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Merge pull request #408 from d3b-center/naqvia/update-readmes
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readme updates
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naqvia authored Aug 22, 2024
2 parents 5823a6f + 483dc4c commit 9204820
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7 changes: 5 additions & 2 deletions analyses/CLK1-splicing-impact-morpholino/README.md
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Expand Up @@ -43,8 +43,10 @@ bash run_module.sh
│   ├── CCMA_crispr_genedependency_042024.csv
│   ├── RBP_known.txt
│   ├── base_excision_repair.txt
│   ├── cancerGeneList.tsv
│   ├── dna_repair_all.txt
│   ├── epi_known.txt
│   ├── genelistreference.txt
│   ├── homologous_recombination.txt
│   ├── mismatch_repair.txt
│   ├── morpholno.merged.rmats.tsv
Expand Down Expand Up @@ -72,6 +74,7 @@ bash run_module.sh
│   ├── dPSI_distr.pdf
│   ├── des-dex-venn-func.pdf
│   ├── des-dex-venn.pdf
│   ├── ds-de-crispr-venn.pdf
│   ├── gene-fam-DE-plot.pdf
│   ├── gsva_heatmap_dna_repair.pdf
│   ├── gsva_heatmap_dna_repair_de.pdf
Expand All @@ -94,9 +97,9 @@ bash run_module.sh
│   ├── ctrl_vs_treated.de.formatted.tsv
│   ├── ctrl_vs_treated.de.tsv
│   ├── de_genes.tsv
│   ├── dex-sign-goi.tsv
│   ├── differential_splice_by_goi_category.tsv
│   ├── ds-de-crispr-events.tsv
│   ├── ds-de-crispr-venn.pdf
│   ├── expr_collapsed_clk1_ctrl_morpho_dna_repair_gsva_scores.tsv
│   ├── expr_collapsed_clk1_ctrl_morpho_hallmark_gsva_scores.tsv
│   ├── expr_collapsed_clk1_ctrl_morpho_kegg_gsva_scores.tsv
Expand Down Expand Up @@ -129,4 +132,4 @@ bash run_module.sh
│   ├── splicing_events.morpho.RI.intersectUnip.ggplot.txt
│   └── splicing_events.morpho.SE.intersectUnip.ggplot.txt
└── run_module.sh
```
```
20 changes: 0 additions & 20 deletions analyses/README.md

This file was deleted.

32 changes: 32 additions & 0 deletions analyses/cohort_summary/README.md
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@@ -0,0 +1,32 @@
# Cohort summary

Module authors: Ammar Naqvi (@naqvia)

The purpose of this module is to summarize cohort in our downstream analyses.

## Usage
<br>**Run shell script to make final tables to be used for plotting below**
```
bash run_module.sh
```
Input files (`data` folder):
```
histologies.tsv
independent-specimens.rnaseqpanel.primary.tsv
```

## Folder content
* `01-generate-cohort-summary-circos-plot.R` creates circos plot of cohort highlighting histology, CNS region and reported gender

## Directory structure
```
.
├── 01-generate-cohort-summary-circos-plot.R
├── input
│   └── plot-mapping.tsv
├── plots
│   └── cohort_circos.pdf
└── results
├── histologies-plot-group.tsv
└── plot_mapping.tsv
```
8 changes: 6 additions & 2 deletions analyses/histology-specific-splicing/README.md
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Expand Up @@ -21,18 +21,22 @@ independent-specimens.rnaseqpanel.primary-plus.tsv
* `run_module.sh` shell script to pre-process histology file and run analysis
* `01-generate_hist_spec_events_tab.pl` processes rMATs output and identifies unique splicing events if it is in 2% of the histology-specific cohort
* `02-plot_histology-specific_splicing_events.R` takes result table frmo above and generates UpSetR plots for each splicing case
* `03-plot-histology-specific-norm-events.R` computes and plots the average number of unique events per histology

## Directory structure
```
.
├── 01-generate_hist_spec_events_tab.pl
├── 02-plot_histology-specific_splicing_events.R
├── 03-plot-histology-specific-norm-events.R
├── README.md
├── plots
│   ├── avg-uniq-hits.pdf
│   ├── upsetR_histology-specific.ei.pdf
│   └── upsetR_histology-specific.es.pdf
├── results
│   ├── recurrent_splice_events_by_histology.tsv
│   ├── unique_events-ei.tsv
│   ├── unique_events-es.tsv
│   └── splicing_events.hist-labeled_list.thr2freq.txt
│   └── unique_events-es.tsv
└── run_module.sh
```
30 changes: 30 additions & 0 deletions analyses/splicing_events_functional_sites/README.md
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Expand Up @@ -44,3 +44,33 @@ results/splicing_events.total.HGG.neg.intersectUnip.ggplot.txt
* `03-format_for_ggplot.sh` formats and appends file into table for plotting
* `04-plot_splicing_across_functional_sites.R` generates ggplot violin plots of average dPSI per event identidied overlapping a functional site, outputting to `plots/*png`
* `05-plot-splice-patterns` generates plots for visualizing splicing event types into `plots` folder

## Directory structure
.
├── 01-extract_recurrent_splicing_events_hgg.pl
├── 02-run_bedtools_intersect.sh
├── 02-run_bedtools_intersect.tmp.sh
├── 03-format_for_ggplot.pl
├── 04-plot_splicing_across_functional_sites.R
├── 05-plot-splice-patterns.R
├── README.md
├── input
│   ├── CLK1-rmats.tsv
│   ├── gene_lists.tsv
│   ├── unipDisulfBond.hg38.col.bed
│   ├── unipDomain.hg38.col.bed
│   ├── unipLocSignal.hg38.col.bed
│   ├── unipMod.hg38.col.bed
│   └── unipOther.hg38.col.bed
├── plots
│   ├── dPSI_across_functional_sites.HGG.pdf
│   ├── dPSI_across_functional_sites_kinase.HGG.pdf
│   ├── kinases-ora-plot.pdf
│   └── splicing_pattern_plot.pdf
├── results
│   ├── kinases-functional_sites.tsv
│   ├── splice_events.diff.SE.txt
│   ├── splicing_events.SE.total.neg.intersectunip.ggplot.txt
│   └── splicing_events.SE.total.pos.intersectunip.ggplot.txt
├── run_module.sh
└── scr
14 changes: 12 additions & 2 deletions analyses/stranded-polyA-assessment/README.md
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Expand Up @@ -5,7 +5,7 @@ This module correlates polyA and stranded PSIs from patient samples known to hav
## Usage
`bash run_module`

## Folder content
## Folder content
`01-plot-str-vs-polyA.Rmd` runs correlation analysis on samples with both stranded and polyA RNA-seq and generates scatter plots.

```
Expand All @@ -17,4 +17,14 @@ This module correlates polyA and stranded PSIs from patient samples known to hav
│   ├── PT_RYMG3M91_polyA_v_stranded_psi.pdf
│   └── PT_W5GP3F6B_polyA_v_stranded_psi.pdf
└── run_module.sh
```
```

## Directory structure
.
├── 01-plot-str-vs-polyA.Rmd
├── 01-plot-str-vs-polyA.html
├── README.md
├── plots
│   ├── PT_RYMG3M91_polyA_v_stranded_psi.pdf
│   └── PT_W5GP3F6B_polyA_v_stranded_psi.pdf
└── run_module.sh

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