@sjcrh/proteinpaint-client 2.224.2 → 2.226.0
This diff represents the content of publicly available package versions that have been released to one of the supported registries. The information contained in this diff is provided for informational purposes only and reflects changes between package versions as they appear in their respective public registries.
- package/dist/2dmaf-CSBPMYHO.js +1362 -0
- package/dist/AggMatrixInput-2HST4LLJ.js +402 -0
- package/dist/AggregateMatrix-UPOAX44L.js +37 -0
- package/dist/AppHeader-H5QBVKUS.js +826 -0
- package/dist/BoxPlot-JTBQA6PL.js +1247 -0
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- package/dist/Cuminc-3BXJVWIH.js +1217 -0
- package/dist/DE-237VV46D.js +85 -0
- package/dist/DEinput-W443UW5T.js +479 -0
- package/dist/DM-TIW623IR.js +86 -0
- package/dist/DifferentialAnalysis-PHUA2GPK.js +236 -0
- package/dist/Disco-WHV52SCI.js +3445 -0
- package/dist/Disco-WHV52SCI.js.map +7 -0
- package/dist/Disco.UI-UDUXNCZX.js +239 -0
- package/dist/DmrPlot-FZCD6FTX.js +366 -0
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- package/dist/GSEA-3CNHMK6M.js +870 -0
- package/dist/GeneExpInput-ZOVP7BFY.js +38 -0
- package/dist/Geomap-JREOIESM.js +80 -0
- package/dist/HicApp-RKAMIUXQ.js +2240 -0
- package/dist/IDCViewer-KXV4FU3V.js +10810 -0
- package/dist/NumBinaryEditor-FNVYUK2J.js +274 -0
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- package/dist/NumContEditor-YLBJW64K.js +100 -0
- package/dist/NumContEditor.unit.spec-6JWBCPFY.js +160 -0
- package/dist/NumCustomBinEditor-42AFCXRN.js +29 -0
- package/dist/NumCustomBinEditor.unit.spec-AFBTF2CL.js +393 -0
- package/dist/NumDiscreteEditor-FJIBZTBP.js +165 -0
- package/dist/NumDiscreteEditor.unit.spec-MC4INDCB.js +229 -0
- package/dist/NumRegularBinEditor-2WRE72TL.js +29 -0
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- package/dist/NumericDensity-BNFAVOFO.js +29 -0
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- package/dist/NumericHandler.unit.spec-76T2IVRS.js +225 -0
- package/dist/ProteomeInput-M5UIO73Q.js +610 -0
- package/dist/Regression-5LB5TLA6.js +1412 -0
- package/dist/RunChart2-HIFXOEKZ.js +744 -0
- package/dist/SC-SMMW5MJG.js +1290 -0
- package/dist/Violin-COAFYZOV.js +1105 -0
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- package/dist/aboutSunburst-3FYJGR6B.js +93 -0
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- package/dist/animatedBubbleChart-QCCIC5IT.js +542 -0
- package/dist/app-IF7YPCGZ.js +28 -0
- package/dist/app-JZ43TSJP.js +38 -0
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- package/dist/block.mds.expressionrank-RKDDKY4J.js +350 -0
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- package/dist/block.mds.junction-MCOG37RA.js +1534 -0
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- package/dist/brainRegions-YUEMTKYH.js +213 -0
- package/dist/bubbleHeatmap-LQCVS4WK.js +374 -0
- package/dist/cellTypeBubbleHeatmap-DFRSPWAY.js +274 -0
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- package/dist/databrowser.ui-EY3H6B4S.js +424 -0
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- package/dist/dnaMethylation-FEB5GGXK.js +29 -0
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- package/dist/dnaMethylation.unit.spec-REOHQOBC.js +95 -0
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"sourcesContent": ["import {\n\tMenu,\n\taddGeneSearchbox,\n\trenderSampleTypeSelect,\n\trenderSampleTypesByTermsSelect,\n\tgetSelectedSampleTypes,\n\tmayGetSampleTypeLabel,\n\ttable2col\n} from '#dom'\nimport { TermTypes } from '#types'\nimport { getGEunit } from '#tw/geneExpression'\n\nexport class SearchHandler {\n\tcallback: any\n\tapp: any\n\tdom: any\n\tquerySampleTypes?: any[]\n\tquerySampleTypesByTerms?: any\n\tsampleTypeSelect?: any\n\tinit(opts) {\n\t\tthis.callback = opts.callback\n\t\tthis.app = opts.app\n\t\tthis.dom = {}\n\t\tconst holder = opts.holder.append('div').style('padding', '10px 