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The test achieves comprehensive gene mutation detection, and serves as a new diagnosis tool for areas from prognosis stratification to targeted drug use.Wide coverage:

    1. Multiple target genes and all clinical hot spots are covered at the same time, and one-stop detection is achieved;

    2. Strong sensitivity: Mutation with a frequency as low as 5% can be detected;

    3. Precise quantification: Difference of 1% can be identified;

    4. High resolution: The change of single base can be detected;

    5. High scalability: facilitates conjoint analysis for multiple sites and multiple genes;

    6. Professional database for localized exploration;

    7. Precise analysis of FLT3-ITD, MLL-PTD and other special variation types.


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