@sjcrh/proteinpaint-client 2.191.3 → 2.191.4

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.
Files changed (888) hide show
  1. package/dist/2dmaf-Z3D2M3FB.js +1373 -0
  2. package/dist/AIProjectAdmin-2OQOQXH4.js +956 -0
  3. package/dist/AppHeader-PXLGVCVS.js +835 -0
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  5. package/dist/CorrelationVolcano-RO6CFLZA.js +619 -0
  6. package/dist/DE-CCA5SBJG.js +95 -0
  7. package/dist/DEinput-MRUQW6X6.js +301 -0
  8. package/dist/DifferentialAnalysis-5YQQLJKR.js +245 -0
  9. package/dist/Disco-4FTOJBLG.js +3237 -0
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  159. package/dist/dnaMethylation-WGJMJL5B.js +38 -0
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+ {
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+ "version": 3,
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+ "sources": ["../../shared/utils/src/common.ts"],
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+ "sourcesContent": ["/*\nshared between client and server\n\nexported functions\n- bplen()\n- mclasstester()\n- basecompliment()\n\n\n*/\nimport { rgb } from 'd3-color'\nimport * as d3scale from 'd3-scale'\nimport * as d3 from 'd3'\n\n// moved from `#shared/terms` to here, so that this can be passed as\n// part of 'common' argument to exported dataset js function, at server runtime\n// 3/30/2026 - changed from literal object to a class with static properties\n// to make it easier for IDEs and tsc compiler to catch typos in consumer code\nexport class TermTypeGroups {\n\tstatic DICTIONARY_VARIABLES = 'Dictionary Variables'\n\tstatic DNA_METHYLATION = 'DNA Methylation'\n\tstatic GENE_DEPENDENCY = 'Gene Dependency'\n\tstatic GENE_EXPRESSION = 'Gene Expression'\n\tstatic ISOFORM_EXPRESSION = 'Isoform Expression'\n\tstatic GSEA = 'GSEA'\n\tstatic METABOLITE_INTENSITY = 'Metabolite Intensity'\n\tstatic PROTEOME_ABUNDANCE = 'Proteome Abundance'\n\tstatic MUTATION_CNV_FUSION = 'Mutation/CNV/Fusion'\n\tstatic MUTATION_SIGNATURE = 'Mutation Signature'\n\tstatic PROTEIN_EXPRESSION = 'Protein Expression'\n\tstatic SINGLECELL_CELLTYPE = 'Single-cell Cell Type'\n\tstatic SINGLECELL_GENE_EXPRESSION = 'Single-cell Gene Expression'\n\tstatic SNP = 'SNP Genotype'\n\tstatic SNP_LIST = 'SNP List'\n\tstatic SNP_LOCUS = 'SNP Locus'\n\tstatic SPLICE_JUNCTION = 'Splice Junction'\n\tstatic SSGSEA = 'Geneset Expression'\n\tstatic TERM_COLLECTION = 'Term Collection'\n\tstatic VARIANT_GENOTYPE = 'Variant Genotype'\n}\n// freeze so that mutating any of the static properties above will throw at runtime\nObject.freeze(TermTypeGroups)\n\nexport const defaultcolor = rgb('#8AB1D4').darker()\nexport const default_text_color = rgb('#aaa').darker().darker()\n\nexport const exoncolor = '#4F8053'\nexport const plotColor = '#ce768e'\n\n// something that has something to do with coding gene reading frame\nexport const IN_frame = true\nexport const OUT_frame = false\n\n/********************************\n* on dt usage *\n*********************************\n- once a dt value is decided and used with actual dataset,\n the value must not be altered, since dataset file may hardcode such value and reassigning to a new integer will break!