This product has selected the coding regions of transcripts of 90 common major fusion genes in tumors and the UTRs (untranslated regions) of some genes for probe design. It supports the detection of fusion, variation, and gene expression information at the RNA level, providing clinical reference for tumor diagnosis and classification, prognosis evaluation, and recurrence monitoring.
| Technical Platform | TargetSeq® Hybridization Capture Sequencing |
| Coverage Size | 582.6 kb |
| Reference Database | RefSeq |
| Reference Genome | GRCh37 (hg19) |
| Coverage | Selected 90 core genes related to solid tumors, including all coding regions of transcripts and UTR regions of selected genes. |
| Storage | -20℃±5℃ |
| Sequence Platform | Illumina / MGI |
| Detection Range | Fusion, transcript variation, and expression, etc. |
| Recommend Sequencing Read Length | PE150 |
| Recommend Sequencing Data | 3 Gb |
| Applications | Adjuvant diagnosis, medication guidance, and prognostic indication |
Designed to target and capture regions of interest across all transcripts, tailored for RNA-level samples.
Efficiently captures target regions, reduces costs, and enables sensitive detection.
Leveraging iGeneTech® TargetSeq® probe hybridization capture sequencing technology, delivering stable and excellent performance.
Offers customizable and semi-customizable services (e.g., probe densification, expanding target regions) based on client needs, meeting personalized requirements.
Capture performance testing
RNA reference material consistency and performance testing. Total RNA was extracted from Seraseq® FFPE fusion RNA Reference Material v4, and libraries were prepared using an RNA library preparation kit with a 50ng input amount. After hybridization capture, sequencing was performed on an Illumina NovaSeq 6000 platform with PE150 read length.
Fusion reference material validation
Fusion reference material detection results

Note: Comparison of fusion detection in positive reference standards analysis results show that under the conditions of the same data volume (~3 Gb) and different input amounts, all fusion events were detected, which is consistent with the expected results.
| Product Name | Set | Cat. No |
| TargetSeq® Core Genes Fusion RNA Panel | 4 rxn | PH2000590 |
| 24 rxn | PH2000595 | |
| 96 rxn | PH2000592 |