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mgatk bcall
has trouble running
#65
Comments
On second thought I wonder if this is just due to these reads not having enough mito. I'll look into that in the meantime. |
Are you doing this to run mgatk-del (based on other comments)?
On Jan 23, 2023, at 5:11 PM, Max Land ***@***.******@***.***>> wrote:
On second thought I wonder if this is just due to these reads not having enough mito. I'll look into that in the meantime.
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Yes I am, I believe this is the second step here. |
ok cool-- depending on where you are at, I'd potentially recommend using the coverage based estimation (discussed in the wiki) if you have cells with low coverage-- it tends to perform a bit better once you have the deletions identified and is less computationally intensive (you can do |
Closed due to inactivity but LMK if there's more that needs to be done here... |
@caleblareau I am facing the same issue, could we reopen this issue and try to figure out why.
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Describe the bug
I was trying to run
mgatk bcall -i ../YfDogmaSeqMtdna-atac-mito/RC-1652_T4i5_D6_multiome/cr-arc-results/atac_possorted_bam.bam -o regular_mgatk_call -n regular_mgatk_call -c 4 -g hg38 -qc -bt CB -b ./short_barcodes.tsv --snake-stdout
but getting errors similar to issues #30, #61 .I spent a bit of time trying to debug based on other issues but nothing seemed to work. At first I thought it was a snakemake issue based on the other issues above, but I was able to successfully run
mgatk bcall -i barcode/test_barcode.bam -n bc2 -o bc2d -bt CB -mb 200 -z
on the test data in the same environment.Any thoughts? Any tips for things I can check to see about my data if it's a data specific issue vs environment/code?
A summary of .log files
Here is output of
cat logs/*
:Post an ls -lRh of mgatk_output_folder
Describe the sequencing assay being analyzed
Dogmaseq data, scRNA and scATAC processed by cellranger.
Clarify if the execution successful on the test data provided in the repository
Test data ran.
Additional Info
Python = 3.7.12
mgatk=0.6.7
snakemake=7.19.1
R = 4.1.1
Java=1.8.0_31
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