I am interested in finding noncoding RNAs, particularly small RNAs from Illumina or SOLiD sequencing data prepared with RNASeq protocol.
Apart from intersecting my mapped reads with mirBASE or other annotated small RNAs, what could I use for detecting noncoding RNAs from from RNASeq data?
I know that we could just do a small RNA prep but I'm sure there are people who have attempted this sort of approach before to maximize what they get out of their RNASeq.
Apart from intersecting my mapped reads with mirBASE or other annotated small RNAs, what could I use for detecting noncoding RNAs from from RNASeq data?
I know that we could just do a small RNA prep but I'm sure there are people who have attempted this sort of approach before to maximize what they get out of their RNASeq.
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