ⓖ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 designed ⓖSEQ analyses to operate in the cloud, where powerful cloud computing resources can be leveraged to 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 traditionally 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 completion of sequencing — time-critical experiments are made easier.