\n- never test dt value by range e.g. if(dt>10), it breaks! only test equality!\n- in code import variable from here and DO NOT use literal values, to make code tractable\n*/\nexport const dtsnvindel = 1\nexport const dtfusionrna = 2\nexport const dtgeneexpression = 3\nexport const dtcnv = 4\nexport const dtsv = 5\nexport const dtitd = 6\nexport const dtdel = 7\nexport const dtnloss = 8\nexport const dtcloss = 9\nexport const dtloh = 10\nexport const dtmetaboliteintensity = 11\nexport const dtssgsea = 12\nexport const dtdnamethylation = 13\nexport const dtproteomeabundance = 14\n// add new dt value here. !!!DO NOT change value of existing dt!!!\n\nexport const dt2label = {\n\t[dtsnvindel]: 'SNV/indel',\n\t[dtfusionrna]: 'Fusion RNA',\n\t[dtcnv]: 'CNV',\n\t[dtsv]: 'SV',\n\t[dtitd]: 'ITD',\n\t[dtdel]: 'Deletion',\n\t[dtnloss]: 'N-loss',\n\t[dtcloss]: 'C-loss',\n\t[dtloh]: 'LOH',\n\t[dtgeneexpression]: 'Gene Expression',\n\t[dtmetaboliteintensity]: 'Metabolite Intensity',\n\t[dtproteomeabundance]: 'Proteome Abundance'\n}\n\n// Maps dt types to UI labels and lesion types for GRIN2\n// All dt types use lesionTypes array for consistency\nexport const dt2lesion = {\n\t[dtsnvindel]: {\n\t\tuilabel: 'SNV/INDEL (Mutation)',\n\t\tlesionTypes: [{ name: 'Mutation', lesionType: 'mutation', color: '#44AA44' }]\n\t},\n\t[dtcnv]: {\n\t\tuilabel: 'CNV (Copy Number Variation)',\n\t\tlesionTypes: [\n\t\t\t{ name: 'Loss', lesionType: 'loss', color: '#4444FF' },\n\t\t\t{ name: 'Gain', lesionType: 'gain', color: '#FF4444' }\n\t\t]\n\t},\n\t[dtsv]: {\n\t\tuilabel: 'SV (Structural Variation)',\n\t\tlesionTypes: [{ name: 'SV', lesionType: 'sv', color: '#9932CC' }]\n\t},\n\t[dtfusionrna]: {\n\t\tuilabel: 'Fusion (RNA Fusion)',\n\t\tlesionTypes: [{ name: 'Fusion', lesionType: 'fusion', color: '#FFA500' }]\n\t}\n}\n\n// Maps GRIN2 option types to their corresponding dt values\nexport const optionToDt = {\n\tsnvindelOptions: dtsnvindel,\n\tcnvOptions: dtcnv,\n\tfusionOptions: dtfusionrna,\n\tsvOptions: dtsv\n}\n\nexport const mclass = {\n\tM: {\n\t\tlabel: 'MISSENSE',\n\t\tcolor: '#3987CC',\n\t\tdt: dtsnvindel,\n\t\tdesc: 'A sequence variant, that changes one or more bases, resulting in a different amino acid sequence but where the length is preserved',\n\t\tkey: 'M'\n\t},\n\tE: { label: 'EXON', color: '#bcbd22', dt: dtsnvindel, desc: 'A variant in the exon of a non-coding RNA.', key: 'E' },\n\tF: {\n\t\tlabel: 'FRAMESHIFT',\n\t\tcolor: 'rgb(200, 61, 61)',\n\t\tdt: dtsnvindel,\n\t\tdesc: 'A sequence variant which causes a disruption of the translational reading frame, because the number of nucleotides inserted or deleted is not a multiple of three',\n\t\tkey: 'F'\n\t},\n\tN: {\n\t\tlabel: 'NONSENSE',\n\t\tcolor: '#ff7f0e',\n\t\tdt: dtsnvindel,\n\t\tdesc: 'A sequence variant whereby at least one base