Literature DB >> 34196785

Massively parallel sequencing of human skeletal remains in Vietnam using the precision ID mtDNA control region panel on the Ion S5™ system.

May Thi Anh Ta1, Nam Ngoc Nguyen1, Duc Minh Tran1, Trang Hong Nguyen2, Tuan Anh Vu1, Dung Thi Le1, Phuong Thi Le1, Thu Thi Hong Do1, Ha Hoang1,2, Hoang Ha Chu3,4.   

Abstract

Mitochondrial DNA (mtDNA) analysis using Sanger sequencing has been a routine practice for the identification of human skeletal remains. However, this process is usually challenging since DNA from the remains is highly degraded and at low concentration. Recently, the advent and implementation of massively parallel sequencing (MPS) have been offered the ability to improve mtDNA sequence data for forensic analysis. To assess the utility of the Ion S5™ system - an MPS platform for mtDNA analysis in challenging samples, we sequenced the mitochondrial control region of 52 age-old skeletal remains. Using the Precision ID mtDNA Control Region Panel, 50 full and two partial control region haplotypes at relatively high mean coverage of 2494 × were achieved for variant calling. Further variant analysis at 10% threshold for point heteroplasmy showed high degradation degree in terms of DNA damage in our bone samples. A higher point heteroplasmy threshold of 20% was required to diminish most of background noise caused by the damage. The results from this study indicated the potential application of the Ion S5™ system in sequencing degraded samples in Vietnam and provided valuable data sources for forensic analyses in the future.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Degraded DNA; Ion S5™; Massively parallel sequencing; Mitochondrial DNA; Point heteroplasmy; Skeletal remains

Mesh:

Substances:

Year:  2021        PMID: 34196785     DOI: 10.1007/s00414-021-02649-1

Source DB:  PubMed          Journal:  Int J Legal Med        ISSN: 0937-9827            Impact factor:   2.686


  36 in total

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Journal:  Croat Med J       Date:  2001-06       Impact factor: 1.351

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Journal:  Pathobiology       Date:  2012-06-21       Impact factor: 4.342

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Journal:  Nat Genet       Date:  1996-04       Impact factor: 38.330

6.  Analysis of Mitochondrial Control Region Using Sanger Sequencing.

Authors:  David Ballard
Journal:  Methods Mol Biol       Date:  2016

7.  Capillary electrophoresis of human mtDNA control region sequences from highly degraded samples using short mtDNA amplicons.

Authors:  Odile M Loreille; Jodi A Irwin
Journal:  Methods Mol Biol       Date:  2012

8.  Assessment of impact of DNA extraction methods on analysis of human remain samples on massively parallel sequencing success.

Authors:  Xiangpei Zeng; Kyleen Elwick; Carrie Mayes; Maiko Takahashi; Jonathan L King; David Gangitano; Bruce Budowle; Sheree Hughes-Stamm
Journal:  Int J Legal Med       Date:  2018-10-19       Impact factor: 2.686

9.  Identification of the remains of King Richard III.

Authors:  Turi E King; Gloria Gonzalez Fortes; Patricia Balaresque; Mark G Thomas; David Balding; Pierpaolo Maisano Delser; Rita Neumann; Walther Parson; Michael Knapp; Susan Walsh; Laure Tonasso; John Holt; Manfred Kayser; Jo Appleby; Peter Forster; David Ekserdjian; Michael Hofreiter; Kevin Schürer
Journal:  Nat Commun       Date:  2014-12-02       Impact factor: 14.919

10.  DNA capture and next-generation sequencing can recover whole mitochondrial genomes from highly degraded samples for human identification.

Authors:  Jennifer E L Templeton; Paul M Brotherton; Bastien Llamas; Julien Soubrier; Wolfgang Haak; Alan Cooper; Jeremy J Austin
Journal:  Investig Genet       Date:  2013-12-02
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  2 in total

1.  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.

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Journal:  Int J Legal Med       Date:  2021-11-06       Impact factor: 2.791

2.  Genetic Background of Kirgiz Ethnic Group From Northwest China Revealed by Mitochondrial DNA Control Region Sequences on Massively Parallel Sequencing.

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Journal:  Front Genet       Date:  2022-02-23       Impact factor: 4.599

  2 in total

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