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Unlocking the mystery of complex diseases

| | November 6, 2017
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This article or excerpt is included in the GLP’s daily curated selection of ideologically diverse news, opinion and analysis of biotechnology innovation.

In our effort to find the answers to some of the most afflicting conditions and diseases known to science, biologists are rapidly turning to mapping the human genome to help us solve some of the great questions, such as: why do some people get certain diseases while others don’t?

One such way [pharma company AbbVie and VP of discovery Jim] Sullivan are figuring that out is with the recent collaboration with Genomics Medicine Ireland (GMI), an Irish life sciences company leading large-scale, population-based genome research studies on the island of Ireland, examining the relationship between genetics, health and disease.

Founded in 2015, GMI earlier this year announced it was to partner with AbbVie and global contract genomics organisation WuXi NextCODE on a 15-year project to sequence 45,000 genomes from volunteer participants across Ireland, to seek new insights into the biological processes that underlie complex diseases.

In the first four to five years of this partnership, Sullivan hopes that quality data science will help it and the other two parties involved to better understand the genetic underpinnings and the genes that are driving many health conditions, and explore ways that could be helpful in clinical trials.

The GLP aggregated and excerpted this blog/article to reflect the diversity of news, opinion, and analysis. Read full, original post: Unlocking human genome’s secrets is the greatest data science challenge

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