Clinical Services
Cancer Panel Analysis
Cancer Panel Analysis
Specimen Management and Interpretation
- Department of Pathology
Service Overview
- We provide comprehensive cancer genomic analysis based on Whole Exome Sequencing (WES) and Whole Transcriptome Sequencing (WTS).
Samples Analyzed
- Paired tumor tissue and normal blood samples (Paired tumor-normal sample)
Analysis Specifications
- Tumor sample: WES 250x + Boosting Panel 250x + WTS 100M reads
- Normal (blood) sample: WES 100x
Reported Results
- SNV/INDEL, CNV, Fusion, Microsatellite Instability (MSI), Tumor Mutational Burden (TMB), Homologous Recombination Deficiency (HRD), Mutational Signature
Reference Genome
- GRCh38
Cancer Panel List (SNUH FiRST Cancer Panel XT)
| Panel | Genes | Fusion Genes | Description |
|---|---|---|---|
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Pan-Cancer Panel
Lung Cancer Panel
Brain Cancer Panel
Lymphoma Panel
|
911 | 278 | SNUH’s comprehensive cancer genomic test based on Whole Exome Sequencing (WES) of paired tumor tissue and normal blood samples and Whole Transcriptome Sequencing (WTS) of tumor tissue. The panel covers 911 clinically validated cancer-related genes and 278 fusion genes and provides comprehensive analysis of SNVs/INDELs, CNVs, fusions, MSI, TMB, HRD, and mutational signatures. |
Pan-Cancer Panel / Lung Cancer Panel /
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Lymphoma & IEI-Specific Panel
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392 | - | A specialized diagnostic panel for lymphoma that analyzes a wide range of genetic variants across 392 genes associated with lymphoma and Inborn Errors of Immunity (IEI). |
Lymphoma & IEI-Specific Panel Gene List
Genetic Variant Detection
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