Hi All,
We have recently done a 454 GS junior run of a rapid library build of some low-copy number aDNA and had an overwhelming number of reads appearing to be dimerisation of our y-adapters. Has anyone else experienced this?
Thanks
We have recently done a 454 GS junior run of a rapid library build of some low-copy number aDNA and had an overwhelming number of reads appearing to be dimerisation of our y-adapters. Has anyone else experienced this?
Thanks
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