Hello. I want to run around 50 samples on a HiSeq lane. I have done this on MiSeq with success and am just scaling up. With the MiSeq I ran 11 samples with 11 barcodes as that's all I was given (they are custom primers). So now I need more barcodes (6 nucleotides). I'm sure I could generate a load of random barcodes but I want to make sure they don't cause havoc. Is there a best practise for barcode generation in this situation?
Are you familiar with dual-indexing?
No. But I guess what I'm asking is whether I can use a load of made up barcodes for single indexing or how I minimise confusion between barcodes when sequencing