Avadis NGS

Avadis NGS supports an extensive workflow for the analysis and visualization of RNA-Seq data. The workflow includes alignment, standard differential expression analysis and differential splicing analysis. Avadis NGS supports novel discovery like identification of novel genes, exons and splice junctions. It also detects transcriptome variants and gene fusion events. Further downstream analysis such as GO and pathway analysis can be performed on the set of interesting genes. The product has an option to create pipelines for time consuming jobs which automates analysis and leaves more time for end data interpretation. This webinar will give an overview of the features in the RNA-Seq data analysis workflow in Avadis NGS and also highlights on parameters within each feature that can be optimized depending on datasets and analysis needs.