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Issue with running tf file #272
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The issue is solved and pipeline ran successfully after I changed the json file "chip.ctl_paired_ends" from true to false.
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Even though I was able to run the all-CTCF.bam file (tf) from above, however, I am having a similar issue with the tf file all-POLR2A.bam I ran I made the same change in the JSON file for all-POLR2A.bam that helped me to get the tf file all-CTCF.bam to run:
However, I still got the error message:
I am not sure how to further debug this, any suggestions would be helpful! |
How did you align your FASTQs into BAM files ( |
For all-CTCF.bam, the FASTQs were aligned using bowtie2 and I got the control BAM from [ENCFF178EJY] (https://www.encodeproject.org/files/ENCFF178EJY/). The same for all-POLR2A.bam and its control bam. |
What reference genome files did you use when you align FASTQs? They should match with files (e.g. FASTA, chromsizes, ...) in the TSV file
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Also the control https://www.encodeproject.org/files/ENCFF178EJY/ is a single-ended one but |
I have been able to successfully run the chip-seq pipeline for the example json and my own histone bam files. However, while passing in a custom tf .bam file, I am running into errors that I am not too sure how to debug. Any suggestions are much appreciated!
Here are more info about the issue:
I ran
caper run chip.wdl -i /mnt/c/users/shirl/Desktop/guttman_lab/CTCF.json --conda
Caper configuration file
Locally run
Input JSON file
Error message:
The text was updated successfully, but these errors were encountered: