-
Notifications
You must be signed in to change notification settings - Fork 77
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
'调用失败' #458
Comments
Hello,
Please test with test data. You will need to reinstall EDTA if it doesn’t
work on the test data.
Shujun
…On Mon, Apr 29, 2024 at 5:01 AM Xxi-GitHub ***@***.***> wrote:
$ perl ../EDTA.pl --genome genome.fa --cds genome.cds.fa --curatedlib
../database/rice7.0.0.liban --exclude genome.exclude.bed --overwrite 1
--sensitive 1 --anno 1 --evaluate 1 --threads 10 > EDTA.test
2024年 04月 29日 星期一 16:53:03 CST EDTA_raw: Check dependencies, prepare
working directories.
2024年 04月 29日 星期一 16:53:04 CST Start to find LTR candidates.
2024年 04月 29日 星期一 16:53:04 CST Identify LTR retrotransposon candidates
from scratch.
Invalid value for shared scalar at
/home/xionglab250/mambaforge/envs/EDTA/share/LTR_retriever/bin/
LTR.identifier.pl line 114, line 11.
cp: 对 'genome.fa.mod.retriever.scn.adj' 调用 stat 失败: 没有那个文件或目录
awk: 致命错误:无法打开文件“genome.fa.mod.pass.list”进行读取:没有那个文件或目录
Warning: LOC list - is empty.
Error: Error while loading sequence
Filter sequence based on TEsorter classifications. Unclassified sequences
will also be output to the clean file.
Usage: perl cleanup_misclas.pl sequence.fa.rexdb.cls.tsv
Author: Shujun Ou ***@***.***) 10/11/2019
mv: 对 'genome.fa.mod.LTR.intact.fa.ori.dusted.cln.cln' 调用 stat 失败:
没有那个文件或目录
mv: 对 'genome.fa.mod.LTR.intact.fa.ori.dusted.cln.cln.list' 调用 stat 失败:
没有那个文件或目录
cp: 对 'genome.fa.mod.LTR.intact.raw.fa.anno.list' 调用 stat 失败: 没有那个文件或目录
ERROR: No such file or directory at
/home/xionglab250/mambaforge/envs/EDTA/share/EDTA/util/output_by_list.pl
line 39.
perl filter_gff3.pl file.gff3 file.list > new.gff3
2024年 04月 29日 星期一 16:53:10 CST Warning: The LTR result file has 0 bp!
2024年 04月 29日 星期一 16:53:10 CST Start to find SINE candidates.
2024年 04月 29日 星期一 16:53:38 CST Warning: The SINE result file has 0 bp!
2024年 04月 29日 星期一 16:53:38 CST Start to find LINE candidates.
2024年 04月 29日 星期一 16:53:38 CST Identify LINE retrotransposon candidates
from scratch.
2024年 04月 29日 星期一 16:54:38 CST Warning: The LINE result file has 0 bp!
2024年 04月 29日 星期一 16:54:38 CST Start to find TIR candidates.
2024年 04月 29日 星期一 16:54:38 CST Identify TIR candidates from scratch.
Species: others
2024年 04月 29日 星期一 16:55:02 CST Finish finding TIR candidates.
2024年 04月 29日 星期一 16:55:02 CST Start to find Helitron candidates.
2024年 04月 29日 星期一 16:55:02 CST Identify Helitron candidates from scratch.
2024年 04月 29日 星期一 16:55:22 CST Finish finding Helitron candidates.
2024年 04月 29日 星期一 16:55:22 CST 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 and
genome.fa.mod.EDTA.raw/genome.fa.mod.LTR.intact.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
###############################################
Is it work in testdata?Shown lack of LTR,and we got the same error for
another species.
Thanks !
—
Reply to this email directly, view it on GitHub
<#458>, or unsubscribe
<https://github.com/notifications/unsubscribe-auth/ABNX4NC4G5XUBI7WRAWFMLTY7YD7FAVCNFSM6AAAAABG55IOAOVHI2DSMVQWIX3LMV43ASLTON2WKOZSGI3DQNBYG42TAOI>
.
