Opens in a new tab

The Archer® FusionPlex® Myeloid Kit is a targeted next-generation sequencing assay to detect and identify fusions, point mutations and expression levels from 84 genes associated with myeloid-origin malignancies.

archer proceso de analisis 1
FusionPlex Myeloid 3

Studies are performed from RNA extracted from several types of starting sample. Using Archer’s proprietary Anchored Multiplex PCR (AMP™)-based enrichment, fusions of all genes in this kit can be identified in a single sequencing assay, even without prior knowledge of fusion partners or breakpoints. Archer Analysis software allows the analysis and interpretation of the data.

Genes:

archer
FusionPlex Myeloid 4

Area:

Myeloid line, Oncohematology

Brand:

Documents:

Consult our experts

Google reCaptcha: Invalid site key.

Related products

FUSIONPlex™ Heme v3 & Pan-Heme v2

RNA-based next-generation sequencing solution for the analytically sensitive identification of known and novel gene fusions, splicing variants, exon-skipping events, SNVs/Indels and gene expression in haematological malignancy research. FUSIONPlex Pan-Heme v2 provides broad coverage of 218 genes associated with haematological malignancies, while FUSIONPlex Heme v3 provides more focused coverage of 121 genes targeting alterations frequently found…
Archer Dx
Next Generation Sequencing (NGS)

RainSure – Digital PCR for Oncohematology

Comprehensive digital PCR (dPCR)-based solution for the quantitative, highly sensitive and low-cost monitoring of genetic mutations and fusions in haematological malignancies, designed for the continuous monitoring of previously identified molecular targets. RainSure offers an extensive catalogue of tests for the individual detection of up to 46 fusions and 121 hotspots. Detailed Description The proposed workflow…
RainSure
Digital PCR

Twist Custom Panels for NGS Applications

Twist custom panels are highly customisable solutions, allowing the exact selection of regions, genes, pathways or variants of interest. They are designed to offer high performance, flexibility and precision in all types of applications and starting samples. Detailed Description Operating principle: In practice, the use of custom panels makes it possible to overcome the limitations…
SOPHIA Genetics
Next Generation Sequencing (NGS)

Franklin by QIAGEN for Somatic Analysis

Advanced cloud-based bioinformatics platform designed for the automated analysis, interpretation, and classification of somatic variants in oncology. Through an integrated environment, the system evaluates clinical evidence in real time, automates classification in accordance with AMP/ASCO/CAP guidelines, and provides access to currently active clinical trials. Detailed description Operating principle End-to-end cloud-based solution for the clinical interpretation…
Qiagen
Next Generation Sequencing (NGS)