Closed iuliachiciudean closed 2 years ago
Hi Iulia,
Some answers to your questions below :)
GAP_FILL
.-i
flag (followed by medium ID) if you want to initialize the model with the same medium you used for gapfilling.Best regards, Daniel
Hi Daniel,
Thank you for the answers and for the article recommendation.
I am not sure I understand the -i flag. What does it mean "to initialize the model with the same medium you used for gapfilling"?
Please let me know if this is correct:
But this does not mean that when constructing the model you will limit the genome growth to the M9 compounds.
Is this correct? Do I also have a model.xml -i M9 command?
Thank you. iulia
Hi Daniel, Hi everyone,
I am a newbie in working with GEMs. I am trying to figure out how to make sense of the CarveMe output and I have a few (most likely, stupid) questions:
Where to find the exact reactions and metabolites added by gap-filling option? I've carve the same .faa file without and with -g M9 and it tells me that some reactions and metabolites are added when using M9 for gap filling, but I don't know where to look for them.
If I use the "gap-filling" option then the model will be constructed only by using the compounds in the media (ex. M9)? If so, then why do I obtain a greater FBA value for the gap filled model (M9) than for the gap unfilled model?
Is there any way to visualize (in a friendly manner) the CarveMe outputs?
Can you please recommend some publications or courses that explain how to deal with the GEMs info. I am planning to use CarveMe and SMETANA in order to figure out the microbial interactions in a bacteria community. But for now, I cant manage to understand the CarveMe outputs for a single organism :). Any help will be very welcome!!!!
Thank you very much. iulia