SOPHiA Genetics software

Other Software

OncoPortal - Reporting Software

Clinical interpretation has been one of the most complex and time-consuming aspects of transforming genomic data into meaningful results, until now.

Alamut Visual - Deep Dive Into Genomic Variants Assessment Software

Alamut Visual Plus™ enables deep assessment of variants on a genomic scale, empowering clinical researchers to make accurate decisions for their data interpretation. Alamut Visual Plus™ is a full genome browser designed to help researchers investigate variations of the human genome. The software combines a wide set of external data with high-quality missense and splicing predictors in one unique interface. As a result, Alamut Visual Plus™ decreases the time and effort required to assess the pathogenicity of genomic variants while maximizing lab workflow efficiency. Furthermore, visualization of different bioinformatics formats is now available in parallel, including Sanger, VCF, BED, and BAM files. Researchers can now also benefit from a simultaneous display of multiple genes in separate tabs.

SOPHiA - Next-Generation Sequencing (NGS) Software for Genomics

Next-generation sequencing (NGS) has the potential to revolutionize the diagnosis and treatment of cancers and rare diseases but creates extremely large, complex, and noisy datasets for analysis. Without the right analytical technology, pinpointing causative variants and obtaining actionable insights from NGS data requires specialist skills, multiple resources, and considerable time. The SOPHiA DDM Platform uses machine learning with patented algorithms to efficiently call, annotate, and pre-classify variants from raw NGS data. User-friendly features streamline prioritization, simplify interpretation, and expedite reporting.