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9.5 years ago
zm20074970
•
0
Hello everyone
I am analyzing small RNA data currently, but there are some questions about Rfam and mirdeep result? could someone give me some advice, thanks!
- I use bowtie to map my reads to Rfam data to annotate the other ncRNA except miRNA, but the Rfam data including ncRNA from many species, I don't know just map my reads to the whole Rfam database or just the data of the species I study?
- I use mirdeep2 to predict the novel miRNA of each sample, but I want to do the differential expression of novel miRNA between different samples, but the name of novel miRNA given by mirdeep are really different, I don't know how to deal with it.
Thank you for your reply, I found that there were about 1/3 same novel precursors between two samples in my data by using bedtools, but it's difficult to compare more than 2 samples
I am very glad that you are in Newcastle, I graduated from Newcastle University O(∩_∩)O~~
I am also facing the same issues. Can you please tell me how to do this using bedtools?