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Advanced mode component hierarchy
Tony Di Sera edited this page Aug 9, 2023
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18 revisions

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TypeAhead (gene search)
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GenesMenu (copy/paste multiple genes)
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PhenotypeSearch
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- SampleData
- SampleDataFile (variants)
- SampleDataFile (alignments)
- SampleData
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SaveAnalysisButton (only shows when launched from Mosaic)
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ImportVariants
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ExportVariants
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SettingsDialog
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Dialogs for disclaimer, terms of service, publications, citations
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NavigationDrawer (left side panel, tabs)
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NOTE: A GeneBadge is created for each DangerSummary
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NOTE: Each entry in the expansion panel represents a flagged variant. The flagged variants are organized by Filter -> Gene -> Variant in CohortModel.organizeVariantsByFilterAndGene().
- FilterSettings
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NavigationDrawer (right side panel)
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LegendPanel
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NavigationDrawer (right side panel)
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AlertPanel
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- GeneLinksMenu
- GeneOMIMTable
- GenePubMedTable
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- TranscriptsMenu
- GeneViz
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- NOTE: The StackedVarChartViz replaces the VariantViz view when the "Counts" radio button is selected.
- NOTE: The StackedVarChartViz replaces the VariantViz view when the "Counts in Exons" radio button is selected.
- VariantToggle (filter by inheritance)
- VariantViz (called variants)
- VariantViz (loaded variants)
- DepthViz (alignment depth)
- GeneViz (selected transcript)
- OptionalTracksMenu
- VariantViz (mother)
- DepthViz (mother)
- VariantViz (father)
- DepthViz (father)
- VariantViz (clinvar)
- StackedBarChartViz (clinvar)
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- VariantLinksMenu
- VariantAliasesMenu
- VariantInterpretation
- GeneAssociationsDialog
- VariantAfPopMenu
- VariantInspectRow
- VariantInspectQualityRow
- VariantInspectInheritanceRow
- DepthViz
- GeneViz
- PedigreeGenotypeViz
- ConservationScoresViz
- MultialignSeqViz
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Developer documentation
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Component organization
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Simplified mode for Nebula Genomics
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Basic mode for MyGene2