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Updated: May 11, 2025

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基于面板的基因测序对·维勒布兰德病的临床实用性

Radha Ramanan1,2,3,4, Christine Van Laer1,5, Sarissa Baert6

  • 1Department of Cardiovascular Sciences, Centre for Molecular and Vascular Biology, KU Leuven, Leuven, Belgium.

Research and practice in thrombosis and haemostasis
|April 17, 2025
PubMed
概括

基于小组的测序显著影响了·维勒布兰德病 (VWD) 患者的诊断和管理,特别是2型和3型VWD患者. 这种基因检测有助于区分VWD基因复制物,并指导治疗决策.

关键词:
基因型 基因型 基因型高通量核酸测序的测序现象型 现象型 是一种现象型.·威勒布兰德病是什么?

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Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
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