Mercurial > repos > bgruening > sailfish
annotate sailfish.xml @ 0:3b4ed0e473dc draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
author | bgruening |
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date | Fri, 16 Oct 2015 15:09:03 -0400 |
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children | 06646e81c543 |
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3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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1 <tool id="sailfish" name="Sailfish" version="0.7.6.0"> |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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2 <description>transcript quantification from RNA-seq data</description> |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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3 <requirements> |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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4 <requirement type="package" version="0.7.6">sailfish</requirement> |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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5 </requirements> |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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6 <macros> |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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7 <xml name="strandedness"> |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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8 <param name="strandedness" type="select" label="Specify the strandedness of the reads"> |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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9 <option value="U" selected="True">Not stranded</option> |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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10 <option value="SF">read 1 (or single-end read) comes from the forward strand</option> |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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11 <option value="SR">read 1 (or single-end read) comes from the reverse strand</option> |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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12 </param> |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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13 </xml> |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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14 </macros> |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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15 <stdio> |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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16 <exit_code range="1:" /> |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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17 <exit_code range=":-1" /> |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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18 <regex match="Error:" /> |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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19 <regex match="Exception:" /> |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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20 </stdio> |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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21 <version_command>sailfish -version</version_command> |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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22 <command> |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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23 <![CDATA[ |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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24 |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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25 #if $refTranscriptSource.TranscriptSource == "history": |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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26 sailfish index |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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27 --transcripts $refTranscriptSource.ownFile |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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28 --kmerSize $refTranscriptSource.kmerSize |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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29 --out ./index_dir |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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30 --threads "\${GALAXY_SLOTS:-4}" |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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31 #set $index_path = './index_dir' |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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32 #else: |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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33 #set $index_path = $refTranscriptSource.index.fields.path |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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34 #end if |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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35 |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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36 && |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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37 |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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38 #if $single_or_paired.single_or_paired_opts == 'single': |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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39 ln -s $single_or_paired.input_singles ./single.$single_or_paired.input_singles.ext && |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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40 #else: |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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41 ln -s $single_or_paired.input_mate1 ./mate1.$single_or_paired.input_mate1.ext && |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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42 ln -s $single_or_paired.input_mate2 ./mate2.$single_or_paired.input_mate2.ext && |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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43 #end if |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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44 |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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45 |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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46 #if $geneMap: |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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47 ln -s "$geneMap" ./geneMap.$geneMap.ext && |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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48 #end if |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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49 |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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50 sailfish quant |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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51 --index $index_path |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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52 #if $single_or_paired.single_or_paired_opts == 'single': |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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53 --libType "${single_or_paired.orientation}${single_or_paired.strandedness}" |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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54 --unmated_reads ./single.$single_or_paired.input_singles.ext |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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55 #else: |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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56 --mates1 ./mate1.$single_or_paired.input_mate1.ext |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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57 --mates2 ./mate2.$single_or_paired.input_mate2.ext |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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58 --libType "${single_or_paired.orientation}${single_or_paired.strandedness}" |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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59 #end if |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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60 --output ./ |
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planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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61 $biasCorrect |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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62 --threads "\${GALAXY_SLOTS:-4}" |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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63 |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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64 #if $fldMean: |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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65 --fldMean $fldMean |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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66 #end if |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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67 |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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68 #if $fldSD: |
