Superior Performance. Reliable Results.

Find It detects common, clinically relevant genomic alterations in solid tumor samples, including single-base substitutions (SNVs), small deletions, and insertions (up to 24bp). It evaluates the mutation status of tumor DNA at 337 hotspots and 26 exons in 37 known cancer-associated genes simultaneously.

Find It detects indications for non-small cell lung cancer, melanoma, colorectal cancer, GIST, basal cell, breast cancer, endometrial, and other solid tumor cancers.

GenePosition
AKT1E17
ALKT1151, L1152, C1156, F1174, L1196, L1198, G1202, D1203, S1206, G1269, R1275, Y1278
ARL702, V716, S741, W742, Q784, H875, F877, T878, M896
BRAF Q201, G464, G466, F468, G469, Y472, D594, F595, G596, L597, V600, K601, part of Exon15 (V600-M620), G606
CCNEAmplification
CTNNB1D32, S33, G34, I35, H36, S37, T41, S45
DDR2L239, I638, S768
DICER1D1705-D1709, G1809, D1810-E1813
EGFRR108, A289, S492, P596, G598, Exon18, Exon19, Exon20, Exon21, & Amplification
ERBB2G309, S310, K753, L755, I767, D769, Exon20, & Amplification
ESR1K303, E380, S463, V534, P535, L536, Y537, D538
FGFR1N546, K656, & Amplification
FGFR2S252, P253, W290, A315, S372, Y375, C382, N549, K659, E731, E777, & Amplification
FGFR3R248, S249, G370, S371, Y373, G380, A391, K650
FOXL2C134
GNA11Q209
GNAQQ209
GNASR201
HRASG12, G13, Q61
IDH1R132
IDH2R140, R172
KITS476, Y553, W557,, V559, V560, L576, K642, V654, T670, D816, D820, N822, Y823, A829, Exon9, Exon11, Exon13, & Amplification
KRASK5, A11, G12, G13, L19, Q22, A59, G60, Q61, K117, A146, & Amplification
MAP2K1(MEK1)F53, Q56, K57, K59, V60, D67, I103, I111, C121, N122, P124, P387
MAP2K2(MEK2)F57, Q60, K61, L119, H123, G132
METT1010, V1112, H1112, G1181, L1213, D1246, Y1248, Y1253, Exon13, Exon14, Exon14 (-50 to+25), Exon18, Amplification
NRASG12, G13, A59, G60, Q61, K117, A146
NTRK1F589, G595, G667
NTRK3G623, G696
PDGFRAR560-E571, P577, N659, L839-Y849, D842
PIK3CAR88, C90, R93, P104, G106, N107, R108, K111, R115, N345, R357, G364, E365, Exon6 [start to P377], C420, E453, P539, E542, E545, Q546, D549, E970, E978, M1043, N1044, A1046, H1047, G1049 + Amplification
POLEExons 9-14 (P286R, M295R, S297F, F367S, D368Y, V411L, L424I, M444K, A456P, S459F)
PTCH1W844, G1093
PTENA126, G129, R130, R173, R233, K254-K267
RETG533, K603, C609, C611, C618, C620, C630, D631, C634, G691, E768, L790, Y791, V804, Y806, A883, R886, S904, M918, A919, Exon10, Exon 13, Exon15
ROS1S1986, G2032, L2026
STK11Q37, P281
TP53Exon4, Exon5, Exon6, Exon7, Exon8, Exon9
MSI21 Loci
Genes37
Hotspots337
Exons26
Turnaround Time3-5 days
Mutation typesSNVs, deletions and insertions(up to 24bp), CNVs and MSI
Sample TypeScrolls/curls & unstained slides
Sample RequirementSample requirements are the same if you are ordering just Find It, just Fusions, or both assays. Please include one H&E slide or a digital image (to test@canexiahealth.com) from the same FFPE block, including the circled tumour area. Please complete specimen details on the TRF including the % tumour content.

Benefits

Key Content

Find It targets genomic content associated with approved therapies, treatment resistance,  disease prognosis, and clinical trials.

Rapid Turnaround Time

A simple laboratory workflow that provides rapid, reliable, results.

Comprehensive Reports

Automated reporting from the Canexia Health Insights Platform provides up-to-date information on interpretations, current treatment options, and available clinical trials

Cost-Effective

Targeted amplicon-based technology provides an economical alternative to single-gene testing or hybrid capture NGS assay.

Conserve Biopsy Tissue

Find It’s single sample panel allows for simultaneous hotspot testing, reducing the amount of biopsy tissue required.

High Quality

All Canexia Health assays and software are developed in our CLIA, CAP, CDPH and DAP accredited laboratory.

View Other Solutions

Follow It®

A minimally invasive option for biopsy, Follow It can also be used to monitor cancer progression or investigate treatment resistance.

Learn About Follow It

Fusions

Rapid, cost-effective, and clinically actionable, Fusions allows you the flexibility to isolate and interrogate relevant fusions.

Learn About Fusions

Canexia Health Insights Platform

Each comprehensive report includes detailed results as well as therapeutic recommendations and expertly curated clinical trials. Our insights can help you make more informed treatment decisions.

Learn About Our Reports

Your Labs, Our Technology

From mutation identification to auto-generated clinical reports, Canexia Health’s proprietary platform allows you to perform mutation assay for cancer patients right from your laboratory.

Learn More

Make Faster Treatment Decisions

Canexia’s Clinical Services can support your local lab bring precision oncology testing in-house.

Get Started Today