F A M E  
 
Welcome to FAME, the Flux Analysis and Modeling Environment!
FAME is your one stop shop for stoichiometric modeling, featuring model construction, model execution, results visualization, and friendly elephants.

RUN/EDIT EXISTING MODEL

BUILD NEW MODEL

MERGE MODELS
ONLY VISUALIZE

LOST YOUR MODEL?

VIEW MANUAL

TUTORIAL
 
If you are unsure what to do, have a look at the tutorial and/or manual, and you'll be on your way soon. If you can come up with questions or unexpected results that the manual didn't count on, please let me know by email: j.boele@vu.nl.
Warning sign FAME is under constant development. If you encounter any malfunctions, bugs, etc. in FAME, please be so kind as to inform me by email, so that I can fix the application if necessary. Please also send me an email (with a snippet of your model's SBML) if you cannot get your model to load properly.
 
© 2011, 2012 Joost Boele / VU University Amsterdam     -     disclaimer, license, and info
Last update: May 15th, 2012
 

FAME is now published in BMC Systems Biology!

We are happy to announce that FAME has just been published in BMC Systems Biology.
If you use FAME in your research, please cite:
 
Boele J, Olivier BG, Teusink B (2012) FAME, the Flux Analysis and Modeling Environment. BMC Syst Biol 6:8.
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Import an existing model

 Back to top Import model to run
1. Select your file
2. Set the default rate for new reactions (when unsure, just leave these values)
Max rate (normal reactions):
Max rate (boundaries):
3. Was this model generated or processed using FAME?

4. All set?
<-- or just click here to load a demo model!
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Build new model

 Back to top Build new model
1. Please select a species:
 2. Please select any number of pathways to include in the model:
 
Pathway options will appear here when you select a species.
3. Choose a name for your model and default max rates for reactions.
You can change the rates for individual reactions later.
Model Name:
Max rate (normal reactions):
Max rate (boundaries):
4. Would you like some fixes?
  Include?MAX objective?
ATP + H2O -> ADP + Pi
DNA synthesis from dNTPs
RNA synthesis from NTPs
Malic enzyme w/ NADP+/NADPH
R00835 (fixes PPP)
FRUCTOSE (fixes PPP)  
 
P/O:
 
   
PPi + H2O -> 2 Pi

5. Ready to go?
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Merge models

 Back to top Merge models
Use this form to merge two models. Objectives from the slave model are ignored, constraints from the slave model are overwritten by those of the master model.
Note that if you have deleted reactions from either model, they may still exist in the other.
 
1. Select your model files
Master model:
Slave model:
2. Set the default rate for reactions (when unsure, just leave these values)
These will not affect reactions currently in the models.
Max rate (normal reactions):
Max rate (boundaries):
3. All set?

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Lost your model?

If you have lost your model or would like to retrieve an old session, enter the model ID here to get the latest version of your model that was kept on our server.		 Back to top Lost your model?
You can find your model ID in the XML in the following line:
<model id="MODEL-ID" name="MODEL-ID">
 
1. Enter your model ID:
 
 
2. All set?

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Only visualize

To visualize data on KEGG-like maps, enter your data in the box below and select the appropriate KEGG maps. Make sure your data are of the form 
KEGG-ID,value
and only enter one key-value pair per line. 		Back to top Only visualize
1. Enter your data

 
2. Select pathways

 
3. All set?

© 2011, 2012 Joost Boele / VU University Amsterdam. All rights reserved     -     disclaimer, license, and info
Last update: May 15th, 2012