Skip to content
New issue

Have a question about this project? Sign up for a free GitHub account to open an issue and contact its maintainers and the community.

By clicking “Sign up for GitHub”, you agree to our terms of service and privacy statement. We’ll occasionally send you account related emails.

Already on GitHub? Sign in to your account

Error: Error while loading sequence perl filter_gff3.pl file.gff3 file.list > new.gff3 #506

Open
huaixiaolu opened this issue Sep 20, 2024 · 1 comment

Comments

@huaixiaolu
Copy link

Hello, thank you for providing such a useful tool. I installed EDTA using conda, and when running the test data, I encountered the following ERROR:

mamba create -n EDTA conda activate EDTA mamba install -c conda-forge -c bioconda edta cd ~/anaconda3/envs/mamba/envs/EDTA/share/EDTA/test EDTA.pl --genome genome.fa --cds genome.cds.fa --curatedlib ../database/rice6.9.5.liban --exclude genome.exclude.bed --overwrite 1 --sensitive 1 --anno 1 --threads 10

########################################################

Extensive de-novo TE Annotator (EDTA) v2.1.0
Shujun Ou ([email protected])

########################################################
Fri Sep 20 17:25:07 CST 2024 Dependency checking:
All passed!
A custom library ../database/rice6.9.5.liban is provided via --curatedlib. Please make sure this is a manually curated library but not machine generated.
A CDS file genome.cds.fa is provided via --cds. Please make sure this is the DNA sequence of coding regions only.
A BED file is provided via --exclude. Regions specified by this file will be excluded from TE annotation and masking.
Fri Sep 20 17:25:09 CST 2024 Obtain raw TE libraries using various structure-based programs:
Fri Sep 20 17:25:09 CST 2024 EDTA_raw: Check dependencies, prepare working directories.
Fri Sep 20 17:25:10 CST 2024 Start to find LTR candidates.
Fri Sep 20 17:25:10 CST 2024 Identify LTR retrotransposon candidates from scratch.
Invalid value for shared scalar at /home/DataDisk/zl_data/anaconda3/envs/mamba/envs/EDTA/share/LTR_retriever/bin/LTR.identifier.pl line 114, line 11.
cp: cannot stat 'genome.fa.mod.retriever.scn.adj': No such file or directory
awk: fatal: cannot open file `genome.fa.mod.pass.list' for reading: No such file or directory
Warning: LOC list - is empty.
Error: Error while loading sequence
perl filter_gff3.pl file.gff3 file.list > new.gff3
Fri Sep 20 17:25:19 CST 2024 Warning: The LTR result file has 0 bp!
Fri Sep 20 17:25:19 CST 2024 Start to find TIR candidates.
Fri Sep 20 17:25:19 CST 2024 Identify TIR candidates from scratch.
Species: others
Fri Sep 20 17:25:29 CST 2024 Finish finding TIR candidates.
Fri Sep 20 17:25:29 CST 2024 Start to find Helitron candidates.
Fri Sep 20 17:25:29 CST 2024 Identify Helitron candidates from scratch.
Fri Sep 20 17:25:59 CST 2024 Finish finding Helitron candidates.
Fri Sep 20 17:25:59 CST 2024 Execution of EDTA_raw.pl is finished!
ERROR: Raw LTR results not found in genome.fa.mod.EDTA.raw/genome.fa.mod.LTR.raw.fa
If you believe the program is working properly, this may be caused by the lack of intact LTRs in your genome. Consider to use the --force 1 parameter to overwrite this check

After running the software, no results were generated. I found that adding the parameter --force 1 still resulted in the ERROR, but it did produce some results.

EDTA.pl --genome genome.fa --cds genome.cds.fa --curatedlib ../database/rice6.9.5.liban --exclude genome.exclude.bed --overwrite 1 --sensitive 1 --anno 1 --threads 10 --force 1

image

I don't know how to resolve this issue, but I feel that it is affecting the results. How can I solve it?

@oushujun
Copy link
Owner

oushujun commented Sep 28, 2024 via email

Sign up for free to join this conversation on GitHub. Already have an account? Sign in to comment
Labels
None yet
Projects
None yet
Development

No branches or pull requests

2 participants