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Description:Industry-leading genetic data analysis software to analyze NGS data in one, complete solution from FASTQ to a physician-ready clinical...
Keywords:Genetic Research, Genetic Analysis, Clinical Genetics, Filtering and Annotation, Clinical Reports,...
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| The Golden Helix Blog https://www.goldenhelix.com/blog/ |
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More Mixed Model Methods! | The Golden Helix Blog https://www.goldenhelix.com/blog/1870/ |
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VarSeq | Golden Helix, Inc. https://www.goldenhelix.com/products/VarSeq/ |
Clinical Variant Interpretation: Part III https://www.goldenhelix.com/blog/clinical_variant_interpretation_part_iii/ |
Genomic Data Analysis Software - Golden Helix https://www.goldenhelix.com/ |
About Golden Helix https://www.goldenhelix.com/company/about.html |
Golden Helix's Next-Gen Sequencing Data Analysis Solutions Explained https://www.goldenhelix.com/blog/next-gen-sequencing-data-analysis-solutions-with-golden-helix-software/ |
The Golden Helix Difference https://www.goldenhelix.com/company/the-golden-helix-difference.html |
Golden Helix Products https://www.goldenhelix.com/products/shop.html |
4 Essential Support Resources for Golden Helix Software Users https://www.goldenhelix.com/blog/4-essential-support-resources-for-golden-helix-software-users/ |
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content="Industry-leading genetic data analysis software to analyze NGS data in one, complete solution from FASTQ to a physician-ready clinical report." data-pgc-field="keywords" name="description"/ |
content="Genetic Research, Genetic Analysis, Clinical Genetics, Filtering and Annotation, Clinical Reports, Clinical Reporting, NGS, Nex-Gen Sequencing, Data Warehousing, Copy Number Analysis, Gene Panels, Exome Analysis, Whole Genome Analysis, Trio Analysis, Secondary Analysis, Deduping, Variant Calling, GATK, Pipeline, GWAS, Genome Wide Association Studies, Genomic Prediction, Genomic Selection, Large N Studies, Imputation, BEAGLE, CNV Analysis, Copy Number Analysis, RNA Analysis, Micro Arrays, NGS, Next-Gen Sequencing" data-pgc-field="Keywords" name="keywords"/ |
Ip Country: United States |
City Name: Ashburn |
Latitude: 39.0469 |
Longitude: -77.4903 |
Toggle navigation Products VarSeq VarSeq Dx VSClinical VS-CNV VSPGx VSPipeline VSReports VSWarehouse SNP & Variation Suite GenomeBrowse Align & Variant Calling Industries Commercial Testing Labs Hospital Labs Human Genetic Research Country-Wide Genome Projects Pharmaceutical R&D GWAS Research Diagnostic Focus Cancer Hereditary Diseases Pharmacogenomics Prenatal Screening Our Difference Blog Resources VarSeq Resources SVS Resources GenomeBrowse Resources eBooks Case StudiesPublished Articles Webcasts White Papers Company About Careers Contact Us Stay Connected Events News Partners Policies ISO Certification Submit Your partner for all NGS workflows Panels to Exomes to Genomes Labs to Regional Hospitals to Genome Centers Germline to Prenatal to Oncology Start Evaluation Scalable NGS Analysis for Hospitals and Clinical Labs Streamline and scale your lab with our comprehensive variant interpretation platform, backed by unparalleled support and a client-centric approach. Use our innovative, scalable, and automated solutions to enable precision medicine at your institution. Institutions 400+ Years in Business 25+ Product Installs 40,000+ Software to power your NGS testing workflows. Variant annotation, filtering, interpretation, and reporting in an integrated package. Scale your tests and your volume with our automation and data warehousing. VarSeq and VS-CNV Repeatable variant annotation and filtering workflows and target-based CNV calling Learn more VSClinical and VSReports Industry standard ACMG and AMP guidelines for variant scoring and clinical evidence reporting Learn more VSWarehouse and VSPipeline Automate workfows and warehousing, enabling continuous improvement and curated insights Learn more Fixed pricing, no per-sample charges Our business model is simple. One annual bundle, no matter how many samples come through your lab. Our Difference Featured webinar Maximizing Profitability in Your NGS Testing Lab Experience the benefits of automating clinical NGS workflows with Golden Helix software, reducing report production time, minimizing human error, and enhancing precision. Our fixed annual subscription model streamlines the entire analysis process, from sequencer to clinical report, maximizing profitability and efficiency in your NGS testing lab. Watch the Webinar Trusted by businesses worldwide. Our software takes a user-centric approach to enable complex workflows to be done repeatedly and efficiently. Users praise the streamlined experience, time savings, and repeatability. VarSeq is like so many birthday presents for my lab in one package! Clinical Director VarSeq is the best in the market. And for new features, the Development Team is always open for suggestions. Head of Bioinformatics The bioinformatic freedom is without parallels. Lead Geneticist VarSeq stood out during