Nanopore-based methods took over 25 years to fully materialise, which involved the collaboration of both academia and industry. It is […]
Illumina’s systems employ short-read sequencing techniques, which has been the predominant NGS technology for the last decade. The company has […]
Introduction It has been over 30 years since the first generation of DNA sequencing technology was developed in 1977. Since […]
ChIP-seq protocol Chromatin immunoprecipitation sequencing, also known as ChIP-seq, is a method used to analyze protein interactions with DNA. Chromatin […]
RNA sequencing is an NGS technique that enables investigation of the transcriptome – the total cellular content of RNAs, including […]
Different sequencing platforms use a variety of read lengths. Both short-read sequencing and long-read sequencing have their own benefits and […]
Since the discovery of the basic double-helix structure of DNA In the 1950’s, scientists have devoted a huge amount of […]
The adoption of single cell analysis approaches is accelerating, leading to rapid progress in our understanding of complex biological systems. […]
Researchers have developed a new approach, called single-cell corrected long-read sequencing (scCOLOUR-seq), that is able to amend errors in long-read […]
Researchers have demonstrated the potential of large-scale whole-exome sequencing in facilitating therapeutic target discovery to combat obesity. The recent upsurge […]
