Mercurial > repos > iuc > scater_normalize
comparison README.md @ 0:87757f7b9974 draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/scater commit 5fdcafccb6c645d301db040dfeed693d7b6b4278
author | iuc |
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date | Thu, 18 Jul 2019 11:13:05 -0400 |
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children | 946179ef029c |
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1 # Wrappers for Scater | |
2 | |
3 This code wraps a number of [scater](https://bioconductor.org/packages/release/bioc/html/scater.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). | |
4 Various filter scripts are provided, along with some plotting functions for QC. | |
5 | |
6 | |
7 ## Typical workflow | |
8 | |
9 1. Read in data with `scater-create-qcmetric-ready-sce`. | |
10 2. Visualise it.\ | |
11 Take a look at the distribution of library sizes, expressed features and mitochondrial genes with `scater-plot-dist-scatter`. | |
12 Then look at the distibution of genes across cells with `scater-plot-exprs-freq`. | |
13 3. Guided by the plots, filter the data with `scater-filter`.\ | |
14 You can either manually filter with user-defined parameters or use PCA to automatically removes outliers. | |
15 4. Visualise data again to see how the filtering performed using `scater-plot-dist-scatter`.\ | |
16 Decide if you're happy with the data. If not, try increasing or decreasing the filtering parameters. | |
17 5. Normalise data with `scater-normalize`. | |
18 6. Investigate other confounding factors.\ | |
19 Plot the data (using PCA) and display various annotated properties of the cells using `scater-plot-pca`. | |
20 | |
21 ## Command-line usage | |
22 | |
23 For help with any of the following scripts, run: | |
24 `<script-name> --help` | |
25 | |
26 --- | |
27 | |
28 `scater-create-qcmetric-ready-sce.R` | |
29 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. | |
30 | |
31 | |
32 ``` | |
33 ./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 | |
34 ``` | |
35 | |
36 --- | |
37 | |
38 `scater-plot-dist-scatter.R` | |
39 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. | |
40 | |
41 ``` | |
42 ./scater-plot-dist-scatter.R -i test-data/scater_qcready.loom -o test-data/scater_reads_genes_dist.pdf | |
43 ``` | |
44 | |
45 --- | |
46 | |
47 `scater-plot-exprs-freq.R` | |
48 Plots mean expression vs % of expressing cells and provides information as to the number of genes expressed in 50% and 25% of cells. | |
49 | |
50 --- | |
51 | |
52 `scater-pca-filter.R` | |
53 Takes SingleCellExperiment object (from Loom file) and automatically removes outliers from data using PCA. Save the filtered SingleCellExperiment object in Loom format. | |
54 | |
55 ``` | |
56 ./scater-pca-filter.R -i test-data/scater_qcready.loom -o test-data/scater_pca_filtered.loom | |
57 ``` | |
58 | |
59 --- | |
60 | |
61 `scater-manual-filter.R` | |
62 Takes SingleCellExperiment object (from Loom file) and filters data using user-provided parameters. Save the filtered SingleCellExperiment object in Loom format. | |
63 | |
64 ``` | |
65 ./scater-manual-filter.R -i test-data/scater_qcready.loom -l 10000 -d 4 -m 33 -o test-data/scater_manual_filtered.loom | |
66 ``` | |
67 | |
68 --- | |
69 | |
70 `scater-normalize.R` | |
71 Compute log-normalized expression values from count data in a SingleCellExperiment object, using the size factors stored in the object. Save the normalised SingleCellExperiment object in Loom format. | |
72 | |
73 ``` | |
74 ./scater-normalize.R -i test-data/scater_manual_filtered.loom -o test-data/scater_man_filtered_normalised.loom | |
75 ``` | |
76 | |
77 --- | |
78 | |
79 `scater-plot-pca.R` | |
80 PCA plot of a normalised SingleCellExperiment object (produced with `scater-normalize.R`). 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`. | |
81 | |
82 ``` | |
83 ./scater-plot-pca.R -i test-data/scater_man_filtered_normalised.loom -c Treatment -p Mutation_Status -o test-data/scater_pca_plot.pdf | |
84 ``` |