Fig. 1: Distribution of genomic features in the Ae. tauschii genome.
From: The Aegilops tauschii genome reveals multiple impacts of transposons

Track a, the seven chromosomes. One scale label indicates 10āMb. The black histogram indicates the distribution of two LTR-RTs (Quinta and Cereba); peaks indicate candidate centromere regions. Track b, miRNA. Track c, Gene density indicated by gene length/5āMb. Track d, pseudogene density, indicated by gene length/5āMb. Track e, recombination, measured by cM/Mb with 5āMb bins. Track f, gene expression, calculated as the average reads per kilobase per million mapped readsĀ (rpkm) in 5āMb bins. Maximum rpkm from eight tissues and normalization of rpkm by log10(rpkmā+ā10-6). Track g, methylation, calculated by methylation base counts/C base counts in Mb bins. Only the most abundant CG methylation contexts are presented. Track h, total TE density across chromosomes, TE length/5āMb. Track i, Gypsy. The distribution of Gypsy TE density across chromosomes: Gypsy length/5āMb. Track j, Copia. The distribution of Copia density across chromosomes: Copia length/5āMb. Track k, DNA TEs. The distribution of DNA transposon density across chromosomes: DNA transposon length/5āMb.