一种检测受者中供者比例的NGS方法

By obtaining mixed cell samples of donor and recipient genotypes, sequencing and analysis are performed, solving the problems of cumbersome operation and high cost in existing technologies, achieving more accurate detection of donor DNA content, and reducing detection costs.

CN119799864BActive Publication Date: 2026-07-17WUHAN KANGSHENGDA MEDICAL LAB CO LTD +1

Patent Information

Authority / Receiving Office
CN · China
Patent Type
Patents(China)
Current Assignee / Owner
WUHAN KANGSHENGDA MEDICAL LAB CO LTD
Filing Date
2024-12-24
Publication Date
2026-07-17

AI Technical Summary

Technical Problem

In existing technologies, when detecting ddcfDNA content in the context of receptor cfDNA, sequencing analysis of receptor gDNA and cfDNA is required, which is cumbersome and costly. If receptor genomic information is not required, the accuracy of the detection will be insufficient.

Method used

By obtaining mixed cell samples of donor and recipient genotypes, sequencing is performed to obtain homozygous and heterozygous gene combinations. Multiple SNP and InDel loci are counted, and the donor ratio is analyzed using probability density maps and Gaussian mixture models, thereby reducing the amount of testing data and lowering costs.

Benefits of technology

By reducing testing data and lowering costs, and by analyzing the genetic combinations of donors and recipients, the accuracy of donor DNA content information is improved, providing more comprehensive molecular genetic evidence.

✦ Generated by Eureka AI based on patent content.

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Abstract

本发明涉及一种检测受者中供者比例的NGS方法,该方法包括获取供者和受者的基因型混合细胞样本;对基因型混合细胞样本进行测序,得到纯合基因组合和杂合基因组合,从而可以减少检测数据,降低检测成本;进一步的,还可以对纯合基因组合和杂合基因组合进行统计,得到多个SNP位点、多个InDel位点和概率密度图;根据概率密度图对纯合基因组合和杂合基因组合中的多个SNP位点和多个InDel位点分别进行分析,得到包括供者的ddcfDNA含量和每个InDel位点的定量信息的检测受者中供者比例的NGS结果;从而可以对供者和受者进行SNP位点和InDel位点的分析,使得到的供体DNA含量信息更加准确。
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