Hi there!
After a miseq Nextera XT run we got a lot of undetermined data (undeterminedbarcode sequences with one mismatch or more). We wouldn't like to throw away so much data , and looking for a possibility to demultiplex sequences with one or more mismatch in the barcode.
Does CLC genomics workbench have this function? there is an option to process tagged sequences, but can the mismatched barcodes be processed?
Thank you for any answers!
After a miseq Nextera XT run we got a lot of undetermined data (undeterminedbarcode sequences with one mismatch or more). We wouldn't like to throw away so much data , and looking for a possibility to demultiplex sequences with one or more mismatch in the barcode.
Does CLC genomics workbench have this function? there is an option to process tagged sequences, but can the mismatched barcodes be processed?
Thank you for any answers!
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