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Multi-Omics ONLINE – January 2022 Webinar Series

Rapid advances in sequencing technologies have enabled the collection of vast quantities of omics data. The coupling of omics technologies on […]

Increasing the genetic diversity in studies of lipids

Researchers have conducted a multi-ancestry GWAS of lipid levels in around 1.65 million individuals, including 350,000 individuals of non-European descent. […]

Down the Rabbit Hole: The genetics of exceptional longevity – Tom Perls

Tom Perls is a Distinguished Professor of Medicine at Boston University School of Medicine and an Attending Physician in Geriatrics […]

UK Biobank whole-genome sequencing data made available

The UK Biobank has released whole-genome sequencing data on 200,000 participants and made it widely available on the platform – […]

Rare variants involved in eczema susceptibility

A recent meta-analysis has identified rare exonic variants that play a role in eczema susceptibility. Eczema Eczema is a chronic […]

New research finds ABI3 gene function in Alzheimer’s disease

Scientists have found that loss of ABI3 function, a protein-coding gene, may increase the risk of developing Alzheimer’s disease by […]

Generating a proteo-genomic map of human health

Researchers at Medical Research Council Epidemiology have carried out a genome-proteome-wide association study that targeted 4,775 distinct proteins, enabling them […]

Interpreting genetic variants in type 2 diabetes

Numerous genetic variants in the human genome have been linked to type 2 diabetes. However, as most of these variants […]

Exploring Alzheimer’s disease using single-cell/nucleus RNA sequencing data

Scientists have developed a network-based methodology that leverages single-cell/nucleus RNA sequencing data to uncover novel therapeutic targets for Alzheimer’s disease. […]

Cancer Genomics Projects: The Collection

The cancer genome has been sequenced for more than a decade. This has created an abundance of relevant information that […]