High myopia gene detection kit and high myopia genetic risk assessment system and method
A genetic risk assessment, high myopia technology, applied in the field of high myopia genetic risk assessment system, high myopia genetic detection kit, can solve the problems of calculation method deviation and error, experimental design difference, inaccuracy, etc., to achieve low detection cost , The effect of large detection throughput and good practical value
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Embodiment 1
[0418] Example 1: Construction of a high myopia genetic risk prediction model
[0419] This example provides a predictive model for assessing the genetic risk of high myopia, which covers the polymorphic sites of the high myopia gene of the Chinese Han population, including 86 SNP sites of human genomic DNA and gender characteristics. The steps for constructing the high myopia genetic risk assessment model of the present invention are as follows: figure 2 shown.
[0420] 1) Obtain high myopia phenotype data. Design a myopia questionnaire, push and distribute the questionnaire, and volunteers voluntarily fill in the questionnaire to collect high myopia phenotype data.
[0421] 2) Obtain genetic data from participants who participated in the myopia questionnaire. Genome-wide loci and their genotype information are obtained through SNP chips or sequencing through bioinformatics analysis.
[0422] 3) Perform preprocessing and set division on the collected questionnaire and ge...
Embodiment 2
[0456] Example 2: Construction of a high myopia genetic risk gene detection kit
[0457] The site and primer design process of the kit:
[0458] According to the high myopia genetic risk prediction model obtained in Example 1, select the SNP site as the gene molecular site of the kit to form a detection PANEL model. For all the SNP sites involved in the detection of the PANEL model for the established high myopia genetic risk level, multiple PCR amplification upstream and downstream primer pairs and single-base extension primer sequences (as shown in the summary of the invention) are designed. The primer design schematic diagram is as follows Figure 10 shown.
[0459] Details about the kit:
[0460] 1.1 Main components
[0461] PCR reaction mixture, Taq enzyme, amplification primer mixture, SAP Buffer, SAP Enzyme, single base extension reaction mixture, iPlex Enzyme, extension primer mixture, ddH2O, positive control, desalting resin, mass spectrometer chip.
[0462] 1.2 S...
Embodiment 3
[0516] Application of Example 3 in Assessing High Myopia and Myopia Genetic Risk Level
[0517] Select a saliva sample from a child with high myopia, numbered mofang-hignmyopia_01, set 3 replicate wells for each sample, and perform SNP typing on the nucleic acid mass spectrometry platform. The process is as follows:
[0518] 1.1 DNA extraction
[0519] DNA extraction involves the following steps:
[0520] 1) Take out the 2ml centrifuge tube and mark it according to the sample number.
[0521] 2) Add 10uL FineMag Particles G, 30μL Proteinase K and 350μL Buffer MLD to each centrifuge tube.
[0522] 3) Transfer 500 μL of saliva sample to a centrifuge tube, mix by inverting 3 times, and vortex at high speed for 15 sec. Put into 45 ℃ constant temperature incubator for 10min.
[0523] 4) Place the centrifuge tube on the magnetic stand and let it stand for 30 sec. After the magnetic beads are completely absorbed, carefully remove the liquid.
[0524] 5) Remove the centrifuge tub...
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