Developmental Validation of a DIP-InDel/DIP-STR System for the Detection of Unbalanced DNA Mixtures.

IF 3 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Mingming Zhang, Yuxin Zhang, Hailing Yang, Huan Yu, Jiajia Fan, Jiaqi Wang, Zidong Liu, Jinding Liu, Jianbo Ren, Gengqian Zhang
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引用次数: 0

Abstract

Extracting "masked" minor donor information from an unbalanced DNA mixture stain is important for the identification of the person of interest. In recent years, a series of compound markers genotyped based on allele-specific amplifications have been proposed to detect minor contributors of mixed stains. In this study, we selected out 18 DIP-InDel markers from previous literatures and established a multiplex system encompassing 18 DIP-InDel markers and 6 DIP-STR markers in two separate reactions. The allele frequencies were estimated based on 200 samples, and 23 of the 24 DIP-linked length polymorphic markers had a relatively high probability of informative markers (I value >0.267), which indicated their potential usefulness in the Chinese Han population. Moreover, the multiplex was highly sensitive (requiring >0.025 ng) and specific to human DNA. This system is capable of detecting the minor contributor comprising 1% in unbalanced mixtures of two individuals. The capacity of profiling cell-free DNA was also analyzed in few cases. At least one paternal allele could be detected in maternal plasma samples with gestation periods ranging from 27 to 40 weeks. To conclude, the DIP-linked length polymorphic markers may serve as a convenient method for detecting the presence of a minor donor in unbalanced mixtures and show promise for noninvasive prenatal diagnosis.

用于检测不平衡 DNA 混合物的 DIP-InDel/DIP-STR 系统的开发验证。
从不平衡的 DNA 混合染色中提取 "被掩盖的 "次要供体信息对于识别相关人员非常重要。近年来,一系列基于等位基因特异性扩增的复合标记基因分型被提出来检测混合染色的次要贡献者。在本研究中,我们从以往的文献中筛选出 18 个 DIP-InDel 标记,并在两个独立的反应中建立了一个包含 18 个 DIP-InDel 标记和 6 个 DIP-STR 标记的多重系统。根据 200 份样本估计等位基因频率,24 个 DIP 连锁长度多态性标记中有 23 个标记的信息概率较高(I 值大于 0.267),这表明它们在中国汉族人群中具有潜在的实用性。此外,该多重系统对人类 DNA 具有高灵敏度(要求大于 0.025 ng)和特异性。该系统能检测出两个个体的不平衡混合物中占 1%的次要贡献者。在少数情况下,还对无细胞 DNA 的分析能力进行了分析。在妊娠期为 27 至 40 周的母体血浆样本中,至少可以检测到一个父系等位基因。总之,DIP连锁长度多态性标记可作为一种便捷的方法,用于检测不平衡混合物中是否存在未成年供体,并有望用于无创产前诊断。
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来源期刊
ELECTROPHORESIS
ELECTROPHORESIS 生物-分析化学
CiteScore
6.30
自引率
13.80%
发文量
244
审稿时长
1.9 months
期刊介绍: ELECTROPHORESIS is an international journal that publishes original manuscripts on all aspects of electrophoresis, and liquid phase separations (e.g., HPLC, micro- and nano-LC, UHPLC, micro- and nano-fluidics, liquid-phase micro-extractions, etc.). Topics include new or improved analytical and preparative methods, sample preparation, development of theory, and innovative applications of electrophoretic and liquid phase separations methods in the study of nucleic acids, proteins, carbohydrates natural products, pharmaceuticals, food analysis, environmental species and other compounds of importance to the life sciences. Papers in the areas of microfluidics and proteomics, which are not limited to electrophoresis-based methods, will also be accepted for publication. Contributions focused on hyphenated and omics techniques are also of interest. Proteomics is within the scope, if related to its fundamentals and new technical approaches. Proteomics applications are only considered in particular cases. Papers describing the application of standard electrophoretic methods will not be considered. Papers on nanoanalysis intended for publication in ELECTROPHORESIS should focus on one or more of the following topics: • Nanoscale electrokinetics and phenomena related to electric double layer and/or confinement in nano-sized geometry • Single cell and subcellular analysis • Nanosensors and ultrasensitive detection aspects (e.g., involving quantum dots, "nanoelectrodes" or nanospray MS) • Nanoscale/nanopore DNA sequencing (next generation sequencing) • Micro- and nanoscale sample preparation • Nanoparticles and cells analyses by dielectrophoresis • Separation-based analysis using nanoparticles, nanotubes and nanowires.
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