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Error: Error while loading sequence perl filter_gff3.pl file.gff3 file.list > new.gff3 #506
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It’s a known issue and resolved. Please search on other issues. Reinstall
LTR_retriever will work.
Shujun
…On Fri, Sep 20, 2024 at 6:36 AM huaixiaolu ***@***.***> wrote:
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 (
***@***.***)
########################################################
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.png (view on web)
<https://github.com/user-attachments/assets/b1d5aec9-cb6d-4ba9-9cc6-1800f894b31a>
I don't know how to resolve this issue, but I feel that it is affecting
the results. How can I solve it?
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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
I don't know how to resolve this issue, but I feel that it is affecting the results. How can I solve it?
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