NeoTYPE® DNA & RNA - Brain

  • Next Generation Sequencing (NGS)

NeoTYPE® DNA & RNA - Brain uses targeted next-generation sequencing (NGS) to detect single nucleotide variants, insertions/deletions, and gene fusions in 83 unique genes (62 genes analyzed by DNA and 28 by RNA), plus microsatellite instability (MSI) and tumor mutational burden (TMB). In addition, FISH is performed to detect nine key copy number alterations and PD-L1 immunohistochemistry is performed. MGMT Promoter Methylation Analysis by PCR is an optional add-on. Results are incorporated into one report providing diagnostic, prognostic, and therapeutic implications, as well as potential clinical trial options. A microsatellite instability NGS result of "indeterminate" will create a reflex to MSI by PCR as long as the tumor percentage is ≥40% and paired normal tissue is available. If the sample is insufficient to produce both DNA and RNA results, the available results will be reported and alternate CPT® Codes may apply. SNVs/Indels (62 genes): AKT1, APC, ATRX, BAP1, BCOR, BCORL1, BRAF, CDK6, CDKN2A, CDKN2B, CIC, CTNNB1, DICER1, EED, EGFR, EPCAM, ERBB2, ERBB4, FGFR1, FGFR2, FGFR3, FUBP1, GNA11, GNAQ, H3F3A (H3-3A), HIST1H3C (H3C3), HRAS, IDH1, IDH2, KDM6A, KRAS, MAP2K1, MET, MLH1, MSH2, MSH6, MYC, MYCN, NOTCH1, NF1, NF2, NRAS, PDGFRA, PIK3CA, PMS2, PTCH1, PTEN, RB1, SETD2, SF3B1, SMAD4, SMARCA4, SMARCB1, SMO, SRC, SUFU, SUZ12, TERT Promoter, TP53, TSC1, TSC2, and VHL RNA Fusions (28 genes): ALK, BRAF, CIC, EGFR including EGFRvIII, EML4, ETV6, EWSR1, FGFR1, FGFR2, FGFR3, FUS, KIAA1549, MAML2, MET, MN1, MYB, MYBL1, NTRK1, NTRK2, NTRK3, PRKCA, RAF1, ROS1, STAT6, TACC3, TFG, YAP1, and ZFTA (C11orf95) CNVs by FISH (9 CNVs): 1p/19q co-deletion, +7/-10 (trisomy 7, monosomy 10), CDKN2A (p16) deletion, EGFR amplification, MET amplification, MYCN amplification, PDGFRA amplification, and PTEN deletion (FISH is global only) IHC:  PD-L1 LDT (tech-only available) Other Biomarkers: Microsatellite Instability (MSI) and Tumor Mutation Burden (TMB) included. MGMT Promoter Methylation Analysis may be added.

Turnaround time
14 Days

Level of Service

  • Global
New York Approved: Yes

Specimen Requirements

FFPE solid tumor tissue: Minimum surface area 10mm2 with 20% tumor content. Please use positively-charged slides and 10% NBF fixative. Do not use zinc fixatives. Paraffin block: Preferred. Cut slides: Send 25 unstained sections cut at 5 microns plus one H&E slide (which NeoGenomics will keep). No additional slides are needed if ordering MGMT Promoter Methylation Analysis.

Storage and Transportation

Storage & Transportation: Use cold pack for transport, making sure cold pack is not in direct contact with specimen. NYS clients please provide date and time of Collection.

CPT Code(s)*

81455x1, 88377x8, 88360x1. Add 81287x1 if ordering MGMT Promoter Methylation Analysis.

*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: January 22, 2025

Get in touch

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