Mercurial > repos > timpalpant > java_genomics_toolkit
annotate galaxy-conf/GreedyCaller.xml @ 25:b43c420a6135 draft default tip
Incorporate fix: https://github.com/timpalpant/java-genomics-toolkit/commit/9a6c61b7c6b8d85a1cd3f595eed657a537b85dc9
author | timpalpant |
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date | Sat, 09 Feb 2019 14:02:24 -0500 |
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1 <tool id="CallNukes" name="Call Nucleosomes" version="1.1.0"> |
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2 <description>in an MNase experiment</description> |
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3 <command interpreter="bash">galaxyToolRunner.sh nucleosomes.GreedyCaller -d $dyads -s $smoothed -n $N -o $output</command> |
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4 <inputs> |
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5 <param name="dyads" type="data" format="bigwig,wig" label="Dyad counts" /> |
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6 <param name="smoothed" type="data" format="bigwig,wig" label="Smoothed dyad counts" /> |
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7 <param name="N" type="integer" value="147" optional="true" label="Assumed nucleosome size" /> |
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8 </inputs> |
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9 <outputs> |
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10 <data name="output" format="tabular" /> |
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11 </outputs> |
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12 |
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13 <help> |
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14 |
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15 Stereotypic nucleosome positions are identified from dyad density maps using an approach similar to the previously reported greedy algorithm in GeneTrack_ (Albert, et al. 2008). Nucleosome calls are identified at peak maxima (p) in the smoothed dyad density map, and then excluded in the surrounding window [p–N, p+N], where N is the assumed nucleosome size in base pairs. This process is continued until all possible sterically hindered nucleosome positions are identified. |
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16 |
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17 .. _GeneTrack: http://atlas.bx.psu.edu/genetrack/docs/genetrack.html |
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18 |
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19 .. class:: warningmark |
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20 |
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21 This tool requires dyad counts and smoothed dyad counts in Wig or BigWig format. Smoothed dyad counts can be generated from dyad counts using the WigMath -> Gaussian smooth tool. |
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22 |
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23 ----- |
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24 |
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25 **Syntax** |
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26 |
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27 - **Dyad counts** is the relative number of nucleosomes positioned at each base pair. |
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28 - **Smoothed dyad counts** should correspond to a smoothed version of the **Dyad counts** |
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29 - **Assumed nucleosome size** is the window size used while identifying maxima to restrict overlapping calls. |
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30 |
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31 ----- |
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32 |
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33 **Output** |
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34 |
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35 The output format has 10 columns defined as follows |
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36 |
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37 - 1. **Chromosome:** the chromosome of this nucleosome call |
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38 - 2. **Start:** the lower coordinate of the call window, equal to the dyad position - N/2 |
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39 - 3. **Stop:** the higher coordinate of the call window, equal to the dyad position + N/2 |
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40 - 4. **Length:** the window size (N) of the nucleosome call, equal to the value specified when the tool was run |
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41 - 5. **Length standard deviation:** the standard deviation of the nucleosome call length (equal to 0 because it is not currently calculated) |
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42 - 6. **Dyad:** the location of the peak maximum (p) in the smoothed dyad density data |
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43 - 7. **Dyad standard deviation:** the standard deviation of dyad density around the dyad mean in the dyad counts data |
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44 - 8. **Conditional position:** the probability that a nucleosome is at this exact dyad location as opposed to anywhere else in the nucleosome call window [p-N/2, p+N/2] |
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45 - 9. **Dyad mean:** the mean of the dyad counts in the window [p-N/2, p+N/2] |
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46 - 10. **Occupancy:** the sum of the dyad counts in the window [p-N/2, p+N/2] |
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47 |
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48 </help> |
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49 </tool> |