Sequencing coverage is a counting ratio over a simplified genome track. Exact arithmetic here means exact results for the stated model inputs; measured inputs still carry uncertainty and significant-figure limits.
highlighted = computed this step
Coverage is total read bases over genome bases
Coverage equals read count times read length divided by genome length.
coverage=genome lengthreads⋅read length
The first toy case gives exact coverage
Read count 10 times read length 100 over genome length 1000 gives coverage 1 x.
100010⋅100=1
More reads increase coverage
With read count 20 and the same lengths, coverage becomes 2 x.
100020⋅100=2
Coverage follows read count in exact rows
Read length and genome length stay fixed. Changing the read count changes only the numerator.