our initial round of evaluations, with all its tools integrated into one workflow. Konstanze Hörtnagel - Deputy Head of Human Genetics My special thanks to the FAS team for their excellent support in helping us to design in-house workflows. Head Analyst Golden Helix provides a market-ready solution for whole exome sequence analysis in a clinical lab. Martin Larsen - Associate Professor and Bioinformatician The excellent support and training are a big reason we decided to go with Golden Helix. Director of Genomics Core We are impressed by the visualization capabilities of VarSeq. Clinical Geneticist Golden Helix’s Clinical Reporting is better than anything we tested. Bioinformatician We are amazed that the analysis of cancer and germline samples is possible within one product. Lab Director We use Golden Helix training materials as our day bible running routine diagnostics. Chief Data Officer We are impressed by the ease of whole genome assay validation. Head of Bioinformatics VarSeq is like so many birthday presents for my lab in one package! Clinical Director VarSeq is the best in the market. And for new features, the Development Team is always open for suggestions. Head of Bioinformatics The bioinformatic freedom is without parallels. Lead Geneticist VarSeq stood out during our initial round of evaluations, with all its tools integrated into one workflow. Konstanze Hörtnagel - Deputy Head of Human Genetics My special thanks to the FAS team for their excellent support in helping us to design in-house workflows. Head Analyst Golden Helix provides a market-ready solution for whole exome sequence analysis in a clinical lab. Martin Larsen - Associate Professor and Bioinformatician The excellent support and training are a big reason we decided to go with Golden Helix. Director of Genomics Core We are impressed by the visualization capabilities of VarSeq. Clinical Geneticist Golden Helix’s Clinical Reporting is better than anything we tested. Bioinformatician We are amazed that the analysis of cancer and germline samples is possible within one product. Lab Director We use Golden Helix training materials as our day bible running routine diagnostics. Chief Data Officer We are impressed by the ease of whole genome assay validation. Head of Bioinformatics We are impressed by the ease of whole genome assay validation. Head of Bioinformatics We use Golden Helix training materials as our day bible running routine diagnostics. Chief Data Officer We are amazed that the analysis of cancer and germline samples is possible within one product. Lab Director Golden Helix’s Clinical Reporting is better than anything we tested. Bioinformatician We are impressed by the visualization capabilities of VarSeq. Clinical Geneticist The excellent support and training are a big reason we decided to go with Golden Helix. Director of Genomics Core Golden Helix provides a market-ready solution for whole exome sequence analysis in a clinical lab. Martin Larsen - Associate Professor and Bioinformatician My special thanks to the FAS team for their excellent support in helping us to design in-house workflows. Head Analyst VarSeq stood out during our initial round of evaluations, with all its tools integrated into one workflow. Konstanze Hörtnagel - Deputy Head of Human Genetics The bioinformatic freedom is without parallels. Lead Geneticist VarSeq is the best in the market. And for new features, the Development Team is always open for suggestions. Head of Bioinformatics VarSeq is like so many birthday presents for my lab in one package! Clinical Director We are impressed by the ease of whole genome assay validation. Head of Bioinformatics We use Golden Helix training materials as our day bible running routine diagnostics. Chief Data Officer We are amazed that the analysis of cancer and germline samples is possible within one product. Lab Director Golden Helix’s Clinical Reporting is better than anything we tested. Bioinformatician We are impressed by the visualization capabilities of VarSeq. Clinical Geneticist The excellent support and training are a big reason we decided to go with Golden Helix. Director of Genomics Core Golden Helix provides a market-ready solution for whole exome sequence analysis in a clinical lab. Martin Larsen - Associate Professor and Bioinformatician My special thanks to the FAS team for their excellent support in helping us to design in-house workflows. Head Analyst VarSeq stood out during our initial round of evaluations, with all its tools integrated into one workflow. Konstanze Hörtnagel - Deputy Head of Human Genetics The bioinformatic freedom is without parallels. Lead Geneticist VarSeq is the best in the market. And for new features, the Development Team is always open for suggestions. Head of Bioinformatics VarSeq is like so many birthday presents for my lab in one package! Clinical Director We are impressed by the visualization capabilities of VarSeq. Clinical Geneticist VarSeq is like so many birthday presents for my lab in one package! Clinical Director The excellent support and training are a big reason we decided to go with Golden Helix. Director of Genomics Core We are...
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