SNP & Variation Suite (SVS) is an integrated collection of powerful analytic tools for managing, analyzing, and visualizing multifaceted genomic and phenotypic data.
Applications include next-generation sequencing studies (DNA/RNA), genome-wide association, and copy number analysis.
Golden Helix introduces a major upgrade to the product used by hundreds of organizations around the world to accelerate their research. Version 8 offers:
- New analysis capabilities including Haplotype Trend Regression, Fst by Marker, and DNA-Seq Additions.
- Taking genomic visualization to the next level with the integration of Golden Helix's advanced, stand-alone genome browser inside of SVS.
- Annotation track and data handling improvements including a new annotation file format, a new Data Conversion Wizard, a new Data Source Library, and more!
- Workflow streamlining through a reorganization of the menus, window management functionality, and the addition of a multi-step dialog for annotating and filtering sequence variants.
