Open jsalignon opened 6 years ago
Silly mistake, great catch! Will update this today, and you're completely right. The genome for those datasets are human. Will update that information.
On Jan 20, 2018 5:15 AM, "Bioninbo" notifications@github.com wrote:
Hi,
Thanks for this pipeline.
I was trying to use it on atac-seq data. I got the following error message: Caused by: Process bamCoverage (1) terminated with an error exit status (127) Command executed: null Checking at the code I find that there is no options for atac seq in this process. I added it line 1016 this way: if (params.mode == "chip" || params.mode == "dnase" || params.mode == "atac") However I am not sure this is correct.
By the way I think the provided example (H3K4me3.500k) lacks instruction: what command to launch? I guess it is chip seq but in which organism? Including the corresponding gtf and fasta file could be nice.
Thanks, Jerome
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Has this error been fixed? I get the exact same error while performing ATAC seq analysis.
May-13 15:23:56.444 [Task submitter] DEBUG nextflow.executor.LocalTaskHandler - Launch cmd line: /bin/bash -ue .c
ommand.run
May-13 15:23:56.446 [Task submitter] INFO nextflow.Session - [1a/b663ef] Submitted process > estimate_fragment_s
ize (2)
May-13 15:23:56.743 [Task monitor] ERROR nextflow.processor.TaskProcessor - Error executing process > 'bamCoverag
e (1)'
Caused by:
Process `bamCoverage (1)` terminated with an error exit status (127)
Command executed:
null
Command exit status:
127
Command output:
(empty)
Command error:
.command.sh: line 2: null: command not found
Let me know if more information is required to understand the source of this error. This information is from .nextflow.log file.
Hi,
Thanks for this pipeline.
I was trying to use it on atac-seq data. I got the following error message:
Caused by: Process bamCoverage (1) terminated with an error exit status (127) Command executed: null
Checking at the code I found that there is no options for atac seq in this process. I added it line 1016 this way:if (params.mode == "chip" || params.mode == "dnase" || params.mode == "atac")
However I am not sure this is correct.By the way I think the provided example (H3K4me3.500k) lacks instruction: what command to launch? I guess it is chip seq but in which organism? Including the corresponding gtf and fasta file could be nice.
Thanks, Jerome