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KCNH2 gene detection kit and detection method

A gene detection and detection method technology, applied in the field of KCNH2 gene detection kits, can solve the problems of false negatives and not being used as a target for the prevention and treatment of sudden cardiac death, etc., and achieve simple operation, reduced sequencing depth, and low cost Effect

Inactive Publication Date: 2021-07-23
郑州普利莱医学检验所有限公司
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Problems solved by technology

However, the currently recognized mutations in genes causing sudden cardiac death are only for the discovered hotspot mutations, and there are still some mutations that have not been used as targets for the prevention and treatment of sudden cardiac death.
(However, not all mutations of any of the aforementioned genes are associated with sudden cardiac death; the diagnosis of sudden cardiac death by detecting the existing few genetic mutations will inevitably lead to false negative test results

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  • KCNH2 gene detection kit and detection method
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  • KCNH2 gene detection kit and detection method

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Embodiment Construction

[0032] The following will clearly and completely describe the technical solutions in the embodiments of the present invention with reference to the accompanying drawings in the embodiments of the present invention. Obviously, the described embodiments are only some, not all, embodiments of the present invention. Based on the embodiments of the present invention, all other embodiments obtained by persons of ordinary skill in the art without making creative efforts belong to the protection scope of the present invention.

[0033] see Figure 1-2 , the present invention provides a kind of technical scheme: a kind of KCNH2 gene detection method, detection method comprises the following steps:

[0034] A. DNA extraction;

[0035] B. Quality inspection of genomic DNA;

[0036] C. Construction of an amplicon targeted capture library;

[0037] D. Perform sequencing on the prepared library;

[0038] E. Standard analysis of data results;

[0039] F. Data quality control;

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Abstract

The invention discloses a KCNH2 gene detection kit and a detection method. The detection method comprises the following steps: A, performing DNA extraction; B, performing quality inspection on the genome DNA; C, constructing an amplicon targeted capture library; D, sequencing the prepared library on a machine; E, performing standard analysis on a data result; F, performing data quality control; and G, obtaining a variation detection result. The detection method in the invention has characteristics of simple operation and low cost, and covers the full coding region of the KCNH2 gene, the 50bp before and after the coding region, and the sites such as chr7:150652688, chr7:150652610, chr7:150646655, chr7:150646928; meanwhile, amplification of 19 pairs of specific primers can be carried out; compared with a traditional first-generation sequencing technology, the operation complexity is reduced; and the cost is reduced while the same sequencing depth as that of a second-generation sequencing technology is kept.

Description

technical field [0001] The invention relates to the technical field of gene detection, in particular to a KCNH2 gene detection kit and detection method. Background technique [0002] Sudden cardiac death refers to natural death caused by cardiac causes characterized by sudden loss of consciousness occurring within 1 hour after the onset of acute symptoms, accounting for the majority of sudden death, and the deceased may or may not have cardiovascular disease before death. Sudden cardiac death has the characteristics of rapid onset, rapid progression, and high mortality. 17 million people die from cardiovascular diseases every year in the world, and sudden cardiac death accounts for about 25%. The incidence rate of sudden cardiac death was 1.40 / 1000 persons / year for women and 6.68 / 1000 persons / year for men. About 50% of cardiac arrests occur in individuals without known cardiac disease, but the majority of patients have undiagnosed ischemic heart disease. It is estimated t...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12Q1/6883
CPCC12Q1/6883C12Q2600/156
Inventor 樊建雨王楚楚李爽王风祁元明陈鲤翔
Owner 郑州普利莱医学检验所有限公司