of a codon is changed, resulting in a premature stop codon, leading to a shortened transcript',\n\t\tkey: 'N'\n\t},\n\tS: {\n\t\tlabel: 'SILENT',\n\t\tcolor: '#2ca02c',\n\t\tdt: dtsnvindel,\n\t\tdesc: 'A sequence variant where there is no resulting change to the encoded amino acid',\n\t\tkey: 'S'\n\t},\n\tD: {\n\t\tlabel: 'PROTEINDEL',\n\t\tcolor: 'rgb(100, 100, 100)',\n\t\tdt: dtsnvindel,\n\t\tdesc: 'An inframe non synonymous variant that deletes bases from the coding sequence',\n\t\tkey: 'D'\n\t},\n\tI: {\n\t\tlabel: 'PROTEININS',\n\t\tcolor: '#8c564b',\n\t\tdt: dtsnvindel,\n\t\tdesc: 'An inframe non synonymous variant that inserts bases into in the coding sequence',\n\t\tkey: 'I'\n\t},\n\tProteinAltering: {\n\t\tlabel: 'PROTEINALTERING',\n\t\tcolor: '#5a0034',\n\t\tdt: dtsnvindel,\n\t\tdesc: 'An inframe complex change to the coding sequence',\n\t\tkey: 'ProteinAltering'\n\t},\n\tP: {\n\t\tlabel: 'SPLICE_REGION',\n\t\tcolor: '#9467bd',\n\t\tdt: dtsnvindel,\n\t\tdesc: 'A sequence variant in which a change has occurred within the region of the splice site, either within 1-3 bases of the exon or 3-8 bases of the intron',\n\t\tkey: 'P'\n\t},\n\tL: {\n\t\tlabel: 'SPLICE',\n\t\tcolor: '#6633FF',\n\t\tdt: dtsnvindel,\n\t\tdesc: 'A variant near an exon edge that may affect splicing functionality',\n\t\tkey: 'L'\n\t},\n\tIntron: { label: 'INTRON', color: '#656565', dt: dtsnvindel, desc: 'An intronic variant.', key: 'Intron' },\n\n\tStopLost: {\n\t\tlabel: 'Stop lost',\n\t\tcolor: '#ff7f0e',\n\t\tdt: dtsnvindel,\n\t\tdesc: 'A sequence variant where at least one base of the terminator codon (stop) is changed, resulting in an elongated transcript',\n\t\tkey: 'StopLost'\n\t},\n\tStartLost: {\n\t\tlabel: 'Start lost',\n\t\tcolor: '#ff7f0e',\n\t\tdt: dtsnvindel,\n\t\tdesc: 'A codon variant that changes at least one base of the canonical start codon',\n\t\tkey: 'StartLost'\n\t},\n\n\t// quick fix!! for showing genes that are not tested in samples (e.g. gene panels) in the heatmap\n\tBlank: { label: 'Not tested', color: '#fff', dt: dtsnvindel, desc: 'This gene is not tested.', key: 'Blank' },\n\n\tWT: { label: 'Wildtype', color: '#D3D3D3', dt: dtsnvindel, desc: 'Wildtype', key: 'WT' }\n}\nexport const mclassitd = 'ITD'\nmclass[mclassitd] = {\n\tlabel: 'ITD',\n\tcolor: '#ff70ff',\n\tdt: dtitd,\n\tdesc: 'In-frame internal tandem duplication',\n\tkey: mclassitd\n}\n\nexport const mclassdel = 'DEL'\nmclass[mclassdel] = {\n\tlabel: 'DELETION, intragenic',\n\tcolor: '#858585',\n\tdt: dtdel,\n\tdesc: 'Intragenic deletion',\n\tkey: mclassdel\n}\n\nexport const mclassnloss = 'NLOSS'\nmclass[mclassnloss] = {\n\tlabel: 'N-terminus loss',\n\tcolor: '#545454',\n\tdt: dtnloss,\n\tdesc: 'N-terminus loss due to translocation',\n\tkey: mclassnloss\n}\n\nexport const mclasscloss = 'CLOSS'\nmclass[mclasscloss] = {\n\tlabel: 'C-terminus loss',\n\tcolor: '#545454',\n\tdt: dtcloss,\n\tdesc: 'C-terminus loss due to translocation',\n\tkey: mclasscloss\n}\n\nexport const mclassutr3 = 