Mercurial > repos > ebi-gxa > seurat_find_markers
comparison seurat_find_markers.xml @ 0:fde95fe95f15 draft
planemo upload for repository https://github.com/ebi-gene-expression-group/container-galaxy-sc-tertiary/ commit 9bf9a6e46a330890be932f60d1d996dd166426c4
author | ebi-gxa |
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date | Wed, 03 Apr 2019 11:17:29 -0400 |
parents | |
children | 7895b4bb6247 |
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1 <tool id="seurat_find_markers" name="Seurat FindMarkers" version="2.3.1+galaxy1"> | |
2 <description>find markers (differentially expressed genes)</description> | |
3 <macros> | |
4 <import>seurat_macros.xml</import> | |
5 </macros> | |
6 <expand macro="requirements" /> | |
7 <expand macro="version" /> | |
8 <command detect_errors="exit_code"><![CDATA[ | |
9 seurat-find-markers.R | |
10 | |
11 --input-object-file '$input' | |
12 --output-text-file output.txt | |
13 | |
14 #if $genes_use: | |
15 --genes-use '$genes_use' | |
16 #end if | |
17 | |
18 #if str($logfc_threshold): | |
19 --logfc-threshold '$logfc_threshold' | |
20 #end if | |
21 | |
22 #if str($adv.min_pct): | |
23 --min-pct '$adv.min_pct' | |
24 #end if | |
25 | |
26 #if str($adv.min_diff_pct): | |
27 --min-diff-pct '$adv.min_diff_pct' | |
28 #end if | |
29 | |
30 #if $adv.only_pos: | |
31 --only-pos '$adv.only_pos' | |
32 #end if | |
33 | |
34 --test-use '$adv.test_use' | |
35 | |
36 #if str($max_cells_per_ident): | |
37 --max-cells-per-ident '$max_cells_per_ident' | |
38 #end if | |
39 | |
40 #if str($min_cells_per_gene): | |
41 --min-cells-gene '$min_cells_per_gene' | |
42 #end if | |
43 | |
44 #if str($min_cells_group): | |
45 --min-cells-group '$min_cells_group' | |
46 #end if | |
47 | |
48 | |
49 ]]></command> | |
50 | |
51 <inputs> | |
52 <param name="input" type="data" format="rdata" label="RDS object" /> | |
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."/> | |
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."/> | |
57 <param name="min_cells_group" label="Min cells in one of the groups" optional="true" argument="--min-cells-group" type="integer"/> | |
58 <section name="adv" title="Advanced Options"> | |
59 <param name="min_pct" type="float" label="Min Pct" optional="true" help="Only test genes that are detected in a minimum fraction of min.pct cells in either of the two populations. Meant to speed up the function by not testing genes that are very infrequently expressed. Default is 0.1."/> | |
60 <param name="min_diff_pct" type="float" label="Min diff Pct" optional="true" help="Only test genes that show a minimum difference in the fraction of detection between the two groups. Set to -Inf by default."/> | |
61 <param name="only_pos" type="boolean" label="Only positive markers" truevalue="TRUE" falsevalue="" help="Only return positive markers (FALSE by default)."/> | |
62 <param name="test_use" type="select" label="Test to use" help=""> | |
63 <option value="wilcox" selected="true">Wilcoxon</option> | |
64 <option value="bimod">Bi-modal</option> | |
65 <option value="roc">ROC</option> | |
66 <option value="t">t-Test</option> | |
67 <option value="tobit">tobit</option> | |
68 <option value="poisson">Poisson</option> | |
69 <option value="negbinom">Negative binomia</option> | |
70 <option value="MAST">MAST</option> | |
71 <option value="DESeq2">DESeq2</option> | |
72 </param> | |
73 </section> | |
74 </inputs> | |
75 | |
76 <outputs> | |
77 <data name="output" format="txt" from_work_dir="output.txt" label="${tool.name} on ${on_string}: Text file"/> | |
78 </outputs> | |
79 | |
80 <tests> | |
81 <test> | |
82 <param name="input" ftype="rdata" value="out_runtsne.rds"/> | |
83 <output name="output" ftype="txt" value="out_findmark.txt"/> | |
84 </test> | |
85 </tests> | |
86 <help><![CDATA[ | |
87 .. class:: infomark | |
88 | |
89 **What it does** | |
90 | |
91 Seurat_ is a toolkit for quality control, analysis, and exploration of single cell RNA sequencing data. | |
92 It is developed and maintained by the `Satija Lab`_ at NYGC. Seurat aims to enable users to identify and | |
93 interpret sources of heterogeneity from single cell transcriptomic measurements, and to integrate diverse | |
94 types of single cell data. | |
95 | |
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.) | |
97 | |
98 ----- | |
99 | |
100 **Inputs** | |
101 | |
102 * RDS object | |
103 | |
104 ----- | |
105 | |
106 **Outputs** | |
107 | |
108 * Text file | |
109 | |
110 .. _Seurat: https://www.nature.com/articles/nbt.4096 | |
111 .. _Satija Lab: https://satijalab.org/seurat/ | |
112 | |
113 @VERSION_HISTORY@ | |
114 ]]></help> | |
115 <expand macro="citations" /> | |
116 </tool> |