NGS-based joint detection system for genetic markers STR and SNP and detection method
A joint detection and genetic marker technology, applied in biochemical equipment and methods, DNA/RNA fragments, microbial determination/inspection, etc., can solve the problems of expensive kits and unfavorable practical application of forensic science, and achieve accuracy assurance, Accurate and reliable results
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Embodiment 1
[0067] Example 1 Evaluating the performance of a NGS-based STR and SNP genetic marker joint detection technology system and detection method for forensic medicine on serially diluted samples
[0068] 1. Sample preparation:
[0069] (1) The FTA blood card samples of 8 unrelated healthy male individuals were taken from the Han population, and the DNA was extracted according to the standard in GA / T383-2014, using the chelex method.
[0070] (2) Repeatability and sensitivity section
[0071] One sample was used to prepare serial dilution series of DNA templates (1ng, 500pg, 200pg, 100pg, 50pg) for sequencing using qubit absolute quantification results, and each sample was tested 3 times in parallel for repeatability and sensitivity studies. In addition, the sequencing data of a standard 2800M Control DNA was analyzed to study the threshold setting.
[0072] 2. Library construction:
[0073] Apply the library construction method described in step S2 of the present invention to c...
Embodiment 2
[0090] Example 2 Evaluating the performance of a NGS-based combined detection technology system and detection method for forensic STR and SNP genetic markers for mixed samples
[0091] 1. Sample preparation (mixed DNA part): According to the quantitative results of Example 1, the DNA quantitative results of 8 male samples were grouped, and 2 DNA samples of single typing were selected to construct 4 groups of DNA samples mixed with two males. Four mixing ratios (1:1, 1:4, 1:9, 1:19) were set for the group mixed samples, and each mixed sample was tested 3 times in parallel.
[0092]2. Library construction: Applying the library construction method in step S2 of the present invention, different mixed samples are used for library construction and sequencing detection with an initial DNA amount of 1 ng. For specific implementation steps, see the implementation method of the library construction link in the specific technical scheme.
[0093] 3. Sequencing and data analysis: Apply th...
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