方法：采用序列特异性引物聚合酶链反应的方法对汉族72例uc患者和314例正常对照者HLA - DRB1基因分型。
Methods: By using polymerase chain reaction-sequence specific primers, frequency of HLADRB1 alleles in 72 patients with UC and 314 healthy controls were detected.
方法运用聚合酶链反应-序列特异性引物（PCR-SSP）法，对38例山东汉族人GPP与94例健康对照进行HLA-DQB1等位基因分型。
Methods The distributing frequencies of HLA-DQB1 alleles were detected with polymerase chain reaction-sequence specific primers (PCR-SSP) in 38 GPP patients and 94 healthy subjects from Shandong.
基因测序分型方法被认为是人类白细胞抗原分型的金标准，它可得出精确的核苷酸序列。
Gene sequencing is considered to be the golden standard for HLA typing, which can obtain exact nucleotide sequence.
采用误差分析方法导出增量型自动厚度控制(agc)模型设定序列的差分方程。
A differential equation of giving series of incremental AGC (Automatic Gauge Control) model has been derived by the error analysis method.
利用紫外光谱结合支持向量机(SVM)模式识别原理建立了短串联重复序列(STR)的分型方法。
An approach for genotyping of STR locus based on ultraviolet (UV) spectroscopy and support vector machine (SVM) was studied.
利用紫外光谱结合支持向量机(SVM)模式识别原理建立了短串联重复序列(STR)的分型方法。
An approach for genotyping of STR locus based on ultraviolet (UV) spectroscopy and support vector machine (SVM) was studied.
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