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@vm11 found that the outputs generated (WS_wEMB10202354.h5ad) do not match sample ID that I inputted (HCA_SkO13919077) into solosis. I also inputted two samples and only 1 output was generated.
-rw-rw-r-- 1 lg28 team298 96041 Dec 4 10:04 low_quality_cells_removed_in_preQC_WS_wEMB10202354.json
-rw-rw-r-- 1 lg28 team298 213836117 Dec 4 10:14 WS_wEMB10202354.h5ad
-rw-rw-r-- 1 lg28 team298 1137998 Dec 4 10:14 HCA_SkO13919077_HCA_SkO13919077.ipynb
## and here
$ ls -lrt reports
total 56
drwxr-xr-x 3 lg28 team298 804 Dec 4 10:08 WS_wEMB10202354
-rw-r--r-- 1 lg28 team298 2199 Dec 4 10:14 index.html
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Description
Updated per sample rna-seq processing pipeline. The main change is python. notebook. Changed the scanpy.py command to accomodate the changes in the notebook.
Fixes # Issue with how one can use the same ipykernel and environment. Numpy deprecated function fixed with new scanpy env.
Type of change
Checklist
pytest)pre-commit run --all-files)