Dear All,
I have just received some RNA Seq data and I noticed that not all reads are at the size I expected: (75bp)
only 64 % are at the correct size,
what should I do? Should I remove all reads below 75?
It is a library selection problem?
Many thanks,
Paolo
I have just received some RNA Seq data and I noticed that not all reads are at the size I expected: (75bp)
only 64 % are at the correct size,
what should I do? Should I remove all reads below 75?
It is a library selection problem?
Many thanks,
Paolo
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