Happy to share the release of Strand NGS v2.5. This release comes with many new exciting features and enhancements. Some of the major enhancements include new workflow for MeDIP-Seq analysis, split read alignment, new structural variant caller using split reads, additional RNA QC plots, enhanced RNA-Seq workflow to handle large-scale projects, correlation analysis, meta-data analysis, new and improved CNV visualisations (genome browser and web browser).
Additionally several enhancements are made with respect to visualizations and for high confidence variant calling. All these new features are available once you update the product by clicking on Update Product from the Help menu. For more information, please see the release notes. In case you need any assistance, please write to us at firstname.lastname@example.org or email@example.com