Optimus RP 4.2.2
SNP & Variation Suite (SVS), Golden Helix GenomeBrowse® visualization tool, HelixTree, ChemTree, and Optimus RP are trademarks of the Golden Helix® company. The common trade name of Golden Helix refers to Golden Helix, Inc., a Montana corporation.
All other company and product names may be trademarks of their respective companies.
About Golden Helix
At Golden Helix® software and analytics company, we strive to enable the genetics research and translational genomics community by making two commitments:
To build high quality software to analyze large genomic datasets.
To empower our end users to perform high end analytics work.
High Quality Software
To meet our first commitment we offer three software tools; SNP & Variation Suite (SVS), VarSeq and Golden Helix GenomeBrowse.
Our SNP & Variation Suite (SVS) is an integrated collection of user-friendly, yet powerful analytic tools for managing, analyzing, and visualizing multifaceted genomic and phenotypic data. SVS was created specifically to empower biologists and other researchers to easily perform complex analyses and visualizations, eliminating the need to rely exclusively on bioinformatics experts or use incompatible freeware. With SVS the focus can be on research instead of learning to be a programmer or waiting in line for bioinformaticians. SVS is compatible with all major genotyping and sequencing platforms and includes extensive data management functionality and a Python scripting interface which allows for fully-programmatic access. SVS also comes with powerful plotting and genome browser visualizations enabling the exploration of many different data types simultaneously in heat maps, variant maps, Manhattan Plots, and more.
SVS is used by hundreds of genetic and pharmacogenomic researchers in academia, government, and industry all over the world. With hundreds of citations in peer reviewed articles, SVS boasts a reputation for performance, usability, reliability, and fast time to results.
The VarSeq software streamlines the process of annotating and filtering variants obtained from next generation sequencing pipelines, allowing both research scientists and clinicians to find variants of interest in a very efficient and straightforward manner. VarSeq simplifies the user interface and provides a scalable architecture featuring repeatable workflows, note taking and reporting, and filter parameter prototyping.
VarSeq additionally offers high throughput environments VSPipeline which allows for the creation of workflow-encoded project templates locking down quality control and filtering parameters, automating bioinformatics pipelines and providing the requirements needed for CLIA and CAP certified analysis. Out of automated pipelines come fully produced VarSeq projects, ready for the technical and medical staff to jump into variant interpretation and reporting.
