More rapid.
More automated.

More complete myeloid genomic profiling
with NGS.

 

Myeloid Testing should
be fast

Myeloid malignancy samples can be challenging to analyze. They are complex, heterogeneous, and have the potential to proliferate rapidly. To get meaningful genetic insights, you need a rapid and streamlined approach for studying all key mutations.

 

Oncomine Myeloid Assay GX V2

The Ion Torrent ™ Oncomine™ Myeloid Assay GX V2 on the Ion Torrent™ Genexus™ System provides a complete next-generation sequencing (NGS) solution that can deliver a comprehensive myeloid mutational report in as little as one day.


Rapid Automated Comprehensive Trusted Insightful
New call-to-action New call-to-action New call-to-action New call-to-action New call-to-action
Go from specimen to report in as little as one day.

 6
 		Process samples with just 20 minutes of hands-on time required.

 7
 		Simultaneously profile 45 key genes (DNA) and 30 fusion drivers (RNA), covering >700 unique fusions.

 29
 		Reliably detect a wide range of variants, including challenging-to-sequence targets like FLT3-ITD.

 79
 		Get an annotated variant report, including links to latest relevant evidence.

 99

Profile All Key Myeloid Mutations with one test

Simultaneously interrogate 45 DNA target genes and 30 fusion driver genes (RNA). This broad fusion panel allows you to sequence over 700 unique fusion transcripts. Gene content on the panel has been curated to cover relevant targets for all the major myeloid disorders—AML, MDS, MPN, CML, CMML, and JMML.

MagGlassDNAGenes

0

Hot Spot Genes

0

Full Genes

0

Fusion Drivers

0

Expression Genes

0

Expression Controls

Complete Coverage of Key Genes

Newly added genes shown in green below.

myeloid-gene-chart-ngs-oncomine

Detect multiple types of mutations
at once

Myeloid samples frequently harbor mutations in difficult-to-sequence regions of the genome.

The Oncomine Myeloid Assay GX v2 has been carefully engineered to reliably detect all relevant mutations associated with myeloid malignancies, including targets in challenging genes like CEBPA, FLT3, CALR and more.

dna-strands

  • Single nucleotide variants
  • Insertions and Deletions
  • Tandem duplications
  • Gene fusions

amp-poster-feature

 

Recent Performance Data

AMP 2021 Poster: Development of an automated genomic profiling assay for myeloid malignancies research

View our e-Poster published in the AMP 2021 Digital Experience Program to see recent data using the Oncomine Myeloid Assay GX v2.

View Poster

Upcoming Live Webinar

Rapid Next-Generation Sequencing for the Study of Acute Myeloid Leukemia


Speaker:

Dr. Diana Morlote

University of Alabama at Birmingham

 

During this presentation, Dr. Diana Morlote, assistant professor of pathology at the University of Alabama at Birmingham, will discuss the recent implementation of a rapid, automated next-generation sequencing (NGS) assay in her research laboratory for genomic profiling of Acute Myeloid Leukemia (AML) and other related hematological disorders. The data collected from several cases using the Oncomine Myeloid Assay GX v2 by Thermo Fisher Scientific will be presented. Analytical performance will be discussed for various key mutations detected using DNA inputs. Morlote will describe how this solution addresses key challenges with molecular analysis of AML and other related malignancies. This research furthers our understanding of malignant hematological disorders and may lead to better care in the future.

 

Morlote-Diana-webinar-feature


Date: Thursday, January 27, 2022
Time: 11:00 AM Eastern Standard Time

 

register-now-cta

 

 

image_5dd6bf98022a6

 

 

It's NGS made easy

A highly integrated workflow lets you go from specimen to report with about 20 minutes of hands-on time required*. It’s never been easier to implement myeloid NGS testing in your lab.

demo-request-cta

 

Automate your workflow from specimen to report

Start with any common myeloid specimen type, including whole blood, bone marrow, or peripheral blood leukocytes. From there, the Genexus System integrates and automates nucleic acid extraction, purification, quantification, library preparation, sequencing, analysis and reporting within a single software ecosystem. 

1-1

All Common Species

Whole Blood

Peripheral Blood Leukocytes (PBLs)

Bone Marrow

3-3

Automated Workflow

Nucleic acid extraction and quantification

Library preparation

Sequencing

Reporting & analysis

2-1

Annotated Variant Report

Biomarkers linked to relevant evidence from public data sources

Clear And Concise Reports


Ion Torrent Oncomine Reporter is a curated knowledgebase and reporting software that links biomarkers to relevant evidence and enables custom reporting. These tools help simplify the bioinformatics workflow and enable you to focus on finding the biological meaning of your data.

See Sample Report

report-example

 

learn-more-about-oncomine-reporter-cta

 

learn-more-about-genexus-system-cta

 

Additional Resources

Book a demo or request a quote

Are you ready to speak to a representative?

request-contact-cta

 

For Research Use Only. Not for use in diagnostic procedures. *The specimen-to-report workflow will be available for  RNA samples once the Total RNA Purification kits are available in approximately early 2022.

Are you a healthcare professional?

あなたは医療関係者ですか?



We've detected your location to be Japan.