Brief Instructions for Using the Phylogenetic Network
Program
L. David Roper (roperld@vt.edu)
(www.roperld.com)
The official brief instructions for using the program are at
http://www.fluxus-engineering.com/netwinfaq.htm.
The phylogenetic network program projects an x-marker dimensional space
onto a 2-dimensional or 3-dimensional space (drawn in 2 dimensions), so there
are many ways to do it. The program does it in three different ways.
Here are some rules I have learned:
- Try a reduced-median calculation first. If it is not too complicated
looking, use it. (I always put RM on the end of the file name for this
calculation.)
- If the reduced-median plot is too messy, then do a median-joined
calculation. If it is not too complicated looking, use it. (I always put MJ on
the end of the file name for this calulation.) Some information about genetic
connections is lost compared to a reduced-median calculation.
- If the median-joined plot is too messy, then do a median-joined
calculation starting from the reduced-median file (*.rmf) file created in the
first item above. (I always put RMMJ on the end of the file name for this
calculation.) Some information about genetic connections is lost compared to a
median-joined calculation.
- Finally, plotting the network (Draw Network menu item in the Network
program) is somewhat complicated. After the drawing is completed, there are
some choices for zooming in out or and panning (called navigating) at the
bottom. When done with those items, click on Finalize at the bottom right
corner to show a menu on the right hand side for selecting various items to
display.
- Then you can print the plot by doing File-Print. You can save the
file by doing File-Save As; then choose file type to be *.bmp and get rid of
the .dia on the end of the file name. You will get a huge bmp file (~6 Mbytes).
Put it in some graphics program and convert it to a very small jpg file. You
can also use a graphics program to annotate it.
Here is an example input file for 12 Y-chromosome markers:
| 393,390,19,391,385a,385b,426,388,439,389a,392,389b |
| (blank line) |
| (blank line) |
| SCL |
| 13,23,15,10,14,15,11,14,11,12,11,17 |
| 1 |
| LLL |
| 13,25,14,12,11,14,12,12,12,13,13,16 |
| DCL |
| 13,25,14,11,11,14,12,12,12,13,13,16 |
| 1 |
| TML |
| 13,24,15,10,12,15,12,13,12,13,12,16 |
| 1 |
| JMAL |
| 13,24,15,10,12,15,12,13,12,13,13,17 |
| 1 |
The first line contains the names of the Y markers (with DYS prefix
understood); only 6 characters are allowed for each marker name. The next two
lines must be blank. The DYS389-1 and DYS389-2 markers must be converted to
DYS389a=(DYS389-1) and DYS389b=(DYS389-2)-(DYS389-1, as they are the true
alleles. The symbols for the participants (e.g. SCL) must not be longer than 6
characters. The line after the marker values is the frequency; i.e., how many
participants have that marker set. (E.g., I use MUR as the symbol for the
Majority USA Roper family and several participants have the same marker
values.)
For 25 markers the first line should be:
393,390,19,391,385a,385b,426,388,439,389a,392,389b,458,459a,459b455,454,447,437,448,449,464a,464b,464c,464d