Abstract

BackgroundWith 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.ResultsHere, 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.ConclusionThis 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.

Highlights

  • 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

  • SSR genotyping has become an extensive application in different fields and has been used for population genetic diversity and structure analysis, the construction of genetic maps, and the investigation of intraspecies relationships [6,7,8]

  • Overview Currently, no suitable genotyping method can achieve tolerance of single nucleotide variations (SNVs) in the SSRs and flanking regions, which may be caused by Polymerase chain reaction (PCR) and sequencing errors or Single nucleotide polymorphisms (SNP) among varieties and can directly affect the sequence alignment and genotyping accuracy

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Summary

Introduction

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. Factors influencing accurate SSR genotyping include the following: 1) The slippage of polymerase is inherent to in vitro SSR polymerase PCR amplification, which leads to incorrect SSR alleles and makes it challenging to genotype SSRs accurately; and 2) the occurrence of variations in the SSR or flanking region will directly affect the genotyping results (Fig. 1) [13, 14] These problems accompanied the SSR genotyping technology development. There is still no suitably accurate SSR genotyping method that can tolerate nucleotide variations in SSRs and flanking regions which may affect the sequence alignment and genotyping accuracy

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