Entering edit mode
8.5 years ago
Cacau
▴
520
I am wondering how the removal of adaptor sequences will impact the transcriptome assembly. For example, in 10% of my reads contain adaptors which are not removed. If I try to assemble the transcriptome, will some of my unigene dataset contain adaptors? Besides, will the result be different if I use a genome-guided or de novo asssembly method?
I've experienced such a catastrophic event. On the other hand you might get cool chimeric proteins.
Reminds me of this blog post: http://www.opiniomics.org/we-need-to-stop-making-this-simple-fcking-mistake/