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planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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69 --fldSD $fldSD |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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70 #end if |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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71 |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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72 #if $maxReadOcc: |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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73 --maxReadOcc $maxReadOcc |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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74 #end if |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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75 |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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76 #if $geneMap: |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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77 --geneMap ./geneMap.${geneMap.ext} |
3b4ed0e473dc
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/sailfish commit bd2dd2419ea52f30cd7de2f7109a12b49b5d0dba-dirty
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78 #end if |
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79 |
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80 $noEffectiveLengthCorrection |
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81 $useVBOpt |
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82 $allowOrphans |
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83 |
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84 $unsmoothedFLD |
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85 --maxFragLen ${maxFragLen} |
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86 --txpAggregationKey "${txpAggregationKey}" |
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87 |
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88 ]]> |
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89 </command> |
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90 <inputs> |
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91 <conditional name="refTranscriptSource"> |
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92 <param name="TranscriptSource" type="select" label="Select a reference transcriptome from your history or use a built-in index?" help="Built-ins were indexed using default options"> |
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93 <option value="indexed">Use a built-in index</option> |
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94 <option value="history" selected="True">Use one from the history</option> |
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95 </param> |
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96 <when value="indexed"> |
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97 <param name="index" type="select" label="Select a reference transcriptome" help="If your transcriptome of interest is not listed, contact your Galaxy admin"> |
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98 <options from_data_table="sailfish_indexes"> |
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99 <filter type="sort_by" column="2"/> |
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100 <validator type="no_options" message="No indexes are available for the selected input dataset"/> |
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101 </options> |
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102 </param> |
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103 </when> <!-- build-in --> |
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104 <when value="history"> |
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105 <param name="ownFile" type="data" format="fasta" metadata_name="dbkey" label="Select the reference transcriptome" /> |
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106 <param argument="kmerSize" type="integer" value="21" max="32" label="The size of the k-mer on which the index is built" |
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107 help="There is a tradeoff here between the distinctiveness of the k-mers and their robustness to errors. |
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108 The shorter the k-mers, the more robust they will be to errors in the reads, but the longer the k-mers, |
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109 the more distinct they will be. We generally recommend using a k-mer size of at least 20."/> |
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110 </when> <!-- history --> |
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111 </conditional> <!-- refTranscriptSource --> |
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112 |
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113 <conditional name="single_or_paired"> |
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114 <param name="single_or_paired_opts" type="select" label="Is this library mate-paired?"> |
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115 <option value="single">Single-end</option> |
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116 <option value="paired">Paired-end</option> |
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117 </param> |
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118 <when value="single"> |
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119 <param name="input_singles" type="data" format="fastq,fasta" label="FASTQ/FASTA file" help="FASTQ file." /> |
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120 <expand macro="strandedness" /> |
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121 </when> |
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122 <when value="paired"> |
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123 <param name="input_mate1" type="data" format="fastq,fasta" label="Mate pair 1" help="FASTQ file." /> |
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124 <param name="input_mate2" type="data" format="fastq,fasta" label="Mate pair 2" help="FASTQ file." /> |
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125 <param name="orientation" type="select" label="Relative orientation of reads within a pair"> |
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126 <option value="M">Mates are oriented in the same direction (M = matching)</option> |
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127 <option value="O">Mates are oriented away from each other (O = outward)</option> |
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128 <option value="I" selected="True">Mates are oriented toward each other (I = inward)</option> |
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129 </param> |
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130 <expand macro="strandedness" /> |
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131 </when> |
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132 </conditional> |
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133 |
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134 <param argument="--geneMap" type="data" format="tabular,gff,gtf" optional="True" label="File containing a mapping of transcripts to genes" |
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135 help="Calculates the aggregated gene-level abundance estimations. This file should be eiher a GTF file or tab-delimited format |
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136 where each line contains the name of a transcript and the gene to which it belongs separated by a tab." /> |
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137 |
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138 <param argument="--biasCorrect" type="boolean" truevalue="--biasCorrect" falsevalue="" checked="False" |
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139 label="Perform bias correction" help=""/> |
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140 |
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141 <param argument="--fldMean" type="integer" value="200" optional="True" label="Calculate effective lengths" |
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142 help="If single end reads are being used for quantification, or there are an insufficient number of uniquely mapping reads when performing paired-end quantification |
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143 to estimate the empirical fragment length distribution, then use this value to calculate effective lengths."/> |
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144 |
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145 <param argument="--fldSD" type="integer" value="80" optional="True" label="Standard deviation" |
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146 help="The standard deviation used in the fragment length distribution for single-end quantification or when an empirical distribution cannot be learned."/> |
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147 |
