An advantage boasted by oxford nanopore is that no PCR is required. However, it is not clear to me how one would target a large genomic region, say 1MB for arguments sake, without a huge PCR at a low number of cycles?
Thinking "nanopore" is new to me so please excuse me if the answer to my questions is elementary.
Cheers,
J
Thinking "nanopore" is new to me so please excuse me if the answer to my questions is elementary.
Cheers,
J
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