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Describe the goals of the changes to the analysis module.
We would like to be able to run AUCell on all samples in SCPCP000015 with all of the marker gene sets that we are interested in. To do that, we should write a script that takes as input a single SCE file, the max rank (chosen in #984), and a table of marker genes and the associated cell type label and outputs a data frame with the AUC value, the AUC threshold determined by AUCell, and the classification based on that threshold.
For some gene sets, I'm not sure AUCell will do a good job of identifying a threshold, but we should record that information to determine if we need to pick a cutoff to use across all samples for that gene set or if we can use the identified threshold.
What will your pull request contain?
This PR should contain a script that runs AUCell on all marker gene sets for a given SCE object and returns the AUC values and the assigned AUC threshold for each gene set.
I think we might want to include all the marker genes in visser-all-marker-genes.tsv, tumor-cell-state-markers.tsv, and our custom gene signatures in references/gene_signatures. So this PR should also contain a single table with all marker genes described above. I'm not sure that we will find information from each gene set useful just yet, but I think it can't hurt to use them all to start.
Will you require additional software beyond what is already in the analysis module?
No
Will you require different computational resources beyond what the analysis module already uses?
No
If known, when do you expect to file the pull request?
This week
The text was updated successfully, but these errors were encountered:
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#696
Describe the goals of the changes to the analysis module.
We would like to be able to run
AUCell
on all samples in SCPCP000015 with all of the marker gene sets that we are interested in. To do that, we should write a script that takes as input a single SCE file, the max rank (chosen in #984), and a table of marker genes and the associated cell type label and outputs a data frame with the AUC value, the AUC threshold determined byAUCell
, and the classification based on that threshold.For some gene sets, I'm not sure
AUCell
will do a good job of identifying a threshold, but we should record that information to determine if we need to pick a cutoff to use across all samples for that gene set or if we can use the identified threshold.What will your pull request contain?
This PR should contain a script that runs
AUCell
on all marker gene sets for a given SCE object and returns the AUC values and the assigned AUC threshold for each gene set.I think we might want to include all the marker genes in
visser-all-marker-genes.tsv
,tumor-cell-state-markers.tsv
, and our custom gene signatures inreferences/gene_signatures
. So this PR should also contain a single table with all marker genes described above. I'm not sure that we will find information from each gene set useful just yet, but I think it can't hurt to use them all to start.Will you require additional software beyond what is already in the analysis module?
No
Will you require different computational resources beyond what the analysis module already uses?
No
If known, when do you expect to file the pull request?
This week
The text was updated successfully, but these errors were encountered: