In recent years, next-generation sequencing (NGS) has evolved from a technology used purely in research settings to being a key […]
We’ve come a long way since the dawn of Sanger sequencing in 1977. The rapid development of next-generation sequencing (NGS) […]
Researchers at the Wellcome Sanger Institute have found that the enzyme APOBEC1 may cause the mutations SBS2 and SBS13 – […]
Introduction The human body contains over 35 trillion cells, with tissues and organs comprising of many different cell types constantly […]
Single-cell RNA sequencing (scRNA-seq) has become the most established and widely used technique within single-cell analysis. Spatial transcriptomics is quickly […]
A team of researchers from Hong Kong have developed a proof-of-concept RNA-sequencing approach to analyse amniotic fluid to diagnose rare […]
In a recent paper, published in Nature Communications, a team of scientists used single nucleus RNA sequencing (snRNAseq) to investigate […]
A new study, published in Nature Biotechnology, presents Spatial PrOtein and Transcriptome Sequencing (SPOTS) for high throughput combined spatial transcriptomics […]
Genomics England have partnered with the NHS to implement the Newborn Genomes Programme. Whole genome sequencing (WGS) will be used […]
The sequencing landscape is changing more rapidly than ever before: The cost of sequencing is decreasing (welcome to the $100 […]
