Entering edit mode
5.2 years ago
panacotaforcota
•
0
Hello!
I try to use Stringtie to generate read coverage tables for prepDE.py. So, I do
./stringtie-2.0.3/stringtie file_sorted.bam -B -e -G merged.gtf > file.gtf
Is it correct that this command return gtf file or not?
Then I do
./prepDE.py -i file.gtf -g ./gene.counts.csv -t ./transc.counts.csv
and get it
Error: Text file with sample ID and path invalid (19 StringTie transcript 3033990 3034589 1000 . . gene_id "MSTRG.1"; transcript_id "MSTRG.1.1"; cov "3.420559"; FPKM "69.257027"; TPM "153.416428";)
Why?
I don't know by heart what stringtie writes to the stdout. I'd rather use the output option for the GTF than writing all output to a file.
The error message shows a line without strand information (+ or -). I'd check where that got lost.
Not helping with this problem but do you really need
stringtie
? If you work with well-annotated transcriptomes there is rarely a reason to assemble the transcriptome. THere are other tools to conveniently get a count matrix for DEG likefeatureCounts
or quantifiers such assalmon
orkallisto
that you might want to check out.Also, please use the code option to hightlight code and error messages. I did it for you this time.