SharedVariantDisplay
Auto-generated config schema for the current JBrowse release — see the
config guide for concepts. Provided by the variants
plugin.
View source.
Related links
- Extended by: LinearMultiSampleVariantDisplay
- Extended by: LinearMultiSampleVariantMatrixDisplay
- Base config: BaseLinearDisplay
- Guide: LD at a selective sweep (human)
- Guide: Variant track
Config slots
SharedVariantDisplay is a shared base schema, not a type you name in a config.
Set these slots on one of the configs under Extended by above, each of which
lists them as inherited and shows the shape in its own example. Slot types
(fileLocation, frozen, ...) are explained in the
config slot types reference. Slots a base
configuration contributes are listed here too, so this table is the whole
surface.
| Slot | Description |
|---|---|
showReferenceAllelesboolean = false | Starting value for drawing reference alleles. When false, the row background is filled solid grey and only ALT alleles are painted on top (makes overlapping variants easier to see); when true, reference alleles are drawn normally. Seeds referenceDrawingMode the first time a config is loaded. |
lineZoneHeightnumber = 0 | Height of the zone above the rows holding the lines that tie each matrix column to its genomic position. 0 (the default here) means no zone at all — only the matrix display, which lays columns out by feature index rather than at their genomic positions, raises it. advanced |
showRowSeparatorsboolean = false | Draw a hairline between adjacent sample rows. Off by default, and only drawn once rows are at least 4px tall — below that the line is as thick as the row it borders. |
showTooltipsboolean = true | Show the hover tooltip naming the genotype, the sample and the record under the pointer. On by default; turning it off leaves every other hover affordance — the crosshairs, the highlighted cell, the cross-display session.hovered channel — alone, so the pointer still says where it is while the panel stops covering the rows beside it.A config slot rather than a display property, so a track config can ship with it off and a figure capture keeps it off across a reload. Both multi-sample displays honor it: they draw the same tooltip off the same hoveredGenotype slot. |
renderingModestringEnum (alleleCount, phased) = 'alleleCount' | 'alleleCount' draws one row per sample colored by allele dosage; 'phased' draws one row per haplotype |
featureColorstring = '' | Optional per-feature color for the genotype cells: a jexl expression (or plain CSS color) evaluated once per variant in the worker, painting every alt-carrying cell with that color while ref/no-call cells keep their normal coloring so "who carries it" still reads. Empty means the default genotype-based coloring (allele dosage / phasing). The "Color by..." menu offers presets like consequence impact (jexl:impactColor(feature)), but any feature jexl works, same as the standard color slot. |
minorAlleleFrequencyFilternumber = 0 | Hide variants whose minor allele frequency is below this threshold advanced |
maxMissingnessFilternumber = 1 | Hide variants whose fraction of no-call (missing) genotypes is above this threshold; 1 keeps every variant advanced |
showLegendmaybeBoolean = true promotable | Whether to draw the floating legend over the display. It is clipped to the display's own bounds, so while it is on it sets a floor under the lane height: turn it off to size a short lane to its rows rather than to its key, which is what a one-record SV call genotyped across a handful of carriers wants. |
colorBystring = '' | Name of a sample-metadata attribute (a column in the adapter's samplesTsvLocation, e.g. 'population') to color the sidebar rows by; empty means no grouping |
groupBystring = '' | Name of a sample-metadata attribute (a column in the adapter's samplesTsvLocation, e.g. 'population') to order the sample rows by, so each group's rows are contiguous and a group-restricted genotype pattern reads as one band; empty means the rows keep their existing order |
referenceDrawingModestringEnum (draw, skip) = 'skip' | A 'draw'/'skip' toggle for reference alleles, settable independent of showReferenceAlleles (the admin-config-only starting default). No fallback derivation at read time — preProcessSnapshot below seeds this from showReferenceAlleles once, the first time a config lacking it is hydrated, so from then on this slot alone is the single source of truth. |
rowHeightnumber = 0 | per-row height in px, scrolling the rows that do not fit; 0 (the default) fits the rows to the display height instead, dividing it between them |
showTreeboolean = true | Show the sample clustering tree in the sidebar |
showBranchLengthboolean = true | position tree nodes by branch length (dendrogram) rather than evenly by topology (cladogram) |
showRowLabelsboolean = true | Show the per-sample row labels in the sidebar |
| Inherited from BaseLinearDisplay | 6 slots |
maxFeatureScreenDensitynumber = 1 | maximum features per pixel before showing a "too many features" message advanced |
heightnumber = 100 | default height for the track |
mouseoverstring = | text to display when the cursor hovers over a feature callback args: feature |
jexlFiltersstringArray = [] | config jexlFilters are deferred evaluated so they are prepended with jexl at runtime rather than being stored with jexl in the config |
fetchSizeLimitnumber = 1_000_000 | maximum data to attempt to download for a given track, used if adapter doesn't specify one advanced |
forceLoadboolean = false | Declarative equivalent of the "Force load" button on the "too much data" banner: when true the display always renders, however large the region or dense the features. Off by default (the gate guards against huge downloads). Set it on a view no one can interact with — an embedded / notebook view, or a screenshot — where the region is known and you want it drawn without a click. advanced |