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7.4 years ago
philgev2
▴
10
Hi
Which is the most correct way to calculate Transcripts read count for differential transcript expression?
I have come across using RSEM software with bam file containing transcript coordinates.
Also using script prepDE.py provided by StringTie assembler that use bam file with genomic coordinates.
Can I opt any one of these option? Or should I use any other option?
Thanks Philge Philip