Streamline variant analysis
Discover how Alamut™ Visual Plus can make advanced variant analysis scalable and accessible in your lab.
Gain time with an intuitive interface and strong customer support
Improve productivity with efficient and user-friendly data-to-report workflows
Enhance variant analysis by accessing 50+ curated sources of information in a single place
Scale your projects with software that remains accessible to all types of users, from beginners to skilled bioinformaticians
Get started with a free trial
Discover how Alamut™ Visual Plus will support
your analysis of disease-associated variants
Supports a large number of file types
Allows you to import and visualize BAM, VCF, BED, and Sanger files
Integrates highly sensitive predictors
Simplifies access to splicing and missense predictors such as MaxEntScan, NNSPLICE, SIFT, and PolyPhen-2
Combines multiple curated databases
Integrates information from databases such as ClinVar, dbSNP, BRIDGES, CADD, PubMed®, and MasterMind®
Simplifies genomic data visualization
Empowers you to visualize flanking and overlapping regions, and explore several genes at once in the nuclear and mitochondrial genomes
Keeps your
data safe
Secures your most sensitive information
Grows with your needs
New features are regularly added to improve your experience and support your needs