Mercurial > repos > iuc > scater_plot_tsne
annotate README.md @ 2:99f912d5af9f draft default tip
"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/scater commit 9961b5acbf9081f10e14bc272406b36854fa2924"
author | iuc |
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date | Mon, 08 Nov 2021 12:03:09 +0000 |
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"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/scater commit 61f3899168453092fd25691cf31871a3a350fd3b"
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1 # Wrappers for Scater |
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"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/scater commit 154318f74839a4481c7c68993c4fb745842c4cce"
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3 This code wraps a number of [scater](https://bioconductor.org/packages/release/bioc/html/scater.html) and [scuttle](https://bioconductor.org/packages/3.13/bioc/html/scuttle.html) functions as Galaxy wrappers. Briefly, the `scater-create-qcmetric-ready-sce` tool takes a sample gene expression matrix (usually read-counts) and a cell annotation file, creates a [SingleCellExperiment](https://bioconductor.org/packages/release/bioc/html/SingleCellExperiment.html) object and runs scater's `calculateQCMetrics` function (using other supplied files such as ERCC's and mitochondrial gene features). |
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4 Various filter scripts are provided, along with some plotting functions for QC. |
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7 ## Typical workflow |
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9 1. Read in data with `scater-create-qcmetric-ready-sce`. |
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10 2. Visualise it. |
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11 Take a look at the distribution of library sizes, expressed features and mitochondrial genes with `scater-plot-dist-scatter`. |
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13 3. Guided by the plots, filter the data with `scater-filter`.\ |
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14 You can either manually filter with user-defined parameters or use PCA to automatically removes outliers. |
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15 4. Visualise data again to see how the filtering performed using `scater-plot-dist-scatter`.\ |
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16 Decide if you're happy with the data. If not, try increasing or decreasing the filtering parameters. |
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18 6. Investigate other confounding factors.\ |
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19 Plot the data (using PCA) and display various annotated properties of the cells using `scater-plot-pca`. |
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21 ## Command-line usage |
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23 The scripts require the installation of scater and few other R/BioConductor packages. An easy way to install them is to create a [conda](https://conda.io/) environment using the `environment.yml` file distributed together with these wrappers: |
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25 ``` |
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26 conda env create -f environment.yml |
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27 conda activate scater |
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28 ``` |
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30 For help with any of the following scripts, run: |
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31 `<script-name> --help` |
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33 --- |
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35 `scater-create-qcmetric-ready-sce.R` |
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36 Takes an expression matrix (usually read-counts) of samples (columns) and gene/transcript features (rows), along with other annotation information, such as cell metadata, control genes (mitochondrail genes, ERCC's), creates a [SingleCellExperiment](https://bioconductor.org/packages/release/bioc/html/SingleCellExperiment.html) object and runs scater's `calculateQCMetrics`. Save the resulting SingleCellExperiment object in Loom format. |
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39 ``` |
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40 ./scater-create-qcmetric-ready-sce.R -a test-data/counts.txt -c test-data/annotation.txt -f test-data/mt_controls.txt -o test-data/scater_qcready.loom |
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41 ``` |
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43 --- |
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45 `scater-plot-dist-scatter.R` |
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46 Takes SingleCellExperiment object (from Loom file) and plots a panel of read and feature graphs, including the distribution of library sizes, distribution of feature counts, a scatterplot of reads vs features, and % of mitochondrial genes in library. |
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47 |
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48 ``` |
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49 ./scater-plot-dist-scatter.R -i test-data/scater_qcready.loom -o test-data/scater_reads_genes_dist.pdf |
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50 ``` |
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55 `scater-pca-filter.R` |
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56 Takes SingleCellExperiment object (from Loom file) and automatically removes outliers from data using PCA. Save the filtered SingleCellExperiment object in Loom format. |
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58 ``` |
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59 ./scater-pca-filter.R -i test-data/scater_qcready.loom -o test-data/scater_pca_filtered.loom |
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60 ``` |
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64 `scater-manual-filter.R` |
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65 Takes SingleCellExperiment object (from Loom file) and filters data using user-provided parameters. Save the filtered SingleCellExperiment object in Loom format. |
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67 ``` |
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68 ./scater-manual-filter.R -i test-data/scater_qcready.loom -l 10000 -d 4 -m 33 -o test-data/scater_manual_filtered.loom |
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69 ``` |
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73 `scater-plot-pca.R` |
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74 PCA plot of a SingleCellExperiment object. The options `-c`, `-p`, and `-s` all refer to cell annotation features. These are the column headers of the `-c` option used in `scater-create-qcmetric-ready-sce.R`. |
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76 ``` |
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77 ./scater-plot-pca.R -i test-data/scater_qcready.loom -c Treatment -p Mutation_Status -o test-data/scater_pca_plot.pdf |
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78 ``` |
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82 `scater-plot-tsne.R` |
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"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/scater commit 154318f74839a4481c7c68993c4fb745842c4cce"
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83 t-SNE plot of a SingleCellExperiment object. The options `-c`, `-p`, and `-s` all refer to cell annotation features. These are the column headers of the `-c` option used in `scater-create-qcmetric-ready-sce.R`. |
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84 |
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85 ``` |
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86 ./scater-plot-tsne.R -i test-data/scater_qcready.loom -c Treatment -p Mutation_Status -o test-data/scater_tsne_plot.pdf |
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"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/scater commit 61f3899168453092fd25691cf31871a3a350fd3b"
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87 ``` |