Literature DB >> 28938154

Massively parallel sequencing of forensic STRs and SNPs using the Illumina® ForenSeq™ DNA Signature Prep Kit on the MiSeq FGx™ Forensic Genomics System.

Fei Guo1, Jiao Yu2, Lu Zhang3, Jun Li3.   

Abstract

The ForenSeq™ DNA Signature Prep Kit (ForenSeq Kit) is designed to detect more than 200 forensically relevant markers in a single reaction on the MiSeq FGx™ Forensic Genomics System (MiSeq FGx System), including Amelogenin, 27 autosomal short tandem repeats (A-STRs), 7 X chromosomal STRs (X-STRs), 24 Y chromosomal STRs (Y-STRs) and 94 identity-informative single nucleotide polymorphisms (iSNPs) with the option to contain 22 phenotypic-informative SNPs (pSNPs) and 56 ancestry-informative SNPs (aSNPs). In this study, we evaluated the MiSeq FGx System on three major parts: methodological optimization (DNA extraction, sample quantification, library normalization, diluted libraries concentration, and sample-to-cell arrangement), massively parallel sequencing (MPS) performance (depth of coverage, sequence coverage ratio, and allele coverage ratio), and ForenSeq Kit characteristics (repeatability and concordance, sensitivity, mixture, stability and case-type samples). Results showed that quantitative polymerase chain reaction (qPCR)-based sample quantification and library normalization and the appropriate number of pooled libraries and concentration of diluted libraries provided a greater level of MPS performance and repeatability. Repeatable and concordant genotypes were obtained by the ForenSeq Kit. Full profiles were obtained from ≥100pg input DNA for STRs and ≥200pg for SNPs. A sample with ≥5% minor contributors was considered as a mixture by imbalanced allele coverage ratio distribution, and full profiles from minor contributors were easily detected between 9:1 and 1:9 mixtures with known reference profiles. The ForenSeq Kit tolerated considerable concentrations of inhibitors like ≤200μM hematin and ≤50μg/ml humic acid, and >56% STR profiles and >88% SNP profiles were obtained from ≥200-bp degraded samples. Also, it was adapted to case-type samples. As a whole, the ForenSeq Kit is a well-performed, robust, reliable, reproducible and highly informative assay, and it can fully meet requirements for human identification. Further, sensitive QC indicator and automated sample comparison function in the ForenSeq™ Universal Analysis Software are quite helpful, so that we can concentrate on questionable genotypes and avoid tedious and time-consuming labor to maximum the time spent in data analysis.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Evaluation; ForenSeq™ DNA Signature Prep Kit; Massively parallel sequencing (MPS); MiSeq FGx(TM) Forensic Genomics System; Short tandem repeat (STR); Single nucleotide polymorphism (SNP)

Mesh:

Year:  2017        PMID: 28938154     DOI: 10.1016/j.fsigen.2017.09.003

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


  22 in total

Review 1.  Separation/extraction, detection, and interpretation of DNA mixtures in forensic science (review).

Authors:  Ruiyang Tao; Shouyu Wang; Jiashuo Zhang; Jingyi Zhang; Zihao Yang; Xiang Sheng; Yiping Hou; Suhua Zhang; Chengtao Li
Journal:  Int J Legal Med       Date:  2018-05-25       Impact factor: 2.686

2.  Utility of ForenSeq™ DNA Signature Prep Kit in the research of pairwise 2nd-degree kinship identification.

Authors:  Miao Xu; Qingqing Du; Guanju Ma; Zifan Chen; Qingxia Liu; Lihong Fu; Bin Cong; Shujin Li
Journal:  Int J Legal Med       Date:  2019-01-28       Impact factor: 2.686

3.  Sequencing of human identification markers in an Uyghur population using the MiSeq FGxTM Forensic Genomics System.

Authors:  Halimureti Simayijiang; Niels Morling; Claus Børsting
Journal:  Forensic Sci Res       Date:  2020-09-10

4.  Mitochondrial genome sequencing with short overlapping amplicons on MiSeq FGx system.

Authors:  Yang Xin; Rulin Jia; Suhua Zhang; Fei Guo
Journal:  Forensic Sci Res       Date:  2021-12-23

5.  Development and validation of a novel 133-plex forensic STR panel (52 STRs and 81 Y-STRs) using single-end 400 bp massive parallel sequencing.

Authors:  Haoliang Fan; Lingxiang Wang; Changhui Liu; Xiaoyu Lu; Xuding Xu; Kai Ru; Pingming Qiu; Chao Liu; Shao-Qing Wen
Journal:  Int J Legal Med       Date:  2021-11-06       Impact factor: 2.791

6.  Massively parallel sequencing analysis of nondegraded and degraded DNA mixtures using the ForenSeq™ system in combination with EuroForMix software.

Authors:  Hsiao-Lin Hwa; Ming-Yih Wu; Wan-Chia Chung; Tsang-Ming Ko; Chih-Peng Lin; Hsiang-I Yin; Tsui-Ting Lee; James Chun-I Lee
Journal:  Int J Legal Med       Date:  2018-10-29       Impact factor: 2.686

7.  Concordance and characterization of massively parallel sequencing at 58 STRs in a Tibetan population.

Authors:  Hui Li; Cheng Zhang; Guoqing Song; Ke Ma; Yu Cao; Xueying Zhao; Qinrui Yang; Jianhui Xie
Journal:  Mol Genet Genomic Med       Date:  2021-02-25       Impact factor: 2.183

8.  Evaluation of the VISAGE Basic Tool for Appearance and Ancestry Prediction Using PowerSeq Chemistry on the MiSeq FGx System.

Authors:  Leire Palencia-Madrid; Catarina Xavier; María de la Puente; Carsten Hohoff; Christopher Phillips; Manfred Kayser; Walther Parson
Journal:  Genes (Basel)       Date:  2020-06-26       Impact factor: 4.096

9.  TIA: algorithms for development of identity-linked SNP islands for analysis by massively parallel DNA sequencing.

Authors:  M Heath Farris; Andrew R Scott; Pamela A Texter; Marta Bartlett; Patricia Coleman; David Masters
Journal:  BMC Bioinformatics       Date:  2018-04-11       Impact factor: 3.169

10.  Sequence investigation of 34 forensic autosomal STRs with massively parallel sequencing.

Authors:  Suhua Zhang; Yong Niu; Yingnan Bian; Rixia Dong; Xiling Liu; Yun Bao; Chao Jin; Hancheng Zheng; Chengtao Li
Journal:  Sci Rep       Date:  2018-05-01       Impact factor: 4.379

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