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Front Plant Sci. 2018 Jun 22;9:849. doi: 10.3389/fpls.2018.00849. eCollection 2018.

Exploiting the Genomic Diversity of Rice (Oryza sativa L.): SNP-Typing in 11 Early-Backcross Introgression-Breeding Populations.

Author information

1
International Rice Research Institute, Los Baños, Philippines.
2
Institute of Crop Science, University of the Philippines Los Baños, Los Baños, Philippines.
3
National Institute of Biotechnology and Genetic Engineering, Faisalabad, Pakistan.
4
Data2Bio, LLC, Ames, IA, United States.
5
Department of Agronomy, Iowa State University, Ames, IA, United States.
6
Department of Plant Genetics and Breeding, China Agricultural University, Beijing, China.
7
National Key Facility for Crop Gene Resources and Genetic Improvement, Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing, China.
8
Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, China.

Abstract

This study demonstrates genotyping-by-sequencing-based single-nucleotide polymorphism (SNP)-typing in 11 early-backcross introgression populations of rice (at BC1F5), comprising a set of 564 diverse introgression lines and 12 parents. Sequencing using 10 Ion Proton runs generated a total of ∼943.4 million raw reads, out of which ∼881.6 million reads remained after trimming for low-quality bases. After alignment, 794,297 polymorphic SNPs were identified, and filtering resulted in LMD50 SNPs (low missing data, with each SNP, genotyped in at least 50% of the samples) for each sub-population. Every data point was supported by actual sequencing data without any imputation, eliminating imputation-induced errors in SNP calling. Genotyping substantiated the impacts of novel breeding strategy revealing: (a) the donor introgression patterns in ILs were characteristic with variable introgression frequency in different genomic regions, attributed mainly to stringent selection under abiotic stress and (b) considerably lower heterozygosity was observed in ILs. Functional annotation revealed 426 non-synonymous deleterious SNPs present in 102 loci with a range of 1-4 SNPs per locus and 120 novel SNPs. SNP-typing this diversity panel will further assist in the development of markers supporting genomic applications in molecular breeding programs.

KEYWORDS:

SNP-typing; conventional genotyping by sequencing (cGBS); introgression breeding; marker-assisted breeding; non-synonymous SNPs; tunable genotyping by sequencing (tGBS)

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