Roche and Garvan Institute of Medical Research partner to develop epigenomics technology

19 August 2014

Roche and the Garvan Institute of Medical Research in Australia are collaborating to develop new technologies to accurately analyze regions of the epigenome using DNA sequencing.

The collaboration brings together the world-leading genomics expertise and infrastructure at the Garvan Institute and the best-in-class products for target enrichment from Roche NimbleGen, part of the Roche Sequencing Unit.

As part of the agreement, the SeqCap Target Enrichment System from Roche will be used by scientists at the Garvan Institute to further their research in epigenetic influences on human diseases.

“This is an excellent example of collaboration between a leading edge company and research institute in the development of advanced technology for genetic analysis, which will empower more research into human biology and disease, and lead to many translational opportunities,” said Professor John Mattick, Executive Director of the Garvan Institute.

“In addition to our recent investments in sequencing platform technologies, our research team is working closely with key opinion leaders to advance sequencing applications of current and future technologies,” said Tom Albert, Head of Research at Roche’s Sequencing Unit. “This collaboration with the Garvan Institute illustrates the potential of SeqCap Target Enrichment products in additional sequencing applications for epigenetic research. This brings us closer to delivering sequencing applications to the clinic that offer truly differentiated medical value.”

Epigenetics is the heritable changes in gene expression that are not caused by changes in the DNA sequence or genetic code, but rather involve secondary chemical modifications of the DNA and the structural proteins in chromosomes. It is being recognized as playing an important role in a host of biological processes and their role in cancer has been increasingly investigated. Due to the myriad of epigenomic events responsible for influencing expression of genes in chromosomes, more advanced methods are being sought to accurately analyze these changes.

Source: Roche