'Utr3'\nmclass[mclassutr3] = {\n\tlabel: 'UTR_3',\n\tcolor: '#998199',\n\tdt: dtsnvindel,\n\tdesc: \"A variant in the 3' untranslated region\",\n\tkey: mclassutr3\n}\n\nexport const mclassutr5 = 'Utr5'\nmclass[mclassutr5] = {\n\tlabel: 'UTR_5',\n\tcolor: '#819981',\n\tdt: dtsnvindel,\n\tdesc: \"A variant in the 5' untranslated region\",\n\tkey: mclassutr5\n}\n\nexport const mclassnonstandard = 'X'\nmclass[mclassnonstandard] = {\n\tlabel: 'NONSTANDARD',\n\tcolor: 'black',\n\tdt: dtsnvindel,\n\tdesc: 'A mutation class that either does not match our notation, or is unspecified',\n\tkey: mclassnonstandard\n}\n\nexport const mclassnoncoding = 'noncoding'\nmclass[mclassnoncoding] = {\n\tlabel: 'NONCODING',\n\tcolor: 'black',\n\tdt: dtsnvindel,\n\tdesc: 'Noncoding mutation',\n\tkey: mclassnoncoding\n}\n\n/*\nincludes full list of consequences from\nhttps://www.ensembl.org/info/genome/variation/prediction/predicted_data.html\neach entry is SO term with matching pp class\nentries that cannot be mapped to dtsnvindel classes are commented off\norder of entries is severity\n\n* since source of data! *\nfrom this array derives multiple types of lookup tables to perform mapping on both ways\n*/\nconst SOterms = [\n\t//transcript_ablation // not supported: 1) do not expect this in maf/vcf 2) should be represented as cnv deletion but not the legacy unused value \"dtdel\"; if needed can reenable\n\t['splice_acceptor_variant', 'L'],\n\t['splice_donor_variant', 'L'],\n\t['stop_gained', 'N'],\n\t['frameshift_variant', 'F'],\n\t['stop_lost', 'StopLost'],\n\t['start_lost', 'StartLost'],\n\t//transcript_amplification // not supported, should be represented by cnv instead\n\t['feature_elongation', mclassnoncoding],\n\t['feature_truncation', mclassnoncoding],\n\t['inframe_insertion', 'I'],\n\t['inframe_deletion', 'D'],\n\t['missense_variant', 'M'],\n\t['protein_altering_variant', 'ProteinAltering'],\n\t['splice_donor_5th_base_variant', 'P'],\n\t['splice_region_variant', 'P'],\n\t['splice_donor_region_variant', 'P'],\n\t['splice_polypyrimidine_tract_variant', 'P'],\n\t['incomplete_terminal_codon_variant', 'N'],\n\t['start_retained_variant', 'S'],\n\t['stop_retained_variant', 'S'],\n\t['synonymous_variant', 'S'],\n\t['coding_sequence_variant', 'E'],\n\t['mature_miRNA_variant', 'E'],\n\t['5_prime_UTR_variant', mclassutr5],\n\t['3_prime_UTR_variant', mclassutr3],\n\t['non_coding_transcript_exon_variant', 'E'],\n\t['intron_variant', 'Intron'],\n\t['NMD_transcript_variant', 'F'],\n\t['non_coding_transcript_variant', 'E'],\n\t['coding_transcript_variant', 'E'],\n\t['upstream_gene_variant', mclassnoncoding],\n\t['downstream_gene_variant', mclassnoncoding],\n\t['TFBS_ablation', mclassnoncoding],\n\t['TFBS_amplification', mclassnoncoding],\n\t['TF_binding_site_variant', mclassnoncoding],\n\t['regulatory_region_ablation', mclassnoncoding],\n\t['regulatory_region_amplification', mclassnoncoding],\n\t['regulatory_region_variant', mclassnoncoding],\n\t['intergenic_variant', mclassnoncoding],\n\t['sequence_variant', mclassnonstandard]\n]\n\n// maps