Genomics

Ireland launches MAGIC-I: First clinical study on genomics in childhood cancer

MAGIC-I, the country's first clinical study of genomics approaches in cancer care, is set to revolutionise childhood cancer care in Ireland.

Genomics and public health: A patent attorney’s perspective

Dr Craig Titmus, Partner and UK and European Patent Attorney at intellectual property firm, Mathys & Squire, turns the spotlight on genomics and public health from a patent attorney’s perspective.

Enabling a global learning health system through genomic standards

Peter Goodhand and Angela Page from Global Alliance for Genomics and Health, explain their thoughts on enabling a global learning health system through genomic standards.

Putting a spotlight on the dark metabolome

David S. Wishart discusses metabolomics, how the field is breaking into biochemical mysteries and the “dark metabolome”.

Bringing genomics into the clinic: Challenges and potential to improve healthcare

Ewan Birney, Director of EMBL’s European Bioinformatics Institute (EMBL-EBI), reveals how genomics could improve healthcare and pave the way to precision medicine.

Genetic testing: What’s wrong with my child?

Dr Katie Finch discusses with Professors Darren Griffin and Alan Thornhill her personal journey involving genetic testing of her son Brandon.

NASA research reveals what happens to human body in space

Results from NASA's landmark Twins Study reveals interesting, surprising and reassuring data about how one human body in space adapted to, then recovered from, that extreme environment.

A look below the surface of marine genomics

Nicolas Pade, Executive Director at EMBRC-ERIC (European Marine Biological Resource Centre) takes a glimpse below the surface of marine genomics, including a fascinating discussion about our oceans and their health.

National Genomic Healthcare Strategy: Improving services for rare disease sufferers

The government will today announce a new National Genomic Healthcare Strategy and measures to improve services for people with rare diseases.

Health research: Applying genome technologies to the study of disease

In this interview, Dr Carolyn M. Hutter, PhD, Director, Division of Genome Sciences at the National Human Genome Research Institute (NHGRI) outlines the important role of research when it comes to applying genome technologies to studying disease.

Harnessing the genetic diversity of a dynamic crop: Cowpea

Shawn Yarnes from The Integrated Breeding Platform highlights harnessing thegenetic diversity of a dynamic crop, cowpea and why it is important today.

Visualising the human genome like beads on a string

The human genome is composed of over 3 billion letters, here Dr Yuval Ebenstein, Principal Investigator, Tel Aviv University sheds light on it.

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