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Is nanopore sequencing the future?

Nanopore-based methods took over 25 years to fully materialise, which involved the collaboration of both academia and industry. It is […]

Nanopore sequencing combined with liquid biopsy analysis

A recent study, published in Clinical Chemistry, has presented a rapid nanopore genotyping strategy to enable amplification-free identification and classification […]

Genetics Unzipped podcast: A brief history of DNA sequencing

In the latest episode of Genetics Unzipped, presenter Dr Kat Arney takes a look at how we learned to read […]

How did Illumina dominate the sequencing market?

Illumina’s systems employ short-read sequencing techniques, which has been the predominant NGS technology for the last decade. The company has […]

DNA amplification techniques

Second- and third-generation NGS platforms are separated by their need for DNA amplification prior to sequencing. Second-generation sequencing technologies are […]

DNA Sequencing: How to Choose the Right Technology

Introduction It has been over 30 years since the first generation of DNA sequencing technology was developed in 1977. Since […]

World of Genomics: The United Kingdom

Being a UK based company in the genomics field, we know the space here better than any other country (or […]

A, C, T to Glossary

Numbers The 1000 Genomes Project: The 1,000 Genome Project (1KGP) launched in January 2008 with the aim of generating the […]

Long-read sequencing vs short-read sequencing

Different sequencing platforms use a variety of read lengths. Both short-read sequencing and long-read sequencing have their own benefits and […]

The progress of NGS platforms

It has been over 30 years since the first generation of DNA sequencing technology was developed in 1977. Since then, […]