Mercurial > repos > iuc > scanpy_plot
diff README.md @ 1:e4c0f5ee8e17 draft
"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/scanpy/ commit 8ef5f7c6f8728608a3f05bb51e11b642b84a05f5"
author | iuc |
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date | Wed, 16 Oct 2019 06:28:57 -0400 |
parents | 397d2c97af05 |
children | 2dfb2227a16c |
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--- a/README.md Mon Mar 04 10:14:25 2019 -0500 +++ b/README.md Wed Oct 16 06:28:57 2019 -0400 @@ -1,138 +1,115 @@ Scanpy ====== -## Classification of methods into steps +1. Inspect & Manipulate (`inspect.xml`) -Steps: + Methods | Description + --- | --- + `pp.calculate_qc_metrics` | Calculate quality control metrics + `pp.neighbors` | Compute a neighborhood graph of observations + `tl.score_genes` | Score a set of genes + `tl.score_genes_cell_cycle` | Score cell cycle gene + `tl.rank_genes_groups` | Rank genes for characterizing groups + `tl.marker_gene_overlap` | Calculate an overlap score between data-deriven marker genes and provided markers (**not working for now**) + `pp.log1p` | Logarithmize the data matrix. + `pp.scale` | Scale data to unit variance and zero mean + `pp.sqrt` | Square root the data matrix -1. Filtering +2. Filter (`filter.xml`) Methods | Description --- | --- `pp.filter_cells` | Filter cell outliers based on counts and numbers of genes expressed. `pp.filter_genes` | Filter genes based on number of cells or counts. - `pp.filter_genes_dispersion` | Extract highly variable genes + `tl.filter_rank_genes_groups` | Filters out genes based on fold change and fraction of genes expressing the gene within and outside the groupby categories (**to fix**) `pp.highly_variable_genes` | Extract highly variable genes `pp.subsample` | Subsample to a fraction of the number of observations - `queries.gene_coordinates` | (Could not find...) - `queries.mitochondrial_genes` | Retrieves Mitochondrial gene symbols for specific organism through BioMart for filtering - -2. Quality Plots - - These are in-between stages used to measure the effectiveness of a Filtering/Normalisation/Conf.Removal stage either after processing or prior to. + `pp.downsample_counts` | Downsample counts so that each cell has no more than target_counts - Methods | Description | Notes - --- | --- | --- - `pp.calculate_qc_metrics` | Calculate quality control metrics - `pl.violin` | violin plot of features, lib. size, or subsets of. - `pl.stacked_violin` | Same as above but for multiple series of features or cells - -3. Normalization +3. Normalize (`normalize.xml`) Methods | Description --- | --- - `pp.normalize_per_cell` | Normalize total counts per cell + `pp.normalize_total` | Normalize counts per cell `pp.recipe_zheng17` | Normalization and filtering as of [Zheng17] `pp.recipe_weinreb17` | Normalization and filtering as of [Weinreb17] `pp.recipe_seurat` | Normalization and filtering as of Seurat [Satija15] - `pp.log1p` | Logarithmize the data matrix. - `pp.scale` | Scale data to unit variance and zero mean - `pp.sqrt` | - `pp.downsample_counts` | Downsample counts so that each cell has no more than target_counts -4. Conf. removal +4. Remove confounders (`remove_confounder.xml`) Methods | Description --- | --- `pp.regress_out` | Regress out unwanted sources of variation `pp.mnn_correct` | Correct batch effects by matching mutual nearest neighbors - `pp.dca` | Deep count autoencoder to denoise the data - `pp.magic` | Markov Affinity-based Graph Imputation of Cells (MAGIC) API to denoise - `tl.sim` | Simulate dynamic gene expression data [Wittman09] - `pp.calculate_qc_metrics` | Calculate quality control metrics - `tl.score_genes` | Score a set of genes - `tl.score_genes_cell_cycle` | Score cell cycle genes - `tl.cyclone` | Assigns scores and predicted class to observations based on cell-cycle genes [Scialdone15] - `tl.sandbag` | Calculates pairs of genes serving as markers for each cell-cycle phase [Scialdone15] + `pp.combat` | ComBat function for batch effect correction -5. Clustering and Heatmaps +5. Clustering, embedding and trajectory inference (`cluster_reduce_dimension.xml`) Methods | Description --- | --- - `tl.leiden` | Cluster cells into subgroups [Traag18] [Levine15] - `tl.louvain` | Cluster cells into subgroups [Blondel08] [Levine15] [Traag17] + `tl.louvain` | Cluster cells into subgroups + `tl.leiden` | Cluster cells into subgroups `tl.pca` | Principal component analysis `pp.pca` | Principal component analysis (appears to be the same func...) `tl.diffmap` | Diffusion