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Wu, Huiyun
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70
@wu-huiyun-5271
Last seen 10.3 years ago
Dear users,
I have a question about miRNA differential profiling between two
groups. Someone suggested a further filtering of other small RNAs such
as mRNA degradation, etc with lengths similar to miRNA after BAM file
(which pre-filtering out longer or shorter ones) read-in. I was
wondering what consequences would be if I do NOT conduct this process.
In this situation, a miRNA count table contains those contaminated
non-coding small RNAs and those small RNAs are brought into DE
analysis. My intuitive understanding is that it should be fine as long
as the miRNA IDs (say, Entrez IDs)are not shared by other small RNAs
during alignment or annotation.
thanks in advance.
sincerely,
William Wu
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