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Genome Giants: Kay Davies – Human Geneticist and Professor of Genetics, University of Oxford

Dame Kay Davies is a human geneticist and Professor of Genetics at the University of Oxford. Davies has spent her […]

Genome Giants: Stephen F. Kingsmore – President and CEO of Rady Children’s Institute for Genomic Medicine

Stephen F. Kingsmore is the President and CEO of Rady Children’s Institute for Genomic Medicine, where they are pioneering the […]

Genome Giants: Heidi Rehm – Chief Genomics Officer, Mass General Hospital

Heidi Rehm is the Chief Genomics Officer in the Department of Medicine and at the Center for Genomic Medicine at […]

Genome Giants – Janet Thornton – Senior Scientist and Director Emeritus at EBI

Dame Janet Thornton is a Senior Scientist and Emeritus Director of EMBL-EBI. Thornton is a pioneer in structural bioinformatics, having […]

AI has been used to rapidly diagnose critically ill patients with rare genetic diseases

Recently, researchers used Fabric GEM, an artificial intelligence algorithm, to detect disease causing variants in newborns and rare disease patients […]

Effect of WGS on clinical management in acutely ill infants

Whole-genome sequencing (WGS) shows promise as a first-line genetic test for acutely ill infants. However, before wide-spread adoption and implementation, […]

A woolly mammoth, an elephant and a scientist walk into a bar…

My idea of the woolly mammoth is limited to the voice of Ray Romano and the unusual pairing with a […]

WGS – The future of consumer genomics

With the falling cost of genome sequencing, it comes as no surprise that there is a growing interest in expanding the availability and accessibility of genomics via consumer testing. Now, Nebula Genomics has entered the market by launching a comprehensive at-home test that analyses the whole genome for just $299.