I have performed PCR validation of an ATAC-seq library targeting known/expected accessible chromatin regions (100bp) but 90% of the products have a smearing banding pattern. Do you perhaps know what could cause this? Could this be inherent to an ATAC-seq library considering that the template is not just one length size but varying lengths?
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Last edited by MzwaneleN; 10-09-2020, 02:12 PM.
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