Oxford Nanopore Technologies PLC has recently highlighted the promising advancement of a research team in Australia that has secured funding for a genomic project utilising Oxford Nanopore sequencing technology.
The renowned company, headquartered in Oxford, England, and specialising in the development and distribution of nanopore sequencing products, announced that the groundbreaking technology will be employed by Ira Deveson in a three-year project at the Garvan Institute of Medical Research.
Deveson, a distinguished researcher whose doctorate focused on genome or transcriptome research and bioinformatics, endeavours to establish a national sequencing programme aimed at simplifying the identification of the genetic causes of rare diseases.
Oxford Nanopore stated that the researchers involved in the project aspire to elevate future diagnostic rates by integrating long nanopore sequencing reads into the characterisation of rare genetic diseases.
The precise amount of the funding granted was not disclosed by the firm. However, Chief Executive Officer Gordon Sanghera expressed, “We are pleased for the team and extend our congratulations to the researchers on securing this vital funding. It is incredibly encouraging to witness substantial research efforts being directed towards rare genetic disorders. With nanopore sequencing data, the team will gain significantly more comprehensive insights.”
He added, “What you’re missing matters, so with Oxford Nanopore’s capability to sequence fragments of DNA of any length, we believe the team will be able to unravel significant blind spots. We eagerly anticipate their progress and discoveries.”
Despite the remarkable achievement, Oxford Nanopore shares experienced a slight decline of 1.2%, trading at 190.90 pence each in London on Thursday morning.
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This strategic development is a testament to the groundbreaking potential of Oxford Nanopore’s technology in advancing genomic research. The collaboration between the company and the Australian research group exemplifies the commitment to innovative solutions in addressing complex medical challenges, particularly in the field of rare genetic diseases. The impact of this partnership is expected to yield invaluable findings that could significantly enhance our understanding of these conditions, consequently paving the way for more effective diagnostic and therapeutic interventions.
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