Hi
I'm planning to sequence some normalised cDNA libraries for transcriptome discovery. Can someone please explain whether there is any discernable difference between using the Illumina DSN protocol vs the Evrogen DSN protocol? Capturing all polyA
+ mRNAs, in full length, is important.
More generally, I've heard that any kind of enzyme-based normalisation results in drop out of small polyA+ transcripts. Does anyone have experience of this, or the contrary, or know of any techniques to mitigate it?
Thanks!
Anar
I'm planning to sequence some normalised cDNA libraries for transcriptome discovery. Can someone please explain whether there is any discernable difference between using the Illumina DSN protocol vs the Evrogen DSN protocol? Capturing all polyA
+ mRNAs, in full length, is important.
More generally, I've heard that any kind of enzyme-based normalisation results in drop out of small polyA+ transcripts. Does anyone have experience of this, or the contrary, or know of any techniques to mitigate it?
Thanks!
Anar
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