Mobile Menu

Search Results

Search results for: Sequencing

64 assembled haplotypes

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

Researchers find 300 proteins that regulate cell division

Researchers from Sweden have published a new molecular mapping of proteins that regulate the cell division process – identifying 300 […]

Genomics week in brief: Week ending 27th February

Enjoy our latest round-up of the most recent genomics new and research. Top stories from the past week A new […]

Largest Middle East GWAS reveals clinically relevant variants

A recent GWAS analysis in the Middle Eastern Qatari population has identified genetic associations in 45 clinically relevant traits. GWAS […]

Filling the Gaps in the Human Genome

Completed 20 years ago this month, the Human Genome Project was a ground-breaking piece of research. However, it was far […]

A well camouflaged zebra

For my undergraduate research project, I studied a rare neurological disease known as Landau-Kleffner Syndrome. It was then that I […]

The Rarest of the Rare

In Europe, a rare disease is defined rare when it affects fewer than 1 in 2,000 people. However, this definition […]

Gene Editing Quality Control – From Humanised Mice to Engineered Human Cells

The ease of new gene editing technologies has opened opportunities to explore in more detail the genetic underpinnings of disease, […]

Genomics week in brief: Week ending 20th February

Another round-up of the latest genomics news and research from the past week – enjoy! Top stories from the past […]

WES uncovers mutations for rare paediatric diseases

Using whole-exome sequencing (WES), researchers have identified underlying variants in children with rare genetic paediatric diseases. Rare genetic paediatric diseases […]