I have Illumina PE data from a MiSeq run and am finding large discrepancies in the number of reads recovered while demultiplexing.
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effective mismatches allowed while demultiplexing
Hi all,
What is the minimum/optimum number of mismatches to be allowed during demultiplexing ?? How do we decide this?
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FASTX Toolkit barcode splitter issue
Hello All,
I've been trying to use the FASTX Toolkit barcode splitter to demultiplex my illumina reads. The following command runs okay...