Golden Helix End-of-Year Bundles 2020

         November 17, 2020

Special pricing offers on our End-of-Year software bundles.

It’s that time of year again! Golden Helix End-of-Year bundles have been released. We are currently offering our industry-leading products in special bundles for you to simplify and accelerate your current workflows. Whether analyzing and classifying variants, detecting large copy number variant events, or automating your workflow, our software bundles have options for your pipeline from secondary analysis to clinical reporting.

At Golden Helix, we recognize that 2020 has been an unprecedented year for many labs around the globe. That’s why along with offering these bundles at discounted rates, we have decided to embrace the season of giving by allowing labs to still reserve bundles into early 2021! We hope that you still take advantage of this limited-time offer, as well as our remote COVID-19 license while it lasts.

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 | $19,995 (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 | $48k (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.

Want More Information?

If you are not sure whether or not a product is a good fit for your organization feel free to check out their in-depth descriptions here. If you would like to learn more about current updates or developments, our blog is a resource used globally by many to stay up to date. Our team is more than happy to speak to you and answer any questions you might have. You can reach us by email at: info@goldenhelix.com Or download one of our free ebooks that covers cutting-edge topics in next-gen sequencing.

free ebook on genetic data warehousing

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