a pp class to an array of consequences\n// k: pp class, v: array of consequences. case sensitive\nexport const class2SOterm = new Map()\nfor (const [csq, cls] of SOterms) {\n\tif (!class2SOterm.has(cls)) class2SOterm.set(cls, [])\n\tclass2SOterm.get(cls).push(csq)\n}\n\n// maps a consequence to a pp class. no severity info. use vepinfo() if needs severity\n// k: consequence, v: pp class. case sensitive.\nexport const SOterm2class = new Map()\nfor (const [csq, cls] of SOterms) {\n\tSOterm2class.set(csq, cls)\n}\n\n// outdated function to match with adhoc nonstandard notations, only used in legacy code utils/src/bulk.snv.js\n// DO NOT USE to map vep consequences\nexport function mclasstester(s) {\n\tswitch (s.toLowerCase()) {\n\t\tcase 'missense_mutation':\n\t\t\treturn 'M'\n\t\tcase 'nonsense_mutation':\n\t\t\treturn 'N'\n\t\tcase 'splice_site':\n\t\t\treturn 'L'\n\t\tcase 'splice_region':\n\t\t\treturn 'P'\n\t\tcase 'rna':\n\t\t\treturn mclassnoncoding\n\t\tcase 'frame_shift_del':\n\t\t\treturn 'F'\n\t\tcase 'frame_shift_ins':\n\t\t\treturn 'F'\n\t\tcase 'in_frame_del':\n\t\t\treturn 'D'\n\t\tcase 'in_frame_ins':\n\t\t\treturn 'I'\n\t\tcase 'protein_altering_variant':\n\t\t\treturn 'ProteinAltering'\n\t\tcase 'translation_start_site':\n\t\t\treturn mclassnonstandard\n\t\tcase 'nonstop_mutation':\n\t\t\treturn 'N'\n\t\tcase \"3'utr\":\n\t\t\treturn mclassutr3\n\t\tcase \"3'flank\":\n\t\t\treturn mclassnoncoding\n\t\tcase \"5'utr\":\n\t\t\treturn mclassutr5\n\t\tcase \"5'flank\":\n\t\t\treturn mclassnoncoding\n\t\tcase 'silent':\n\t\t\treturn 'S'\n\t\tcase 'blank':\n\t\t\treturn 'Blank'\n\t\tdefault:\n\t\t\treturn null\n\t}\n}\n\nexport const mclassfusionrna = 'Fuserna'\nmclass[mclassfusionrna] = {\n\tlabel: 'Fusion transcript',\n\tcolor: '#545454',\n\tdt: dtfusionrna,\n\tdesc:\n\t\t'Marks the break points leading to fusion transcripts.<br>' +\n\t\t'<span style=\"font-size:150%\">&#9680;</span> - 3\\' end of the break point is fused to the 5\\' end of another break point in a different gene.<br>' +\n\t\t'<span style=\"font-size:150%\">&#9681;</span> - 5\\' end of the break point is fused to the 3\\' end of another break point in a different gene.',\n\tkey: mclassfusionrna\n}\nexport const mclasssv = 'SV'\nmclass[mclasssv] = {\n\tlabel: 'Structural variation',\n\tcolor: '#858585',\n\tdt: dtsv,\n\tdesc:\n\t\t'<span style=\"font-size:150%\">&#9680;</span> - 3\\' end of the break point is fused to the 5\\' end of another break point in a different gene.<br>' +\n\t\t'<span style=\"font-size:150%\">&#9681;</span> - 5\\' end of the break point is fused to the 3\\' end of another break point in a different gene.',\n\tkey: mclasssv\n}\n\n// \"CNV_amp\" represents \"CNV Gain\" and is used in both 2-category and 5-category CNV data representation\n// \"CNV_amplification\" represents CNV amplification and is used in 5-category CNV\n// \"CNV_amp\" have to stay as-is since it may be hardcoded in lots of data beyond portal code.