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Overview

This operation provides an advanced genome VCF merging to provide a multisample dataset suitable for cohort analysis. 

Family-based Aggregation


Example

In the next figure we can see an example of aggregating multiple variants, from different single-sample files.

The variants from samples 1 and 2 have two overlapping variants. Variants from samples 3 and 4 are reference blocks from a gVCF.



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