The Wellcome Trust Sanger Institute has sequenced the equivalent of 300 human genomes in just over six months, reaching a staggering 1,000,000,000,000 letters of genetic code that will be read by researchers worldwide and aiding in the quest to understand the role of genes in health and disease.
The amount of data is remarkable: every two minutes, the Institute produces as much sequence as was deposited in the first five years of the international DNA sequence databases, which started in 1982.
The Institute has major roles in projects such as The 1000 Genomes Project, The International Cancer Genome Consortium and the second round of the Wellcome Trust Case Control Consortium, all of which will depend on DNA sequence to uncover genetics variants that are important for human disease. Next-generation sequencing is also enabling the Institute's own research portfolio.