Closed sternp closed 2 years ago
Hi,
Your issue is caused by assigning fragmented or conventional RNA-Seq data to tex-notex_libs. Since you are using "fragment", you should assign your wig files to --frag_libs not --tex-notex_libs.
Best, Sung-Huan
WIG_FOLDER="ANNOgesic/input/wigs/fragment"
LIBS="$WIG_FOLDER/rev2.wig:notex:1:a:- $WIG_FOLDER/fwd2.wig:notex:1:a:+"
#Run TSS
singularity exec -B /lustre/work-lustre/microbiome/users/sternesp/annogesic/ANNOgesic annogesic.img \
annogesic \
tss_ps \
--fasta_files MGYG-HGUT-00001.fna \
--annotation_files GUT_GENOME000001.gff \
--project_path ANNOgesic \
--program TSS \
--tex_notex_libs $LIBS \
--condition_names fileName \
--replicate_tex all_1
Error: The --tex_notex_libs was assinged incorrectly. Please check it again.
I still get the same error unfortunately.
I should also mention that I'm using the Docker version and that --tex_notex_libs is an essential parameter as there is no --frag_libs option
Sorry, my bad. I didn't notice you are running TSS prediction. For TSS and processing site prediction, dRNA-seq are needed. Thus, the conventional RNA-seq is not acceptable for TSS prediction currently. We are still developing new feature for using conventional RNA-seq to detect TSSs. But you still can use --frag-lib for other predictions. If you want to detect sRNA for example, you can do so without assigning TSS information.
Ah yes. I see now. Thanks for the clarification.
Since I don't have dRNA-seq data, which parts of the analysis can I complete without TSS prediction. I'm interested in array of features such as sRNA, sORF, riboswitches, UTRs, CRISPRs and operons
I think you can do all of them, otherwise, the error message will let you know. But, of course, having TSS information can get more accurate results.
Hi,
I'm trying to execute the command shown below however I keep getting the following error:
Command:
Example wiggle file:
I've been scratching my head about what the issue is. Can you please help?
Thanks!.