Nanopore-based methods took over 25 years to fully materialise, which involved the collaboration of both academia and industry. It is […]
A recent study, published in Clinical Chemistry, has presented a rapid nanopore genotyping strategy to enable amplification-free identification and classification […]
In the latest episode of Genetics Unzipped, presenter Dr Kat Arney takes a look at how we learned to read […]
Illumina’s systems employ short-read sequencing techniques, which has been the predominant NGS technology for the last decade. The company has […]
Second- and third-generation NGS platforms are separated by their need for DNA amplification prior to sequencing. Second-generation sequencing technologies are […]
Introduction It has been over 30 years since the first generation of DNA sequencing technology was developed in 1977. Since […]
Being a UK based company in the genomics field, we know the space here better than any other country (or […]
Numbers The 1000 Genomes Project: The 1,000 Genome Project (1KGP) launched in January 2008 with the aim of generating the […]
Different sequencing platforms use a variety of read lengths. Both short-read sequencing and long-read sequencing have their own benefits and […]
It has been over 30 years since the first generation of DNA sequencing technology was developed in 1977. Since then, […]
