ⓖSEQ allows doctors and clinicians to spend less time on setting up experiments and more time
analyzing the results. Each run allows the simultaneous sequencing of up to 48 multiplexed
samples, prepared using a single-step protocol which eliminates the need for many of the
time-consuming steps required in traditional protocols.
We understand that the decision to have a child via IVF is no small matter --- and that it’s
important to have as much information as possible about possible outcomes. That’s why we’ve
ⓖSEQ analyses to operate in the cloud, where powerful cloud computing resources can be leveraged
implement cutting-edge statistical methods and machine-learning techniques to identify not only
whole-chromosome abnormalities, but also a variety of chromosomal disorders that are
notoriously difficult to detect.
ⓖSEQ seamlessly integrates the experimental and the computational, making PGS easier and faster
than ever before, eliminating any need for manual intervention after sample preparation by
performing real-time uploading and analysis of raw sequence data. By completing analyses and
providing automatic email notifications thereof — no more than one hour after the
of sequencing — time-critical experiments are made easier.