It’s the most wonderful time of the year; our software specials are here!
Now is the time to implement a Golden Helix solution to automate your workflows and analyze variants quick, easy, and affordably with our Year-End Bundles. Select packages which come once a year… these deals have been designed to fit your lab’s needs – and budget.
Please note the limited availability of these bundles, so you will have to act quick before they sell out! All packages will expire on December 31, 2019.
SVS with CADD & OMIM | $5,995 (3-User License)
Most annotations tend to exploit a single information type (e.g., conservation) and are restricted in scope (e.g., to missense changes). CADD is a tool for scoring the deleteriousness of single nucleotide variants as well as insertion/deletions variants in the human genome.
OMIM is a comprehensive database of human genes and genetic phenotypes for all known mendelian disorders and over 15,000 genes.
SVS Imputation Module with CADD & OMIM | $7,995 (2-User License)
Are you working with different SNP arrays? Alternatively, do you have historical SNP array data that you need to combine with modern SNP array outputs? In this case, you could use our imputation capabilities within SVS to conduct a meta-analysis on data based on different SNP arrays with varying resolutions.
VSClinical with VS-CNV & Sentieon Tier 1 | $19,995 (2-User License)
A complete solution for labs to take any clinical interpretation from FASTQ to report while complying with applicable ACMG guidelines. This package also provides a lab the capability to conduct a thorough CNV analysis within an NGS sample. All findings are captured in a clinical report that can be generated with a single mouse click.
VSClinical with AMP Workflow | $23,995 (2-User License)
This bundle is our solution for the interpretation of somatic variants in accordance with the AMP guidelines, as well as ACMG guidelines for germline. Included with our AMP Workflow is the professionally curated Golden Helix CancerKB to jump-start your clinical report.
VSClinical with AMP Workflow, VS-CNV & Sentieon Tier 1 | $29,995 (2-User License)
A complete solution for labs to take any clinical interpretation from FASTQ to report while complying with applicable ACMG and AMP guidelines. This package also provides a lab the capability to conduct a thorough CNV analysis within an NGS sample. All findings are captured in a clinical report that can be generated with a single mouse click. Included with our AMP Workflow is the professionally curated Golden Helix CancerKB to jump-start your clinical report.
Small Warehouse License: VSClinical, AMP Workflow, VS-CNV, VSReports, VSPipeline, Sentieon Tier 1 | $47k (2-User License)
The perfect package for small clinical labs. It has all the capabilities discussed in the VSClinical, CNV & Sentieon Package (see above). In addition, the VSWarehouse allows a lab to query efficiently if a variant has been seen before. It gives a lab the option to build powerful assessment catalogs to standardize the clinical variant interpretation across any number of analysts within a lab. It provides a lab with the ability to share variants with other collaborators.
Large Warehouse License: VSClinical, AMP Workflow, VS-CNV, VSReports, VSPipeline, Sentieon Tier 1 | $120k (Up to 10-User License)
The ultimate package for clinical labs. It has all the capabilities discussed in the VSClinical, CNV & Sentieon Package (see above). In addition, the VSWarehouse allows a lab to query efficiently if a variant has been seen before. It gives a lab the option to build powerful assessment catalogs to standardize the clinical variant interpretation across any number of analysts within a lab. It provides a lab with the ability to share variants with other collaborators. VSPipeline enables bioinformatic cores to automate the entire tertiary analysis process to achieve higher throughput.