Nucleus

Easy ordering & networking platform for clinicians

Nucleus offers the possibility to place orders for genetic testing, follow progress, and read results. Nucleus also provides a feature, Connecting Clinicians, that connects clinicians based on variants, for knowledge sharing and further collaboration. The portal is free for all users. With this service we want to provide clinicians with the possibility to connect according to your own preference, to share knowledge and phenotypes in rare cases of VUS or Likely Pathogenic variants.

Key features of Nucleus

  1. Order and follow-up

    Place the order easily through our online ordering portal. By logging in at any point of the analysis you can follow the progress of your order.

  2. Read results

    Results can be read, archived and shared with your colleagues in a secure way.

  3. Support

    FAQ provides answers to frequently asked questions. You can also reach our customer support or genetics experts at any point of the analysis.

  4. Connect with clinicians

    Our own professional network that enables to connect with clinicians from all over the world to gain and share knowledge and better serve your patients with rare inherited diseases.

  1. Order & follow-up
    order process image
  2. Read results
    order process image
  3. Support
    order process image
  4. Connecting Clinicians
    order process image

Order & follow-up

Place the order easily by filling in the requisition form and uploading clinical documents. By logging in at any point of the analysis you can follow the progress of your order. The progress bar clearly shows the stage a single order is at, which makes the list of orders clear and easy to follow. The notification bar will notify you whenever results are ready, updated or there is a new suggested connection.

Read & share results

We will send you a notification when the results are available. Results can easily be viewed online, printed, or shared in safe and secure way with a colleague treating the same patient. Archive function gives the possibility to archive patient cases in order to make your personal view of ordered tests shorter and clearer. You can access the archived cases easily with a click and unarchive them if needed.

Support

We will guide you through the whole diagnostic process. You may contact our Clinical Genetics Support team or log in to browse by topic and find information to frequently asked questions.

Connect with clinicians

Nucleus offers a unique possibility for ordering clinicians to get connected with other clinicians from all over the world, that share patients with identical matching variants. A connection is suggested when variant is classified as a VUS (Variants of uncertain significance) or Likely Pathogenic. With this service we want to provide you with the possibility to connect according to own preferences, to share knowledge and phenotypes to better serve your patients with rare inherited diseases.

Interested?

To register for an account, click here to submit your account request. If you have any questions about Nucleus or ordering, please contact our customer support: support[at]blueprintgenetics.com, US & CANADA: support.us[at]blueprintgenetics.com.

#GeneticKnowledge

We developed Nucleus to gain, share, and build life changing genetic knowledge.