Last updated: 2021-08-16
Checks: 2 0
Knit directory: Turati_NatCancer_2021/
This reproducible R Markdown analysis was created with workflowr (version 1.6.2). The Checks tab describes the reproducibility checks that were applied when the results were created. The Past versions tab lists the development history.
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Ignored files:
Ignored: .Rhistory
Ignored: .Rproj.user/
Ignored: bulkRNA/
Ignored: data/bulk4_counts.rda
Ignored: data/bulk4_dds.rda
Ignored: data/paper_palette.rda
Ignored: data/signatures.rda
Ignored: output/deseq2-mini_bulk4_dds.3pts-Treated-vs-Untreated.rds
Ignored: output/deseq2-mini_bulk4_dds.pt1-Treated-vs-Untreated.rds
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Ignored: output/deseq2-mini_bulk4_dds.pt13-Treated-vs-Untreated.rds
Ignored: output/deseq2-mini_bulk4_dds.pt2-Acutely treated-vs-Chronically treated.rds
Ignored: output/deseq2-mini_bulk4_dds.pt2-Acutely treated-vs-Never treated.rds
Ignored: output/deseq2-mini_bulk4_dds.pt2-Chronically treated-vs-Never treated.rds
Ignored: output/deseq2-mini_bulk4_dds.pt2-Relapse-vs-Never treated.rds
Ignored: output/deseq2-mini_bulk4_dds.pt2-Treatment withdrawn-vs-Never treated.rds
Ignored: output/fgsea_results.RDS
Ignored: output/figures/ExtFig5a_pca_3patients.pdf
Ignored: output/figures/ExtFig5b_pca_treatment_response.pdf
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Ignored: output/figures/ItemS2.pdf
Ignored: output/tables/ExtFig5a_bulkRNAseq_data.xlsx
Ignored: output/tables/ExtFig5b_bulkRNAseq_data.xlsx
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These are the previous versions of the repository in which changes were made to the R Markdown (analysis/bulkRNA-index.Rmd
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File | Version | Author | Date | Message |
---|---|---|---|---|
Rmd | 01ec959 | Javier Herrero | 2021-08-16 | wflow_publish(all = T) |
html | 01ec959 | Javier Herrero | 2021-08-16 | wflow_publish(all = T) |
html | e02ea6e | Javier Herrero | 2021-08-16 | Build site. |
html | cfa55c7 | Javier Herrero | 2021-08-16 | Build site. |
Rmd | 6f629e4 | Javier Herrero | 2021-08-16 | Bulk RNA pages are now complete |
html | 80a3f49 | Javier Herrero | 2021-08-16 | Build site. |
Rmd | 1a35752 | Javier Herrero | 2021-08-16 | Adding Bulk RNA / GSEA page |
html | b6f5b35 | Javier Herrero | 2021-08-13 | Build site. |
html | a7a695e | Javier Herrero | 2021-08-13 | Build site. |
Rmd | c2ccafd | Javier Herrero | 2021-08-13 | Add “Bulk RNAseq / DESeq2” page |
html | c2ccafd | Javier Herrero | 2021-08-13 | Add “Bulk RNAseq / DESeq2” page |
Rmd | 146911e | Javier Herrero | 2021-08-13 | Adding Bulk RNAseq / PCA page |
html | 146911e | Javier Herrero | 2021-08-13 | Adding Bulk RNAseq / PCA page |
Rmd | 42e5864 | Javier Herrero | 2021-08-13 | Init workflowr website |
html | 42e5864 | Javier Herrero | 2021-08-13 | Init workflowr website |
This analysis is used in Figure S5A and S5B of the mss.
DESeq2 uses the top 500 most variable genes by default to draw the PCA. In this case, we are using the top 1000 genes (for historical reasons).
Generates Extended Figure 5a and Extended Figure 5b
This runs DESeq2 and stores the results in the output folder.
This runs fGSEA and stores the results in the output folder.
Generates Figure 5c