You are receiving this because you are subscribed to this thread.Message
ID: ***@***.***>
|
$ perl ../EDTA.pl --genome genome.fa --cds genome.cds.fa --curatedlib ../database/rice7.0.0.liban --exclude genome.exclude.bed --overwrite 1 --sensitive 1 --anno 1 --evaluate 1 --threads 40 > EDTA.test 2024年 04月 30日 星期二 00:49:46 CST Start to find LTR candidates. 2024年 04月 30日 星期二 00:49:46 CST Identify LTR retrotransposon candidates from scratch. Warning: LOC list genome.fa.mod.ltrTE.veryfalse is empty. 2024年 04月 30日 星期二 00:49:59 CST Start to find SINE candidates. 2024年 04月 30日 星期二 00:50:34 CST Warning: The SINE result file has 0 bp! 2024年 04月 30日 星期二 00:50:34 CST Start to find LINE candidates. 2024年 04月 30日 星期二 00:50:34 CST Identify LINE retrotransposon candidates from scratch. cp: 无法获取'genome.fa.mod.RM2.raw.fa' 的文件状态(stat): 没有那个文件或目录 2024年 04月 30日 星期二 00:50:34 CST Start to find TIR candidates. 2024年 04月 30日 星期二 00:50:34 CST Identify TIR candidates from scratch. Species: others Error: Error while loading sequence mv: 无法获取'genome.fa.mod.TIR.ext30.fa.pass.fa.dusted.cln.cln' 的文件状态(stat): 没有那个文件或目录 2024年 04月 30日 星期二 00:50:36 CST Start to find Helitron candidates. 2024年 04月 30日 星期二 00:50:36 CST Identify Helitron candidates from scratch. 2024年 04月 30日 星期二 00:51:01 CST Finish finding Helitron candidates. 2024年 04月 30日 星期二 00:51:01 CST Execution of EDTA_raw.pl is finished! ERROR: Raw TIR results not found in genome.fa.mod.EDTA.raw/genome.fa.mod.TIR.intact.raw.fa |
You need to provide the environment settings and your list of installed packages otherwise its hard to help |
Thanks for your help!We have uploaded the conda env package list to github issue, did it lack any package?Or we can try another way to install?Thanks!
…------------------ 原始邮件 ------------------
发件人: "oushujun/EDTA" ***@***.***>;
发送时间: 2024年5月1日(星期三) 上午10:51
***@***.***>;
***@***.******@***.***>;
主题: Re: [oushujun/EDTA] '调用失败' (Issue #458)
You need to provide the environment settings and your list of installed packages otherwise its hard to help
—
Reply to this email directly, view it on GitHub, or unsubscribe.
You are receiving this because you authored the thread.Message ID: ***@***.***>
|
Have you resolved your issue? I encountered a similar problem when running EDTA. |
I didn't look in detail and I am not the author of the software however for the Line and repeat modeler I found that the consensus file is created with Line sequences inside of the fasta but it seems that the consensus.fa file in LINE/ is probably not named with $genome prefix so it seems that EDTA can't read it because of its name / path |
File "/home/xionglab250/mambaforge/envs/edta/lib/python3.9/site-packages/numpy/init.py", line 324, in getattr That is part of error reports , it seems that numpy function 'object' did not work...emmmm |
The initial error Thanks! |
Thank you very much! I will reinstall EDTA later.
Lizhen
李珍
***@***.***
…------------------ 原始邮件 ------------------
发件人: "oushujun/EDTA" ***@***.***>;
发送时间: 2024年10月7日(星期一) 晚上9:13
***@***.***>;
***@***.******@***.***>;
主题: Re: [oushujun/EDTA] '调用失败' (Issue #458)
The initial error Invalid value for shared scalar was solved in the LTR_retriever repo. Reinstalling EDTA should solve the issue. please refer to #497
Thanks!
