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Methods to study cell-cell communication from single-cell sequencing data

This feature on cell-cell communication is adapted from part of Chapter 4 of the upcoming Spatial and Single-cell Playbook, due […]

New method improves next-generation sequencing accuracy 1000-fold

A new method has been published in Nature Genetics that offers a 1000-fold increase in accuracy compared to next-generation sequencing […]

The Sequencing Buyer’s Guide: 5th Edition

In recent years, next-generation sequencing (NGS) has evolved from a technology used purely in research settings to being a key […]

Sequencing options for cancer genomics

We’ve come a long way since the dawn of Sanger sequencing in 1977. The rapid development of next-generation sequencing (NGS) […]

Comprehensive sequencing of the small intestine reveals “collateral damage” by APOBEC1 enzyme may lead to cancer

Researchers at the Wellcome Sanger Institute have found that the enzyme APOBEC1 may cause the mutations SBS2 and SBS13 – […]

RNA-sequencing of amniotic fluid cells for prenatal diagnosis of rare disorders

A team of researchers from Hong Kong have developed a proof-of-concept RNA-sequencing approach to analyse amniotic fluid to diagnose rare […]

Insights Into The Danish National Genome Center

Bettina Lundgren, CEO of the Danish National Genome Center, joins us to discuss the incredible work being undertaken in Denmark […]

A Spotlight On: Genomics in Qatar – Said Ismail, Director of Qatar Genome

Said Ismail is the Director of Qatar Genome, a national programme trying to spearhead Qatar’s vision to become a pioneer […]

Californian biotech company claims $100 genome

California-based Ultima Genomics emerged from stealth mode on 31st May to announce a new high-throughput, low-cost sequencing platform that it […]

Exome sequencing in bipolar disorder identifies new risk gene

A study published in Nature Genetics from a consortium of researchers — the BipEx collaboration — is the largest whole-exome […]