Data and code for the Multiomics surface receptor profiling of the NCI-60 tumor cell panel uncovers novel theranostics for cancer immunotherapy
paper.
We can clone via:
git clone git@github.com:qbicsoftware/QMSFC.git
If the following error is appearing:
Error downloading object: Curate_ArrayData_April2022/GSE32474_series_matrix.txt (b9a6057): Smudge error: Error downloading Curate_ArrayData_April2022/GSE32474_series_matrix.txt (b9a6057e68823732e88825d5bd2d62236342bab40cb6d59bacbc25ced9783bc8): batch response: This repository is over its data quota. Account responsible for LFS bandwidth should purchase more data packs to restore access.
Errors logged to /home/heumos/QBiC/QMSFC/.git/lfs/logs/20240425T101004.638820054.log
Use `git lfs logs last` to view the log.
error: external filter 'git-lfs filter-process' failed
fatal: Curate_ArrayData_April2022/GSE32474_series_matrix.txt: smudge filter lfs failed
warning: Clone succeeded, but checkout failed.
You can inspect what was checked out with 'git status'
and retry with 'git restore --source=HEAD :/'
Then please follow the guidance given at https://stackoverflow.com/questions/62905325/this-repository-is-over-its-data-quota-account-responsible-for-lfs-bandwidth-sh to fork and archive this repository and downlaod it as ZIP.
Then change your directory:
cd QMSFC
Some basic software is required in order to run the R analysis scripts. Please install Rstudio
as described in https://www.rstudio.com/products/rstudio/download/#download. To get a miniconda
installation please follow https://conda.io/projects/conda/en/latest/user-guide/install/index.html.
Once you have installed miniconda
you can add the QMSFC environment as follows:
conda env create -f QMSFC_environment_21042022.yml
For the QMSFC_2 environment, you have to execute:
conda env create -f QMSFC_environment_22042022.yml
Ensure that you are in the QMSFC environment:
conda activate QMSFC
For Rstudio
to work properly, we tell it the path to th R version used in the conda environment:
export RSTUDIO_WHICH_R=~/miniconda3/envs/QMSFC/bin/R
If you installed miniconda
to a different location than your home folder, please adjust the path above.
Now open Rstudio
from the command line:
rstudio
Depending on your OS, it may also be rstudio-bin
.
Navigate to File
and click on Open File...
. Navigate to the IsotypeControl_QC
folder and open IsotypeControl_QC.R
. Select all lines and press SHIFT+ENTER
in order to re-run the analysis.
Ensure that you have the QMSFC environment activated and Rstudio
is open as in Run quality control analysis.
Navigate to File
and click on Open File...
. Navigate to the week1_week2
folder and open week1_week2.R
. Select all lines and press SHIFT+ENTER
in order to re-run the analysis.
Ensure that you have the QMSFC environment activated and Rstudio
is open as in Run quality control analysis.
Navigate to File
and click on Open File...
. Navigate to the Homogenize_Identifiers
folder and open harmonize_IDs.R
. Select all lines and press SHIFT+ENTER
in order to re-run the analysis.
Ensure that you are in the QMSFC_2 environment:
conda activate QMSFC_2
For Rstudio
to work properly, we tell it the path to th R version used in the conda environment:
export RSTUDIO_WHICH_R=~/miniconda3/envs/QMSFC_2/bin/R
If you installed miniconda
to a different location than your home folder, please adjust the path above.
Now open Rstudio
from the command line:
rstudio
Depending on your OS, it may also be rstudio-bin
.
Navigate to File
and click on Open File...
. Navigate to the Curate_ArrayData_April2022
folder and open curate_array_April2022.R
. Select all lines and press SHIFT+ENTER
in order to re-run the analysis.
Ensure that you have the QMSFC_2 environment activated and Rstudio
is open as in Run Tx curation.
Navigate to File
and click on Open File...
. Navigate to the Curate_Px_April2022
folder and open curate_px_gholami_April2022.R
. Select all lines and press SHIFT+ENTER
in order to re-run the analysis.
Ensure that you have the QMSFC environment activated and Rstudio
is open as in Run quality control analysis.
Navigate to File
and click on Open File...
. Navigate to the multiomics_March2022_NO_LOX_NO_ISOTYPE_CONTORLS
folder and open omicade4_March2022_NO_LOX_NO_ISOTYPE_CONTROLS.R
. Select all lines and press SHIFT+ENTER
in order to re-run the analysis.
For each of the folders starting with recount2
you can run the same analysis steps. In the following an example for COLON.
Ensure that you have the QMSFC_2 environment activated and Rstudio
is open as in Run Tx curation.
Navigate to File
and click on Open File...
. Navigate to the recount2_co_April2022
folder and open curate_px_gholami_April2022.R
. Select all lines and press SHIFT+ENTER
in order to re-run the analysis.