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              +86 400-821-9890


              By utilizing our big panel comprehensive genomic
              profiling test, we collaborate with our partners in
              biomarker discovery and biomarker-driven drug
              development-from target discovery to
              commercial launch.

              Fusion-Based Biomarkers
              for Targeted Therapy

              We have integrated DNA and RNA sequencing results
              for detection of fusion genes with higher sensitivity.

              DNA+RNA-based analysis
              of Fusion

              RNA sequencing is a supplement to fusion detection

              In Chinese solid tumor cohort, 60.2% of fusion could be identified both in DNA&RNA, 21.4% of fusion was DNA only and 18.4% was RNA only.

              Gene fusions

              Overview of gene rearrangement in Chinese cohort including kinase gene fusions and LOF rearrangement of tumor suppressor genes. Different driver genes and their partners were identified in the cohort. The thickness of the line indicated the number of cases with relative gene rearrangement.

              NTRK family gene fusions

              Among 5,388 clinical cases, 22 ( 0.4% ) patients were found harboring NTRK1/3 fusions by next-generation sequencing testing, which was further confirmed by pan-Trk IHC or PCR.
              NTRK fusions were detected more in fibrosarcoma and colorectal cancer at a ratio of 11.1% and 1.1%, respectively.

              FGFR family gene fusions

              From over 4,000 solid tumor patients, 6.6% had FGFR 1-4 variations. The incidences of genomic alterations on FGFR1, 2, 3, and 4 were 2.8%, 1.6%, 1.2% and 1%, respectively. Amplification was the most common variation type of FGFR, which accounted for 47% of all the genomic alterations, followed by mutations (41.5%) and fusions (11.4%).

              Targeted Therapy


              The 5000+ Chinese solid tumor patients included 58.3% males and 41.7% females. Among patients with BRCA1/2 mutations,74.7% patients harbored somatic mutations. 24.3% patients harbored germline mutations and 1.0% patients harbored both somatic and germline mutations.


              Distriution and frequency of ERBB2 variants in 5000+ Chinese solid tumor patients.


              We have leveraged multiple techniques (DNA, RNA, IHC, etc.) to help identify
              immunotherapy-related biomarkers for our patients.


              The landscape of tumor mutational burden (TMB)in 10,000+ Chinese solid tumor patients.


              The landscape of PD-L1 expression on varoius types of tumor cells in 3,000+ Chinese solid tumor patients.

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