From targeted gene panels to whole genomes, Golden Helix provides the end-to-end software infrastructure to master the complexity of next-generation sequencing.
The transition from raw sequencing data to a clinical report is a complex journey requiring precision at every step. While secondary analysis handles the initial alignment and variant calling, the true diagnostic insight is revealed through rigorous tertiary analysis and clinical interpretation.
Our solutions are engineered to handle the massive scale of modern genomics, providing labs with the tools to detect SNVs, CNVs, and structural variants with clinical-grade accuracy and automated efficiency.
Streamline your whole exome sequencing (WES) and targeted gene panel workflows. From alignment and variant calling to ACMG classification and clinical reporting, VarSeq provides the end-to-end solution for clinical laboratories.
Explore the full workflow, technical capabilities, and clinical evidence for exome analysis.
Address the unique challenges of whole genome sequencing (WGS) analysis. From petabyte-scale data management to clinical structural variant detection and non-coding region interpretation, VarSeq provides the end-to-end genomic analysis software solution.
Explore the full workflow, technical capabilities, and clinical evidence for genome analysis.
Resolve complex genomic regions, tandem repeats, and structural variants with PacBio and Oxford Nanopore support. Integrate long-read data into your clinical workflow to resolve variants missed by short-read platforms.
Explore the full workflow, technical capabilities, and clinical evidence for long-read analysis.
Join leading clinical labs and genome centers worldwide using Golden Helix to automate high-throughput pipelines and maintain clinical standards.