Hi (i'm new in this forum and new in sequencing analysis, please be patient )
I’m comparing some solexa re-sequence experiment in which different DNA sharing treatment were used.
I there any statistic I can use to compare coverage evenness between sequencing experiments?
I’m comparing some solexa re-sequence experiment in which different DNA sharing treatment were used.
I there any statistic I can use to compare coverage evenness between sequencing experiments?
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