4.7 Article

High-throughput genomics in sorghum: from whole-genome resequencing to a SNP screening array

期刊

PLANT BIOTECHNOLOGY JOURNAL
卷 11, 期 9, 页码 1112-1125

出版社

WILEY
DOI: 10.1111/pbi.12106

关键词

Illumina; Infinium; single-nucleotide polymorphism; SNP chip

资金

  1. German Federal Ministry of Education and Research (BMBF) [0315421B]
  2. Federal Ministry for Consumer Affairs, Nutrition and Agriculture (BMVEL) [23/12-13C HN12]
  3. DAAD

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With its small, diploid and completely sequenced genome, sorghum (Sorghum bicolor L. Moench) is highly amenable to genomics-based breeding approaches. Here, we describe the development and testing of a robust single-nucleotide polymorphism (SNP) array platform that enables polymorphism screening for genome-wide and trait-linked polymorphisms in genetically diverse S.bicolor populations. Whole-genome sequences with 6x to 12x coverage from five genetically diverse S.bicolor genotypes, including three sweet sorghums and two grain sorghums, were aligned to the sorghum reference genome. From over 1 million high-quality SNPs, we selected 2124 Infinium Type II SNPs that were informative in all six source genomes, gave an optimal Assay Design Tool (ADT) score, had allele frequencies of 50% in the six genotypes and were evenly spaced throughout the S.bicolor genome. Furthermore, by phenotype-based pool sequencing, we selected an additional 876 SNPs with a phenotypic association to early-stage chilling tolerance, a key trait for European sorghum breeding. The 3000 attempted bead types were used to populate half of a dual-species Illumina iSelect SNP array. The array was tested using 564 Sorghum spp. genotypes, including offspring from four unrelated recombinant inbred line (RIL) and F-2 populations and a genetic diversity collection. A high call rate of over 80% enabled validation of 2620 robust and polymorphic sorghum SNPs, underlining the efficiency of the array development scheme for whole-genome SNP selection and screening, with diverse applications including genetic mapping, genome-wide association studies and genomic selection.

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