0px')\n\t\tthis.dom.sampleTypeDiv = holder.append('div')\n\t\tthis.mayRenderSampleTypeSelect()\n\t\tconst geneSearch = addGeneSearchbox({\n\t\t\ttip: new Menu({ padding: '0px' }),\n\t\t\tgenome: opts.genomeObj,\n\t\t\trow: holder,\n\t\t\tsearchOnly: 'gene',\n\t\t\tcallback: () => this.selectGene(geneSearch)\n\t\t})\n\t\tholder.select('.sja_genesearchinput').style('margin', '0px')\n\t}\n\n\tmayRenderSampleTypeSelect() {\n\t\tthis.dom.sampleTypeDiv.selectAll('*').remove()\n\t\tthis.querySampleTypes = this.app.vocabApi.termdbConfig?.queries.geneExpression.sampleTypes\n\t\tthis.querySampleTypesByTerms = this.app.vocabApi.termdbConfig?.queries.geneExpression.sampleTypesByTerms\n\t\tif ((Array.isArray(this.querySampleTypes) && this.querySampleTypes.length >= 2) || this.querySampleTypesByTerms) {\n\t\t\t// render sample type select\n\t\t\tconst table = table2col({ holder: this.dom.sampleTypeDiv, margin: '0px 0px 15px 0px' })\n\t\t\tconst [td1, td2] = table.addRow()\n\t\t\ttd1.text('Sample Type')\n\t\t\ttd2.style('padding-left', '10px')\n\t\t\tif (this.querySampleTypesByTerms) {\n\t\t\t\tthis.sampleTypeSelect = renderSampleTypesByTermsSelect(\n\t\t\t\t\ttd2,\n\t\t\t\t\tthis.querySampleTypesByTerms,\n\t\t\t\t\tthis.app.vocabApi.termdbConfig\n\t\t\t\t)\n\t\t\t} else {\n\t\t\t\tthis.sampleTypeSelect = renderSampleTypeSelect(td2, this.querySampleTypes, this.app.vocabApi.termdbConfig)\n\t\t\t}\n\t\t}\n\t}\n\n\tasync selectGene(geneSearch) {\n\t\tconst gene = geneSearch?.geneSymbol\n\t\tif (!gene) throw new Error('No gene selected')\n\t\tconst sampleTypes = getSelectedSampleTypes({\n\t\t\tsampleTypeSelect: this.sampleTypeSelect,\n\t\t\tquerySampleTypes: this.querySampleTypes,\n\t\t\tquerySampleTypesByTerms: this.querySampleTypesByTerms\n\t\t})\n\t\tif (this.sampleTypeSelect && !sampleTypes?.length) {\n\t\t\treturn\n\t\t}\n\t\tconst unit = getGEunit(this.app.vocabApi)\n\t\tconst name = `${gene} ${unit}`\n\t\tconst term: any = { gene, name, type: TermTypes.GENE_EXPRESSION, sampleTypes }\n\t\tterm.sampleTypeLabel = mayGetSampleTypeLabel({\n\t\t\tsampleTypeSelect: this.sampleTypeSelect,\n\t\t\tquerySampleTypes: this.querySampleTypes,\n\t\t\tquerySampleTypesByTerms: this.querySampleTypesByTerms,\n\t\t\ttermdbConfig: this.app.vocabApi.termdbConfig\n\t\t})\n\t\tthis.callback(term)\n\t}\n}\n"],
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|
-
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|
-
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}
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|
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}
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|
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|
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|
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|
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|
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|
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if (hasHypoCpg) items.push({ text: "Hypo (FDR sig.)", color: colors.hypo });
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|
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rows.push({ label: "Sig. CpGs", items });
|
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|
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}
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return rows;
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|
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}
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|
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/**
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|
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|
-
* Render the per-CpG means scatter plot to an offscreen canvas and return
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|
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|
-
* a data URI suitable for the bigwig imgData track.
