Rare and not so rare variants can be easily searched from inventory FFPE samples or on tissue microarrays. Multiplatform data (IHC and RNAseq) may be available for selected cohorts.
Samples are annotated using standard ThermoFisher Oncomine or Illumina Spike in NGS panels. Inventory can be queried for SNV, CNV, Indels, and Fusions.
QC outputs from these NGS platforms can be provided upon request and purchase. Tumor mutation burden (TMB), microsatellite instability (MSI), HLA-DR genotype, TCR and BCR sequences are additionally reported from the Illumina platform.