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ABSTRACT: Background
Genotype-by-sequencing (GBS) is a cost-effective method for large-scale genotyping, widely used across various species, particularly those with large genomes. A critical aspect of GBS lies in the selection of restriction enzymes for genome digestion and the optimization of data analysis pipelines. However, few studies have comprehensively examined the combined effects of enzyme choice and pipeline configuration.Results
In this study, we created GBS libraries using three commonly used restriction enzyme combinations (HindIII-NlaIII, PstI-MspI, and ApeKI) and assessed multiple SNP-calling pipelines in 15 soybean varieties. We tested four aligners (BWA-MEM, Bowtie2, BBMap, and Strobealign) and seven SNP callers (Bcftools, Stacks, DeepVariant, FreeBayes, VarScan, BBC
SUBMITTER: Zamalutdinov A
PROVIDER: S-EPMC12330036 | biostudies-literature | 2025 Aug
REPOSITORIES: biostudies-literature