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|
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|
-
*/
|
|
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|
-
renderBetaTrack(diagnostic, config, blockWidth, showLoess, showDots, queryStart, queryStop) {
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|
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|
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|
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if (!probes.positions.length) return void 0;
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|
-
const { colors, fdr_cutoff, minProbesForCi } = config.settings.dmr;
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|
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|
-
const dpr = typeof window !== "undefined" && window.devicePixelRatio > 1 ? window.devicePixelRatio : 1;
|
|
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|
-
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|
|
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|
-
const height = 150;
|
|
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|
-
const canvas = document.createElement("canvas");
|
|
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|
-
canvas.width = width * dpr;
|
|
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|
-
canvas.height = height * dpr;
|
|
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|
-
const ctx = canvas.getContext("2d");
|
|
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|
-
if (!ctx) return void 0;
|
|
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|
-
ctx.scale(dpr, dpr);
|
|
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|
-
const xMin = queryStart ?? probes.positions[0];
|
|
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|
-
const xMax = queryStop ?? probes.positions[probes.positions.length - 1];
|
|
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|
-
const xRange = xMax - xMin || 1;
|
|
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|
-
const scaleX = (val) => (val - xMin) / xRange * width;
|
|
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|
-
const scaleY = (val) => height - val * height;
|
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{
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"sources": ["../plots/dmr/settings/defaults.ts", "../plots/dmr/viewModel/DmrViewModel.ts"],
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"sourcesContent": ["import type { DMRSettings } from './Settings.ts'\n\n// direction colours are shared with the server-rendered scan Manhattan\nexport { HYPER_COLOR, HYPO_COLOR } from '#shared/dmrColors.js'\nimport { HYPER_COLOR, HYPO_COLOR } from '#shared/dmrColors.js'\n\nexport function getDefaultDMRSettings(opts: any): DMRSettings {\n\tconst overrides = opts.settings || {}\n\t/* A dataset with no CpG-level matrix runs the region analysis on its element matrix, where one\n\trow is a cCRE, not a CpG. Those sit ~10kb apart against a CpG's ~100bp, so the CpG-scale window\n\tand kernel below would frame one element and smooth nothing. Scaled to element spacing instead.