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NEO PanTracer LBx

  • Next Generation Sequencing (NGS)

PanTracer LBx is a liquid biopsy next-generation sequencing panel for advanced stage pan-solid tumor indications. The assay detects single nucleotide variants (SNVs), insertions/deletions (InDels), copy number variants (CNVs), and fusions in a total of 514 genes, plus microsatellite instability status (MSI-High status) and blood tumor mutational burden (bTMB) score. 

ctDNA GENE LIST:

DETECTION OF SNVs, INDELS AND CNVs
ABL1, ABL2, ABRAXAS1, ACVR1, ACVR1B, ADGRA2, AKT1, AKT2*, AKT3, ALK*, ALOX12B, AMER1, ANKRD11, ANKRD26, APC, AR*, ARAF, ARFRP1, ARID1A, ARID1B, ARID2, ARID5B, ASXL1, ASXL2, ATM*, ATR, ATRX, AURKA, AURKB, AXIN1, AXIN2, AXL, B2M, BAP1, BARD1, BBC3, BCL10, BCL2, BCL2L1, BCL2L11, BCL6, BCOR, BCORL1, BCR, BCR-ABL1, BDG, BMP1, BTG1, BTK, CBL, CCDC6, CD274, CD276, CDK12, CDK4*, CDK6*, CDK8, CENPA, CHEK1, CHEK2, CIC, CLCN6, CMTM6, CNKSR1, COP1, CRKL, CRLF2, CTLA4, CTNNB1, CUX1, CYLD, DAXX, DNAJB1, DDX41, DICER1, DIS3, DNMT1, DNMT3A, DNMT3B, E2F3, EDC4, EGFR*, EGR1, EIF4A2, EIF4E, EML4, ERBB2*, ERBB3*, ERBB4, ERCC1*, ERCC2*, ERCC3, ERCC4, ESR1*, ETS1, ETV1, ETV4, ETV5, F3, FAD2, FAS, FAT1, FGF1*, FGF2*, FGF3*, FGF4*, FGF5*, FGF6*, FGF7*, FGF8*, FGF9*, FGF10*, FGF14*, FGF19*, FGF23*, FLT1, FLT3, FOXC1, FOXI1, FOXO1, FOXO3, FRZB, FYN, GABRA6, GATA1, GATA2, GATA3, GATA4, GATA6, GEN1, GLI1, GNAS, H3-3A, H3-3B, H3-4, H3C1, H3C10, H3C11, H3C12, H3C13, H3C14, H3C15, HRAS, HSP90AA1, IKBKE, IGF1, IGF2, IGF1R, IL10, IL7R, INHA, INS, IRS1, IRS2, JAK1, JAK2*, JAK3, JAK4, JUN, KDM5A, KDM5C, KDR, KLHL6, KIT*, KRAS*, LATS1, LATS2, LRP1B, LYN, MAGI2, MAP2K1, MAP2K2, MAP2K3, MAP2K4, MAP3K1, MAP3K13, MAP3K14, MAP3K15, MDM2*, MDM4, MDS, MET*, MGA, MLLT3, MRE11, MST1, MYB, MYC, MYCN*, NBN, NF1, NF2, NRAS*, NTRK1, NTRK2, NTRK3, NUP93, NUTM1, PAX3, PAX5, PAX7, PIK3CA*, PIK3CB*, PIK3CD, PIK3CG, PIK3C2B, PIK3C2G, PMS1, PMS2, POLD1, POLE, PRDM1, PRKDC, PRKCI, PRKAR1A, RAB35, RAD21, RAD50, RAD51, RAD51B, RAD51C, RAD51D, RAD54L, RASA1, RECQL4, REL, RHEB, RHOA, RUNX1, RUNX1T1, SMC1A, SMC3, SMARCA4, SMARCB1, SMARCD1, SOCS1, SPOP, SRC, STAT1, STAT3, STAT4, STAT5A, STAT5B, STAT6, STAG1, STAG2, STK11, SUFU, TAF1, TBC1D2, TCF3, TCF7L2, TFE3, TFRC, TMEM127, TNFAIP3, TNFRSF14, TOP1, TOP2A, TSHR, TSC1, TSC2, TET1, TET2, VEGFA, VHL, WT1, XIAP, YAP1, ZBTB2, ZBTB7A, ZNF217*, ZRSR2, ZSYNT3.
* Denotes genes with CNV detection

DETECTION OF FUSIONs
ABL1, BCR, CD74, ETV1, ETV6, FGFR2, NAB2, NTRK2, PAX3, PPARG, ROS1, TMPRSS2, ALK, BRAF, EGFR, ETV4, EWSR1, FGFR3, NTRK1, NUTM1, PAX8, RET, TFE3

ADDITIONAL BIOMARKERS: MSI-H, bTMB score

Turnaround time
7 Days

Level of Service

  • Global
New York Approved: No

Specimen Requirements

Peripheral blood: two x 10 mL Streck Cell-Free DNA BCT® tubes

Storage and Transportation

Use cold pack for transport, making sure cold pack is not in direct contact with specimen.

CPT Code(s)*

81464

*The CPT codes provided with our test descriptions are based on AMA guidelines and are for informational purposes only. Correct CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payor being billed.

Last Updated: July 30, 2025

Get in touch

Our Client Services team is on hand to help. Please call us at 866.776.5907, Option 3.