Hello,
in some of my prepared sequencing libraries I observe multiple peaks in the bioanalyzer run after library pcr (see attached file). Many of the peaks have an average distance of arround 60 bp. Are these adaptor concatameres or something like this?
Is there any way to avoid these peaks?
I know the peak at 126 bp are adaptor dimers... But this is a different story.
Best Harry
in some of my prepared sequencing libraries I observe multiple peaks in the bioanalyzer run after library pcr (see attached file). Many of the peaks have an average distance of arround 60 bp. Are these adaptor concatameres or something like this?
Is there any way to avoid these peaks?
I know the peak at 126 bp are adaptor dimers... But this is a different story.
Best Harry
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