Maps `tl.tsne` | t-SNE `tl.umap` | Embed the neighborhood graph using UMAP - `tl.phate` | PHATE - `pp.neighbors` | Compute a neighborhood graph of observations - `tl.rank_genes_groups` | Rank genes for characterizing groups - `pl.rank_genes_groups` | - `pl.rank_genes_groups_dotplot` | - `pl.rank_genes_groups_heatmap` | - `pl.rank_genes_groups_matrixplot` | - `pl.rank_genes_groups_stacked_violin` | - `pl.rank_genes_groups_violin` | - `pl.matrix_plot` | - `pl.heatmap` | - `pl.highest_expr_genes` | - `pl.diffmap` | + `tl.draw_graph` | Force-directed graph drawing + `tl.dpt` | Infer progression of cells through geodesic distance along the graph + `tl.paga` | Mapping out the coarse-grained connectivity structures of complex manifolds + +6. Plot (`plot.xml`) + + 1. Generic + + Methods | Description + --- | --- + `pl.scatter` | Scatter plot along observations or variables axes + `pl.heatmap` | Heatmap of the expression values of set of genes + `pl.dotplot` | Makes a dot plot of the expression values + `pl.violin` | Violin plot + `pl.stacked_violin` | Stacked violin plots + `pl.matrixplot` | Heatmap of the mean expression values per cluster + `pl.clustermap` | Hierarchically-clustered heatmap -6. Cluster Inspection and plotting + 2. Preprocessing - Methods that draw out the clusters computed in the previous stage, not heatmap or pseudotime related. + Methods | Description + --- | --- + `pl.highest_expr_genes` | Plot the fraction of counts assigned to each gene over all cells + `pl.highly_variable_genes` | Plot dispersions versus means for genes + + 3. PCA - Methods | Description - --- | --- - `pl.clustermap` | - `pl.phate` | - `pl.dotplot` | - `pl.draw_graph` | (really general purpose, would not implement directly) - `pl.filter_genes_dispersion` | (depreciated for 'highly_variable_genes') - `pl.matrix` | (could not find in API) - `pl.pca` | - `pl.pca_loadings` | - `pl.pca_overview` | - `pl.pca_variance_ratio` | - `pl.ranking` | (not sure what this does...) - `pl.scatter` | ([very general purpose](https://icb-scanpy.readthedocs-hosted.com/en/latest/api/scanpy.api.pl.scatter.html), would not implement directly) - `pl.set_rcParams_defaults` | - `pl.set_rcParams_scanpy` | - `pl.sim` | - `pl.tsne` | - `pl.umap` | + Methods | Description + --- | --- + `pl.pca` | Scatter plot in PCA coordinates + `pl.pca_loadings` | Rank genes according to contributions to PCs + `pl.pca_variance_ratio` | Scatter plot in PCA coordinates + `pl.pca_overview` | Plot PCA results -7. Branch/Between-Cluster Inspection + 4. Embeddings - Pseudotime analysis, relies on initial clustering. + Methods | Description + --- | --- + `pl.tsne` | Scatter plot in tSNE basis + `pl.umap` | Scatter plot in UMAP basis + `pl.diffmap` | Scatter plot in Diffusion Map basis + `pl.draw_graph` | Scatter plot in graph-drawing basis - Methods | Description - --- | --- - `tl.dpt` | Infer progression of cells through geodesic distance along the graph [Haghverdi16] [Wolf17i] - `pl.dpt_groups_pseudotime` | - `pl.dpt_timeseries` | - `tl.paga_compare_paths` | - `tl.paga_degrees` | - `tl.paga_expression_entropies` | - `tl.paga` | Generate cellular maps of differentiation manifolds with complex topologies [Wolf17i] - `pl.paga` | - `pl.paga_adjacency` | - `pl.paga_compare` | - `pl.paga_path` | - `pl.timeseries` | - `pl.timeseries_as_heatmap` | - `pl.timeseries_subplot` | + 5. Branching trajectories and pseudotime, clustering + Methods | Description + --- | --- + `pl.dpt_groups_pseudotime` | Plot groups and pseudotime + `pl.dpt_timeseries` | Heatmap of pseudotime series + `pl.paga` | Plot the abstracted graph through thresholding low-connectivity edges + `pl.paga_compare` | Scatter and PAGA graph side-by-side + `pl.paga_path` | Gene expression and annotation changes along paths -Methods to sort | Description ---- | --- -`tl.ROC_AUC_analysis` | (could not find in API) -`tl.correlation_matrix` | (could not find in API) -`rtools.mnn_concatenate` | (could not find in API) -`utils.compute_association_matrix_of_groups` | (could not find in API) -`utils.cross_entropy_neighbors_in_rep` | (could not find in API) -`utils.merge_groups` | (could not find in API) -`utils.plot_category_association` | (could not find in API) -`utils.select_groups` | (could not find in API) \ No newline at end of file + 6. Marker genes + + Methods | Description + --- | --- + `pl.rank_genes_groups` | Plot ranking of genes using dotplot plot + `pl.rank_genes_groups_violin` | Plot ranking of genes for all tested comparisons