We are hopefully going to release a new version soon with several enhanced analysis features. In doing so, we have begun to support the new ontology file format OBO 1.2.
In working with this new format, I have been trying to decide whether to consider terms that denote regulation of a GO-term (e.g., regulation of apoptosis versus apoptosis) as children of that term or as separate, and thus not a part of the GO category they are regulating. Currently, they are considered children. If do not consider these children, this will have a profound effect on which terms are ultimately reported by GO-Elite.
For example, the GO term calcium-independent cell-cell adhesion (GO:0016338), has three regulation terms; negative regulation of calcium-independent cell-cell adhesion, positive regulation of calcium-independent cell-cell adhesion and regulation of calcium-independent cell-cell adhesion (http://amigo.geneontology.org/cgi-bin/amigo/term_details?term=GO:0016338). In the current version of GO-Elite (version 1.20), these three "regulation" terms are considered children, however, It is unclear to me whether this should be the case. If we consider them children, then the associated genes will be considered a part of (nested with) the parent (calcium-independent cell-cell adhesion) for pathway over-representation analysis, otherwise, they will be evaluated independently. Right now I am leaning towards not including these as children. My rationale for this is that if one process is regulating another (e.g., regulation of apoptosis and apoptosis), then these should be considered independent terms.
Keeping them as children makes sense. Here's a question that might help clarify the decision. Are most of the "regulators" of a process also members of the process term? If so, then nesting them makes sense. If not, then I would agree with you that these are indeed separate processes and should be not be included as children.
- Alex
On May 31, 2011, at 9:50 PM, Nathan Salomonis <nsalomo...@gmail.com> wrote:
> We are hopefully going to release a new version soon with several > enhanced analysis features. In doing so, we have begun to support the > new ontology file format OBO 1.2.
> In working with this new format, I have been trying to decide whether > to consider terms that denote regulation of a GO-term (e.g., > regulation of apoptosis versus apoptosis) as children of that term or > as separate, and thus not a part of the GO category they are > regulating. Currently, they are considered children. If do not > consider these children, this will have a profound effect on which > terms are ultimately reported by GO-Elite.
> For example, the GO term calcium-independent cell-cell adhesion > (GO:0016338), has three regulation terms; negative regulation of > calcium-independent cell-cell adhesion, positive regulation of > calcium-independent cell-cell adhesion and regulation of > calcium-independent cell-cell adhesion > (http://amigo.geneontology.org/cgi-bin/amigo/term_details?term=GO:0016338). > In the current version of GO-Elite (version 1.20), these three > "regulation" terms are considered children, however, It is unclear to > me whether this should be the case. If we consider them children, then > the associated genes will be considered a part of (nested with) the > parent (calcium-independent cell-cell adhesion) for pathway > over-representation analysis, otherwise, they will be evaluated > independently. Right now I am leaning towards not including these as > children. My rationale for this is that if one process is regulating > another (e.g., regulation of apoptosis and apoptosis), then these > should be considered independent terms.
> Thanks in advance for you feedback. > Best, > Nathan
A different consideration/question: If all gene names in 'regulation' are summarized in X, the gene names in 'positive regulation' called Y and in 'negative regulation' called Z. Would X always be equal to Y + Z ? i.e. shouldn't Y and Z then be children of X (instead of 3 seperate processes right now)
-- Stan
________________________________________ From: go-elite@googlegroups.com [go-elite@googlegroups.com] On Behalf Of Alexander Pico [ap...@gladstone.ucsf.edu] Sent: 01 June 2011 18:09 To: Nathan Salomonis Cc: go-elite@googlegroups.com Subject: GO-Elite User Group Post Re: Question to GO-Elite users
Keeping them as children makes sense. Here's a question that might help clarify the decision. Are most of the "regulators" of a process also members of the process term? If so, then nesting them makes sense. If not, then I would agree with you that these are indeed separate processes and should be not be included as children.
- Alex
On May 31, 2011, at 9:50 PM, Nathan Salomonis <nsalomo...@gmail.com> wrote:
> We are hopefully going to release a new version soon with several > enhanced analysis features. In doing so, we have begun to support the > new ontology file format OBO 1.2.
> In working with this new format, I have been trying to decide whether > to consider terms that denote regulation of a GO-term (e.g., > regulation of apoptosis versus apoptosis) as children of that term or > as separate, and thus not a part of the GO category they are > regulating. Currently, they are considered children. If do not > consider these children, this will have a profound effect on which > terms are ultimately reported by GO-Elite.
> For example, the GO term calcium-independent cell-cell adhesion > (GO:0016338), has three regulation terms; negative regulation of > calcium-independent cell-cell adhesion, positive regulation of > calcium-independent cell-cell adhesion and regulation of > calcium-independent cell-cell adhesion > (http://amigo.geneontology.org/cgi-bin/amigo/term_details?term=GO:0016338). > In the current version of GO-Elite (version 1.20), these three > "regulation" terms are considered children, however, It is unclear to > me whether this should be the case. If we consider them children, then > the associated genes will be considered a part of (nested with) the > parent (calcium-independent cell-cell adhesion) for pathway > over-representation analysis, otherwise, they will be evaluated > independently. Right now I am leaning towards not including these as > children. My rationale for this is that if one process is regulating > another (e.g., regulation of apoptosis and apoptosis), then these > should be considered independent terms.
> Thanks in advance for you feedback. > Best, > Nathan
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