Shujun
—
Reply to this email directly, view it on GitHub, or unsubscribe.
You are receiving this because you commented.Message ID: ***@***.***>
|
Just use the conda version Follow the instructions. However I noticed that sometimes the SINEs don't appear so you need to add the SINEs as -lib as in the tutorial too. Overall this EDTA version works quite well. But I think it is a bit sad that we cannot choose what run to restart if we want to redo only one type of TE like helitron, if we do EDTA it doesn't ask us which type unless we use EDTA.raw but it's annoying to have to merge the Types of TE. It's better to let the user choose to continue an EDTA run and to redo from row only 1 superfamily |
$ perl ../EDTA.pl --genome genome.fa --cds genome.cds.fa --curatedlib ../database/rice7.0.0.liban --exclude genome.exclude.bed --overwrite 1 --sensitive 1 --anno 1 --evaluate 1 --threads 10 > EDTA.test
2024年 04月 29日 星期一 16:53:03 CST EDTA_raw: Check dependencies, prepare working directories.
2024年 04月 29日 星期一 16:53:04 CST Start to find LTR candidates.
2024年 04月 29日 星期一 16:53:04 CST Identify LTR retrotransposon candidates from scratch.
Invalid value for shared scalar at /home/xionglab250/mambaforge/envs/EDTA/share/LTR_retriever/bin/LTR.identifier.pl line 114, line 11.
cp: 对 'genome.fa.mod.retriever.scn.adj' 调用 stat 失败: 没有那个文件或目录
awk: 致命错误:无法打开文件“genome.fa.mod.pass.list”进行读取:没有那个文件或目录
Warning: LOC list - is empty.
Error: Error while loading sequence
Filter sequence based on TEsorter classifications. Unclassified sequences will also be output to the clean file.
Usage: perl cleanup_misclas.pl sequence.fa.rexdb.cls.tsv
Author: Shujun Ou ([email protected]) 10/11/2019
mv: 对 'genome.fa.mod.LTR.intact.fa.ori.dusted.cln.cln' 调用 stat 失败: 没有那个文件或目录
mv: 对 'genome.fa.mod.LTR.intact.fa.ori.dusted.cln.cln.list' 调用 stat 失败: 没有那个文件或目录
cp: 对 'genome.fa.mod.LTR.intact.raw.fa.anno.list' 调用 stat 失败: 没有那个文件或目录
ERROR: No such file or directory at /home/xionglab250/mambaforge/envs/EDTA/share/EDTA/util/output_by_list.pl line 39.
2024年 04月 29日 星期一 16:53:10 CST Warning: The LTR result file has 0 bp!
2024年 04月 29日 星期一 16:53:10 CST Start to find SINE candidates.
2024年 04月 29日 星期一 16:53:38 CST Warning: The SINE result file has 0 bp!
2024年 04月 29日 星期一 16:53:38 CST Start to find LINE candidates.
2024年 04月 29日 星期一 16:53:38 CST Identify LINE retrotransposon candidates from scratch.
2024年 04月 29日 星期一 16:54:38 CST Warning: The LINE result file has 0 bp!
2024年 04月 29日 星期一 16:54:38 CST Start to find TIR candidates.
2024年 04月 29日 星期一 16:54:38 CST Identify TIR candidates from scratch.
Species: others
2024年 04月 29日 星期一 16:55:02 CST Finish finding TIR candidates.
2024年 04月 29日 星期一 16:55:02 CST Start to find Helitron candidates.
2024年 04月 29日 星期一 16:55:02 CST Identify Helitron candidates from scratch.
2024年 04月 29日 星期一 16:55:22 CST Finish finding Helitron candidates.
2024年 04月 29日 星期一 16:55:22 CST 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 and genome.fa.mod.EDTA.raw/genome.fa.mod.LTR.intact.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
###############################################
Is it work in testdata?Shown lack of LTR,and we got the same error for another species.
Thanks !
The text was updated successfully, but these errors were encountered: