Hello.
I have two human single end RNA seq data generated from Solexa.
Yesterday, I ran fastqc using my data and the program reported that two data have a little amount of duplicated reads.
Should I remove this before processing Tophat?
And is there any programs which can be used for such purpose?
Thanks!!
I have two human single end RNA seq data generated from Solexa.
Yesterday, I ran fastqc using my data and the program reported that two data have a little amount of duplicated reads.
Should I remove this before processing Tophat?
And is there any programs which can be used for such purpose?
Thanks!!
Comment