I think the second line should read:
On a genome it means that each base has on average been sequenced a number of time.
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how is average sequence depth calculated from number of reads and read length
I understand this concept as equivalent to coverage.
On a genome it means that each base has been sequenced a number of time.
Coverage = (Nb of Reads)*(Read Length) / (Genome Size)
I think the second line should read:
On a genome it means that each base has on average been sequenced a number of time.
Relevant questions are:
@Istvan Albert pointed to the "Coverage" section of "Shotgun sequencing" on Wiki, same as @pasta.
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