Customizable Classification
VarSome Clinical allows you to modify the default classification verdict by activating/inactivating specific rules according to your best knowledge.
No matter how good your clinical NGS pipeline is, you can still find yourself trying to validate an unclear variant. While you can validate it through Sanger sequencing, a much faster and cheaper alternative is variant calling orthogonal validation. VarSome Clinical is ideally suited to being your variant validation and interpretation pipeline.
VarSome Clinical allows you to modify the default classification verdict by activating/inactivating specific rules according to your best knowledge.
In addition to the automatic ACMG and AMP classification offered by VarSome Clinical, you have various options to build your own private database of classifications according to your patient's history.
Continuous contributions from the VarSome Global Community or novel scientific data may lead to the update of certain variants' annotation. With the regular re-annotation of your past analyses in VarSome Clinical, you can locate variants with an updated verdict, reflecting the most recent scientific knowledge which was not available at the time of the initial analysis.
You can add comments to specific variants and choose whether you will share them with the global VarSome community or keep them private. Our platform provides several ways to share your experience and benefit from global knowledge with the purpose of increasing the diagnostic yield!
All your samples in VarSome Clinical are linked in the variant level, enabling you to compare current and past cases with great ease.
Our platform has patient confidentiality and data protection as a top priority and security procedures are continuously monitored. You can always review all actions of your group’s users in the Audit Trail. Finally, sharing your data with partner institutions processed in VarSome Clinical is entirely your own choice and requires written consent from both parties.