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TEST:
Hemasalus™

Company:
Geneseeq
Type:
CE Marked
Related tests:
Evidence

News

4ms
The Clinical Utility of Plasma Circulating Tumor DNA in the Diagnosis and Disease Surveillance in non-DLBCL non-Hodgkin’s Lymphomas (ACMG 2024)
Plasma ctDNA demonstrated high concordance with tumor biopsy in detecting genetic aberrations for non-DLBCL NHLs and serves as a promising surrogate of tumor biopsy in monitoring treatment response and disease progression in non-DLBCL NHLs.
Clinical • Tumor mutational burden • IO biomarker • Circulating tumor DNA
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TMB (Tumor Mutational Burden) • BCL2 (B-cell CLL/lymphoma 2) • CCND1 (Cyclin D1)
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EZH2 mutation
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Hemasalus™
9ms
Geneseeq Gains CE Marks for NGS-based Test Kits for Solid Tumors and Hematological Cancer (Canada Newswire)
"Geneseeq Technology Inc. has announced that three of our next-generation sequencing (NGS)-based cancer genetic testing kits, GENESEEQPRIME NGS Tumor Gene Detection Kit (GeneseeqPrime ™), GENESEEQ Homologous Recombination Deficiency Detection Kit (GeneseeqPrime™ HRD), and GENESEEQ Blood Cancer Gene Detection Kit (Hemasalus™ DNA/Hemarna™ RNA), have obtained the European Union's CE Mark approval. These approvals signify that GeneseeqPrime™ and GeneseeqPrime™ HRD are suitable for solid tumor genomic profiling, while Hemasalus™ DNA/Hemarna™ RNA is cleared for hematological cancer genomic profiling."
European regulatory
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GeneseeqPrime™ • GeneseeqPrime™HRD • Hemarna™ • Hemasalus™