Closed Ferossitiziano closed 4 years ago
Hi, Please which HiC-Pro version are you using ? Could you try to install the latest version ? 2.11.3 Thanks
Hi,
I am already using version 2.11.3
It looks to me the pipeline is expecting the read file to be named with "fq" instead of "fastq.gz", but the "fq" file has not been created.
Thanks, Federico
H, Strange, we did a lot of test on this version. Could you check that you have rights on the test_data ? it seems that the file are not readable ? What about the bowte log ? could you check in the log what is the bowtie command ?
Hi,
I think I have permission to access the test_data folder as it comes with "drwxr-xr-x".
This is the bowtie command:
bowtie2 --very-sensitive -L 30 --score-min L,-0.6,-0.2 --end-to-end --reorder --un bowtie_results/bwt2_global/WT/WTRing1bFP75m_00_R1_mm10.bwt2glob.unmap.fastq --rg-id BMG --rg SM:WTRing1bFP75m_00_R1 -p 3 -x bowtie2_index/mm10 -U rawdata/WT/WTRing1bFP75m_00_R1.fastq.gz 2>> logs/WT/WTRing1bFP75m_00_R1_bowtie2.log| /hpcnfs/home/ieo5073/miniconda3/envs/HiCpro/bin/samtools view -F 4 -bS - > bowtie_results/bwt2_global/WT/WTRing1bFP75m_00_R1_mm10.bwt2glob.bam
I'm not able to reproduce the issue :(
Where is the error ? because your bowtie command looks good with .fastq
file (not .fq
)
Is it in the bowtie2 log file ?
or could you check the rawdata folder please ? it should contain links to the rawdata file. Are they correct ?
Yes, the bowtie2 command works fine, I tried it myself as well straight from the command line. I am running a generic bowtie2 alignment in local mode as this should be the following step in the pipeline, if I'm not wrong. It is working fine.
The link to rawdata looks fine, it points to my raw data. The "inputfiles_test.txt" looks wired to me as in only include the R1 file and not the corresponding R2 file. Is that fine?
I added the R2 file to the "inputfiles_test.txt" and it gave me the same issue: bowtie_global Error 1. So that was not the problem.
Yes, it's normal. You are using the '-p' option ?
Yes, I have used the command
HiC-Pro -c config-hicpro.txt -i test_data/ -o Results -p
indeed ! I do have an error on my side too ... let me check that and I come back to you ... Does it work without -p option ?
Using the interactive mode without "-p" all the jobs work fine. Thanks
Hi Frederico, I just make a fix on the devel branch. Many thanks for reporting this issue. I removed the 2.11.3 tag, and will release the 2.11.4 as soon as I will be sure that this version is ok. Thanks again !
Thank you for your help!! I will try to download the files you modified on the devel branch and I will test them.
Hi, I just made a pre-relase 2.11.4 if you want to test. I hope this one is fine ! thanks
Hi,
I have downloaded all the files on the level branch on the Github page and installed HiC-Pro again. Unfortunately, as already occurred, HiC-Pro works fine in the interactive mode but fail when it is launched with the -p option.
The error I get is still the same:
stat: Bad file descriptor Warning: Could not open read file "rawdata/dixon_2M/SRR400264_00_R2.fq" for reading; skipping... Error: No input read files were valid (ERR): bowtie2-align exited with value 1
It cannot find the file rawdata/dixon_2M/SRR400264_00_R2.fq, but I don't really know why it is not looking for rawdata/dixon_2M/SRR400264_00_R2.fastq.gz, which exist.
Best, Federico
Sorry, it looks like I still got version 2.11.3, I'll try to download 2.11.4.
Federico
The pipeline in parallel mode worked fine with test_data using version 2.11.4. Thank you very much!
great !
Hi! I have the same problem with the Bowtie_global error 1. How do I get the 2.11.4 version? I somehow always end up installing version 2.11.3.
Thanks, Best, Mlad
thank you!
Hi, Would you have more info ? logs please ? Look at the bowtie logs please. Nicolas
Le 15/05/2020 à 15:20, baishengjun a écrit :
Hi, I have the same problem with the Bowtie_global error 1. and I use hic-pro version 2.11.4 . my genome size 530M , I get errors. when I run genome size 430M , no errors. I use the same operation with hicpro. that is strange . how can I fix it ?
thanks
— You are receiving this because you modified the open/close state. Reply to this email directly, view it on GitHub https://github.com/nservant/HiC-Pro/issues/326#issuecomment-629232006, or unsubscribe https://github.com/notifications/unsubscribe-auth/ACSHM27GGOFM74WME54QGZ3RRU6RLANCNFSM4LVVNL6A.
Hi. I am suing HiC-Pro 3.1.0 When I run ./bin/HiC-Pro -i rawdata -o hic_results -c config-hicpro.txt
Fri Oct 27 10:33:53 PDT 2023 Bowtie2 alignment step1 ... Logs: logs/Sample1/mapping_step1.log [main_samview] fail to read the header from "-". [main_samview] fail to read the header from "-". Exit: Error in reads alignment - Exit make: *** [/home/HiC-Pro_3.1.0/bin/../scripts//Makefile:88: bowtie_global] Error 1
Hi. I am suing HiC-Pro 3.1.0 When I run ./bin/HiC-Pro -i rawdata -o hic_results -c config-hicpro.txt
Run HiC-Pro 3.1.0
Fri Oct 27 10:33:53 PDT 2023 Bowtie2 alignment step1 ... Logs: logs/Sample1/mapping_step1.log [main_samview] fail to read the header from "-". [main_samview] fail to read the header from "-". Exit: Error in reads alignment - Exit make: *** [/home/HiC-Pro_3.1.0/bin/../scripts//Makefile:88: bowtie_global] Error 1
I have the same issue! Some samples are working, others I get this error, here is the log which seems related to the file descriptor:
stat: Bad file descriptor Warning: Could not open read file "rawdata/501mel_sgCHD7-2/501mel-sgCHD7-2_S15_L004_R1_001.fastq.gz.fastq" for reading; skipping... Error: No input read files were valid
@nservant any help would be extremely grateful, I am using the last release of HiC-Pro 3.1.0 like @Oksanak22
Best Pietro
Dear Nicolas,
I made a test run in interactive mode with both test_data and my own data, using the following command, and it worked.
HiC-Pro -c config-hicpro.txt -i test_data/ -o Results
When I tried to repeat the analysis by adding "-p" to the previous command line to the submit the job with qsub, I had the following error message:
Exit: Error in reads alignment - Exit make: *** [HiC-Pro_2.11.3/scripts/Makefile:88: bowtie_global] Error 1
I checked the logs and they reported the following:
HiC-Pro mapping
stat: Bad file descriptor Warning: Could not open read file "rawdata/dixon_2M/SRR400264_00_R1.fq" for reading; skipping... Error: No input read files were valid (ERR): bowtie2-align exited with value 1
The test fastq files are dixon_2M/SRR400264_00_R1.fastq.gz and dixon_2M/SRR400264_00_R2.fastq.gz
Could you help me with this issue?
Federico