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G3 (Bethesda). 2015 Jan 13;5(3):385-98. doi: 10.1534/g3.114.016501.

Rapid and inexpensive whole-genome genotyping-by-sequencing for crossover localization and fine-scale genetic mapping.

Author information

1
Department of Molecular Biology, Max Planck Institute for Developmental Biology, 72076 Tübingen, Germany.
2
Department of Developmental Biology, Max Planck Institute for Plant Breeding Research, 50829 Cologne, Germany.
3
Department of Molecular Biology, Max Planck Institute for Developmental Biology, 72076 Tübingen, Germany weigel@weigelworld.org.

Abstract

The reshuffling of existing genetic variation during meiosis is important both during evolution and in breeding. The reassortment of genetic variants relies on the formation of crossovers (COs) between homologous chromosomes. The pattern of genome-wide CO distributions can be rapidly and precisely established by the short-read sequencing of individuals from F2 populations, which in turn are useful for quantitative trait locus (QTL) mapping. Although sequencing costs have decreased precipitously in recent years, the costs of library preparation for hundreds of individuals have remained high. To enable rapid and inexpensive CO detection and QTL mapping using low-coverage whole-genome sequencing of large mapping populations, we have developed a new method for library preparation along with Trained Individual GenomE Reconstruction, a probabilistic method for genotype and CO predictions for recombinant individuals. In an example case with hundreds of F2 individuals from two Arabidopsis thaliana accessions, we resolved most CO breakpoints to within 2 kb and reduced a major flowering time QTL to a 9-kb interval. In addition, an extended region of unusually low recombination revealed a 1.8-Mb inversion polymorphism on the long arm of chromosome 4. We observed no significant differences in the frequency and distribution of COs between F2 individuals with and without a functional copy of the DNA helicase gene RECQ4A. In summary, we present a new, cost-efficient method for large-scale, high-precision genotyping-by-sequencing.

KEYWORDS:

genetic mapping; hidden Markov model; next-generation sequencing; quantitative trait; recombination

PMID:
25585881
PMCID:
PMC4349092
DOI:
10.1534/g3.114.016501
[Indexed for MEDLINE]
Free PMC Article

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