ebi-ait / hca-ebi-wrangler-central

This repo is for tracking work related to wrangling datasets for the HCA, associated tasks and for maintaining related documentation.
https://ebi-ait.github.io/hca-ebi-wrangler-central/
Apache License 2.0
7 stars 2 forks source link

GSE147944 - cutaneousTcellLymphoma #856

Open idazucchi opened 2 years ago

idazucchi commented 2 years ago

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

Series: GSE147947

scRNA-Seq data: GSE147944 - count cell matrices only

Bulk data: GSE147911

Key Events

ami-day commented 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).

ami-day commented 2 years ago

Downloading bulk RNA sequencing data.

ami-day commented 2 years ago

76b72ab5-702e-4057-b0a5-c1ebdea8c03c d9ae6035-2385-4b68-aba0-e3b805eda861 420c20f8-34c2-4aa2-b4fb-4533c8ededea 8bbb6b78-1e08-4a52-9ee4-b2e52f78be1c

gabsie commented 2 years ago

Data is being uploaded.

ami-day commented 2 years ago

Graph is valid

idazucchi commented 2 years ago

Hi ami, I'm done with the review! It looks good, I have just a few comments

Project

Collection

Enrichment

Cell suspension

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

Analysis file

ami-day commented 2 years ago

Hi 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 | from the computational methods, it't a reserved character

Analysis 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.

ami-day commented 2 years ago

submitted

ami-day commented 2 years ago

Exported and import form submitted.

ami-day commented 2 years ago

Looks good

idazucchi commented 1 year ago

This project can't be found in the data Portal Was this dropped due to import issues?

idazucchi commented 1 year ago

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:

idazucchi commented 1 year ago

import failed - slack + ticket

idazucchi commented 1 month ago

this was part of the initial skin list but is not on Dave's tracker do we want to: