Coverage Size | 1.2 Mb |
Coverage | All coding regions of transcripts from 298 core genes related to solid tumors and the UTR regions of selected genes. |
Detection Range | Fusion, transcript variation, and expression, etc. |
Recommend Sequencing Data | 4 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: Detection comparison of fusion events in positive reference materials. Analysis results show that under the conditions of the same data volume (~4G) and different input amounts, all fusion events were detected, consistent with the expected results.
Product Name | Set | Cat. No |
TargetSeq® Solid Tumor Fusion RNA Panel | 4 rxn | PH2000470 |
24 rxn | PH2000475 | |
96 rxn | PH2000472 |