The goal of the “Research Catalyst Network: Expediting collaboration between basic and clinician scientists in functional studies of novel rare disease genes” is to establish a national consortium that will enable clinical geneticists who are identifying rare disease gene mutations to collaborate with model organism researchers with expertise in the cognate gene’s function.
Canada’s federal research granting agencies—the Social Sciences and Humanities Research Council (SSHRC), the Natural Sciences and Engineering Research Council (NSERC), the Canadian Institutes of Health Research (CIHR), as well as the Canada Foundation for Innovation (CFI), and in collaboration with Genome Canada—have joined forces to help address digital infrastructure challenges through the consultation document
Hundreds of researchers from North America, Europe, Australia and Asia have joined together in a consortium to identify the genetic basis of the five most common forms of cancer – breast, prostate, lung, ovarian and colorectal. The group, called the OncoArray Consortium, developed a new customized genotyping tool – the OncoArray – manufactured by the U.S. genomics firm Illumina, Inc.
The Ontario Genomics Institute (OGI) today announced the launch of Scintelligence, a new industry-focused division to help companies in a variety of sectors capitalize on research and innovation in the life sciences. This division will engage the private sector to identify challenges and business needs, and facilitate collaborations between partners in industry, academia and government.
In 1988, Walter Hiebert was given what amounted to a death sentence: he was diagnosed with HIV and given just six months to live. “I didn’t have any hope at all,” says 56 year-old Hiebert, who had to go on disability from his job as a registered nurse.
Since the sequence map of the human genome, the cost of sequencing the genome of an individual has fallen rapidly. This has resulted in a tremendous increase in the amount of human genomic data available to the international research community for the advancement of biomedical research. Yet, there is an absence of international mechanisms to support researchers in ensuring ethical and legal interoperability.