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I am now following the tutorial for single cell, RNA seq, somatic mutation calling.
I am wondering if the input fastq file had to be spliced (spicing introns) in advance of the workflow?
Otherwise, does CTAT automatically remove intron part for analysis?
Thank you.
The text was updated successfully, but these errors were encountered:
Hello,
I am now following the tutorial for single cell, RNA seq, somatic mutation calling.
I am wondering if the input fastq file had to be spliced (spicing introns) in advance of the workflow?
Otherwise, does CTAT automatically remove intron part for analysis?
Thank you.
The text was updated successfully, but these errors were encountered: