Hi,
I am new to RNA-seq library preparation. I made some libraries with NuGEN Ovation RNA-seq kit for Arabidopsis. The library was made with rice leaf RNA. The bioanalyzer trace of the final library show a split peak (rather than a smooth, bell shaped one generally seen). Is it usable for sequencing? If you guys have any suggestions for improvement for me, I will appreciate that. The trace is attached.
Thank you
IKay
I am new to RNA-seq library preparation. I made some libraries with NuGEN Ovation RNA-seq kit for Arabidopsis. The library was made with rice leaf RNA. The bioanalyzer trace of the final library show a split peak (rather than a smooth, bell shaped one generally seen). Is it usable for sequencing? If you guys have any suggestions for improvement for me, I will appreciate that. The trace is attached.
Thank you
IKay
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