Entering edit mode
12.0 years ago
Dan D
7.4k
We have an Illumina HiSeq2000 paired-end 100 run that had a clog, so the data for all lanes are junk after ~cycle 160. We would like to demultiplex the good data we have, but I've never demultiplexed a partial flowcell and the user's guide doesn't go into detail about how to perform such an operation. Has anyone done this before?
were the barcodes sequenced properly?
Yes, the data were beautiful until the clog. Thanks, and good question!