Table 3.
Sequencing and mapping statistics.
Sample name | Number of mapped unique reads | % mapped reads | % genome covered* by unique reads | Average coverage by unique reads |
---|---|---|---|---|
BY2961 | 11,155,487 | 96.13 | 94.97 | 87.9× |
EMS1 | 5,406,681 | 96.94 | 94.81 | 42.2× |
EMS2 | 6,240,554 | 97.26 | 94.85 | 48.7× |
EMS3 | 5,275,583 | 98.12 | 94.81 | 41.2× |
EMS4 | 4,502,271 | 97.17 | 94.80 | 35.2× |
EMS5 | 4,113,345 | 96.27 | 94.83 | 32.1× |
Mutator 1 | 9,612,541 | 93.93 | 94.90 | 75.8× |
Mutator 2 | 5,111,531 | 92.39 | 94.79 | 39.9× |
Mutator 3 | 5,649,822 | 96.11 | 94.95 | 44.1× |
Mutator 4 | 4,226,405 | 98.79 | 94.85 | 33.0× |
Mutator 5 | 9,855,938 | 97.36 | 95.10 | 77.6× |
*Coverage is defined as the percentage of bases in the genome that have at least 1 uniquely mapped read at that position.