\n\tponytail: fixed values, not derived from the matrix's actual spacing \u2014 worth deriving only if a\n\tdataset shows up whose element density is far off this one's. The user can pan/zoom either way. */\n\tconst dm = opts?.app?.vocabApi?.termdbConfig?.queries?.dnaMethylation\n\t/* Per chromosome, not per dataset: a cohort with some shards built runs CpG resolution where one\n\texists and elements everywhere else (server resolveMethylationMatrix), so a dataset-wide flag gave\n\tthe fallback chromosomes a CpG-scale window over rows ~10 kb apart. cpgChroms is sent only for a\n\tshard-backed dataset without a genome-wide file. */\n\tconst chr = opts?.coordinateOverride?.chr\n\tconst elementScale =\n\t\tdm?.regionAnalysis == 'element' || (Array.isArray(dm?.cpgChroms) && !!chr && !dm.cpgChroms.includes(chr))\n\tconst defaults = {\n\t\tblockWidth: 800,\n\t\tpad: elementScale ? 100_000 : 2000,\n\t\tlambda: elementScale ? 50_000 : 1000,\n\t\tC: 2,\n\t\tfdr_cutoff: 0.05,\n\t\tcolors: {\n\t\t\tgroup1: '#3b5ee6',\n\t\t\tgroup2: '#c04e00',\n\t\t\thyper: HYPER_COLOR,\n\t\t\thypo: HYPO_COLOR\n\t\t},\n\t\tmaxLoessRegion: 250_000,\n\t\tminProbesForCi: 10,\n\t\tmaxRegionSize: 5_000_000\n\t}\n\n\t// Deep-merge colors so hyper/hypo defaults are preserved\n\t// when only group colors are overridden\n\tif (overrides.colors) {\n\t\tObject.assign(defaults.colors, overrides.colors)\n\t\tdelete overrides.colors\n\t}\n\n\treturn Object.assign(defaults, overrides)\n}\n", "import { first_genetrack_tolist } from '#common/1stGenetk'\n\n/** Name of the regulatory-element track in the genome config, if it declares one. */\nexport const CCRE_TRACK_NAME = 'ENCODE cCREs'\nimport type { TermdbDmrSuccessResponse, DmrDiagnostic } from '#types'\nimport type { DmrConfig, BedItem, LegendRow, DmrViewData } from '../DmrTypes.ts'\n\nexport class DmrViewModel {\n\tviewData: DmrViewData\n\n\tconstructor(\n\t\tdmrResult: TermdbDmrSuccessResponse,\n\t\tconfig: DmrConfig,\n\t\tgenomeObj: any,\n\t\tqueryChr: string,\n\t\tqueryStart?: number,\n\t\tqueryStop?: number\n\t) {\n\t\tconst { settings } = config\n\t\tconst dmrBedItems = this.makeDmrBedItems(dmrResult, settings)\n\t\tconst sigCpgBedItems = this.makeSigCpgBedItems(dmrResult, settings, queryChr, queryStart, queryStop)\n\n\t\tconst xRange = (queryStop ?? 0) - (queryStart ?? 0)\n\t\tconst loess = dmrResult.diagnostic?.loess\n\t\tconst showLoess = !!(loess && loess.group1_fitted.length > 0 && loess.group2_fitted.length > 0)\n\t\tconst showDots = xRange <= settings.dmr.maxLoessRegion\n\n\t\tconst betaTrackResult = dmrResult.diagnostic\n\t\t\t? this.renderBetaTrack(\n\t\t\t\t\tdmrResult.diagnostic,\n\t\t\t\t\tconfig,\n\t\t\t\t\tsettings.dmr.blockWidth,\n\t\t\t\t\tshowLoess,\n\t\t\t\t\tshowDots,\n\t\t\t\t\tqueryStart,\n\t\t\t\t\tqueryStop\n\t\t\t )\n\t\t\t: undefined\n\n\t\tthis.viewData = {\n\t\t\ttklst: this.buildTrackList(dmrBedItems, sigCpgBedItems, genomeObj, betaTrackResult?.img),\n\t\t\tlegendRows: this.buildLegendData(\n\t\t\t\tconfig,\n\t\t\t\tdmrResult.dmrs,\n\t\t\t\tsigCpgBedItems,\n\t\t\t\tshowLoess,\n\t\t\t\tshowDots,\n\t\t\t\tbetaTrackResult?.showCi ?? false\n\t\t\t),\n\t\t\tdiagnostic: dmrResult.diagnostic,\n\t\t\tdmrs: dmrResult.dmrs,\n\t\t\tdmrBedItems,\n\t\t\tshowLoess,\n\t\t\tshowDots\n\t\t}\n\t}\n\n\tprivate buildTrackList(\n\t\tdmrBedItems: BedItem[],\n\t\tsigCpgBedItems: BedItem[],\n\t\tgenomeObj: