1 | #Please insert up references in the next lines (line starts with keyword UP) |
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2 | UP arb.hlp |
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3 | UP glossary.hlp |
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4 | |
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5 | #Please insert subtopic references (line starts with keyword SUB) |
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6 | #SUB subtopic.hlp |
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7 | |
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8 | # Hypertext links in helptext can be added like this: LINK{ref.hlp|http://add|bla@domain} |
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9 | |
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10 | #************* Title of helpfile !! and start of real helpfile ******** |
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11 | TITLE Calculate Branch Lengths |
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12 | |
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13 | OCCURRENCE ARB_PARSIMONY/Tree/Calculate Branch Lengths |
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14 | |
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15 | |
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16 | DESCRIPTION Calculates branchlengths for the current tree. |
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17 | |
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18 | |
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19 | SECTION Inner branches |
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20 | |
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21 | To calculate the lengths of non-terminal branches, branch swapping |
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22 | is used on them. |
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23 | |
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24 | Branch swapping (aka NNI=Nearest Neighborhood Interchange) is the most |
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25 | atomic operation possible at an inner branch and has as such an effect on |
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26 | the overall costs of the tree. |
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27 | |
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28 | That effect is used as branchlength of the inner branch. |
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29 | |
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30 | The branchlength reflects the significance of the branch, i.e. |
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31 | |
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32 | - the exact topology around SHORT inner branches has little influence |
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33 | on the overall tree costs, i.e. the calculated topology does most |
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34 | likely NOT reflect the "real phylogentic topology". |
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35 | |
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36 | - Opposed, the exact topology around LONG inner branches has big influence |
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37 | on the overall tree costs, i.e. the calculated topology does most |
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38 | likely reflect the "real phylogentic topology". |
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39 | |
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40 | SECTION Terminal branches |
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41 | |
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42 | For terminal branches ARB_PARSIMONY checks how much the overall |
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43 | tree costs changed by adding this species to the tree. The price |
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44 | is weighted by the base-count of the species. |
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45 | |
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46 | i.e. |
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47 | - if the species has an identical relative in the tree and is added |
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48 | as neighbor of that relative, the resulting branchlength will be zero. |
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49 | - if added the species increases the tree costs by 50 and the species |
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50 | contains 100 bases, the resulting branchlength will be 0.5 |
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51 | |
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52 | This does quite accurately reflect the percentage of residues changed |
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53 | against the rest of the tree. |
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54 | |
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55 | SECTION Partial sequences |
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56 | |
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57 | If you add species with partial sequences as fulllength-species, they will |
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58 | group together in distant subtrees. |
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59 | |
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60 | But if species are flagged to contain "partial sequences" (this is done by |
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61 | "Add marked partial species"), they are handled differently: |
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62 | |
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63 | - Each partial species corresponds to one non-partial species |
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64 | - The partial-species is always inserted "below" the corresponding full-species. |
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65 | Multiple partials may correspond to the same full-species. |
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66 | - By adding that partial sequence to the tree, the tree costs only raise |
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67 | by the weighted mismatches in the region that overlaps (opposed, non-partial |
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68 | sequences would as well count the missing part as "gap insertions", i.e. |
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69 | the costs for adding a sequence as "partial" are MUCH cheaper). |
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70 | |
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71 | Species with partial sequences have the field "ARB_partial" set to 1 |
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72 | |
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73 | SECTION Used terms |
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74 | |
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75 | - overall tree costs: minimum number of mutation in the tree |
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76 | - base-count: without filtered positions. affected by specified weights. |
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77 | |
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78 | |
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79 | EXAMPLES None |
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80 | |
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81 | WARNINGS None |
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82 | |
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83 | BUGS No bugs known |
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