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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 […]

Genomics week in brief: Week ending 3rd July

Another month, another genomics week in brief, jam-packed with all of the latest news and research within the genomics space. […]

Twin studies have disentangled the common genes in post-traumatic stress disorder (PTSD) and migraine

A recent study of monozygotic twins revealed certain genes and pathways that overlap between post-traumatic stress disorder (PTSD) and migraine, […]

Human and mouse astrocytes have crucial differences

Researchers have discovered crucial physiological differences between human and mouse astrocytes, with implications for studies on neurological disorders. Mice are […]

HLA-DR4: The human antigen with subtypes that are strongly linked to type 1 diabetes

Researchers have identified three amino acid residues that are responsible for the variable association of HLA-DR4 subtypes with type 1 […]

What genes did humans inherit from Neanderthals?

Recently, researchers have developed a novel method that uses convolutional neural networks to detect adaptive introgression in the human genome. […]

Genomics week in brief: Week ending 19th June

Here, is a summary of all of the latest genomics news and research from the past week! Top stories from […]

Multi-Omics ONLINE – July Series

Sequencing technologies are continuously improving, making it easier to obtain more in-depth molecular information than ever before. As such, we […]

Understanding the role of genetic resistance in the UK ash tree population

This article was compiled from a recent webinar, delivered by Professor Richard Buggs and supported by Novogene, a genomic services […]

Genomics week in brief: Week ending 12th June

We have got you covered for another week with all of the latest genomics news and research in one place! […]