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. 2021 Apr 8;19(9):1725–1742. doi: 10.1111/pbi.13586

Figure 1.

Figure 1

Landscape of the safflower genome and expression data. (a) Pseudochromosomes identified using Hi‐C. (b) The genetic linkage map from 248 simple sequence repeats (SSR). (c–h) The distribution of the SSR density, GC density, gene density, long terminal repeat retrotransposons density, long noncoding RNA density and differential alternative splicing events. (i–k) Expression of genes in different tissues. (i) Seeds at 0 days after flowering (DAF), 10 DAF and 20 DAF. (j) Flowers at initial flowering stage, middle bud stage, initial flowering stage, peak flowering stage and decayed flowering stage. (k) Cotyledons at 1 day after germination (DAG), 3 DAG, 5 DAG, 7 DAG and 10 DAG. (l) Syntenic blocks. The band width is proportional to the syntenic block size.