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Myeloid Panel

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Myeloid Panel

The Myeloid Panel is a robust NGS assay that interrogates 58 genes of interest* most relevant to myeloid cancers. The panel uses proprietary Stem-Loop Inhibition-Mediated amplification (SLIMamp®) technology, a tiled amplicon-based library prep chemistry, designed by AI-empowered VersaTile™ Primer Design tool, for efficient single-tube target enrichment.

Myeloid Panel (58 genes)

ABL1 BRAF CEBPA ETV6 HRAS KDM6A NPM1 PTEN SMC1A TP53
ANKRD26 CALR CSF3R EZH2 IDH1 KIT NRAS PTPN11 SMC3 U2AF1
ASXL1 CBL CUX1 FLT3 IDH2 KMT2A PDGFRA RAD21 SRSF2 WT1
ATRX CBLB DDX41 GATA1 IKZF1 KRAS PHF6 RUNX1 STAG1 ZRSR2
BCOR CBLC DNMT3A GATA2 JAK2 MPL PIGA SETBP1 STAG2
BCORL1 CDKN2A ETNK1 GNAS JAK3 NF1 PPM1D SF3B1 TET2

Genes marked in green indicate full CDS coverage

Panel Flow

Simple NGS library prep workflow

Maintain control of samples and results with single-tube, tiled amplification that can be performed in-house by any NGS lab.

Sensitive and robust chemistry

Achieve variant detection as low as 1% VAF† without UIDs ‡ even with limited DNA input or poor sample quality.

Reduced fully-loaded lab costs

Improve lab efficiency and reduce “no calls”, repeat testing, and difficult interpretation decisions

Simple, one-day workflow

DNA sample

DNA sample

Library preparation

Library preparation

Sequencing

Sequencing

Data analysis

Data analysis

Reporting

Reporting

Gene-specific PCR & cleanup
Indexing PCR & cleanup
Quantitation & normalization
Load sequencer

Panel Attribites

Parameter Description / Value
Enrichment chemistry Multiplex PCR using tiled amplicons
Number of genes / amplicons 58/766
Number of targets Full CDS coverage of 18 genes, hotspots in 40 additional genes, FLT3 ITDs; 107.9kb total size
Variant types SNVs, indels, ITD (internal tandem duplicates)
Average amplicon size 217bp
Recommended DNA input range 20ng to 60ng (20ng recommended)
Sample types DNA from whole blood, PBMCs
Mapping rate 99.6% ± 0.2%
% on-target aligned reads 92.0% ± 5.3%
Coverage uniformity (% targets with >0.2X mean coverage) 96.8% ± 1.0%
Recommended Reads Per Sample ~4 million paired-end reads

*Mapping rate, % of on-target aligned reads, and coverage uniformity metrics are based on internal testing performed using reference standard materials.

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