Mercurial > repos > ebi-gxa > seurat_find_markers
comparison seurat_find_markers.xml @ 1:7895b4bb6247 draft
planemo upload for repository https://github.com/ebi-gene-expression-group/container-galaxy-sc-tertiary/ commit 0463f230d18201c740851d72e31a5024f391207f
author | ebi-gxa |
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date | Mon, 25 Nov 2019 06:09:57 -0500 |
parents | fde95fe95f15 |
children | 4039a99ae846 |
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0:fde95fe95f15 | 1:7895b4bb6247 |
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1 <tool id="seurat_find_markers" name="Seurat FindMarkers" version="2.3.1+galaxy1"> | 1 <tool id="seurat_find_markers" name="Seurat FindMarkers" version="@SEURAT_VERSION@_@VERSION@+galaxy0"> |
2 <description>find markers (differentially expressed genes)</description> | 2 <description>find markers (differentially expressed genes)</description> |
3 <macros> | 3 <macros> |
4 <import>seurat_macros.xml</import> | 4 <import>seurat_macros.xml</import> |
5 </macros> | 5 </macros> |
6 <expand macro="requirements" /> | 6 <expand macro="requirements" /> |
7 <expand macro="version" /> | 7 <expand macro="version" /> |
8 <command detect_errors="exit_code"><![CDATA[ | 8 <command detect_errors="exit_code"><![CDATA[ |
9 seurat-find-markers.R | 9 seurat-find-markers.R |
10 | 10 |
11 --input-object-file '$input' | 11 @INPUT_OBJECT@ |
12 --output-text-file output.txt | 12 --output-text-file output.txt |
13 | 13 |
14 #if $genes_use: | 14 #if $genes_use: |
15 --genes-use '$genes_use' | 15 --genes-use '$genes_use' |
16 #end if | 16 #end if |
47 | 47 |
48 | 48 |
49 ]]></command> | 49 ]]></command> |
50 | 50 |
51 <inputs> | 51 <inputs> |
52 <param name="input" type="data" format="rdata" label="RDS object" /> | 52 <expand macro="input_object_params"/> |
53 <expand macro="genes-use-input"/> | 53 <expand macro="genes-use-input"/> |
54 <param name="logfc_threshold" label="LogFC logfc_threshold" optional="true" argument="--logfc-threshold" type="float" help="Limit testing to genes which show, on average, at least X-fold difference (log-scale) between the two groups of cells. Default is 0.25 Increasing logfc.threshold speeds up the function, but can miss weaker signals."/> | 54 <param name="logfc_threshold" label="LogFC logfc_threshold" optional="true" argument="--logfc-threshold" type="float" help="Limit testing to genes which show, on average, at least X-fold difference (log-scale) between the two groups of cells. Default is 0.25 Increasing logfc.threshold speeds up the function, but can miss weaker signals."/> |
55 <param name="max_cells_per_ident" label="Max cells per ident" optional="true" argument="--max-cells-per-ident" type="integer" help="Down sample each identity class to a max number. Default is no downsampling. Not activated by default (set to Inf)."/> | 55 <param name="max_cells_per_ident" label="Max cells per ident" optional="true" argument="--max-cells-per-ident" type="integer" help="Down sample each identity class to a max number. Default is no downsampling. Not activated by default (set to Inf)."/> |
56 <param name="min_cells_per_gene" label="Min cells per gene" optional="true" argument="--min-cells-gene" type="integer" help="Minimum number of cells expressing the gene in at least one of the two groups, currently only used for poisson and negative binomial tests."/> | 56 <param name="min_cells_per_gene" label="Min cells per gene" optional="true" argument="--min-cells-gene" type="integer" help="Minimum number of cells expressing the gene in at least one of the two groups, currently only used for poisson and negative binomial tests."/> |
57 <param name="min_cells_group" label="Min cells in one of the groups" optional="true" argument="--min-cells-group" type="integer"/> | 57 <param name="min_cells_group" label="Min cells in one of the groups" optional="true" argument="--min-cells-group" type="integer"/> |
72 </param> | 72 </param> |
73 </section> | 73 </section> |
74 </inputs> | 74 </inputs> |
75 | 75 |
76 <outputs> | 76 <outputs> |
77 <data name="output" format="txt" from_work_dir="output.txt" label="${tool.name} on ${on_string}: Text file"/> | 77 <data name="output" format="csv" from_work_dir="output.txt" label="${tool.name} on ${on_string}: Text file"/> |
78 </outputs> | 78 </outputs> |
79 | 79 |
80 <tests> | 80 <tests> |
81 <test> | 81 <test> |
82 <param name="input" ftype="rdata" value="out_runtsne.rds"/> | 82 <param name="input" ftype="rdata" value="out_runtsne.rds"/> |
86 <help><![CDATA[ | 86 <help><![CDATA[ |
87 .. class:: infomark | 87 .. class:: infomark |
88 | 88 |
89 **What it does** | 89 **What it does** |
90 | 90 |
91 Seurat_ is a toolkit for quality control, analysis, and exploration of single cell RNA sequencing data. | 91 This tool finds markers (differentially expressed genes) for each of the identity classes in a dataset. |
92 It is developed and maintained by the `Satija Lab`_ at NYGC. Seurat aims to enable users to identify and | 92 It outputs a text file containing a ranked list of putative markers, and associated statistics (p-values, ROC score, etc.) |
93 interpret sources of heterogeneity from single cell transcriptomic measurements, and to integrate diverse | |
94 types of single cell data. | |
95 | 93 |
96 This tool finds markers (differentially expressed genes) for each of the identity classes in a dataset. It outputs a text file containing a ranked list of putative markers, and associated statistics (p-values, ROC score, etc.) | 94 p-value adjustment is performed using bonferroni correction based on the total |
95 number of genes in the dataset. Other correction methods are not recommended, | |
96 as Seurat pre-filters genes using the arguments above, reducing the number of | |
97 tests performed. Lastly, as Aaron Lun has pointed out, p-values should be | |
98 interpreted cautiously, as the genes used for clustering are the same genes | |
99 tested for differential expression. | |
100 | |
101 @SEURAT_INTRO@ | |
97 | 102 |
98 ----- | 103 ----- |
99 | 104 |
100 **Inputs** | 105 **Inputs** |
101 | 106 |