any,\n\t\tbetaTrackImg?: { minv: number; maxv: number; src: string }\n\t): any[] {\n\t\tconst tklst: any[] = []\n\t\tfirst_genetrack_tolist(genomeObj, tklst)\n\t\t/* Regulatory context, switched on here rather than left in the Tracks menu. A DMR next to a\n\t\tgene model says where it is; a DMR next to the cCREs says what it is sitting on, which is the\n\t\tquestion the element-level view was answering. Taken from the genome's own declaration by\n\t\tname, so a genome that does not declare it simply renders without the row. */\n\t\tconst ccre = (genomeObj?.tracks || []).find((t: any) => t.name == CCRE_TRACK_NAME)\n\t\tif (ccre) tklst.push(structuredClone(ccre))\n\t\ttklst.push({ type: 'bedj', name: 'DMRs', bedItems: dmrBedItems })\n\t\ttklst.push({ type: 'bedj', name: 'Sig. CpGs', bedItems: sigCpgBedItems })\n\t\tif (betaTrackImg) {\n\t\t\ttklst.push({\n\t\t\t\ttype: 'bigwig',\n\t\t\t\tname: 'Per-CpG Means',\n\t\t\t\theight: 150,\n\t\t\t\timgData: betaTrackImg\n\t\t\t})\n\t\t}\n\t\treturn tklst\n\t}\n\n\tprivate buildLegendData(\n\t\tconfig: DmrConfig,\n\t\tdmrs: TermdbDmrSuccessResponse['dmrs'],\n\t\tsigCpgBedItems: BedItem[],\n\t\tshowLoess: boolean,\n\t\tshowDots: boolean,\n\t\tshowCi: boolean\n\t): LegendRow[] {\n\t\tconst { colors } = config.settings.dmr\n\t\tconst g1 = config.group1Name || 'Group 1'\n\t\tconst g2 = config.group2Name || 'Group 2'\n\t\tconst meansItems: LegendRow['items'] = []\n\t\tif (showDots) {\n\t\t\tmeansItems.push({ text: `${g1} (control)`, color: colors.group1 }, { text: `${g2} (case)`, color: colors.group2 })\n\t\t}\n\t\tif (showLoess) {\n\t\t\tconst ciLabel = showCi ? ' + 95% CI' : ''\n\t\t\tmeansItems.push(\n\t\t\t\t{ text: `${g1} LOESS trend${ciLabel}`, color: colors.group1, style: showCi ? 'shaded' : 'dashed' },\n\t\t\t\t{ text: `${g2} LOESS trend${ciLabel}`, color: colors.group2, style: showCi ? 'shaded' : 'dashed' }\n\t\t\t)\n\t\t}\n\t\tconst rows: LegendRow[] = [{ label: 'Per-CpG Means', items: meansItems }]\n\t\t// Only show DMR legend entries for directions present in the results\n\t\tconst hasHyper = dmrs.some(d => d.direction === 'hyper')\n\t\tconst hasHypo = dmrs.some(d => d.direction === 'hypo')\n\t\tif (hasHyper || hasHypo) {\n\t\t\tconst items: LegendRow['items'] = []\n\t\t\tif (hasHyper) items.push({ text: 'Hypermethylated', color: colors.hyper })\n\t\t\tif (hasHypo) items.push({ text: 'Hypomethylated', color: colors.hypo })\n\t\t\trows.push({ label: 'DMR', items })\n\t\t}\n\t\tif (sigCpgBedItems.length) {\n\t\t\tconst items: LegendRow['items'] = []\n\t\t\tconst hasHyperCpg = sigCpgBedItems.some(b => b.color === colors.hyper)\n\t\t\tconst hasHypoCpg = sigCpgBedItems.some(b => b.color === colors.hypo)\n\t\t\tif (hasHyperCpg) items.push({ text: 'Hyper (FDR sig.)', color: colors.hyper })\n\t\t\tif (hasHypoCpg) items.push({ text: 'Hypo (FDR sig.)', color: colors.hypo })\n\t\t\trows.push({ label: 'Sig. CpGs', items })\n\t\t}\n\t\treturn rows\n\t}\n\n\t/**\n\t * Render the per-CpG means scatter plot to an offscreen canvas and return\n\t * a data URI suitable for the bigwig imgData track.