Overview of Analysis Features

Below are a few features that make Strand NGS an effective tool for analyzing sequence data. However, this list of features is by no means comprehensive; the best way to learn all the features is by getting a free trial of Strand NGS and analyzing either your own sample data or our demo data bundles.

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Genome Browser

The Genome Browser is a representation of a complete genome on which the sequenced reads can be visualized. Learn more

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Variant Support View

The Variant Support View displays SNPs and small InDels independently from the reference genome and groups identical reads together. Learn more