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DNA Sequencing: How to Choose the Right Technology

Introduction It has been over 30 years since the first generation of DNA sequencing technology was developed in 1977. Since […]

A Spotlight On: Science Communication – Jonathan Roberts

Jonathan Roberts is a Registered Genetic Counsellor at Addenbrooke’s Hospital in Cambridge and a Researcher at the Society and Ethics […]

World of Genomics: Canada

For the latest in the World of Genomics series, we head over to the Great White North and home of […]

Long-read sequencing vs short-read sequencing

Different sequencing platforms use a variety of read lengths. Both short-read sequencing and long-read sequencing have their own benefits and […]

Working to improve pipeline efficiency using genomics

Although the Food and Drug Administration approved a record number of novel therapeutics in 2020, only one drug out of […]

How Finnish genetics have shifted

A new analysis by researchers at the University of Finland has detailed how Finnish genetics have changed throughout the 20th […]

Induced pluripotent stem cells map variants of disease

Scientists have compiled data from induced pluripotent stem cells to link genetic variants to many different diseases. Linking variants Researchers […]

64 assembled haplotypes

Researchers have assembled 64 haplotypes from 32 diverse human genomes in order to serve as a new reference for genetic […]

“The Silent Liver Disease”: How one company is helping biopharma tackle this growing epidemic

The growing epidemic of “The Silent Liver Disease” Non-alcoholic fatty liver disease (NAFLD) is experiencing a meteoric rise globally. NAFLD […]

On the horizon: In situ sequencing

Advancements in technologies, including single cell and spatial transcriptomics, have provided us with a finer view of our complex biology […]