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=Agenda=
=Agenda=


===Transferring annotations to geneproducts in other strains===
===Transferring annotations to geneproducts in between strains===
<pre>
<pre>
Hi Rama,
Hi Rama,
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cases where I was looking at conservative ortholog calls for genes of the same species, different strains?  
cases where I was looking at conservative ortholog calls for genes of the same species, different strains?  
Or should I use the ISO code and the with_from value (e.g. PseudoCAP:PA1777) to indicate the strain the  
Or should I use the ISO code and the with_from value (e.g. PseudoCAP:PA1777) to indicate the strain the  
function/process was observed in? I used the former approach when I originally did some GO mapping to  
function/process was We observed in? I used the former approach when I originally did some GO mapping to  
Pseudomonas aeruginosa strains in our database, but I'm now leaning toward the latter approach in order to  
Pseudomonas aeruginosa strains in our database, but I'm now leaning toward the latter approach in order to  
make the logic behind the call more transparent.  
make the logic behind the call more transparent.  
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</pre>
</pre>


The most accurate representation for the bacterial strains would be to use ISS as the evidence because it is not an ortholog. Use the strain ID in the taxon column. We currently use K12 for the taxon for E. coli, so we don't make annotations at the species level for this. Should we allow annotation at the strain level? We think this should be allowed. Do we ever want to have strain information for mice? Eventually, we probably do, there are 17 strains to consider.


[[Category:Meetings]]
===Trello board===
https://trello.com/b/IdtTLGEt/go-priorities
 
[[Category:GO Managers Meetings‏‎]]

Latest revision as of 09:51, 15 April 2019

Agenda

Transferring annotations to geneproducts in between strains

Hi Rama,
I have a quick question for you regarding how your group manually maps curated GO annotations 
from one bacterial strain to another of the same species.
I was wondering if the best practice would be to use the same evidence code (e.g. IDA) for 
cases where I was looking at conservative ortholog calls for genes of the same species, different strains? 
Or should I use the ISO code and the with_from value (e.g. PseudoCAP:PA1777) to indicate the strain the 
function/process was We observed in? I used the former approach when I originally did some GO mapping to 
Pseudomonas aeruginosa strains in our database, but I'm now leaning toward the latter approach in order to 
make the logic behind the call more transparent. 
Do you have any opinion on which approach is best?
Thanks for any help you can offer!
Geoff

The most accurate representation for the bacterial strains would be to use ISS as the evidence because it is not an ortholog. Use the strain ID in the taxon column. We currently use K12 for the taxon for E. coli, so we don't make annotations at the species level for this. Should we allow annotation at the strain level? We think this should be allowed. Do we ever want to have strain information for mice? Eventually, we probably do, there are 17 strains to consider.

Trello board

https://trello.com/b/IdtTLGEt/go-priorities