@genomics/*Install any piece as local React + Tailwind source, then adapt it inside your own design system. Every viewer speaks the shared reference-residue coordinate from coordinate-link.
The shared selection substrate.
The readable half of every colored viewer.
Loading, error, and empty states for async viewers.
Margins derived from the data, not hand-tuned.
Ticks from the scale that placed the data.
Design tokens a draw callback can actually read.
Hover without repainting a million points.
What's under the cursor, answered once.
Pan and zoom, shared across an axis.
Click, extend, brush, clear — one state machine.
A viewer declares what it exports; the frame renders it.
The cartesian archetype, assembled.
The rows × columns archetype.
Lanes stacked over one shared window.
The character-cell axis.
Node-link diagrams: transform, hit-test, labels.
The 3Dmol lifecycle, owned once.
Fetch what the window shows, and nothing twice.
The encoding picker, bound to its own scale.
Virtualized DNA/RNA/protein, to megabase scale.
Two-axis virtualized multiple alignment.
3Dmol.js wrapper with a linked confidence strip.
Predicted aligned error / contact map.
Rectangular phylogram from Newick.
Linear coordinate browser (IGV-in-a-box).
Information-content logo over an alignment.
Pfam-style protein architecture.
IGV-style alignment pileup.
Chromosome overview + navigation.
Pairwise comparison by shared k-mers.
Genome-wide association results.
Differential-expression volcano.
Genes × samples, row z-scored.
Align and overlay structures, colored by RMSD.
φ/ψ dihedral scatter for structure validation.
Circular DNA map for plasmids and small genomes.
Sanger sequencing trace (.ab1-style) viewer.
Query/subject alignment with midline.
UMAP / t-SNE cell embedding.
Single-cell marker dot plot.
Distributions across groups.
Genome-wide copy-number profile.
RNA-seq coverage + junction arcs.
1D protein SS ribbon (DSSP-style).
2D small-molecule depiction from SMILES.
Molecular surface colored by residue property.
LigPlot-style 2D ligand–residue contacts.
Ribbon comparison between two sequences.
Linear DNA map of restriction sites.
Whole-genome chromosome grid.
Chromatin contact map with TADs and loops.
Interaction, regulatory, and pathway networks.
Six-frame translation and ORFs under a DNA sequence.
Expression heatmap with row and column dendrograms.
96- and 384-well plates, as a first-class view.
Gene model on a genomic axis, linked to protein residues.
Kaplan–Meier with numbers at risk and a log-rank test.
Observed vs expected p-values, with λGC.
Set intersections past the point Venn diagrams break.
The three-panel GSEA figure.
Family structure in standard clinical notation.
Figure and data out, in the formats the field uses.
Coordinates or gene symbols, resolved.
Pointer-following detail panel for canvas viewers.
Dependency-free single-value slider.
Compact dependency-free dropdown.