1 | <tool id="rmapq_wrapper" name="RMAPQ" version="1.0.0"> |
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2 | <description>for Solexa Short Reads Alignment with Quality Scores</description> |
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3 | <command interpreter="python"> |
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4 | #if $trim.choice=="No": #rmapq_wrapper.py $database $input_seq $input_score $high_score $high_len 0 $align_len $mismatch $output1 |
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5 | #else: #rmapq_wrapper.py $database $input_seq $input_score $high_score $high_len $trim.read_len $align_len $mismatch $output1 |
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6 | #end if |
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7 | </command> |
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8 | <inputs> |
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9 | <param name="database" type="select" display="radio" label="Target database"> |
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10 | <options from_file="faseq.loc"> |
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11 | <column name="name" index="0"/> |
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12 | <column name="value" index="0"/> |
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13 | </options> |
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14 | </param> |
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15 | <param name="input_seq" type="data" format="fasta" label="Sequence file"/> |
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16 | <param name="input_score" type="data" format="qualsolexa" label="Quality score file"/> |
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17 | <param name="high_score" type="float" size="15" value="40" label="Minimum score for high-quality base (-q)"/> |
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18 | <param name="high_len" type="integer" size="15" value="36" label="Minimal high-quality bases (-M)"/> |
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19 | <param name="align_len" type="integer" size="15" value="11" label="Minimal length of a hit (-h)" help="seed"/> |
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20 | <param name="mismatch" type="select" label="Number of mismatches allowed (-m)"> |
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21 | <option value="0">0</option> |
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22 | <option value="1">1</option> |
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23 | <option value="3">3</option> |
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24 | <option value="5">5</option> |
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25 | </param> |
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26 | <conditional name="trim"> |
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27 | <param name="choice" type="select" label="To trim the reads"> |
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28 | <option value="No">No</option> |
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29 | <option value="Yes">Yes</option> |
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30 | </param> |
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31 | <when value="No"> |
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32 | </when> |
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33 | <when value="Yes"> |
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34 | <param name="read_len" type="integer" size="15" value="36" label="Read length (-w)" /> |
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35 | </when> |
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36 | </conditional> |
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37 | </inputs> |
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38 | <outputs> |
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39 | <data name="output1" format="bed"/> |
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40 | </outputs> |
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41 | <requirements> |
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42 | <requirement type="binary">rmapq</requirement> |
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43 | </requirements> |
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44 | <!-- |
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45 | <tests> |
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46 | <test> |
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47 | <param name="database" value="/galaxy/data/faseq/test" /> |
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48 | <param name="input_seq" value="rmapq_wrapper_test1.fasta" ftype="fasta"/> |
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49 | <param name="input_score" value="rmapq_wrapper_test1.qual" ftype="qualsolexa" /> |
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50 | <param name="high_score" value="40" /> |
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51 | <param name="high_len" value="36" /> |
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52 | <param name="read_len" value="36" /> |
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53 | <param name="align_len" value="36" /> |
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54 | <param name="mismatch" value="3" /> |
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55 | <output name="output1" file="rmapq_wrapper_test1.bed"/> |
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56 | </test> |
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57 | </tests> |
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58 | --> |
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59 | <help> |
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60 | |
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61 | .. class:: warningmark |
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62 | |
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63 | RMAPQ was developed for **Solexa** reads. |
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64 | |
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65 | .. class:: infomark |
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66 | |
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67 | **TIP**. The tool will guess the length of the reads, however, if you select to trim the reads, the *Maximal Length of the Reads* must be between 20 and 64. Reads with lengths longer than the specified value will be trimmed at the 3'end. |
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68 | |
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69 | ----- |
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70 | |
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71 | **What it does** |
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72 | |
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73 | This tool runs **rmapq** (for more information, please see the reference below), searching against a genome build with sequence qualities. |
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74 | |
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75 | ----- |
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76 | |
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77 | **Parameters** |
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78 | |
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79 | - *Minimal High-quality Bases* (**-M**): the minimal length of the high quality score bases |
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80 | - *Minimum Score for High-quality Base* (**-q**) : the minimal quality score |
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81 | - *Minimal Length of a Hit* (**-h**) : the minimal length of an exact match or seed |
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82 | - *Number of Mismatches Allowed* (**-m**) : the maximal number of mismatches allowed in an alignment |
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83 | - *Read Length* (**-w**) : maximal length of the reads; reads longer than the threshold will be truncated at 3' end. |
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84 | |
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85 | ----- |
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86 | |
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87 | **Reference** |
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88 | |
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89 | **RMAP** is developed by Dr. Andrew D Smith and Dr. Zhenyu Xuan at the Cold Spring Harbor Laboratory. Please see http://rulai.cshl.edu/rmap/ |
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90 | |
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91 | </help> |
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92 | </tool> |
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