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curation_guide [2013/02/11 18:40]
biogridadmin [Adding Interactions]
curation_guide [2013/11/06 19:24]
jenn [Curation Questions and Answers]
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   - **What about genes that are 'not physically mapped'​ in SGD or genes that only encode RNA products?**   - **What about genes that are 'not physically mapped'​ in SGD or genes that only encode RNA products?**
     * Currently, the tool will not allow you to enter genes that are 'not physically mapped'​ in SGD. This is also true for genes that only encode RNA products (e.g. Tlc1, Snr1). However, you can use the "force interactions"​ option to enter the gene names for now. The IMS system will eventually be updated to recognize these features.     * Currently, the tool will not allow you to enter genes that are 'not physically mapped'​ in SGD. This is also true for genes that only encode RNA products (e.g. Tlc1, Snr1). However, you can use the "force interactions"​ option to enter the gene names for now. The IMS system will eventually be updated to recognize these features.
 +  - **What is the difference between “Affinity Capture-MS/​Western” and “Reconstituted Complex"?​**
 +    * If the relevant proteins are co-expressed in the cell, then the interaction is considered to occur //in vivo// and can be classified as "​Affinity Capture-Western"​ or "​Affinity Capture-MS"​. ​ If the bait is not co-expressed in the cell, but merely purified and incubated with a cell lysate //in vitro// or even purified recombinant proteins (e.g. GST pull-down), then we use the //in vitro// option of "​Reconstituted Complex"​. ​   ​
   - **What if an interaction can't be assigned one of the available experimental system categories?​**   - **What if an interaction can't be assigned one of the available experimental system categories?​**
     * Occasionally,​ an interaction cannot be readily assigned a protein or genetic interaction category, in which case, the closest substitute should be chosen and an explanation of the exact experimental context should be given in the qualification text box.     * Occasionally,​ an interaction cannot be readily assigned a protein or genetic interaction category, in which case, the closest substitute should be chosen and an explanation of the exact experimental context should be given in the qualification text box.
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    - ** Do we curate cross-species interactions?​**    - ** Do we curate cross-species interactions?​**
      * We curate cross-species interactions,​ e.g. between a yeast and a human protein. The curation tool allows us to select separate species for the bait and hit using the relevant pulldown menus. However, this does not include cross-species complementation experiments because they are not really genetic interactions between two genes, but rather a test to determine functional orthologs in other species. ​      * We curate cross-species interactions,​ e.g. between a yeast and a human protein. The curation tool allows us to select separate species for the bait and hit using the relevant pulldown menus. However, this does not include cross-species complementation experiments because they are not really genetic interactions between two genes, but rather a test to determine functional orthologs in other species. ​
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 ===== BioGRID Team Members, References, and Funding Details ===== ===== BioGRID Team Members, References, and Funding Details =====
 For more information on the BioGRID and the history of the BioGRID, a full list of our publications,​ team members, and funding sources can be found on our [[aboutus|About Us Page]]. For more information on the BioGRID and the history of the BioGRID, a full list of our publications,​ team members, and funding sources can be found on our [[aboutus|About Us Page]].
 
curation_guide.txt · Last modified: 2017/08/08 12:52 (external edit)