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Multi-omics: Exploring Inside Cells

Introduction Multi-omics is an emerging field. ‘Omics’ refers to the comprehensive collection of a set of biological molecules. Essentially, the […]

Researchers have revealed novel ultra-rare risk genes for autism

Researchers have identified ultra-rare, likely gene-disruptive variants unique to autism families, revealing 28 novel candidate risk genes. The genetics of […]

How to do RNA sequencing

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

Sample Preparation for NGS – A Comprehensive Guide

Introduction Sample preparation is the process of getting DNA ready for Next Generation Sequencing (NGS). This requires a few steps… […]

scCOLOUR-seq: The new method that corrects errors in single-cell sequencing

Researchers have developed a new approach, called single-cell corrected long-read sequencing (scCOLOUR-seq), that is able to amend errors in long-read […]

Frontiers in Pediatric Genomic Medicine 2021

For a second year running, the annual ‘Frontiers in Pediatric Genomic Medicine’ conference has gone virtual – bringing together the […]

Rare VEXAS syndrome is more common than originally thought

Researchers at the University of Leeds have found that a rare disease first discovered in 2020 – VEXAS syndrome – […]

All Wales, All the way!

Megan Fealey, NovaSeq Implementation Lead, and Joseph Halstead, Bioinformatician, from All Wales Medical Genomics Service (AWMGS) joined us to discuss […]

Transposon expression impacts neuronal function

Research at the University of Oxford has revealed that transposon expression within the brain is not random and is in […]

Researchers identify five gene candidates linked to insomnia

A team of researchers from China have performed an integrative genomic analysis and identified five genes associated with insomnia. Insomnia […]