Mercurial > repos > iuc > scanpy_cluster_reduce_dimension
diff README.md @ 0:0e212e42ef88 draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/scanpy/ commit 92f85afaed0097d1879317a9f513093fce5481d6
author | iuc |
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date | Mon, 04 Mar 2019 10:13:44 -0500 |
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children | 20cfb9f3dded |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/README.md Mon Mar 04 10:13:44 2019 -0500 @@ -0,0 +1,138 @@ +Scanpy +====== + +## Classification of methods into steps + +Steps: + +1. Filtering + + 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 + `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. + + 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 + + Methods | Description + --- | --- + `pp.normalize_per_cell` | Normalize total 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 + + 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] + +5. Clustering and Heatmaps + + Methods | Description + --- | --- + `tl.leiden` | Cluster cells into subgroups [Traag18] [Levine15] + `tl.louvain` | Cluster cells into subgroups [Blondel08] [Levine15] [Traag17] + `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` | + +6. Cluster Inspection and plotting + + Methods that draw out the clusters computed in the previous stage, not heatmap or pseudotime related. + + 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` | + +7. Branch/Between-Cluster Inspection + + Pseudotime analysis, relies on initial clustering. + + 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` | + + +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