Hello,
I have tried running Trinity multiple times now, but I'm always running into an empty output Trinity-GG.fasta file, and I was hoping you could help me out with it.
I downloaded the Trinity Docker image through Singularity on the cluster, and I am using a sorted .bam file for a genome-guided transcriptome assembly. This is the command I used:
module load singularity; singularity exec -e trinityrnaseq_latest.sif Trinity --genome_guided_bam $SCRATCH/reannot/merged_aligned_reads.bam --genome_guided_max_intron 50000 --jaccard_clip --output $SCRATCH/reannot/trinity_GG --max_memory 15G --CPU 4 --SS_lib_type RF
The log file is too big to attach, but it seems to be giving no obvious error messages for the inputs, so I'm not sure what the issue is.
Thanks so much!
Best,
Meera