Read about our novel technology in the Nature Biotechnology journal here
Our single-base-resolution sequencing methodology sequences complete genetics and the two most common cytosine modifications in a single workflow. This approach is accurate, requires low DNA input and has a low-barrier-to-entry as it works with existing sequencing instruments and our software deploys on existing computational set-ups. Simultaneous, phased reading of genetic and epigenetic bases provides a more complete picture of the information stored in genomes and has applications throughout biomedicine.
