comparison QDNAseq.xml @ 6:beb7abe277b3 draft

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author stef
date Fri, 13 Jun 2014 11:01:25 -0400
parents 75d96e0555d1
children 9f4e0192de10
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5:d4747215fa6b 6:beb7abe277b3
1 <tool id="QDNAseq" name="QDNAseq" version="0.0.1"> 1 <tool id="QDNAseq" name="QDNAseq" version="0.0.1">
2 2
3 <requirements> 3 <requirements>
4 <!-- <requirement type="set_environment">QDNASEQ_SCRIPT_PATH</requirement> --> 4 <requirement type="set_environment">QDNASEQ_SCRIPT_PATH</requirement>
5 <requirement type="package" version="3.0.3">R</requirement> 5 <requirement type="package" version="3.0.3">R</requirement>
6 <requirement type="package" version="1.0.4">bioc_qdnaseq</requirement>
6 </requirements> 7 </requirements>
7 8
8 <description>Quantitative copy number abberation detection</description> 9 <description>Quantitative copy number abberation detection</description>
9 10
10 <command interpreter="Rscript"> 11 <command interpreter="Rscript">
290 291
291 ----- 292 -----
292 293
293 .. class:: warningmark 294 .. class:: warningmark
294 295
295 Requires internet access for downloading bin-annotations from bitbucket and to show css styling of the final report 296 The input BAMs are expected to be **single end reads of 50bp length** mapped to GRCh37/hg19 genome build. Other experiment setups are currently not supported within galaxy. See the documentation of QDNAseq at bioconductor on how to deal with different setups.
296 297
297 .. class:: warningmark 298 .. class:: warningmark
298 299
299 All R stderr is rerouted to stdout due to limitations in R. This means the tool might be marked succesful (green) while it actually isn't, closer inspection of the stdout output is required in that case. 300 Requires **internet access** for downloading bin-annotations from bitbucket and to show css styling of the final report
300 301
301 .. class:: warningmark 302 .. class:: warningmark
302 303
303 The smaller the binsize, the longer the analysis takes
304
305 .. class:: warningmark
306
307 If the data is noisy, a **larger binsize** should be chosen 304 If the data is noisy, a **larger binsize** should be chosen
308
309 .. class:: warningmark
310
311 The input BAMs are expected to be **single end reads of 50bp length** mapped to GRCh37/hg19 genome build. Other experiment setups are currently not supported within galaxy. See the documentation of QDNAseq at bioconductor on how to deal with different setups.
312 305
313 ----- 306 -----
314 307
315 **Example** 308 **Example**
316 309