DNA library prep for MiSeq NGS platform
Our experience is that the library yield is affected by the quality of the input DNA (presence of contaminants, etc) as much as by the concentration.
I am struggling with it as well. No matter I do, regardless additional purification steps with beads or columns, the yield is too low
I am working with DNA from fecal samples, thus, the purity of DNA might be an issue
Just tried to increase the number of cycles for the indexing step and got perfect results: try to go to 15 cycles instead of 12
Good luck!)
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