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148 <param argument="--maxReadOcc" type="integer" value="200" optional="True" label="Maximal read mapping occurence" |
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149 help="Reads mapping to more than this many places won't be considered."/> |
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150 |
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151 <param argument="--noEffectiveLengthCorrection" type="boolean" truevalue="--noEffectiveLengthCorrection" falsevalue="" checked="False" |
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152 label="Disable effective length correction" help="Disables effective length correction when computing the probability that a fragment was generated from a transcript. |
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153 If this flag is passed in, the fragment length distribution is not taken into account when computing this probability."/> |
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154 |
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155 <param argument="--useVBOpt" type="boolean" truevalue="--useVBOpt" falsevalue="" checked="False" |
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156 label="Use Variational Bayesian EM algorithm for optimization" help=""/> |
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157 |
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158 <param argument="--allowOrphans" type="boolean" truevalue="--allowOrphans" falsevalue="" checked="False" |
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159 label="Consider orphaned reads as valid hits when performing lightweight-alignment" |
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160 help="This option will increase sensitivity (allow more reads to map and more transcripts to be detected), but may decrease specificity as orphaned alignments are more likely to be spurious."/> |
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161 |
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162 <param argument="--unsmoothedFLD" type="boolean" truevalue="--unsmoothedFLD" falsevalue="" checked="False" |
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163 label="Use the un-smoothed approach to effective length correction" help="This traditional approach works by convolving the FLD with the characteristic function over each transcript."/> |
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164 |
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165 <param argument="--maxFragLen" type="integer" value="1000" optional="True" |
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166 label="The maximum length of a fragment to consider when building the empirical fragment length distribution" |
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167 help=""/> |
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168 |
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169 <param argument="--txpAggregationKey" value="gene_id" type="text" label="The key for aggregating transcripts during gene-level estimates" |
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170 help="The default is the gene_id field, but other fields (e.g. gene_name) might be useful depending on the specifics of the annotation being used." /> |
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171 |
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172 </inputs> |
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173 <outputs> |
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174 <data name="output_quant" format="tabular" from_work_dir="quant.sf" label="${tool.name} on ${on_string} (Quantification)" /> |
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175 <data name="output_bias_corrected_quant" format="tabular" from_work_dir="quant_bias_corrected.sf" label="${tool.name} on ${on_string} (Bias corrected Quantification)"> |
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176 <filter>bias_correct == '--biasCorrect'</filter> |
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177 </data> |
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178 <data name="output_gene_quant" format="tabular" from_work_dir="quant.genes.sf" label="${tool.name} on ${on_string} (Gene Quantification)"> |
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179 <filter>geneMap is True</filter> |
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180 </data> |
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181 </outputs> |
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182 <tests> |
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183 <test> |
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184 <param name="single_or_paired_opts" value="paired" /> |
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185 <param name="input_mate1" value="reads_1.fastq" /> |
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186 <param name="input_mate2" value="reads_2.fastq" /> |
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187 <param name="biasCorrect" value="True" /> |
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188 <param name="TranscriptSource" value="history" /> |
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189 <param name="ownFile" value="transcripts.fasta" ftype="fasta" /> |
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190 <output file="sailfish_quant_result1.tab" ftype="tabular" name="output_quant" /> |
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191 <output file="sailfish_bias_result1.tab" ftype="tabular" name="output_bias_corrected_quant" /> |
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192 </test> |
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193 </tests> |
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194 <help> |
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195 <![CDATA[ |
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196 **What it does** |
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197 |
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198 Sailfish is a tool for transcript quantification from RNA-seq data. It |
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199 requires a set of target transcripts (either from a reference or _de-novo_ |
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200 assembly) to quantify. All you need to run Sailfish is a fasta file containing |
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201 your reference transcripts and a (set of) fasta/fastq file(s) containing your |
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202 reads. Sailfish runs in two phases; indexing and quantification. The indexing |
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203 step is independent of the reads, and only need to be run one for a particular |
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204 set of reference transcripts and choice of k (the k-mer size). The |
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205 quantification step, obviously, is specific to the set of RNA-seq reads and is |
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206 thus run more frequently. |
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207 |
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208 When the quantification output contains a number of columns: |
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209 (1) Transcript ID, |
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210 (2) Transcript Length, |
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211 (3) Transcripts per Million (TPM) and |
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212 (4) Estimated number of reads (an estimate of the number of reads drawn from this transcript given the transcript’s relative abundance and length). |
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213 |
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214 The first two columns are self-explanatory, the next four are measures of transcript abundance and the final is a commonly used input for differential expression tools. |
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215 The Transcripts per Million quantification number is computed as described in [1], and is meant as an estimate of the number of transcripts, per million observed transcripts, |
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216 originating from each isoform. Its benefit over the F/RPKM measure is that it is independent of the mean expressed transcript length |
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217 (i.e. if the mean expressed transcript length varies between samples, for example, this alone can affect differential analysis based on the K/RPKM.). |
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218 |
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219 |
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220 |
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221 Fragment Library Types |
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222 ====================== |
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223 |
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224 There are numerous library preparation protocols for RNA-seq that result in |
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225 sequencing reads with different characteristics. For example, reads can be |
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226 single end (only one side of a fragment is recorded as a read) or paired-end |
