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Old 07-11-2016, 04:03 AM   #1
Location: Sweden

Join Date: Nov 2014
Posts: 18
Default Trinity assembly and qPCR

Hi folks,

I have new RNAseq data assembled with Trinity, and now I am trying to use qPCR for validation. I blasted a gene of interest from another species against the RNAseq data for primer design, but I have got something like this in return.


All of them are best hits and have identical score and E value. They only have tiny gap differences when I aligned them.

May you explain what are diffrences between them and which one I shall use for primer design? I want a primer to amplify both gene of interest and the closest hit from the new RNAseq data.

Thank you very much for your time and help!
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