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Genome Giants: Stephen Scherer – Director, The Centre for Applied Genomics, SickKids

Stephen Scherer is a Canadian scientist who founded Canada’s first human genome centre, the Centre for Applied Genomics (TCAG) at […]

Genome Giants – Leroy Hood, Co-founder and Professor, Institute for Systems Biology

Leroy Hood is a pioneer of systems biology and Professor and Co-founder of the Institute for Systems Biology, Seattle. He […]

Genome Giants – Tak Mak, Senior Scientist, Princess Margaret Cancer Centre

Tak Mak is a world leader in the genetics of immunology and cancer. He is currently a Senior Scientist at […]

Genome Giants – Janina Jeff, Staff Bioinformatics Scientist, Illumina

Janina Jeff is an American geneticist and Staff Bioinformatics Scientist at Illumina. Jeff is particularly interested in identifying genetic variants […]

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 […]

A History of Sequencing

Nucleic acid sequencing has become an integral part of modern biomedical research. The advances in sequencing technology, from its invention […]

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 […]