Mercurial > repos > nilesh > rseqc
comparison read_NVC.xml @ 49:6b33e31bda10 draft
Uploaded tar based on https://github.com/lparsons/galaxy_tools/tree/master/tools/rseqc 1a3c419bc0ded7c40cb2bc3e7c87bfb01ddfeba2
author | lparsons |
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date | Thu, 16 Jul 2015 17:43:43 -0400 |
parents | eb339c5849bb |
children | 09846d5169fa |
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48:2e6190c29c54 | 49:6b33e31bda10 |
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1 <tool id="rseqc_read_NVC" name="Read NVC" version="2.4"> | 1 <tool id="rseqc_read_NVC" name="Read NVC" version="2.4galaxy1"> |
2 <description>to check the nucleotide composition bias</description> | 2 <description>to check the nucleotide composition bias</description> |
3 | |
4 <macros> | |
5 <import>rseqc_macros.xml</import> | |
6 </macros> | |
7 | |
3 <requirements> | 8 <requirements> |
4 <requirement type="package" version="3.0.3">R</requirement> | 9 <expand macro="requirement_package_r" /> |
5 <requirement type="package" version="1.7.1">numpy</requirement> | 10 <expand macro="requirement_package_numpy" /> |
6 <requirement type="package" version="2.4">rseqc</requirement> | 11 <expand macro="requirement_package_rseqc" /> |
7 </requirements> | 12 </requirements> |
13 | |
14 <expand macro="stdio" /> | |
15 | |
16 <version_command><![CDATA[read_NVC.py --version]]></version_command> | |
17 | |
8 <command> | 18 <command> |
9 read_NVC.py -i $input -o output $nx | 19 read_NVC.py |
20 --input-file $input | |
21 --out-prefix output | |
22 $nx | |
23 --mapq $mapq | |
10 </command> | 24 </command> |
11 <stdio> | 25 |
12 <exit_code range="1:" level="fatal" description="An error occured during execution, see stderr and stdout for more information" /> | |
13 <regex match="[Ee]rror" source="both" description="An error occured during execution, see stderr and stdout for more information" /> | |
14 </stdio> | |
15 <inputs> | 26 <inputs> |
16 <param name="input" type="data" format="bam,sam" label="input bam/sam file" /> | 27 <param name="input" type="data" format="bam,sam" label="input bam/sam file" help="(--input-file)"/> |
17 <param name="nx" type="boolean" value="false" truevalue="-x" falsevalue="" label="Include N,X in NVC plot"/> | 28 <param name="nx" type="boolean" value="false" truevalue="--nx" falsevalue="" label="Include N,X in NVC plot" help="(--nx)"/> |
29 <param name="mapq" type="integer" label="Minimum mapping quality (default=30)" help="Minimum phred scale mapping quality to consider a read 'uniquely mapped' (--mapq)" value="30" /> | |
18 </inputs> | 30 </inputs> |
31 | |
19 <outputs> | 32 <outputs> |
20 <data format="xls" name="outputxls" from_work_dir="output.NVC.xls" label="${tool.name} on ${on_string} (XLS)" /> | 33 <data format="xls" name="outputxls" from_work_dir="output.NVC.xls" label="${tool.name} on ${on_string} (XLS)" /> |
21 <data format="txt" name="outputr" from_work_dir="output.NVC_plot.r" label="${tool.name} on ${on_string} (R Script)" /> | 34 <data format="txt" name="outputr" from_work_dir="output.NVC_plot.r" label="${tool.name} on ${on_string} (R Script)" /> |
22 <data format="pdf" name="outputpdf" from_work_dir="output.NVC_plot.pdf" label="${tool.name} on ${on_string} (PDF)" /> | 35 <data format="pdf" name="outputpdf" from_work_dir="output.NVC_plot.pdf" label="${tool.name} on ${on_string} (PDF)" /> |
23 </outputs> | 36 </outputs> |
24 <help> | 37 |
38 <tests> | |
39 <test> | |
40 <param name="input" value="pairend_strandspecific_51mer_hg19_chr1_1-100000.bam"/> | |
