Docs Library

A collection of learning materials covering the core features of VarSome.com as well as VarSome Clinical.

Learning Videos

Watch Learning VarSome Clinical Series on YouTube, to better understand the functionalities and benefits of the platform.

Learn VarSome Clinical

READ APP NOTE

Learn about how VarSome Clinical analyzes exome-wide CNVs using Agilent's proprietary exon-proximal region design.

READ WHITEPAPER

Learn more about the validation program for VarSome Clinical. This process will help you adopt VarSome Clinical as the end-to-end bioinformatics solution for the processing and interpretation of your NGS data.

READ WHITEPAPER

Learn how we ensure that your data is always protected and how we deliver business resilience with the right data protection and safety measures in place. 

READ WHITEPAPER

Learn how you can detect low-frequency variants with VarSome Clinical by utilizing UMIs in your NGS workflow.

READ WHITEPAPER

Learn about VarSome and VarSome Clinical's ACMG-based variant classification engine which implements advanced machine learning techniques. 

READ WHITEPAPER

Learn how VarSome Clinical increases your diagnostic yield through sample cross-referencing, custome classifications and other advanced data mining features.

READ WHITEPAPER

Learn about MolecularDB, VarSome's proprietary high-throughput database system allowing seamless integration of genomics Big Data and data retrival.

READ WHITEPAPER

Learn about VarSome.com as the Global Human Genomics Community, and how you may laverage it for outcomes of your work.

READ WHITEPAPER

Learn more about how VarSome Clinical offers you the opportunity to share your data with other institutions. 

READ WHITEPAPER

Learn about VarSome Clinical's implementation of AMP's cancer variant classification guidelines.

READ WHITEPAPER

Learn about how you could be saving time and money by using VarSome Clinical as a validation pipeline.