Simao F.A., Waterhouse R.M., Ioannidis P., Kriventseva E.V., Zdobnov E.M. Hoff K.J., Lange S., Lomsadze A., Borodovsky M., Stanke M. Quevillon E., Silventoinen V., Pillai S., et al.Â, Llorens C., Futami R., Covelli L., et al.Â, Tatusov R.L., Fedorova N.D., Jackson J.D., et al.Â, Kurtz S., Phillippy A., Delcher A.L., et al.Â. Genome sizes of bacteriophages and viruses range from about 2 kb to over 1 Mb. 3 released the first rose genome sequence from the wild and heterozygous Rosa multiflora.It was still a genome in pieces (low N50 and 83,189 scaffolds, Table Table1). The training set for R. multiflora was constructed by BRAKER1,35 and used for gene prediction by Augustus 184.108.40.206 As a result, we predicted 178,512 genes on the genome sequence. 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1, a rose aquaporin gene, is involved in ethylene-regulated petal expansion, Cell wall extensibility and effect of cell-wall-loosening proteins during rose flower opening, Isolation of Rh-TIP1; 1, an aquaporin gene and its expression in rose flowers in response to ethylene and water deficit, RhNAC2 and RhEXPA4 are involved in the regulation of dehydration tolerance during the expansion of rose petals, Involvement of rose aquaporin RhPIP1; 1 in ethylene-regulated petal expansion through interaction with RhPIP2; 1, Evolution of Rosaceae fruit types based on nuclear phylogeny in the context of geological times and genome duplication, Filling gaps with construction of a genetic linkage map in tetraploid roses, Genetic linkage maps of rose constructed with new microsatellite markers and locating QTL controlling flowering traits, Microsatellite marker development in rose and its application in tetraploid mapping. However, the R. multiflora MASAKO C1 (Rmu_sc0003469.1_g000007.1) have an intact open reading frame without a frame shift or transposon insertion.