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When I started REDItoolDnaRna.py on REP NON ALU and NON REP sites using strict criteria to recover RNAseq reads that contained reference mismatches, why were there more RNA editing events generated this time than the first time? #24
When I started REDItoolDnaRna.py on REP NON ALU and NON REP sites using strict criteria to recover RNAseq reads that contained reference mismatches, why were there more RNA editing events generated this time than the first time?
When I started REDItoolDnaRna.py on REP NON ALU and NON REP sites using strict criteria to recover RNAseq reads that contained reference mismatches, why were there more RNA editing events generated this time than the first time?