GO Pathology Workbench
GO Pathology Workbench is an end-to-end tertiary analysis solution for NGS and non-NGS data that integrates directly with lab systems, automates somatic and germline variant interpretation, matches patients to personalized therapy and clinical trial options, and produces a fully custom report. The flexible and customizable process enhancement tool enables users to go from order entry to quality control to variant interpretation and reporting, quickly and easily.
We help you easily interpret and report NGS data.
Our Solution
Easily process, validate, and report genetic test results (somatic or hereditary) into actionable insights for clinicians.
Solution Features
Integration with Lab Systems
Directly integrates with current infrastructure, including EHR, LIMS, and sequencers, for a seamless flow of data.
Somatic Variant Analysis
Automated variant interpretation for oncogenicity and AMP/ASCO/CAP tiers, plus best-in-class therapy, clinical trial, prognosis, and diagnosis recommendations based on approvals, guidelines, evidence, eligibility criteria, and drug targets.
Germline Variant Analysis
Variant interpretation using the ACMG guidelines and ClinGen, with support for all panels including WES/WGS, and use cases ranging from hereditary cancer to rare disease.
Fully-Customized Reporting
Create fully customized reports, with the ability to change layout, formatting, and content, as well as output format (PDF, XML, DOCX, TXT, HL7).
Assay-Agnostic
The solution supports any instrument/assay/file format, and handles both NGS results (DNA and RNA-Seq, SNVs, CNVs, fusions, splice variants, expression, MSI, TMB, HRD, HLA, etc) and non-NGS results (FISH, IHC, karyotype, PCR, etc).
Broad Annotation Coverage
Annotate variants using one database with 15+ sources, including ClinVar, ClinGen, GENIE, and prediction algorithms.
User Roles & Permissions
Customize permissions, access levels, and capabilities based on assigned user roles or responsibilities.
Single Installation
All assays and tests can be run through one central installation, maximizing ease of use by allowing molecular laboratories to seamlessly analyze and report any NGS test in a singular, unified workflow.
Our Process
Quality Control
The GO Pathology Workbench provides you with recommendations to pass or fail a run based on sample level QC metrics defined by your assay validation metrics. This information can be tracked to help comply with CAP guidelines and can be exported for audit purposes.
Variant Review
The GO Pathology Workbench presents you with the information required to review variants (read counts, quality info, BAM cartoon, pile-ups, platform recommendation, etc.) while providing relevant clinical interpretations. All information is presented in a single view for a comprehensive and streamlined analysis.
Custom Report
Create fully customized reports, with the ability to change layout, formatting, and content, as well as output format (PDF, XML, DOCX, TXT, HL7).