Difference between revisions of "User Guide/Gene/Phenotype Graph"

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(Created page with "== Widget: Phenotype Graph == Phenotype graph provides a summary view of phenotypes caused by gene perturbations, e.g. mutations and RNAi. In the graph, relevant phenotypes a...")
 
 
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== Widget: Phenotype Graph ==
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Phenotype graph widget provides a summary view of phenotypes caused by gene perturbations, e.g. mutations and RNAi. In the graph, relevant phenotypes are represented as nodes and the relationships among them as arrows. The size (area) of a node is proportional to the total number of annotations for that node, combining RNAi and allele annotations. Phenotypes used directly in annotations are red with a solid border, whereas those that are relevant only by inference are dash-bordered blue.
 
 
Phenotype graph provides a summary view of phenotypes caused by gene perturbations, e.g. mutations and RNAi. In the graph, relevant phenotypes are represented as nodes and the relationships among them as arrows. The size (area) of a node is proportional to the total number of annotations for that node, combining RNAi and allele annotations. Phenotypes used directly in annotations are red with a solid border, whereas those that are relevant only by inference are dash-bordered blue.
 

Latest revision as of 22:21, 5 January 2016

Phenotype graph widget provides a summary view of phenotypes caused by gene perturbations, e.g. mutations and RNAi. In the graph, relevant phenotypes are represented as nodes and the relationships among them as arrows. The size (area) of a node is proportional to the total number of annotations for that node, combining RNAi and allele annotations. Phenotypes used directly in annotations are red with a solid border, whereas those that are relevant only by inference are dash-bordered blue.