Open idazucchi opened 2 years ago
Need to add a treatment protocol: Cells were activated by the Dynabeads CD3/CD28 T cell Expander (ThermoFisher, bead-to-cell ratio: 1:1).
Downloading bulk RNA sequencing data.
76b72ab5-702e-4057-b0a5-c1ebdea8c03c
d9ae6035-2385-4b68-aba0-e3b805eda861
420c20f8-34c2-4aa2-b4fb-4533c8ededea
8bbb6b78-1e08-4a52-9ee4-b2e52f78be1c
Data is being uploaded.
Graph is valid
Hi ami, I'm done with the review! It looks good, I have just a few comments
samples were cultured for 48 hours with or without the STAT6 inhibitor and then analyzed with RNAseq
You can also apply the timecourse to the controls as well, something like 48h RNA collected after 48h in culture, to show that the controls were under the same conditions as the treated samples
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from the computational methods, it't a reserved charactercount matrix
for the scRNAseq because the ontology definition is more accurate that that for gene expression matrixHi ami, I'm done with the review! It looks good, I have just a few comments
Project
- you should add yourself as curator!
Collection
- remove healthy/ disease from description since the protocols are used for both disease and healthy
Enrichment
- you can add CD4+ to the markers
Cell suspension
- you can add the INSDC sample accession for the bulk RNAseq
- I think that the treatment protocol should be applied to all bulk RNAseq cell suspension, the controls go through the same treatment as the STAT6 ones but without any drug
samples were cultured for 48 hours with or without the STAT6 inhibitor and then analyzed with RNAseq
You can also apply the timecourse to the controls as well, something like 48h RNA collected after 48h in culture, to show that the controls were under the same conditions as the treated samples
Analysis protocol
- remove the
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from the computational methods, it't a reserved characterAnalysis file
- I'd use
count matrix
for the scRNAseq because the ontology definition is more accurate that that for gene expression matrix
Thank you, I have made most of the suggested changes and re-submitting it now.
submitted
Exported and import form submitted.
Looks good
This project can't be found in the data Portal Was this dropped due to import issues?
the import team had issues with this project due to the new treatment protocol - the project was removed from R22 this was not handed off when Ami left so no one ever followed up on it
next steps:
this was part of the initial skin list but is not on Dave's tracker do we want to:
Project short name:
CutaneousTcellLymphomaSTAT6
Primary Wrangler:
Ami
Secondary Wrangler:
Ida
Associated files
https://docs.google.com/spreadsheets/d/1SN-9T3V0FFfOZ9VGvTEQ8JEHDokPJoFzgIdgGprY8iE/edit#gid=1868030719
Published study links
Paper: Genome-wide transcriptome analysis of the STAT6-regulated genes in advanced-stage cutaneous T-cell lymphoma
Accessioned data:
Series: GSE147947
scRNA-Seq data: GSE147944 - count cell matrices only
Bulk data: GSE147911
Key Events