Sequence output of high throughput sequencing experiments.
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https://figshare.com/articles/dataset/_Sequence_output_of_high_throughput_sequencing_experiments_/444087
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资源简介：
1Source was BAC DNA encoding the AD169 or Toledo genome, or urine samples collected from neonates (<2 weeks from birth) with congenital HCMV infections.
2Depth is the average number of reads that cover each position of the genome.
3Coverage is expressed as percentage of the genome for which sequence data was generated. For AD169 and Toledo resequencing, the published sequence was used to calculate coverage. For clinical material sequencing, the coverage is estimated by using the Merlin strain reference genome.
创建时间：
2011-05-19
