oncoReveal®
Myeloid v2 Panel

The oncoReveal® Myeloid v2 Panel is a robust NGS assay that interrogates 80 genes of interest most relevant to myeloid cancer. The panel uses proprietary Stem-Loop Inhibition-Mediated amplification (SLIMamp®) technology, a tiled amplicon-based library prep chemistry for efficient single-tube target enrichment

oncoReveal® Myeloid v2 Panel (80 genes)

ABL1CALRCSF3REZH2IDH2MAP2K1NPM1RAD21SMC1ATET2
ANKRD26CBLCUX1FLT3IKZF1MBD4NRASRBBP6SMC3TP53
ARAFCBLBDDX41GATA1JAK2MEN1PDGFRARUNX1 SRSF2U2AF1
ASXL1CBLCDNMT3A GATA2 JAK3MPLPHF6 SAMD9STAG1U2AF2
ATRXCCND2ELANEGNASKDM6AMYCPIGA SAMD9LSTAG2UBA1
BCORCDKN2A ERCC6L2GNB1KITMYD88PPM1DSETBP1STAT3UBTF
BCORL1 CEBPA ETNK1HRASKMT2ANF1PTENSF3B1STAT5BWT1
BRAFCHEK2ETV6IDH1KRASNOTCH1PTPN11SH2B3TERT
(promoter)
ZRSR2
ABL1DDX41KDM6ARUNX1
ANKRD26DNMT3A KITSETBP1
ASXL1ETNK1KMT2ASF3B1
ATRXETV6KRASSMC1A
BCOREZH2MPLSMC3
BCORL1 FLT3NF1SRSF2
BRAFGATA1NPM1STAG1
CALRGATA2 NRASSTAG2
CBLGNASPDGFRATET2
CBLBHRASPHF6 TP53
CBLCIDH1PIGA U2AF1
CDKN2A IDH2PPM1DWT1
CEBPAIKZF1PTENZRSR2
CSF3RJAK2PTPN11
CUX1JAK3RAD21
Genes marked in green indicate full CDS coverage

Simple, Rapid NGS Library Prep Workflow

  • Single-tube library prep simplifies assay setup and reduces hands-on time
  • Flexible stopping points support efficient sample batching
  • Faster turnaround times with sample-to-result in <48 hours

Accurate, Reproducible Results

  • Detect variants down to 1% VAF*
  • Consistent performance across low-input and degraded DNA samples
  • Robust assay design supports reproducible results across runs 

Scalable NGS Testing with Intuitive Informatics

  • Facilitates an efficient and economic adoption of in-house NGS workflows
  • Low read requirements support scalable, high-throughput testing
  • Integrated informatics with a user-friendly Graphical User Interface (GUI)
  • Streamlined analysis supports a clear path from sample to results

*VAF (variant allele frequency) listed is for select variants.
For Research Use Only. Not for use in diagnostic procedures.

Panel Specifications*

Enrichment chemistryMultiplex PCR using tiled amplicons
Number of pools1 pool
Number of genes | amplicons80 | 874
Total panel size124.3kb
Variant typesSNVs, indels, ITD (internal tandem duplications)
Average amplicon size215bp
Recommended DNA input range 20ng to 60ng
Sample types DNA from whole blood or PBMCs
Mapping rate~98.9%
% on-target aligned reads ~87.5%
Coverage uniformity
(% targets with >0.2X mean coverage)
~97.4%
Recommended Reads Per Sample~5.14 million paired-end reads
Total assay time (from DNA to sequencer)<8.5 hours

*Mapping rate, percentage of on-target aligned reads, and coverage uniformity metrics are averages based on internal testing performed using reference standard materials and analysis using PiVAT®

Ordering Information

Select the panel and one of the index kit options listed below.

PanelPart Number
oncoReveal® Myeloid v2 Panel (24 reactions) HDA-MY-1010-24
Pillar Index Kit OptionsReactionsPart Number
Pillar Custom Indexing Kit A32 Combinations, 96 ReactionsIDX-PI-1001-96
Pillar Custom Indexing Kit D96 Combinations, 192 Reactions IDX-PI-1004-192

User Guide

Myeloid v2 User Guide

Product Sheet

Myeloid v2 Product Sheet

SDS Sheet

Myeloid v2 SDS Sheet

App Note

Myeloid v2 Application Notes