Additional file 1 of Towards reliable whole genome sequencing for outbreak preparedness and response

Additional file 1: Figure S1. Overview of variants across the genomes before cleanup of read mapping. The x axis shows the variants found across the 4 genomes. The color scale represents the fraction of mapped reads containing the indicated variant in the read alignment. A darkgrey tile color indicates coverage below the coverage threshold (5x Illumina, 100x Nanopore). Figure S2. Overview of true variants across the genomes. The x axis shows the variants found across the 4 genomes. The color scale represents the fraction of mapped reads containing the indicated variant in the read alignment. A darkgrey tile color indicates coverage below the coverage threshold (5x Illumina, 100x Nanopore).

附加文件1：图S1。读段比对清理前全基因组变异概览。横轴展示4个基因组中鉴定到的变异位点，色阶代表读段比对中携带目标变异的比对读段占比，深灰色色块代表测序覆盖度低于阈值（Illumina平台为5倍，Nanopore平台为100倍）。
附加文件1：图S2。全基因组真实变异位点概览。横轴展示4个基因组中鉴定到的变异位点，色阶代表读段比对中携带目标变异的比对读段占比，深灰色色块代表测序覆盖度低于阈值（Illumina平台为5倍，Nanopore平台为100倍）。