Are you interested in learning more about AION? Join our new biweekly demo sessions, open to the public. Our team will guide you through a case start-to-finish, covering:
- How to upload your case and add details such as family members, HPO terms, and adding in-silico panels or removing secondary findings.
- How to understand the details of your analysis based on AION's prioritization algorithm and the provided rank of variant/disease pairs, considering the most likely genetic disease based on the patient's symptoms, but also detailed information about inheritance patterns, zygosity, or frequency, according to gnomAD and more.
- How to adapt the analysis to your needs by applying and removing ACMG classification criteria as you see fit dynamically to update your final classification or considering all annotated variants in the VCF files by manually filtering them.
- Finally, product and science team members will be available to answer all questions about how AION can improve your lab's workflow from testing to diagnosis, helping you solve more cases faster.
To participate, fill out the form and choose a date that works for you. Our team is looking forward to seeing you in the next session!
