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. 2018 May 9;557(7705):424–428. doi: 10.1038/s41586-018-0108-0

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© Macmillan Publishers Ltd., part of Springer Nature 2018

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Extended Data Fig. 1 — a, Schematic workflow for genome sequencing, assembly and chromosomal assignment with a high-density SNP map. b, Statistics of sequencing data. *Calculated from the estimated genome size of 4.94 Gb. LIS, library insert size; ARL, average read length; RD, raw data; UD, usable data; ED, effective depth. c, Summary of the Tu genome assembly. *Contig: contiguous sequence without Ns assembled with Illumina reads, corrected by PacBio reads. ^#Scaffold: Sequence with Ns, in which two or more contigs were connected by mate-pair reads, BioNano genome maps and 10× Genomics linked reads. d, High-resolution genetic map of T. urartu using SNP markers. The SNP markers were identified from an F2 population (475 individuals) derived from a cross between accessions G1812 and G3146 of Tu. e, Summary of physical length and genetic map of seven pseudomolecules. Chr, chromosome; GLDAccu, genetic linkage distance accumulation; GLDAvg, genetic linkage distance on average; PDPCM, physical distance per centiMorgen (cM).