Literature DB >> 29778045

Massively parallel sequencing of 124 SNPs included in the precision ID identity panel in three East Asian minority ethnicities.

Jing Liu1, Zheng Wang1, Guanglin He1, Xueying Zhao2, Mengge Wang1, Tao Luo3, Chengtao Li4, Yiping Hou5.   

Abstract

Massively parallel sequencing (MPS) technologies can sequence many targeted regions of multiple samples simultaneously and are gaining great interest in the forensic community. The Precision ID Identity Panel contains 90 autosomal SNPs and 34 upper Y-Clade SNPs, which was designed with small amplicons and optimized for forensic degraded or challenging samples. Here, 184 unrelated individuals from three East Asian minority ethnicities (Tibetan, Uygur and Hui) were analyzed using the Precision ID Identity Panel and the Ion PGM System. The sequencing performance and corresponding forensic statistical parameters of this MPS-SNP panel were investigated. The inter-population relationships and substructures among three investigated populations and 30 worldwide populations were further investigated using PCA, MDS, cladogram and STRUCTURE. No significant deviation from Hardy-Weinberg equilibrium (HWE) and Linkage Disequilibrium (LD) tests was observed across all 90 autosomal SNPs. The combined matching probability (CMP) for Tibetan, Uygur and Hui were 2.5880 × 10-33, 1.7480 × 10-35 and 4.6326 × 10-34 respectively, and the combined power of exclusion (CPE) were 0.999999386152271, 0.999999607712827 and 0.999999696360182 respectively. For 34 Y-SNPs, only 16 haplogroups were obtained, but the haplogroup distributions differ among the three populations. Tibetans from the Sino-Tibetan population and Hui with multiple ethnicities with an admixture population have genetic affinity with East Asian populations, while Uygurs of a Eurasian admixture population have similar genetic components to the South Asian populations and are distributed between East Asian and European populations. The aforementioned results suggest that the Precision ID Identity Panel is informative and polymorphic in three investigated populations and could be used as an effective tool for human forensics.
Copyright © 2018 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Forensic genetics; Genetic polymorphism; Massively parallel sequencing (MPS); Precision ID identity panel

Mesh:

Year:  2018        PMID: 29778045     DOI: 10.1016/j.fsigen.2018.05.002

Source DB:  PubMed          Journal:  Forensic Sci Int Genet        ISSN: 1872-4973            Impact factor:   4.882


  5 in total

1.  An alternate workflow for preparing Precision ID Ancestry and Identity Panel libraries for Illumina sequencing.

Authors:  Melissa Kr Scheible; Emma K Timpano; Laura M Boggs; Kelly A Meiklejohn
Journal:  Int J Legal Med       Date:  2021-03-04       Impact factor: 2.686

2.  A new strategy to confirm the identity of tumour tissues using single-nucleotide polymorphisms and next-generation sequencing.

Authors:  Lijuan Sun; Qi Liu; Shujin Li; Guanju Ma; Zhandong Wang; Chunling Ma; Bin Cong; Lihong Fu
Journal:  Int J Legal Med       Date:  2019-12-06       Impact factor: 2.686

3.  The Heart of Silk Road "Xinjiang," Its Genetic Portray, and Forensic Parameters Inferred From Autosomal STRs.

Authors:  Atif Adnan; Adeel Anwar; Halimureti Simayijiang; Noor Farrukh; Sibte Hadi; Chuan-Chao Wang; Jin-Feng Xuan
Journal:  Front Genet       Date:  2021-12-17       Impact factor: 4.599

4.  Genetic diversity and phylogenetic analysis of Chinese Han and Li ethnic populations from Hainan Island by 30 autosomal insertion/deletion polymorphisms.

Authors:  Jing Liu; Ziwei Ye; Zheng Wang; Xing Zou; Guanglin He; Mengge Wang; Shouyu Wang; Yiping Hou
Journal:  Forensic Sci Res       Date:  2019-12-13

5.  Systematic selections and forensic application evaluations of 111 individual identification SNPs in the Chinese Inner Mongolia Manchu group.

Authors:  Congying Zhao; Hui Xu; Yating Fang; Ming Zhao; Qiong Lan; Man Chen; Shuyan Mei; Bofeng Zhu
Journal:  Front Genet       Date:  2022-09-05       Impact factor: 4.772

  5 in total

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