Sentences with phrase «whole genome sequencing where»

«Especially with what's called next generation sequencing or whole genome sequencing where it's not just one patent holder you have to deal with there is a real fear Canadian hospitals and researchers will be locked out of this domain and it could hurt us in terms of delivery of the service, health - care costs, and being locked out of innovation — those were the three important things at stake,» says Gold.
«People we've spoken with at Health Canada are delighted because they're grappling with whole exome / whole genome sequencing where you literally sequence a patient's genes and even one patent on one mutation could be enough to thwart the power of the test, so they've been happy with the result and looking at how it might affect them,» he says.

Not exact matches

«Studies like the current one involving rhabdomyosarcoma are giving us a close - up look at the way cancer evolves in response to treatment,» said study co-author Richard K. Wilson, Ph.D., director of The Genome Institute at Washington University School of Medicine in St. Louis, where scientists have extensive expertise analyzing tumor recurrence using whole - genome sequeGenome Institute at Washington University School of Medicine in St. Louis, where scientists have extensive expertise analyzing tumor recurrence using whole - genome sequegenome sequencing.
The research groups then examined the landscape of the pancreatic cancer epigenome using a combination of stains on patient tissues, direct examination of the proteins that wrap DNA and whole - genome sequencing of the detected epigenetic changes to map precisely where they were located.
RGC will provide these centers whole exome sequencing and genome - wide association (with phenotype, where applicable) data free - of - charge.
The Family - Based study includes whole genome sequencing (WGS) on multiplex families where DNA for at least two members per family was available and includes Caucasians and Caribbean Hispanic families.
We used whole - genome sequencing to analyse B. pseudomallei isolates collected from an historical 2 - year long case cluster that occurred in a remote northern Australian indigenous island community, where infections were previously linked to a contaminated communal water supply.
We aimed to demonstrate the possibility and advantages of transitioning to whole genome sequencing (WGS) for surveillance within existing networks across a continent where S. sonnei is endemic.
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