Leveraging mRNA cMH and machine learning for the deconvolution of mixed body fluid stains in East Asian populations.

IF 7.3 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Qinglin Liu, Xiaolian Wu, Fanzhang Lei, Xi Yuan, Meiming Cai, Yiman Wu, Qiong Lan, Chunmei Shen, Bofeng Zhu
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引用次数: 0

Abstract

Body fluid identification methods have become increasingly well-established, but deconvoluting multi-component mixtures remains a significant challenge. When dealing with complex mixtures, methods based on mRNA coding-region SNPs (cSNPs) still face limitations such as limited polymorphisms of markers and insufficient population specificity. mRNA coding-region microhaplotypes (cMHs), combining tissue specificity with high discrimination power, offer a promising alternative for donor attribution in body fluid stains. In this study, we developed a targeted RNA sequencing panel for East Asian populations, comprising 36 body fluid-specific genes containing 48 cMHs (including 108 cSNPs), along with five genes lacking cMHs. This panel enables both tissue source identification and donor attribution for five types of body fluids and their mixtures. Through specificity evaluation of single-source body fluid stains, we identified six novel body fluid-specific genes. Furthermore, by integrating machine learning algorithms with an in silico mixing strategy, we developed a body fluid classifier that achieved accurate inference for both single-source fluids and complex mixtures. The panel's cumulative discrimination power across the five body fluid types ranged from 0.99568126 (peripheral blood) to 0.99999999 (vaginal secretion). In conclusion, the dual-purpose panel demonstrates robust performance in both tissue source identification and donor attribution for single-source body fluids and complex mixtures.

利用mRNA cMH和机器学习对东亚人群混合体液污渍进行反卷积。
体液识别方法已经变得越来越完善,但反卷积多组分混合物仍然是一个重大挑战。在处理复杂混合物时,基于mRNA编码区SNPs (cSNPs)的方法仍然面临标记多态性有限和群体特异性不足等局限性。mRNA编码区微单倍型(cMHs)结合了组织特异性和高分辨能力,为体液染色供体鉴定提供了一种有希望的替代方法。在这项研究中,我们为东亚人群开发了一个靶向RNA测序小组,包括36个含有48个cMHs(包括108个csnp)的体液特异性基因,以及5个缺乏cMHs的基因。该小组能够对五种体液及其混合物进行组织来源鉴定和供体归属。通过对单一来源体液染色的特异性评价,我们鉴定出6个新的体液特异性基因。此外,通过将机器学习算法与计算机混合策略相结合,我们开发了一种体液分类器,可以对单源流体和复杂混合物进行准确的推断。该小组对五种体液类型的累积辨别能力从0.99568126(外周血)到0.99999999(阴道分泌物)不等。总之,双重用途面板在组织来源识别和单一来源体液和复杂混合物的供体归属方面表现出强大的性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Briefings in bioinformatics
Briefings in bioinformatics 生物-生化研究方法
CiteScore
13.20
自引率
13.70%
发文量
549
审稿时长
6 months
期刊介绍: Briefings in Bioinformatics is an international journal serving as a platform for researchers and educators in the life sciences. It also appeals to mathematicians, statisticians, and computer scientists applying their expertise to biological challenges. The journal focuses on reviews tailored for users of databases and analytical tools in contemporary genetics, molecular and systems biology. It stands out by offering practical assistance and guidance to non-specialists in computerized methodologies. Covering a wide range from introductory concepts to specific protocols and analyses, the papers address bacterial, plant, fungal, animal, and human data. The journal's detailed subject areas include genetic studies of phenotypes and genotypes, mapping, DNA sequencing, expression profiling, gene expression studies, microarrays, alignment methods, protein profiles and HMMs, lipids, metabolic and signaling pathways, structure determination and function prediction, phylogenetic studies, and education and training.
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