Identify Variants (WGS-HD)

You can use the Identify Variants (WGS-HD) ready-to-use workflow to call variants in the mapped and locally realigned reads. The workflow removes false positives and, in case of a targeted experiment, removes variants outside the targeted region. Variant calling is performed with the Fixed Ploidy Variant Detection tool.

The Identify Variants (WGS-HD) ready-to-use workflow accepts sequencing reads as input.



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