Closed sdwien closed 5 years ago
@sdwien In the example, U>T conversiont was carried out before nanofilt, so converted fastqs were mapped with minimap2. And yes, a reference transcriptome should be used. Otherwise, a reference genome will also wokr if alternative splicing is 'very' rare.
In the example command for minimap2, you use the output of NanoFilt instead of the U>T converted fastq, is that correct? Also, I assume you use a transcriptome fasta as input for minimap2, right? Thank you, best, Sophia