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tutorials:eccb_t2_badasp [2012/09/07 12:28] romainstuder old revision restored |
tutorials:eccb_t2_badasp [2012/09/08 16:15] (current) romainstuder |
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| ==== BADASP ==== | ==== BADASP ==== | ||
| - | BADASP can produce different kind of measure: | + | BADASP can produce different measures: |
| * bad: similar the **Type II** of functional divergence. The threshold to choose depend if we want to be stringeant (i.e. BAD > 4) or more relaxed (BAD > 2). | * bad: similar the **Type II** of functional divergence. The threshold to choose depend if we want to be stringeant (i.e. BAD > 4) or more relaxed (BAD > 2). | ||
| Line 22: | Line 22: | ||
| </code> | </code> | ||
| - | === Execution === | + | === Analysis of the V-type proton ATPase 116 kDa subunit a gene family === |
| We want to identify the residues making differences between the **isoforms 1** and **isoforms 4** of the V-type proton ATPase 116 kDa subunit a. | We want to identify the residues making differences between the **isoforms 1** and **isoforms 4** of the V-type proton ATPase 116 kDa subunit a. | ||
| + | First, visualise briefly the multiple alignment in Jalview. (File "badasp_eg.fas" in the badasp folder. | ||
| - | <code> | ||
| - | cd ./badasp # Folder of installation | ||
| - | </code> | ||
| Execute **badasp** by importing the multiple alignment in FASTA format ("badasp_eg.fas") and activating the interactive mode (i=1): | Execute **badasp** by importing the multiple alignment in FASTA format ("badasp_eg.fas") and activating the interactive mode (i=1): | ||
| - | <code>python badasp.py seqin=badasp_eg.fas i=1</code> | + | |
| + | <code> | ||
| + | cd ./badasp # Folder of installation | ||
| + | python badasp.py seqin=badasp_eg.fas i=1</code> | ||
| Badasp will ask for the associated tree, in newick format ("badasp_eg.nsf"): | Badasp will ask for the associated tree, in newick format ("badasp_eg.nsf"): | ||
| Line 42: | Line 43: | ||
| => Press enter | => Press enter | ||
| + | </code> | ||
| Display Tree, with two groups of sequences: | Display Tree, with two groups of sequences: | ||
| V-type proton ATPase 116 kDa subunit a | V-type proton ATPase 116 kDa subunit a | ||
| - | - VPP1 = VPP Isoform 1 (8 genes) | + | * VPP1 = VPP Isoform 1 (8 genes) |
| - | - NVL = VPP Isoform 4 (3 genes) | + | * NVL = VPP Isoform 4 (3 genes) |
| + | <code> | ||
| Rooted Tree (1000 bootstraps). Branch Lengths given. 21 nodes. <ENTER> to continue. | Rooted Tree (1000 bootstraps). Branch Lengths given. 21 nodes. <ENTER> to continue. | ||
| => Press enter | => Press enter | ||
| Line 62: | Line 63: | ||
| </code> | </code> | ||
| - | We have a tree and we need to define the two groups to analyse: | + | The tree is now loaded and we need to define the two groups to analyse: |
| <code> | <code> | ||
| Line 70: | Line 71: | ||
| => Press enter | => Press enter | ||
| - | # We need to split the tree on the node 21, so we need to define two groups from the children nodes 20 (= VPP1 subfamily) and 19 (= VPP4 subfamily) . | + | # We need to split the tree on the node 21, |
| + | # so we need to define two groups from the children nodes 20 (= VPP1 subfamily) and 19 (= VPP4 subfamily) . | ||
| => Press M, then enter. # Manual grouping | => Press M, then enter. # Manual grouping | ||
| (Tree displayed) | (Tree displayed) | ||
| - | Choice? [default=Q]: c # We collapse node | + | Choice? [default=Q]: c # We collapse nodes |
| Node [default=0]: 20 | Node [default=0]: 20 | ||
| => Type VPP1, then Press enter | => Type VPP1, then Press enter | ||
| - | Choice? [default=Q]: c # We collapse node | + | Choice? [default=Q]: c # We collapse nodes |
| Node [default=0]: 19 | Node [default=0]: 19 | ||
| => Type VPP4, then Press enter | => Type VPP4, then Press enter | ||
| Line 95: | Line 97: | ||
| </code> | </code> | ||
| - | Badasp will now perform some computation. It will reconstruct the ancestral sequences at each node of the tree, using the [[http:dx.doi.org/10.1186/1471-2105-5-123|GASP (Gapped Ancestral Sequence Prediction) method]]: | + | Badasp will now perform some computations. It will reconstruct the ancestral sequences at each node of the tree, using GASP (ref: http:dx.doi.org/10.1186/1471-2105-5-123 ) |
| + | <code> | ||
| Making Ancestral Sequences - Variable PAM Weighting | Making Ancestral Sequences - Variable PAM Weighting | ||
| Reading PAM1 matrix from jones.pam | Reading PAM1 matrix from jones.pam | ||
| Line 181: | Line 183: | ||
| Put a vertical line a the root of the tree to split the tree in two. | Put a vertical line a the root of the tree to split the tree in two. | ||
| - | Positon 3 BAD | + | Some sites are interesting, i.e.: |
| - | Position 762 BAD | + | * Positon 3 BAD |
| - | Position 223 BADX | + | * Position 762 BAD |
| + | * Position 223 BADX | ||
| + | |||
| + | There are only three genes in the group de VPP4, that explains why the BADX score are very close to the BAD score. | ||
