Hi! Good Afternoon
I think I'm having some trouble with my sequences. I have an Escherichia coli genome and the sequences have very dissimilar sizes. Should I do something specific during my trial in this case?
It is possible that the sequences are already scanned and trimmed to remove adapters. It is normal to have a size spread in that case.
What is it that you are looking to do downstream? Just align to a reference?
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