- Health Minister provided blood samples on Great Ormond Street for a genome sequencing program
- Genomics England’s diverse data initiatives aim to reduce medical disparities
Health Minister Sajid Javid visited Great Ormond Street Hospital today to provide blood samples from a genome sequencing program aimed at addressing health inequality.
Genomics England’s Diverse Data Initiative works with researchers and the NHS to ensure that life-changing work to sequence genomes benefits everyone, regardless of ethnic socio-economic or geographical background. It is working.
His data is analyzed by researchers to speed up the diagnosis of patients with cancer and rare diseases and develop new therapies as part of an ongoing effort to make health care more diverse and comprehensive. Helps to do.
Secretary of State Sajid Javid said:
“I am very proud to be able to participate in this study. This study will help everyone, regardless of background, benefit from the world’s leading genomics research program. ..
“A key initiative of Genomics England is to sequence the genomes of people who are underestimated in research data, develop better therapies, and enable the transformation of health care for everyone.”
To date, human genetics research is often based on European volunteers, which means that these communities may not be benefiting the genomic healthcare revolution. It also misdiagnoses the relationship between genes and diseases, the low “generalizability” of research results across different populations, and the safe and effective translation of genomic studies into clinical care for all. It contributes to a substantial barrier.
Genomics England works with the community to analyze data from an increasingly diversified population and help reduce health inequality by rapidly improving the representation of underrepresented groups in genetic datasets and studies. I am.
Chris Wigley, CEO of Genomics England, said:
“Genomics has the potential to transform healthcare. This technology provides new, faster diagnostics and enables the development of life-changing therapies for people with rare diseases, cancer and other conditions. ..
“But it needs to work for all of us, and people with non-European ancestry are underestimated in the study data, so this becomes mainstream in patient care and does not provide the same benefits. There are risks. Through a variety of data initiatives, we have made significant progress in addressing that issue. “
By participating in the initiative, the Minister of Health is now part of a community of research participants, whose data is safely and anonymously stored by Genomics England in the over 140,000 human genome.
His blood samples are mapped by the Sequence Lab at the Sanger Center near Cambridge and stored in the National Genome Research Library along with the 100,000 Genome Project and other participants in the GenOMICC COVID-19 study.
New office for health improvement and inequality (OHID)-Started October 1st-to improve public health by preventing illness and helping people of all ages and all parts of the country lead healthier lives. Lead nationwide efforts.
NS OHID An important part of the Ministry of Health, it promotes a government-wide preventive agenda to reduce health inequalities exacerbated by the COVID-19 pandemic.
Minister of Health has determined the genome sequence for a project to address health inequalities
SourceMinister of Health has determined the genome sequence for a project to address health inequalities