GenVision Pro supports visualization and analysis of multiple samples from a single genome. The application lets you visually navigate between single-segment chromosomes and/or contigs of a genome, and can also export data and publication-quality images.
If a reference sequence was used in data assembly, GenVision Pro provides powerful tools for examining variants and structural variations, including for filtering variants based on functional impact, on making selections in a Venn diagram, on alignment statistics and many more.
GenVision Pro is also an essential tool for displaying and comparing multiple genome-wide data sets for RNA-seq, ChIP-seq and copy number variation (CNV) studies, where coverage and peak plots are compared and used to interpret gene expression and regulation.
These support pages contain written help and tutorials, as well as video tutorials.
- For help INSTALLING Lasergene, see our separate Installation Guide.
- For written TUTORIALS with free data, see GenVision Pro Tutorials.
- Click here for a list of all topics that include VIDEOS.
- To PRINT the current page of the User Guide, click the printer icon in the top right corner (
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).- To download a PDF of the entire User Guide, scroll to the bottom of the table of contents on the left, and press Download as PDF.
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