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.
The Genome Browser is a representation of a complete genome on which the sequenced reads can be visualized. Learn more
The Variant Support View displays SNPs and small InDels independently from the reference genome and groups identical reads together. Learn more
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