Mercurial > repos > bgruening > deeptools_multi_bam_summary
comparison multiBamSummary.xml @ 1:f2a582e0314d draft
planemo upload for repository https://github.com/fidelram/deepTools/tree/master/galaxy/wrapper/ commit fef8b344925620444d93d8159c0b2731a5777920
author | bgruening |
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date | Mon, 15 Feb 2016 10:27:26 -0500 |
parents | 04b612e24e62 |
children | b319edc108a7 |
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0:04b612e24e62 | 1:f2a582e0314d |
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39 #end if | 39 #end if |
40 ]]> | 40 ]]> |
41 </command> | 41 </command> |
42 | 42 |
43 <inputs> | 43 <inputs> |
44 <expand macro="multiple_input_bams" /> | 44 <expand macro="multiple_input_bams_min2" /> |
45 | 45 |
46 <conditional name="mode"> | 46 <conditional name="mode"> |
47 <param name="modeOpt" type="select" label="Choose computation mode" | 47 <param name="modeOpt" type="select" label="Choose computation mode" |
48 help="In the bins mode, the coverage is computed for equally | 48 help="In the bins mode, the coverage is computed for equally |
49 sized bins. In the BED file mode, a list of genomic regions in BED | 49 sized bins. \nIn BED file mode, a list of genomic regions |
50 format has to be given. For each region in the BED file the number of | 50 in BED or INTERVAL format has to be given. For each region |
51 overlapping reads is counted in each of the BAM files. | 51 in the BED file, the number of overlapping reads from each BAM file is counted. |
52 "> | 52 "> |
53 <option value="bins" selected="true">Bins</option> | 53 <option value="bins" selected="true">Bins</option> |
54 <option value="BED-file">Limit calculation to certain regions (BED file)</option> | 54 <option value="BED-file">Limit calculation to certain regions (BED file)</option> |
55 </param> | 55 </param> |
56 <when value="bins"> | 56 <when value="bins"> |
61 <expand macro="distanceBetweenBins" /> | 61 <expand macro="distanceBetweenBins" /> |
62 | 62 |
63 </when> | 63 </when> |
64 <when value="BED-file"> | 64 <when value="BED-file"> |
65 <param name="region_file" type="data" format="bed" | 65 <param name="region_file" type="data" format="bed" |
66 label="Region file in BED format" | 66 label="Region file in BED or INTERVAL format" |
67 help="Coverage is computed for the number of reads that overlap such regions."/> | 67 help="Coverage is computed for the number of reads that overlap such regions."/> |
68 </when> | 68 </when> |
69 </conditional> | 69 </conditional> |
70 | 70 |
71 <expand macro="region_limit_operation" /> | 71 <expand macro="region_limit_operation" /> |
100 | 100 |
101 </tests> | 101 </tests> |
102 <help> | 102 <help> |
103 <![CDATA[ | 103 <![CDATA[ |
104 | 104 |
105 **What it does** | 105 What it does |
106 ------------- | |
106 | 107 |
107 This tool generates a matrix of read-coverages for a list of genomic regions and at least two samples (BAM files). | 108 This tool generates a matrix of read coverages for a list of genomic regions and at least two samples (BAM files). |
108 The genome is split into bins of the given size. For each bin, the number of reads found in it in each BAM file is counted. | 109 The genome is split into bins of the given size. For each bin, the number of reads found in each BAM file is counted. |
109 Alternatively, a bed file with pre-defined genomic regions can be provided. In each case the calculation can further be limited to | 110 Alternatively, an interval file with pre-defined genomic regions can be provided. |
110 a given genomic interval (e.g. a given chromosome). This option is mostly used for testing and efficiency. | |
111 A typical follow-up application is to check and visualize the similarity between replicates or published data sets (see: plotPCA and plotCorrelation). | |
112 | 111 |
113 **Output files**: | 112 In principle, this tool does the same as ``multiBigwigSummary``, but for BAM files. |
114 | 113 |
115 - **score matrix**: a compressed matrix where every row corresponds to a genomic region (or bin) and each column corresponds to a sample (BAM file) | 114 A typical follow-up application is to check and visualize the similarity and variability between replicates or published data sets (see: ``plotPCA`` and ``plotCorrelation``). |
116 - Optional : Uncompressed **score matrix**, in case you want to analyse the coverage scores yourself. (Select to "Save raw counts" from above) | |
117 | 115 |
118 ======= | 116 Output |
117 -------- | |
119 | 118 |
120 .. image:: $PATH_TO_IMAGES/QC_multiBamSummary_humanSamples.png | 119 The default output is a **compressed file** that can only be used with ``plotPCA`` or ``plotCorrelation``. |
121 :alt: Heatmap of RNA Polymerase II ChIP-seq | |
122 | 120 |
121 To analyze the coverage scores yourself, you can get the **uncompressed score matrix** where every row corresponds to a genomic region (or bin) and each column corresponds to a sample (BAM file). (To obtain this output file, select "Save raw counts (coverages) to file" ) | |
123 | 122 |
124 You can find more details on the multiBamSummary doc page: https://deeptools.readthedocs.org/en/master/content/tools/multiBamSummary.html | 123 .. image:: $PATH_TO_IMAGES/multiBamSummary_output.png |
124 :width: 600 | |
125 :height: 443 | |
125 | 126 |
126 ----- | 127 ----- |
127 | 128 |
128 @REFERENCES@ | 129 @REFERENCES@ |
129 ]]> | 130 ]]> |