Hi,
How to calculate coverage for Illumina Genome Analyzer sequencing data?
Wikipedia says: It can be calculated from the length of the original genome (G), the number of reads(N), and the average read length(L) as NL / G.
The question is how to get N?
Kind regards
Maria
How to calculate coverage for Illumina Genome Analyzer sequencing data?
Wikipedia says: It can be calculated from the length of the original genome (G), the number of reads(N), and the average read length(L) as NL / G.
The question is how to get N?
Kind regards
Maria
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