Hello,
I have 4 samples of RNA-seq library made with scriptseq kit.
Bioanalyzer shows that for one sample the peak size is about 30 bp smaller than others and the size distribution is overall shifted too.
(270 bp for this one and 300 bp for others)
Would this make a huge problem when I analyze the final result?
Or all 4 libraries should be made again?
I have 4 samples of RNA-seq library made with scriptseq kit.
Bioanalyzer shows that for one sample the peak size is about 30 bp smaller than others and the size distribution is overall shifted too.
(270 bp for this one and 300 bp for others)
Would this make a huge problem when I analyze the final result?
Or all 4 libraries should be made again?
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