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Title: Anchoring and ordering NGS contig assemblies by population sequencing (POPSEQ)

Journal Article · · The Plant Journal
DOI:https://doi.org/10.1111/tpj.12319· OSTI ID:1625934
 [1];  [2];  [3];  [4];  [5];  [4];  [6];  [7];  [8];  [9];  [1];  [10];  [1];  [11];  [1];  [12]
  1. Leibniz Inst. of Plant Genetics and Crop Plant Research (IPK), Gatersleben (Germany)
  2. Univ. of Minnesota, St Paul, MN (United States). Dept. of Agronomy and Plant Genetics; Univ. of Minnesota, St Paul, MN (United States). Dept. Plant Biology
  3. USDOE Joint Genome Institute (JGI), Walnut Creek, CA (United States); Univ. of California, Berkeley, CA (United States). Dept. of Molecular and Cell Biology
  4. USDOE Joint Genome Institute (JGI), Walnut Creek, CA (United States)
  5. USDOE Joint Genome Institute (JGI), Walnut Creek, CA (United States); HudsonAlpha Inst. of Biotechnology, Huntsville, AL (United States)
  6. Univ. of Minnesota, St Paul, MN (United States). Dept. of Agronomy and Plant Genetics
  7. Univ. of California, Riverside, CA (United States). Dept. of Botany & Plant Sciences
  8. US Dept. of Agriculture (USDA)., Ames, IA (United States). Agricultural Research Service (ARS). Iowa State Univ.
  9. Univ. of Helsinki (Finland). MTT Agrifood Research. Inst. of Biotechnology
  10. Helmholtz Zentrum München, Neuherberg (Germany). Munich Information Center for Protein Sequences. Inst. of Bioinformatics and Systems Biology
  11. Kansas State Univ., Manhattan, KS (United States). US Dept. of Agriculture. Agricultural Research Service (ARS). Hard Winter Wheat Genetics Research Unit. Dept. of Agronomy
  12. Univ. of Dundee (United Kingdom). The James Hutton Inst. Division of Plant Sciences

Next-generation whole-genome shotgun assemblies of complex genomes are highly useful, but fail to link nearby sequence contigs with each other or provide a linear order of contigs along individual chromosomes. Here, we introduce a strategy based on sequencing progeny of a segregating population that allows de novo production of a genetically anchored linear assembly of the gene space of an organism. We demonstrate the power of the approach by reconstructing the chromosomal organization of the gene space of barley, a large, complex and highly repetitive 5.1 Gb genome. We evaluate the robustness of the new assembly by comparison to a recently released physical and genetic framework of the barley genome, and to various genetically ordered sequence-based genotypic datasets. The method is independent of the need for any prior sequence resources, and will enable rapid and cost-efficient establishment of powerful genomic information for many species.

Research Organization:
Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Biological and Environmental Research (BER). Earth and Environmental Systems Science Division
Grant/Contract Number:
AC02-05CH11231
OSTI ID:
1625934
Journal Information:
The Plant Journal, Vol. 76, Issue 4; ISSN 0960-7412
Publisher:
Society for Experimental BiologyCopyright Statement
Country of Publication:
United States
Language:
English

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