Hello there
I've made 2 new libraries out of totalRNA, with the Illumina tru-seq kit and manual.
I've tested them both on the Bioanalyzer.
The ladder seems to be good and the main peak is ok but I don't know why I have all those little peaks in the range between 100-400 bp.
Does anyone know why?
I thought that maybe they could be adapter-dimers, but why do they run higher than 150bp?
thanks
I've made 2 new libraries out of totalRNA, with the Illumina tru-seq kit and manual.
I've tested them both on the Bioanalyzer.
The ladder seems to be good and the main peak is ok but I don't know why I have all those little peaks in the range between 100-400 bp.
Does anyone know why?
I thought that maybe they could be adapter-dimers, but why do they run higher than 150bp?
thanks