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* add enh. volcano * update docu * add comment * rm comments, add omitNa * ch version to dev * add volcano to tests * fix deprecated key-value * update docs,changelog * prettier test rsem profile * fix contrast names
* add colors to plotly volcano * add color scale
* hotfix switch volcano colors * fix colors * add abs, rm space * rm "feature" text * update titles, legends * add subtitle for interactive plot * ch y-axis label * rm outcommented lines
* put gprofiler in tabs * revert * linting * trim whitespace * mod plot title
* raise max dimensions limit * concat ensembl ids with gene names * update changelog & usage update changelog & usage update changelog & usage Co-authored-by: Famke Bäuerle <45968370+famosab@users.noreply.github.com> fix typo
* change report name * modify report * update report & tests & fix volcano colors * add to changelog, references * fix citation * fix df RIN * fix linting & ci * fix padding * update md5sums due to sampleNames * apply suggestions * update confs * apply suggestion * add num all genes * change icon * adjust docs text
* incorporate feedback * update report * fix typos * update changelog * fix pre-commit * fix spaces * fix colored cells * linting * fix typos * adjust table border * fix typos * apply suggestions * apply suggestions
* fix contrast * update usage * add to changelog * update test * PR num * ch md5sum
* adjust md5sums due to gtf biotypes * update branch * fix assignment * add biotype to final DE table * update md5sums
This PR is against the
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Linting fails in CI due to latest nf-core tools version 3.3.1 and the pipeline here relies on nf-core tools 2.14.1 |
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Branch protection could probably be fixed in the |
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locally, the download works with |
I'm playing around with the CI right now for my pipeline. So what i saw in my |
famosab
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To me this looks good but note that I am not an expert on pytests and R haha :D
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Awesome, thanks! |
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Branch protection is failing because of a typo in the rnadeseq/.github/workflows/branch.yml Line 16 in e53bbae |
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| The image below displays the two-step analysis workflow from your input data to differential gene expression analysis. | ||
| In the first step, reads were aligned and assigned to genomic features using nf-core pipelines. | ||
| In the second step, the gene counts were analyzed for differential expression with the secondary analysis pipeline rnadeseq. |
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we have 2x second in here, nut-picking maybe...but could be modified to : "In the next step, the resulting gene counts were analyzed for differential expression with the secondary analysis pipeline rnadeseq."
| # Workflow overview | ||
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| The image below displays the two-step analysis workflow from your input data to differential gene expression analysis. | ||
| In the first step, reads were aligned and assigned to genomic features using nf-core pipelines. |
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"In the first step, reads were aligned and assigned to genomic features (e.g. genes) using nf-core pipelines.
| - `Heatmaps_of_distances.pdf/.png/.svg`: heatmap of the pairwise Euclidean distances among samples, when the `r norm_method_text` normalized gene counts are considered. | ||
| - `PCA_plot.pdf`: PCA of the `r norm_method_text` normalized gene counts. | ||
| - **DE_genes_tables:** folder containing one tab-separated table for each of the contrasts in the analysis. Each table contains a list of all differentially expressed genes in the contrast, specifying the mean gene expression across all samples (baseMean), and the log2 fold change value and p-adjusted values (padj) for this contrast. If a `gtf` file is provided, the tables will also contain a column with the gene biotypes of the differentially expressed genes. | ||
| - **final_gene_table/final_gene_list_DESeq2.tsv**: table containing a list of all genes considered in the analysis. Here a summary of the log2 Fold Change and p-adjusted values for all contrasts is displayed. Additionally, the column **filter** shows if this gene was differentially expressed (DE) in any of the contrasts, or not (not_DE). The column **contrast_vector** contains for each contrast considered in the analysis a 1 if the gene was differentially expressed for this contrast or a 0 if it was not. |
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I would also add this sentence here as that column is also added to the final aggregated DE table: "If a gtf file is provided, the tables will also contain a column with the gene biotypes of the differentially expressed genes."
qbicStefanC
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Overall looks fine to me. Before merging let us wait for the checks on the 4 mentioned previously run projects and then see what is missing.
* fix thresholds in enhanced volcano * add to changelog
* prettify long contrast names in plot titles * add new test profile but not for ci * rename files * correct pr nums
Are there any updates on the runs of the 4 projects? @qbicStefanC @MAKirch |
* switch back to githubusercontent * add to changelog
Note: 4 Projects passed the tests |
PR checklist
nf-core lint).nextflow run . -profile test,docker --outdir <OUTDIR>).docs/usage.mdis updated.docs/output.mdis updated.CHANGELOG.mdis updated.README.mdis updated (including new tool citations and authors/contributors).