\n\t */\n\tprivate renderBetaTrack(\n\t\tdiagnostic: DmrDiagnostic,\n\t\tconfig: DmrConfig,\n\t\tblockWidth: number,\n\t\tshowLoess: boolean,\n\t\tshowDots: boolean,\n\t\tqueryStart?: number,\n\t\tqueryStop?: number\n\t): { img: { minv: number; maxv: number; src: string }; showCi: boolean } | undefined {\n\t\tconst { probes } = diagnostic\n\t\tif (!probes.positions.length) return undefined\n\n\t\tconst { colors, fdr_cutoff, minProbesForCi } = config.settings.dmr\n\t\tconst dpr = typeof window !== 'undefined' && window.devicePixelRatio > 1 ? window.devicePixelRatio : 1\n\t\tconst width = blockWidth\n\t\tconst height = 150\n\n\t\tconst canvas = document.createElement('canvas')\n\t\tcanvas.width = width * dpr\n\t\tcanvas.height = height * dpr\n\t\tconst ctx = canvas.getContext('2d')\n\t\tif (!ctx) return undefined\n\t\tctx.scale(dpr, dpr)\n\n\t\t// Use the full block view range so dots align with bedj tracks above.\n\t\t// The block stretches the image to fill the view from queryStart to queryStop.\n\t\tconst xMin = queryStart ?? probes.positions[0]\n\t\tconst xMax = queryStop ?? probes.positions[probes.positions.length - 1]\n\t\tconst xRange = xMax - xMin || 1\n\t\tconst scaleX = (val: number) => ((val - xMin) / xRange) * width\n\t\tconst scaleY = (val: number) => height - val * height // beta 0-1\n\n\t\t// Transparent background so block mouse events (yellow line) show through\n\t\tctx.clearRect(0, 0, width, height)\n\n\t\t// DMR region shading omitted \u2014 already shown as a bedj track above\n\n\t\t// Draw LOESS curves with shaded CI regions, clipped to probe data range.\n\t\t// Only show CIs when there are enough probes for a reliable estimate.\n\t\tlet showCi = false\n\t\tif (showLoess && diagnostic.loess) {\n\t\t\tconst { loess } = diagnostic\n\t\t\tconst firstProbePos = probes.positions[0]\n\t\t\tconst lastProbePos = probes.positions[probes.positions.length - 1]\n\t\t\tshowCi = probes.positions.length >= minProbesForCi\n\n\t\t\tfor (const [fitted, ciLower, ciUpper, color] of [\n\t\t\t\t[loess.group1_fitted, loess.group1_ci_lower, loess.group1_ci_upper, colors.group1],\n\t\t\t\t[loess.group2_fitted, loess.group2_ci_lower, loess.group2_ci_upper, colors.group2]\n\t\t\t] as [number[], number[], number[], string][]) {\n\t\t\t\tif (!fitted.length) continue\n\t\t\t\tconst lPos = loess.positions\n\n\t\t\t\t// Find LOESS indices within the range of actual probe positions\n\t\t\t\tlet iStart = 0\n\t\t\t\tlet iEnd = lPos.length - 1\n\t\t\t\twhile (iStart < lPos.length && lPos[iStart] < firstProbePos) iStart++\n\t\t\t\twhile (iEnd >= 0 && lPos[iEnd] > lastProbePos) iEnd--\n\t\t\t\tif (iStart > iEnd) continue\n\n\t\t\t\tif (showCi) {\n\t\t\t\t\t// Draw CI as shaded region\n\t\t\t\t\tctx.globalAlpha = 0.12\n\t\t\t\t\tctx.fillStyle = color\n\t\t\t\t\tctx.beginPath()\n\t\t\t\t\tfor (let i = iStart; i <= iEnd; i++) {\n\t\t\t\t\t\tctx.lineTo(scaleX(lPos[i]), scaleY(Math.max(0, Math.min(1, ciUpper[i]))))\n\t\t\t\t\t}\n\t\t\t\t\tfor (let i = iEnd; i >= iStart; i--) {\n\t\t\t\t\t\tctx.lineTo(scaleX(lPos[i]), scaleY(Math.max(0, Math.min(1, ciLower[i]))))\n\t\t\t\t\t}\n\t\t\t\t\tctx.closePath()\n\t\t\t\t\tctx.fill()\n\t\t\t\t}\n\n\t\t\t\t// Draw LOESS fitted curve (dashed when no CI, solid otherwise)\n\t\t\t\tctx.globalAlpha = 0.8\n\t\t\t\tctx.strokeStyle = color\n\t\t\t\tctx.lineWidth = 2\n\t\t\t\tctx.setLineDash(showCi ? [] : [6, 4])\n\t\t\t\tctx.beginPath()\n\t\t\t\tfor (let i = iStart; i <= iEnd; i++) {\n\t\t\t\t\tctx.lineTo(scaleX(lPos[i]), scaleY(Math.max(0, Math.min(1, fitted[i]))))\n\t\t\t\t}\n\t\t\t\tctx.stroke()\n\t\t\t\tctx.setLineDash([])\n\t\t\t}\n\t\t}\n\n\t\t// Draw dots (hidden for large regions where only LOESS is shown)\n\t\tif (!showDots) {\n\t\t\tctx.globalAlpha = 1\n\t\t\treturn { img: { minv: 0, maxv: 1, src: canvas.toDataURL('image/png') }, showCi }\n\t\t}\n\t\tfor (let i = 0; i < probes.positions.length; i++) {\n\t\t\tconst x = scaleX(probes.positions[i])\n\t\t\tconst isSig = probes.fdr[i] < fdr_cutoff\n\t\t\tconst alpha = isSig ? 0.85 : 0.3\n\n\t\t\t// Group 1 (control)\n\t\t\tctx.globalAlpha = alpha\n\t\t\tctx.fillStyle = colors.group1\n\t\t\tconst m1 = probes.mean_group1[i]\n\t\t\tif (m1 != null) {\n\t\t\t\tctx.beginPath()\n\t\t\t\tctx.arc(x, scaleY(m1), 4, 0, Math.PI * 2)\n\t\t\t\tctx.fill()\n\t\t\t}\n\n\t\t\t// Group 2 (case)\n\t\t\tctx.fillStyle = colors.group2\n\t\t\tconst m2 = probes.mean_group2[i]\n\t\t\tif (m2 != null) {\n\t\t\t\tctx.beginPath()\n\t\t\t\tctx.arc(x, scaleY(m2), 4, 0, Math.PI * 2)\n\t\t\t\tctx.fill()\n\t\t\t}\n\t\t}\n\t\tctx.globalAlpha = 1\n\n\t\treturn { img: { minv: 0, maxv: 1, src: canvas.toDataURL('image/png') }, showCi }\n\t}\n\n\tprivate makeDmrBedItems(dmrResult: TermdbDmrSuccessResponse, settings: DmrConfig['settings']): BedItem[] {\n\t\treturn dmrResult.dmrs.map(dmr => {\n\t\t\t// Map -log10(min_smoothed_fdr) to alpha: more significant = more opaque\n\t\t\tconst negLog = -Math.log10(Math.max(dmr.min_smoothed_fdr, 1e-300))\n\t\t\tconst alpha = Math.round(Math.min(255, Math.max(50, (negLog / 10) * 255)))\n\t\t\tconst hex = alpha.toString(16).padStart(2, '0')\n\t\t\tconst base = dmr.direction === 'hyper' ? settings.dmr.colors.hyper : settings.dmr.colors.hypo\n\t\t\treturn { chr: dmr.chr, start: dmr.start, stop: dmr.stop, color: base + hex }\n\t\t})\n\t}\n\n\tprivate makeSigCpgBedItems(\n\t\tdmrResult: TermdbDmrSuccessResponse,\n\t\tsettings: DmrConfig['settings'],\n\t\tchr: string,\n\t\tqueryStart?: number,\n\t\tqueryStop?: number\n\t): BedItem[] {\n\t\tconst diag = dmrResult.diagnostic\n\t\tif (!diag) return []\n\t\tconst { probes } = diag\n\t\tconst items: BedItem[] = []\n\t\tconst minDeltaBeta = 0.05\n\t\tfor (let i = 0; i < probes.positions.length; i++) {\n\t\t\tif (probes.fdr[i] >= settings.dmr.fdr_cutoff) continue\n\t\t\tconst pos = probes.positions[i]\n\t\t\tif (queryStart != null && queryStop != null && (pos < queryStart || pos > queryStop)) continue\n\t\t\tconst mg1 = probes.mean_group1[i]\n\t\t\tconst mg2 = probes.mean_group2[i]\n\t\t\tif (mg1 == null || mg2 == null) continue\n\t\t\tconst deltaBeta = mg2 - mg1\n\t\t\tif (Math.abs(deltaBeta) < minDeltaBeta) continue\n\t\t\tconst color = deltaBeta >= 0 ? settings.dmr.colors.hyper : settings.dmr.colors.hypo\n\t\t\titems.push({ chr, start: pos, stop: pos + 1, color })\n\t\t}\n\t\treturn items\n\t}\n}\n"],
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5
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6
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-
"names": []
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7
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-
}
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