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Genplex单核苷酸多态性分型系统及49重法医标记物组合的评估。

Evaluation of the Genplex SNP typing system and a 49plex forensic marker panel.

作者信息

Phillips C, Fang R, Ballard D, Fondevila M, Harrison C, Hyland F, Musgrave-Brown E, Proff C, Ramos-Luis E, Sobrino B, Carracedo A, Furtado M R, Syndercombe Court D, Schneider P M

机构信息

Forensic Genetics Department, Genomic Medicine Group, University of Santiago de Compostela, Galicia, Spain.

出版信息

Forensic Sci Int Genet. 2007 Jun;1(2):180-5. doi: 10.1016/j.fsigen.2007.02.007. Epub 2007 Mar 23.

Abstract

Using a 52 SNP marker set previously developed for forensic analysis, a novel 49plex assay has been developed based on the Genplex typing system, a modification of SNPlex chemistry (both Applied Biosystems) using oligo-ligation of pre-amplified DNA and dye-labeled, mobility modified detection probes. This gives highly predictable electrophoretic mobility of the allelic products generated from the assay to allow detection with standard capillary electrophoresis analyzers. The loci chosen comprise the 48 most informative autosomal SNPs from the SNPforID core discrimination set supplemented with the amelogenin gender marker. These SNPs are evenly distributed across all 22 autosomes, exhibit balanced polymorphisms in three major population groups and have been previously shown to be effective markers for forensic analysis. We tested the accuracy and reproducibility of the Genplex system in three SNPforID laboratories, each using a different Applied Biosystems Genetic Analyzer. Genotyping concordance was measured using replicates of 44 standardized DNA controls and by comparing genotypes for the same samples generated by the TaqMan, SNaPshot and Sequenom iPLEX SNP typing systems. The degree of informativeness of the 48 SNPs for forensic analysis was measured using previously estimated allele frequencies to derive the cumulative match probability and in paternity analysis using 24 trios previously typed with 18 STRs together with three CEPH families with extensive sibships typed with the 15 STRs in the Identifiler kit.

摘要

利用先前为法医分析开发的52个单核苷酸多态性(SNP)标记集,基于Genplex分型系统开发了一种新型的49重检测方法,该系统是对SNPlex化学方法(均为应用生物系统公司产品)的改进,采用预扩增DNA的寡核苷酸连接以及染料标记、迁移率修饰的检测探针。这使得该检测方法产生的等位基因产物具有高度可预测的电泳迁移率,从而能够使用标准毛细管电泳分析仪进行检测。所选择的位点包括来自SNPforID核心鉴别集的48个信息量最大的常染色体SNP,并补充了牙釉蛋白性别标记。这些SNP在所有22条常染色体上均匀分布,在三个主要人群中表现出平衡的多态性,并且先前已被证明是法医分析的有效标记。我们在三个SNPforID实验室测试了Genplex系统的准确性和可重复性,每个实验室使用不同的应用生物系统公司基因分析仪。通过对44个标准化DNA对照的重复样本进行基因分型,并比较由TaqMan、SNaPshot和Sequenom iPLEX SNP分型系统生成的相同样本的基因型,来测量基因分型的一致性。使用先前估计的等位基因频率来推导累积匹配概率,从而测量48个SNP在法医分析中的信息量,并在亲子关系分析中使用先前用18个短串联重复序列(STR)分型的24个三联体以及在Identifiler试剂盒中用15个STR分型的三个具有广泛同胞关系的CEPH家族。

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