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Sequence investigation of 34 forensic autosomal STRs with massively parallel sequencing
STRs vary not only in the length of the repeat units and the number of repeats but also in the region with which they conform to an incremental repeat pattern. Massively parallel sequencing (MPS) offers new possibilities in the analysis of STRs since they can simultaneously sequence multiple targets...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5931506/ https://www.ncbi.nlm.nih.gov/pubmed/29717145 http://dx.doi.org/10.1038/s41598-018-24495-9 |
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author | Zhang, Suhua Niu, Yong Bian, Yingnan Dong, Rixia Liu, Xiling Bao, Yun Jin, Chao Zheng, Hancheng Li, Chengtao |
author_facet | Zhang, Suhua Niu, Yong Bian, Yingnan Dong, Rixia Liu, Xiling Bao, Yun Jin, Chao Zheng, Hancheng Li, Chengtao |
author_sort | Zhang, Suhua |
collection | PubMed |
description | STRs vary not only in the length of the repeat units and the number of repeats but also in the region with which they conform to an incremental repeat pattern. Massively parallel sequencing (MPS) offers new possibilities in the analysis of STRs since they can simultaneously sequence multiple targets in a single reaction and capture potential internal sequence variations. Here, we sequenced 34 STRs applied in the forensic community of China with a custom-designed panel. MPS performance were evaluated from sequencing reads analysis, concordance study and sensitivity testing. High coverage sequencing data were obtained to determine the constitute ratios and heterozygous balance. No actual inconsistent genotypes were observed between capillary electrophoresis (CE) and MPS, demonstrating the reliability of the panel and the MPS technology. With the sequencing data from the 200 investigated individuals, 346 and 418 alleles were obtained via CE and MPS technologies at the 34 STRs, indicating MPS technology provides higher discrimination than CE detection. The whole study demonstrated that STR genotyping with the custom panel and MPS technology has the potential not only to reveal length and sequence variations but also to satisfy the demands of high throughput and high multiplexing with acceptable sensitivity. |
format | Online Article Text |
id | pubmed-5931506 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59315062018-08-29 Sequence investigation of 34 forensic autosomal STRs with massively parallel sequencing Zhang, Suhua Niu, Yong Bian, Yingnan Dong, Rixia Liu, Xiling Bao, Yun Jin, Chao Zheng, Hancheng Li, Chengtao Sci Rep Article STRs vary not only in the length of the repeat units and the number of repeats but also in the region with which they conform to an incremental repeat pattern. Massively parallel sequencing (MPS) offers new possibilities in the analysis of STRs since they can simultaneously sequence multiple targets in a single reaction and capture potential internal sequence variations. Here, we sequenced 34 STRs applied in the forensic community of China with a custom-designed panel. MPS performance were evaluated from sequencing reads analysis, concordance study and sensitivity testing. High coverage sequencing data were obtained to determine the constitute ratios and heterozygous balance. No actual inconsistent genotypes were observed between capillary electrophoresis (CE) and MPS, demonstrating the reliability of the panel and the MPS technology. With the sequencing data from the 200 investigated individuals, 346 and 418 alleles were obtained via CE and MPS technologies at the 34 STRs, indicating MPS technology provides higher discrimination than CE detection. The whole study demonstrated that STR genotyping with the custom panel and MPS technology has the potential not only to reveal length and sequence variations but also to satisfy the demands of high throughput and high multiplexing with acceptable sensitivity. Nature Publishing Group UK 2018-05-01 /pmc/articles/PMC5931506/ /pubmed/29717145 http://dx.doi.org/10.1038/s41598-018-24495-9 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zhang, Suhua Niu, Yong Bian, Yingnan Dong, Rixia Liu, Xiling Bao, Yun Jin, Chao Zheng, Hancheng Li, Chengtao Sequence investigation of 34 forensic autosomal STRs with massively parallel sequencing |
title | Sequence investigation of 34 forensic autosomal STRs with massively parallel sequencing |
title_full | Sequence investigation of 34 forensic autosomal STRs with massively parallel sequencing |
title_fullStr | Sequence investigation of 34 forensic autosomal STRs with massively parallel sequencing |
title_full_unstemmed | Sequence investigation of 34 forensic autosomal STRs with massively parallel sequencing |
title_short | Sequence investigation of 34 forensic autosomal STRs with massively parallel sequencing |
title_sort | sequence investigation of 34 forensic autosomal strs with massively parallel sequencing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5931506/ https://www.ncbi.nlm.nih.gov/pubmed/29717145 http://dx.doi.org/10.1038/s41598-018-24495-9 |
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