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The future of precision medicine: at the forefront of advances in genomics

6.9.2021

Our mission at Euformatics is to accelerate the transition to precision medicine. But what exactly does that mean? And how does NGS software from a

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PRESS RELEASE | Euformatics receives funding from Amazon Web Services and is selected by SYNLAB to design and deploy cloud-based genomic variant analysis software including COVID-19 variant surveillance

2.8.2021

HELSINKI, Finland, August 2021. Finnish bioinformatics software company Euformatics has been awarded funding through the Amazon Web Services (AWS)

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PRESS RELEASE | Euformatics further expands channel partner network through agreement with Quimiolab, Colombian distributor of NGS technologies

30.7.2021

HELSINKI, Finland, July 2021. Euformatics, a bioinformatics software company providing world-leading NGS interpretation and quality control tools

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PRESS RELEASE | Euformatics partners with Solaria Biodata, Mexican company specialised in bioinformatics solutions

27.7.2021

HELSINKI, Finland, July 2021. Euformatics, a bioinformatics software company providing world-leading NGS interpretation and quality control tools

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PRESS RELEASE | King Chulalongkorn Memorial Hospital chooses Omnomics Suite from Euformatics for NGS QC and analysis software as test offering expands

26.7.2021

HELSINKI, Finland, July 2021. King Chulalongkorn Memorial Hospital in Bangkok, Thailand, has chosen Finnish software company Euformatics as the

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PRESS RELEASE | Euformatics and Kemomed in distribution partnership for world-leading NGS bioinformatics software in Slovenia and Croatia

9.7.2021

HELSINKI, Finland, July 2021. Finnish bioinformatics software company Euformatics, which develops and sells world-leading NGS interpretation and

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PRESS RELEASE | Euformatics in distribution agreement with Illumina reseller in Indonesia, PT Pandu Biosains

9.7.2021

HELSINKI, Finland, July 2021. Finnish bioinformatics software company Euformatics, which develops and sells world-leading NGS interpretation and

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Evidencing the quality of clinical service next-generation sequencing for germline and somatic variants.

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