oncoReveal®
Solid Tumor v2 Panel

The oncoReveal® Solid Tumor v2 Panel is a robust 48-gene assay that simultaneously tests for key mutations present in solid tumors, including NSCLC, colorectal, melanoma, endometrial, pancreatic, GIST, bladder, thyroid, and gliomas. Additionally, genes with potential importance in immuno-oncology such as POLD1 and POLE are analyzed. The panel uses proprietary Stem-Loop Inhibition-Mediated amplification (SLIMamp®) technology, a tiled amplicon-based library prep chemistry, designed by Pillar’s AI-empowered VersaTile Primer Design tool, for efficient single-tube target enrichment.

oncoReveal® Solid Tumor v2 Panel (48 genes)

AKT1CYSLTR2FBXW7GNASKEAP1NTRK1PTEN*SMAD4
ALKDDR2FGFR1H3F3A (H3-3A)KITPDGFRAPTPN11SRSF2
ARAFEGFRFGFR2HIST1H3B (H3C2)KRASPIK3CARAC1STK11
BRAFEIF1AXFGFR3HRASMAP2K1PLCB4RAF1TERT
CDKN2AERBB2GNA11IDH1METPOLD1RETTP53
CTNNB1ERBB4GNAQIDH2NRASPOLESF3B1TSHR
AKT1FBXW7KEAP1PTEN*
ALKFGFR1KITPTPN11
ARAFFGFR2KRASRAC1
BRAFFGFR3MAP2K1RAF1
CDKN2AGNA11METRET
CTNNB1GNAQNRASSF3B1
CYSLTR2GNASNTRK1SMAD4
DDR2H3F3A (H3-3A)PDGFRASRSF2
EGFRHIST1H3B (H3C2)PIK3CASTK11
EIF1AXHRASPLCB4TERT
ERBB2IDH1POLD1TP53
ERBB4IDH2POLETSHR

Genes marked in green indicate full CDS coverage
* indicates full CDS with exception of exon 9, chr10; 89725157-89725229

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* 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

Panel Specifications*

Enrichment chemistryMultiplex PCR using tiled amplicons
Number of pools1 pool
Number of genes/amplicons48/246
Total panel sizeFull CDS coverage of 3 genes; hotspots in 45 additional genes; 25.2kb total size
Variant typesSNVs, small and medium indels
Average amplicon size154bp
Recommended DNA input range20ng to 80ng
Sample typesDNA from tissue, blood, or FFPE
Mapping rate98%
% on-target aligned reads98%
Coverage uniformity
(% targets with >0.2X mean coverage)98%
Recommended Reads Per Sample~2 million paired-end reads
Total assay time (from DNA to sequencer)<8 hours

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

Ordering Information

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

PanelPart number
oncoReveal® Solid Tumor v2 Panel (24 reactions)HDA-CH-3003-24
Pillar Index Kit optionsReactionsPart number
Pillar Custom Index Primers Kit A32 Combinations, 96 reactionsIDX-PI-1001-96
Pillar Custom Index Primers Kit D96 Combinations, 192 reactionsIDX-PI-1004-192

User Guide

Solid Tumor v2 Panel

Product Sheet

Solid Tumor v2 Panel

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