Genotyping, statistical analysis and gene function research are the three key parts of modern genetics.
基因分型，统计分析和基因功能研究是现代遗传学研究中的三个核心组成部分。
Genotyping error has become one of important issues during the molecular marker detection studies, especially for the trace sample genotyping and forensic analysis.
基因分型错误已成为目前分子标记检测(如痕量样品分析、法医学鉴定)过程中愈发受到重视的问题。
SSR markers as an effective genotyping technology that can generate enough allelic polymorphism, has become an effective means of breeding pedigree analysis.
SSR标记作为一种有效的基因型鉴定技术，能够产生足够多的等位多态性，已成为育种系谱分析的有效手段。
ResultsThe results of genotyping in two-step PCR-CTPP were consistent with those conducted by PCR-RFLP and DNA sequence analysis.
结果通过两步法PCR-CTPP得到的基因分型结果与PCR-RFLP和DNA测序得到的基因分型结果完全一致。
DRD2P and COMT genotyping were carried out using PCR followed by RFLP and statistical analysis of genotype frequencies between ts patients and healthy controls was performed using SPSS programme.
采用病例对照研究的方法，用聚合酶链反应(PCR)和限制性片段长度多态性分析(RFLP)研究TS患者与健康对照间DRD2P、COMT基因的基因型频率有无统计学差异。
REP-PCR is a valid and rapid genotyping method for homological analysis and tracking the source of infection during epidemic outbreak.
REP-PCR是一种有效快捷的基因分型法，可为细菌同源性分析以及爆发流行时追根溯源建立简便可行的方法。
REP-PCR is a valid and rapid genotyping method for homological analysis and tracking the source of infection during epidemic outbreak.
REP-PCR是一种有效快捷的基因分型法，可为细菌同源性分析以及爆发流行时追根溯源建立简便可行的方法。
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