biosample sharing and database interoperability, is mounting. Within this changing environment, the need to develop appropriate, legitimate and effective human genetic database governance frameworks - at national, regional and international levels - is...

Leave a Reply Cancel reply

You must be logged in to post a comment.

« Heated car seats may reduce male fertility

Data-Label The UK's Leading Supplier Of Medical Labels & Asset Labels

RetiringDentist.co.uk The UK's Leading M&A Company.
easyfundraising
amazon

This month in BioNews

  • Popular
  • Recent
13 June 2022 • 2 minutes read

Drop in diversity of blood stem cells leads to old-age health issues

27 June 2022 • 2 minutes read

UK report reveals public attitudes to fertility, genomics and embryo research

27 June 2022 • 2 minutes read

Shortage of sperm donors despite men willing to donate

27 June 2022 • 2 minutes read

North East London CCG proposes offering three funded IVF cycles

27 June 2022 • 2 minutes read

Fibrosis drugs reverse ovarian ageing in mice

27 June 2022 • 2 minutes read

Gene implicated in motor neurone diseases discovered

Subscribe to BioNews and other PET updates for free.

Subscribe
  • Twitter
  • Facebook
  • Instagram
  • LinkedIn
  • YouTube
  • RSS
Wellcome
Website redevelopment supported by Wellcome.

Website by Impact Media Impact Media

  • Privacy Statement
  • Advertising Policy
  • Thanks and Acknowledgements

© 1992 - 2022 Progress Educational Trust. All rights reserved.

Limited company registered in England and Wales no 07405980 • Registered charity no 1139856

Subscribe to BioNews and other PET updates for free.

Subscribe
PET PET

PET is an independent charity that improves choices for people affected by infertility and genetic conditions.

  • Twitter
  • Facebook
  • Instagram
  • LinkedIn
  • YouTube
  • RSS
Wellcome
Website redevelopment supported by Wellcome.

Navigation

  • About Us
  • Get Involved
  • Donate
  • BioNews
  • Events
  • Engagement
  • Jobs & Opportunities
  • Contact Us

BioNews

  • News
  • Comment
  • Reviews
  • Elsewhere
  • Topics
  • Glossary
  • Newsletters

Other

  • My Account
  • Subscribe

Website by Impact Media Impact Media

  • Privacy Statement
  • Advertising Policy
  • Thanks and Acknowledgements

© 1992 - 2022 Progress Educational Trust. All rights reserved.

Limited company registered in England and Wales no 07405980 • Registered charity no 1139856