Thermo Fisher launches a new NGS kit for myeloid hematological tumors

Every year, approximately 1.

Traditional molecular detection of blood diseases requires multiple single analyte methods, complicated workflows, and different testing laboratories, often requiring a detection cycle of more than 2-3 weeks

Thermo Fisher provides a comprehensive NGS solution for hematological tumors

Choose the mature Ion Torrent™ NGS platform according to the throughput.

Oncomine™ has report analysis software, which simplifies the biometric analysis process, automatically generates customized reports, and integrates variation annotations and related evidence

Brand new upgrade to the market, accelerating the detection of myeloid blood diseases

The high complexity and heterogeneity of myeloid malignant tumors, coupled with the rapid development of the disease, make rapid clinical and research detection challenging

One sample, one test can analyze all key mutations

Oncomine Myeloid Assay GX v2 only requires a very low sample starting volume (10-20ng), which can simultaneously detect 45 DNA targets and 30 fusion driver genes

Detect multiple types of mutations at once

The undetectable areas and high GC content areas of myeloid samples usually contain important mutant genes

Really automated process from sample to report

For all common sample types of myeloid diseases, including whole blood, bone marrow or peripheral blood leukocytes, nucleic acid extraction, purification, quantification, library preparation, sequencing, analysis and report generation can be automatically completed on the Genexus system, which can be obtained in one day Variant annotation report with relevant evidence reduces laboratory load and releases testing capabilities

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If you are interested in the Thermo Scientific Hematology Oncology NGS solution, please scan the code or click the link to fill in the questionnaire

*For scientific research use only, not for diagnostic purposes

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