I am trying to see if I can find possible RNA editing at genome level. Is there a reference protocol how to prepare sample for sequencing. Can I just follow the protocol of RNA- seq?
How much coverage may be optimal? Finally is there any tool available which can help me to analyze the aligned data. I know I can use Sam tool but looking for any commercial software.
Thanks for your help
How much coverage may be optimal? Finally is there any tool available which can help me to analyze the aligned data. I know I can use Sam tool but looking for any commercial software.
Thanks for your help
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