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Single-cell RNA sequencing suggests new treatment options for diabetic kidney disease

A new study using a 1-million-cell atlas shows heterogeneity in kidney cell responses to diabetic kidney disease and treatments. Published […]

Single-cell RNA sequencing: How to optimize the workflow from tissue through analysis – Webinar

Today, researchers can analyze 10 000+ cells from one tissue sample or patient to understand individual cell populations and their […]

RNA sequencing detects fusion genes in childhood cancer

A new study, carried out by scientists from the Princess Máxima Centre, has shown that RNA sequencing can identify more […]

RNA sequencing can predict pregnancy health from single blood draw

Researchers from a global collaboration have identified patterns of gene expression associated with a healthy pregnancy using circulating RNA. Pregnancy […]

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. […]

How to do RNA sequencing

RNA sequencing is an NGS technique that enables investigation of the transcriptome – the total cellular content of RNAs, including […]

Biologically-validated AI is how scientists are realising the full potential of single-cell RNA sequencing

The promise of single-cell gene expression data Genomic data are an excellent source of novel disease biomarkers and targets. In […]

How to: Choose the best RNA sequencing method for quantitative miRNA profiling

This article has been based upon this blog post, written by Dr Karolina Szczesna. RNA sequencing (RNA-seq) uses next generation […]

FoG 2020 Presentation Michael Barnes, QMUL: RNA Sequencing and Machine Learning as Molecular Scalpels

Professor of Bioinformatics, Director, the Centre for Translational Bioinformatics, William Harvey Research Institute, Queen Mary University of London Co-Investigator, Health […]

Spatial and temporal RNA-sequencing

Sam Rodriques, Group Leader, Francis Crick Institute