Overview of Analysis Features
Below are a few features that make Avadis 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 Avadis NGS and analyzing either your own sample data or our demo data bundles.
Genome Browser
The Genome Browser is a representation of a complete genome on which the sequenced reads can be visualized. Learn more
Variant Support View
The Variant Support View displays SNPs and small InDels independently from the reference genome and groups identical reads together. Learn more
Pathway Analysis
Analyzing interactions between genes and small molecules may provide insights and contexts to biological functions. Learn more
Alternative Splicing
For RNA-Seq experiments, the differential expression of genes and transcripts can be shown in a special visualization plot. Learn more
SNP Detection
The SNP detection feature identifies variants like SNPs, MNPs, and InDels by comparing the aligned reads against the reference genome. Learn more
BIOBASE Genome Trax
Genome Trax biological databases and annotations can be accessed within Avadis NGS in a matter of mouse clicks. Learn more