41 <output name="outputxls" file="output.NVC.xls"/> | |
42 <output name="outputr" file="output.NVC_plot.r"/> | |
43 </test> | |
44 </tests> | |
45 | |
46 <help><![CDATA[ | |
25 read_NVC.py | 47 read_NVC.py |
26 +++++++++++ | 48 +++++++++++ |
27 | 49 |
28 This module is used to check the nucleotide composition bias. Due to random priming, certain | 50 This module is used to check the nucleotide composition bias. Due to random priming, certain |
29 patterns are over represented at the beginning (5'end) of reads. This bias could be easily | 51 patterns are over represented at the beginning (5'end) of reads. This bias could be easily |
30 examined by NVC (Nucleotide versus cycle) plot. NVC plot is generated by overlaying all | 52 examined by NVC (Nucleotide versus cycle) plot. NVC plot is generated by overlaying all |
31 reads together, then calculating nucleotide composition for each position of read | 53 reads together, then calculating nucleotide composition for each position of read |
32 (or each sequencing cycle). In ideal condition (genome is random and RNA-seq reads is | 54 (or each sequencing cycle). In ideal condition (genome is random and RNA-seq reads is |
33 randomly sampled from genome), we expect A%=C%=G%=T%=25% at each position of reads. | 55 randomly sampled from genome), we expect A%=C%=G%=T%=25% at each position of reads. |
34 | 56 |
35 NOTE: this program expect a fixed read length | 57 NOTE: this program expect a fixed read length |
36 | 58 |
37 Inputs | 59 Inputs |
38 ++++++++++++++ | 60 ++++++++++++++ |
55 | 77 |
56 | 78 |
57 .. image:: http://rseqc.sourceforge.net/_images/NVC_plot.png | 79 .. image:: http://rseqc.sourceforge.net/_images/NVC_plot.png |
58 :height: 600 px | 80 :height: 600 px |
59 :width: 600 px | 81 :width: 600 px |
60 :scale: 80 % | 82 :scale: 80 % |
61 | 83 |
62 ----- | 84 ----- |
63 | 85 |
64 About RSeQC | 86 About RSeQC |
65 +++++++++++ | 87 +++++++++++ |
66 | 88 |
67 The RSeQC_ package provides a number of useful modules that can comprehensively evaluate high throughput sequence data especially RNA-seq data. "Basic modules" quickly inspect sequence quality, nucleotide composition bias, PCR bias and GC bias, while "RNA-seq specific modules" investigate sequencing saturation status of both splicing junction detection and expression estimation, mapped reads clipping profile, mapped reads distribution, coverage uniformity over gene body, reproducibility, strand specificity and splice junction annotation. | 89 The RSeQC_ package provides a number of useful modules that can comprehensively evaluate high throughput sequence data especially RNA-seq data. "Basic modules" quickly inspect sequence quality, nucleotide composition bias, PCR bias and GC bias, while "RNA-seq specific modules" investigate sequencing saturation status of both splicing junction detection and expression estimation, mapped reads clipping profile, mapped reads distribution, coverage uniformity over gene body, reproducibility, strand specificity and splice junction annotation. |
68 | 90 |
69 The RSeQC package is licensed under the GNU GPL v3 license. | 91 The RSeQC package is licensed under the GNU GPL v3 license. |
70 | 92 |
71 .. image:: http://rseqc.sourceforge.net/_static/logo.png | 93 .. image:: http://rseqc.sourceforge.net/_static/logo.png |
72 | 94 |
73 .. _RSeQC: http://rseqc.sourceforge.net/ | 95 .. _RSeQC: http://rseqc.sourceforge.net/ |
96 ]]> | |
97 </help> | |
74 | 98 |
99 <expand macro="citations" /> | |
75 | 100 |
76 </help> | |
77 </tool> | 101 </tool> |