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Accelerated Combined Extraction & Sequencing Services: | Construction Tenders

Construction Companies, News, Jobs - The Construction Index is a building industry news and construction company directory

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Are We Ready for Systematic Newborn Genome Sequencing?

Routine sampling and analysis of newborn DNA would enable screening for hundreds of childhood genetic diseases, but also raises concerns about privacy and ethics.

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Richard Scott highlights the role AI plays in the work of Genomics England

Richard Scott, chief medical officer, acting CEO and soon to be the new interim CEO of Genomics England, has delved deep into the work the organisation does and how AI fits in ahead of speaking at the inaugural Digital Health AI and Data next week. Speaking to host Jordan Sollof on the Digital Health Unplugged podcast, Scott discussed his background and career to date and explained the work of Genomics England and the importance of AI before previewing his session at AI and Data on Monday 30 October. Scott is a trained doctor by background but confirmed that he was "really into genetics" and "did a project on genetics and my third year scientific bit was very much focused on genetics. "I didn't know that I'd end up so immersed in it (genetics/genomics), it was just one of those things that captured my imagination," he said. He eventually specialised in genomics and is now a clinical genetics consultant at Great Ormond Street. Whilst doing his PhD, "next generation sequencing, so the

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Oliver, one, was saved from unnecessary chemo by gene mapping technology

Oliver, one, (pictured) was just days old when his family were told he had cancer and would need chemotherapy.

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Genomics Are a Lifesaver for Patients With Rare Diseases

The 100,000 Genomes Project has a massive database to help doctors and patients solve baffling medical cases and diagnose cancers.

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Government-funded research to screen genomes of 100,000 babies for rare diseases

The Pharmaceutical Journal from the Royal Pharmaceutical Society

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Expert predicts genetic codes of babies could be read by the NHS in as little as five years

Rare diseases in children would be much easier to spot said Chief Scientific Officer of Genomics England who predicted in five years all parents could have their baby's genetic code read by the NHS.

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Genomics England receives government funding for cutting-edge genomics research

Genomics England receives government funding for cutting-edge genomics research
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New £105m scheme aims to speed up diagnosis of rare genetic diseases in newborns

‘We want to be able to offer speedy diagnosis, quicker access to treatment, and better outcomes and quality of life,’ Dr Rich Scott said.

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Babies will get blood tests to see if they have rare childhood cancers

Experts say it has the potential to help 3,000 children a year in England if rolled out, helping many young patients before symptoms appear.

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