Hi... I did a RNAseq to small RNAs (18-30nt). But the last (27-30) bases are with bad quality. Should I to cut that reads or not? I trimmed the last reads to obtain 18-25 reads and analized with this approuch but I dont know this is correct.
Question: Problem with bad quality bases in RNAseq
4.6 years ago by
silas008 • 100
silas008 • 100 wrote:
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