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An integrated strategy for target SSR genotyping with toleration of nucleotide variations in the SSRs and flanking regions

BACKGROUND: With the broad application of high-throughput sequencing and its reduced cost, simple sequence repeat (SSR) genotyping by sequencing (SSR-GBS) has been widely used for interpreting genetic data across different fields, including population genetic diversity and structure analysis, the co...

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Autores principales: Huo, Yongxue, Zhao, Yikun, Xu, Liwen, Yi, Hongmei, Zhang, Yunlong, Jia, Xianqing, Zhao, Han, Zhao, Jiuran, Wang, Fengge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8424866/
https://www.ncbi.nlm.nih.gov/pubmed/34496768
http://dx.doi.org/10.1186/s12859-021-04351-w
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author Huo, Yongxue
Zhao, Yikun
Xu, Liwen
Yi, Hongmei
Zhang, Yunlong
Jia, Xianqing
Zhao, Han
Zhao, Jiuran
Wang, Fengge
author_facet Huo, Yongxue
Zhao, Yikun
Xu, Liwen
Yi, Hongmei
Zhang, Yunlong
Jia, Xianqing
Zhao, Han
Zhao, Jiuran
Wang, Fengge
author_sort Huo, Yongxue
collection PubMed
description BACKGROUND: With the broad application of high-throughput sequencing and its reduced cost, simple sequence repeat (SSR) genotyping by sequencing (SSR-GBS) has been widely used for interpreting genetic data across different fields, including population genetic diversity and structure analysis, the construction of genetic maps, and the investigation of intraspecies relationships. The development of accurate and efficient typing strategies for SSR-GBS is urgently needed and several tools have been published. However, to date, no suitable accurate genotyping method can tolerate single nucleotide variations (SNVs) in SSRs and flanking regions. These SNVs may be caused by PCR and sequencing errors or SNPs among varieties, and they directly affect sequence alignment and genotyping accuracy. RESULTS: Here, we report a new integrated strategy named the accurate microsatellite genotyping tool based on targeted sequencing (AMGT-TS) and provide a user-friendly web-based platform and command-line version of AMGT-TS. To handle SNVs in the SSRs or flanking regions, we developed a broad matching algorithm (BMA) that can quickly and accurately achieve SSR typing for ultradeep coverage and high-throughput analysis of loci with SNVs compatibility and grouping of typed reads for further in-depth information mining. To evaluate this tool, we tested 21 randomly sampled loci in eight maize varieties, accompanied by experimental validation on actual and simulated sequencing data. Our evaluation showed that, compared to other tools, AMGT-TS presented extremely accurate typing results with single base resolution for both homozygous and heterozygous samples. CONCLUSION: This integrated strategy can achieve accurate SSR genotyping based on targeted sequencing, and it can tolerate single nucleotide variations in the SSRs and flanking regions. This method can be readily applied to divergent sequencing platforms and species and has excellent application prospects in genetic and population biology research. The web-based platform and command-line version of AMGT-TS are available at https://amgt-ts.plantdna.site:8445 and https://github.com/plantdna/amgt-ts, respectively. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-021-04351-w.
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spelling pubmed-84248662021-09-10 An integrated strategy for target SSR genotyping with toleration of nucleotide variations in the SSRs and flanking regions Huo, Yongxue Zhao, Yikun Xu, Liwen Yi, Hongmei Zhang, Yunlong Jia, Xianqing Zhao, Han Zhao, Jiuran Wang, Fengge BMC Bioinformatics Software BACKGROUND: With the broad application of high-throughput sequencing and its reduced cost, simple sequence repeat (SSR) genotyping by sequencing (SSR-GBS) has been widely used for interpreting genetic data across different fields, including population genetic diversity and structure analysis, the construction of genetic maps, and the investigation of intraspecies relationships. The development of accurate and efficient typing strategies for SSR-GBS is urgently needed and several tools have been published. However, to date, no suitable accurate genotyping method can tolerate single nucleotide variations (SNVs) in SSRs and flanking regions. These SNVs may be caused by PCR and sequencing errors or SNPs among varieties, and they directly affect sequence alignment and genotyping accuracy. RESULTS: Here, we report a new integrated strategy named the accurate microsatellite genotyping tool based on targeted sequencing (AMGT-TS) and provide a user-friendly web-based platform and command-line version of AMGT-TS. To handle SNVs in the SSRs or flanking regions, we developed a broad matching algorithm (BMA) that can quickly and accurately achieve SSR typing for ultradeep coverage and high-throughput analysis of loci with SNVs compatibility and grouping of typed reads for further in-depth information mining. To evaluate this tool, we tested 21 randomly sampled loci in eight maize varieties, accompanied by experimental validation on actual and simulated sequencing data. Our evaluation showed that, compared to other tools, AMGT-TS presented extremely accurate typing results with single base resolution for both homozygous and heterozygous samples. CONCLUSION: This integrated strategy can achieve accurate SSR genotyping based on targeted sequencing, and it can tolerate single nucleotide variations in the SSRs and flanking regions. This method can be readily applied to divergent sequencing platforms and species and has excellent application prospects in genetic and population biology research. The web-based platform and command-line version of AMGT-TS are available at https://amgt-ts.plantdna.site:8445 and https://github.com/plantdna/amgt-ts, respectively. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-021-04351-w. BioMed Central 2021-09-08 /pmc/articles/PMC8424866/ /pubmed/34496768 http://dx.doi.org/10.1186/s12859-021-04351-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Software
Huo, Yongxue
Zhao, Yikun
Xu, Liwen
Yi, Hongmei
Zhang, Yunlong
Jia, Xianqing
Zhao, Han
Zhao, Jiuran
Wang, Fengge
An integrated strategy for target SSR genotyping with toleration of nucleotide variations in the SSRs and flanking regions
title An integrated strategy for target SSR genotyping with toleration of nucleotide variations in the SSRs and flanking regions
title_full An integrated strategy for target SSR genotyping with toleration of nucleotide variations in the SSRs and flanking regions
title_fullStr An integrated strategy for target SSR genotyping with toleration of nucleotide variations in the SSRs and flanking regions
title_full_unstemmed An integrated strategy for target SSR genotyping with toleration of nucleotide variations in the SSRs and flanking regions
title_short An integrated strategy for target SSR genotyping with toleration of nucleotide variations in the SSRs and flanking regions
title_sort integrated strategy for target ssr genotyping with toleration of nucleotide variations in the ssrs and flanking regions
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8424866/
https://www.ncbi.nlm.nih.gov/pubmed/34496768
http://dx.doi.org/10.1186/s12859-021-04351-w
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