In the last two runs/cbot clusterings, we've had an interesting phenomenon. Lanes 1-6 are PE noamp DNA libraries (same pool of 24 samples in each lane), lanes 7 and 8 are 2 separate pools of 24 stranded RNAseq libraries.
Trying to figure out what could be making a difference that affects only no amp libraries only on the top surface. (note: on the cbot this is the surface in contact with the heating element) Any ideas??
Trying to figure out what could be making a difference that affects only no amp libraries only on the top surface. (note: on the cbot this is the surface in contact with the heating element) Any ideas??