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Barley whole exome capture: a tool for genomic research in the genus Hordeum and beyond
Authors:Martin Mascher  Todd A Richmond  Daniel J Gerhardt  Axel Himmelbach  Leah Clissold  Dharanya Sampath  Sarah Ayling  Burkhard Steuernagel  Matthias Pfeifer  Mark D'Ascenzo  Eduard D Akhunov  Pete E Hedley  Ana M Gonzales  Peter L Morrell  Benjamin Kilian  Frank R Blattner  Uwe Scholz  Klaus FX Mayer  Andrew J Flavell  Gary J Muehlbauer  Robbie Waugh  Jeffrey A Jeddeloh  Nils Stein
Institution:1. Leibniz Institute of Plant Genetics and Crop Plant Research (IPK), , D‐06466 Stadt Seeland (OT) Gatersleben, Germany;2. Roche NimbleGen, Inc., , Madison, WI, 53719 USA;3. The Genome Analysis Centre, Norwich Research Park, , Norwich, NR4 7UH UK;4. MIPS/IBIS, Helmholtz Zentrum München, , D‐85764 Neuherberg, Germany;5. Department of Plant Pathology, Kansas State University, , Manhattan, KS, 66506 USA;6. The James Hutton Institute, , Dundee, DD2 5DA UK;7. Department of Agronomy and Plant Genetics, University of Minnesota, , St. Paul, MN, 55108 USA;8. University of Dundee at JHI, , Dundee, DD2 5DA UK;9. Department of Plant Biology, University of Minnesota, , St. Paul, MN, 55108 USA
Abstract:Advanced resources for genome‐assisted research in barley (Hordeum vulgare) including a whole‐genome shotgun assembly and an integrated physical map have recently become available. These have made possible studies that aim to assess genetic diversity or to isolate single genes by whole‐genome resequencing and in silico variant detection. However such an approach remains expensive given the 5 Gb size of the barley genome. Targeted sequencing of the mRNA‐coding exome reduces barley genomic complexity more than 50‐fold, thus dramatically reducing this heavy sequencing and analysis load. We have developed and employed an in‐solution hybridization‐based sequence capture platform to selectively enrich for a 61.6 megabase coding sequence target that includes predicted genes from the genome assembly of the cultivar Morex as well as publicly available full‐length cDNAs and de novo assembled RNA‐Seq consensus sequence contigs. The platform provides a highly specific capture with substantial and reproducible enrichment of targeted exons, both for cultivated barley and related species. We show that this exome capture platform provides a clear path towards a broader and deeper understanding of the natural variation residing in the mRNA‐coding part of the barley genome and will thus constitute a valuable resource for applications such as mapping‐by‐sequencing and genetic diversity analyzes.
Keywords:barley  genomics  genetic diversity     Hordeum bulbosum        Hordeum pubiflorum        Hordeum vulgare     targeted resequencing  Triticeae
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