Hi
We are running a genomic library on a multiplexed miseq but we have space left for another library and were wondering if it is technically feasible to fill the space with a cDNA library?
I figure that the nucleic content is equivalent but the read structure may bias the samples? but I hope not.
Thanks
We are running a genomic library on a multiplexed miseq but we have space left for another library and were wondering if it is technically feasible to fill the space with a cDNA library?
I figure that the nucleic content is equivalent but the read structure may bias the samples? but I hope not.
Thanks
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