Wong M, Liew B, Hum M, Lee NY, Lee ASG. Benchmarking of variant calling software for whole-exome sequencing using gold standard datasets. Sci Rep. 2025;15(1):13697. doi:10.1038/s41598-025-97047-7

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Benchmarking Variant Calling Tools - Wong et al., 2025

By Jason Armstrong on May 13, 2025

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Genomics and the Future of Maternal and Newborn Health: Closing Gaps, Saving Lives

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World Health Day 2025 - Genomics in Maternal & Newborn Health

By Jason Armstrong on April 7, 2025

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This collaboration will provide selected EU clinical laboratories with a digital solution for meeting IVDR documentation requirements for in-house NGS workflows. Lausanne, Vienna, September 2024 — Saphetor, creator of VarSome and the CE-IVD NGS...

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Saphetor and Platomics announce agreement to support labs with IVDR compliance

By Carl Smith on September 9, 2024

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Lausanne, Switzerland 24th July 2024 - Saphetor SA, the creators of the global human genetics community VarSome, today announced European CE mark approval of the VarSome Clinical platform for the automated variant discovery, annotation, and...

Press Releases VarSome Clinical News

Saphetor SA receives IVDR Certification for clinical diagnosis support NGS data analysis platform, VarSome Clinical, ensuring enhanced safety and performance standards

By Carl Smith on July 24, 2024

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Saphetor at ASHG 2023

By Carl Smith on October 30, 2023

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This new partnership will provide integrated end-to-end solutions from sample to report for whole genome nanopore sequencing in future clinical applications.

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Oxford Nanopore Technologies and Saphetor announce a new partnership to deliver tertiary analysis for comprehensive interpretation of nanopore sequencing

By Carl Smith on October 25, 2023

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Lausanne, Switzerland, October 17,2023 – Saphetor SA today announces that it is partnering with world-leading healthcare intelligence and clinical research organization ICON to develop an innovative approach to support the planning and execution of...

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Saphetor partners with ICON to develop innovative data-centric approach to precision medicine clinical trial strategies to help support unique patients

By Carl Smith on October 17, 2023

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Saphetor are taking part in the Genomics Unlocked Webinar Series, as part of a partnership with MGI Europe. The webinar, Clinical Exomes: Sequencing to Reporting, demonstrates the full clinical exome workflow from sample to report generation...

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Webinar: Clinical Exomes to Reporting

By Carl Smith on May 30, 2023

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Saphetor is exhibiting at this year's European Society of Human Genetics conference in Glasgow, Scotland.

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Saphetor at ESHG 2023

By Carl Smith on May 15, 2023

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Our Head of Regulatory Affairs and Quality Assurance, Amélie Martinez, was featured in Inside Precision Medicine in an interview covering the upcoming impact and practical considerations labs are facing regarding IVDR.

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Inside Precision Medicine IVDR Interview

By Carl Smith on January 4, 2023

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Abu Dhabi, October 24, 2022: In a step aimed at boosting its clinical genomics capabilities in the region and beyond, G42 Healthcare, Abu Dhabi-based leading AI health-tech company, has announced a partnership with Saphetor SA, a Swiss precision...

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G42 Healthcare strengthens clinical genomics offering with Saphetor’s VarSome bioinformatics platform, strengthens UAE’s position as a global leader in healthcare innovation

By Carl Smith on October 24, 2022

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VarSome is exhibiting at this year's ASHG annual meeting in Los Angeles.

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VarSome at ASHG 2022

By Carl Smith on October 20, 2022

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