Closed Cristinex closed 6 months ago
Please specify your bam file using option "-bam"
Here was my command.
liqa -task quantify -refgene <path>/xx.refgene -bam <path>/yy.bam -out <path>/output -max_distance 20 -f_weight 1
And I did not add any suffix for output since I did not know what format should be.
I did specified my bam file with -bam. Thank you for your reply!!!
Please use "ls -l
Thank you!! It work after indexing.
Another question, is it possible to use LIQA for hpv genome annotation? Since I downloaded hpv's gtf from https://www.ncbi.nlm.nih.gov/assembly/GCF_000863945.3/ and executed -task refgene. It turned out that 0 genes were processed. Was there any problem for this .gtf to be process?
Hi yes, I did the same and I was able to output processed genes. Perhaps as done above, sort/index the BAM before LIQA, and ensure you have the latest version of LIQA as you run the quantify task again.
This step also usually only outputs genes with 2 or more isoforms, which is why you may be running into this issue
It turned out to be error: .bam does not exist!
I run the command and the bam file in the same folder, it cannot find it. How to solve this problem?
Thank you!