Suppr超能文献

法医科学中InDel遗传标记的研究进展

Research Progress on InDel Genetic Marker in Forensic Science.

作者信息

Sheng X, Bao Y, Zhang J S, Li M, Li Y N, Xu Q N, Zhang S H, Li C T

机构信息

Department of Forensic Medicine, Medical College of Soochow University, Suzhou 215123, China.

Shanghai Key Laboratory of Forensic Medicine, Shanghai Forensic Service Platform, Academy of Forensic Science, Shanghai 200063, China.

出版信息

Fa Yi Xue Za Zhi. 2018 Aug;34(4):420-427. doi: 10.12116/j.issn.1004-5619.2018.04.016. Epub 2018 Aug 25.

Abstract

Genetic markers in forensic DNA typing experienced the variable number of tandem repeats (VNTR) sequences and the short tandem repeats (STR) sequences. With the emerge of sequencing technology, the third generation of genetic markers were found out, which usually have two alleles including single nucleotide polymorphism (SNP) and insertion/deletion (InDel), also known as biallelic genetic markers. Because of the insertions or deletions of DNA fragments, InDel genetic marker reveals DNA fragment length polymorphism and widely distributes across the whole genome. InDel genetic marker is numerous and has the characteristics of STR and SNP genetic markers, which has been applied in the fields of genetics and anthropology. This review focuses on the research progress of InDel genetic marker in forensic science, aiming to review and summarize the main research findings in recent years and provide clues for future researches.

摘要

法医DNA分型中的遗传标记经历了可变数目串联重复序列(VNTR)和短串联重复序列(STR)。随着测序技术的出现,发现了第三代遗传标记,其通常有两个等位基因,包括单核苷酸多态性(SNP)和插入/缺失(InDel),也被称为双等位基因遗传标记。由于DNA片段的插入或缺失,InDel遗传标记揭示了DNA片段长度多态性,并广泛分布于整个基因组。InDel遗传标记数量众多,具有STR和SNP遗传标记的特点,已应用于遗传学和人类学领域。本综述重点关注InDel遗传标记在法医学中的研究进展,旨在回顾和总结近年来的主要研究成果,并为未来的研究提供线索。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验