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227 (reads are generated from both ends of a fragment). Further, the sequencing |
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228 reads themselves may be unstraned or strand-specific. Finally, paired-end |
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229 protocols will have a specified relative orientation. To characterize the |
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230 various different typs of sequencing libraries, we've created a miniature |
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231 "language" that allows for the succinct description of the many different types |
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232 of possible fragment libraries. For paired-end reads, the possible |
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233 orientations, along with a graphical description of what they mean, are |
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234 illustrated below: |
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235 |
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236 .. image:: ReadLibraryIllustration.png |
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237 |
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238 The library type string consists of three parts: the relative orientation of |
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239 the reads, the strandedness of the library, and the directionality of the |
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240 reads. |
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241 |
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242 The first part of the library string (relative orientation) is only provided if |
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243 the library is paired-end. The possible options are: |
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244 |
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245 :: |
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246 |
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247 I = inward |
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248 O = outward |
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249 M = matching |
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250 |
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251 The second part of the read library string specifies whether the protocol is |
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252 stranded or unstranded; the options are: |
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253 |
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254 :: |
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255 |
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256 S = stranded |
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257 U = unstranded |
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258 |
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259 If the protocol is unstranded, then we're done. The final part of the library |
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260 string specifies the strand from which the read originates in a strand-specific |
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261 protocol — it is only provided if the library is stranded (i.e. if the |
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262 library format string is of the form S). The possible values are: |
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263 |
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264 :: |
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265 |
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266 F = read 1 (or single-end read) comes from the forward strand |
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267 R = read 1 (or single-end read) comes from the reverse strand |
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268 |
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269 So, for example, if you wanted to specify a fragment library of strand-specific |
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270 paired-end reads, oriented toward each other, where read 1 comes from the |
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271 forward strand and read 2 comes from the reverse strand, you would specify ``-l |
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272 ISF`` on the command line. This designates that the library being processed has |
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273 the type "ISF" meaning, **I**\ nward (the relative orientation), **S**\ tranted |
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274 (the protocol is strand-specific), **F**\ orward (read 1 comes from the forward |
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275 strand). |
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276 |
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277 The single end library strings are a bit simpler than their pair-end counter |
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278 parts, since there is no relative orientation of which to speak. Thus, the |
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279 only possible library format types for single-end reads are ``U`` (for |
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280 unstranded), ``SF`` (for strand-specific reads coming from the forward strand) |
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281 and ``SR`` (for strand-specific reads coming from the reverse strand). |
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282 |
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283 A few more examples of some library format strings and their interpretations are: |
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284 |
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285 :: |
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286 |
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287 IU (an unstranded paired-end library where the reads face each other) |
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288 |
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289 :: |
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290 |
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291 SF (a stranded single-end protocol where the reads come from the forward strand) |
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292 |
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293 :: |
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294 |
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295 OSR (a stranded paired-end protocol where the reads face away from each other, |
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296 read1 comes from reverse strand and read2 comes from the forward strand) |
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297 |
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298 .. note:: Correspondence to TopHat library types |
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299 |
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300 The popular `TopHat <http://ccb.jhu.edu/software/tophat/index.shtml>`_ RNA-seq |
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301 read aligner has a different convention for specifying the format of the library. |
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302 Below is a table that provides the corresponding sailfish/salmon library format |
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303 string for each of the potential TopHat library types: |
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304 |
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305 |
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306 +---------------------+-------------------------+ |
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307 | TopHat | Salmon (and Sailfish) | |
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308 +=====================+============+============+ |
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309 | | Paired-end | Single-end | |
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310 +---------------------+------------+------------+ |
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311 |``-fr-unstranded`` |``-l IU`` |``-l U`` | |
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312 +---------------------+------------+------------+ |
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313 |``-fr-firststrand`` |``-l ISR`` |``-l SR`` | |
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314 +---------------------+------------+------------+ |
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315 |``-fr-secondstrand`` |``-l ISF`` |``-l SF`` | |
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316 +---------------------+------------+------------+ |
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317 |
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318 The remaining salmon library format strings are not directly expressible in terms |
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319 of the TopHat library types, and so there is no direct mapping for them. |
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320 |
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321 |
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322 ]]> |
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323 </help> |
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324 </tool> |