Literature DB >> 30780121

Forensic characterization of Brazilian regional populations through massive parallel sequencing of 124 SNPs included in HID ion Ampliseq Identity Panel.

Eduardo Avila1, Aline Brugnera Felkl2, Pietra Graebin2, Cláudia Paiva Nunes2, Clarice Sampaio Alho3.   

Abstract

Use of Massive Parallel Sequencing (MPS) techniques has been investigated by forensic community aiming introduction of such methods in routine forensic casework analyses. Interesting features presented by MPS include high-throughput, ability to simultaneous genotyping of significant number of samples and forensic markers, workflow automation, among others. Emergence of single nucleotide polymorphism (SNP) as forensic relevant markers was facilitated in this process, since concurrent typing of larger marker sets is necessary for obtaining same levels of individual discrimination provided by other marker categories. In this context, HID Ion Ampliseq Identity Panel is a commercial solution with forensic purposes comprising simultaneous analysis of 90 highly informative autosomal SNPs and 34 Y -chromosome superior clade SNPs for male lineage haplotyping. SNP typing can be obtained with smaller amplicons, and this panel was designed for efficient processing of critical or challenging forensic samples. In this work, a sample of 432 individuals from all five Brazilian geopolitical regions was evaluated with this panel, in order to access feasibility of this panel use in a national basis. Results obtained for all five regions, including forensic parameters, show that this marker set can be efficiently employed for Brazilian nationals in human identification or kinship determination applications, due to high levels of genetic discriminative information content displayed by Brazilians. Interpopulation comparison studies were executed among Brazilian regional populations and 26 worldwide populations, in order to access genetic stratification occurrence. Some levels of population structure were identified, and impact on database design was discussed. Y-chromosome haplotyping of Brazilian samples revealed high levels of European ancestry in Brazilian male lineages, and utility of haplotyping in real forensic casework is addressed. Finally, genotyping and sequencing efficiency with this panel were addressed, as an effort to appraise the adequacy of this panel use in Brazilian national forensic demands.
Copyright © 2019 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Brazilian population; Forensics; HID Ion Ampliseq Identity Panel; Massive Parallel Sequencing; SNP; Y-haplotypes

Mesh:

Year:  2019        PMID: 30780121     DOI: 10.1016/j.fsigen.2019.02.012

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


  6 in total

1.  A novel forensic panel of 186-plex SNPs and 123-plex STR loci based on massively parallel sequencing.

Authors:  Xinyao Miao; Yuesheng Shen; Xiaojuan Gong; Huiyun Yu; Bowen Li; Liao Chang; Yinan Wang; Jingna Fan; Zuhuan Liang; Bowen Tan; Shengbin Li; Bao Zhang
Journal:  Int J Legal Med       Date:  2020-08-26       Impact factor: 2.686

2.  HIV-1 Drug Resistance Assay Using Ion Torrent Next Generation Sequencing and On-Instrument End-to-End Analysis Software.

Authors:  Michael T Pyne; Keith E Simmon; Melanie A Mallory; Weston C Hymas; Jeffery Stevenson; Adam P Barker; David R Hillyard
Journal:  J Clin Microbiol       Date:  2022-06-14       Impact factor: 11.677

3.  Forensic characterization of 124 SNPs in the central Indian population using precision ID Identity Panel through next-generation sequencing.

Authors:  Hirak Ranjan Dash; Eduardo Avila; Soumya Ranjan Jena; Kamlesh Kaitholia; Radhika Agarwal; Clarice Sampaio Alho; Ankit Srivastava; Anil Kumar Singh
Journal:  Int J Legal Med       Date:  2021-11-08       Impact factor: 2.791

4.  A New Computational Deconvolution Algorithm for the Analysis of Forensic DNA Mixtures with SNP Markers.

Authors:  Yu Yin; Peng Zhang; Yu Xing
Journal:  Genes (Basel)       Date:  2022-05-15       Impact factor: 4.141

5.  Sequence variations, flanking region mutations, and allele frequency at 31 autosomal STRs in the central Indian population by next generation sequencing (NGS).

Authors:  Hirak Ranjan Dash; Kamlesh Kaitholia; R K Kumawat; Anil Kumar Singh; Pankaj Shrivastava; Gyaneshwer Chaubey; Surajit Das
Journal:  Sci Rep       Date:  2021-12-01       Impact factor: 4.379

Review 6.  An Introductory Overview of Open-Source and Commercial Software Options for the Analysis of Forensic Sequencing Data.

Authors:  Tunde I Huszar; Katherine B Gettings; Peter M Vallone
Journal:  Genes (Basel)       Date:  2021-10-29       Impact factor: 4.096

  6 in total

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