\nexport const mclasscnvgain = 'CNV_amp'\nmclass[mclasscnvgain] = {\n\tlabel: 'Copy number gain', // TODO change to 'Gain'\n\tcolor: '#e9a3c9',\n\tdt: dtcnv,\n\tdesc: 'Copy number gain',\n\tkey: mclasscnvgain\n}\n\nexport const mclasscnvloss = 'CNV_loss'\nmclass[mclasscnvloss] = {\n\tlabel: 'Copy number loss',\n\tcolor: '#a1d76a',\n\tdt: dtcnv,\n\tdesc: 'Copy number loss',\n\tkey: mclasscnvloss\n}\n\n// mclasscnvAmp is next level above mclasscnvgain and is used in 5-category CNV data\nexport const mclasscnvAmp = 'CNV_amplification'\nmclass[mclasscnvAmp] = {\n\tlabel: 'Copy number amplification',\n\tcolor: '#ff0000',\n\tdt: dtcnv,\n\tdesc: 'Copy number amplification',\n\tkey: mclasscnvAmp\n}\n\nexport const mclasscnvHomozygousDel = 'CNV_homozygous_deletion'\nmclass[mclasscnvHomozygousDel] = {\n\tlabel: 'Copy number homozygous deletion',\n\tcolor: '#0000ff',\n\tdt: dtcnv,\n\tdesc: 'Copy number homozygous deletion',\n\tkey: mclasscnvHomozygousDel\n}\n\nexport const mclasscnvloh = 'CNV_loh'\nmclass[mclasscnvloh] = { label: 'LOH', color: '#12EDFC', dt: dtcnv, desc: 'Loss of heterozygosity', key: mclasscnvloh }\n\n// for VCF\nexport const mclasssnv = 'snv'\nmclass[mclasssnv] = {\n\tlabel: 'SNV',\n\tcolor: '#92a2d4',\n\tdt: dtsnvindel,\n\tdesc: 'Single nucleotide variation',\n\tkey: mclasssnv\n}\n\nexport const mclassmnv = 'mnv'\nmclass[mclassmnv] = {\n\tlabel: 'MNV',\n\tcolor: '#92a2d4',\n\tdt: dtsnvindel,\n\tdesc: 'Multiple nucleotide variation',\n\tkey: mclassmnv\n}\n\nexport const mclassinsertion = 'insertion'\nmclass[mclassinsertion] = {\n\tlabel: 'Sequence insertion',\n\tcolor: '#bd8e91',\n\tdt: dtsnvindel,\n\tdesc: 'Sequence insertion',\n\tkey: mclassinsertion\n}\n\nexport const mclassdeletion = 'deletion'\nmclass[mclassdeletion] = {\n\tlabel: 'Sequence deletion',\n\tcolor: '#b5a174',\n\tdt: dtsnvindel,\n\tdesc: 'Sequence deletion',\n\tkey: mclassdeletion\n}\n// TODO complex indel\n\n/* tricky\nwhen a mds3 tk uses numeric cnv, data points from tk.cnv.cnvLst[] has .class=dtcnv but no class!\na \"cnv\" entry needs to be present in mclass legend, and thus this wrapper function over mclass{} to allow dtcnv as key\nthe tricky case doesn't apply to other plots\n*/\nexport function mds3tkMclass(k) {\n\tif (k == dtcnv) {\n\t\treturn {\n\t\t\tcolor: '#858585',\n\t\t\tlabel: 'CNV',\n\t\t\tdesc: 'Copy number variation'\n\t\t}\n\t}\n\treturn mclass[k]\n}\n\nexport const dt2color = {\n\t[dtsnvindel]: mclass.M.color // general color for snvindel irrespective of class (when class is not available)\n\t// add new dt as needed\n}\n\n// option to override mutation class attribute values\nexport function applyOverrides(overrides: Record<string, any> = {}) {\n\tif (overrides.mclass) {\n\t\tfor (const key in overrides.mclass) {\n\t\t\t// allow to fill-in mutation class that are missing from mclass;\n\t\t\t// may be useful for things like 'Not tested', etc, that may not be in mclass by default\n\t\t\t// but are used by a customer with its own PP server instance\n\t\t\tif (!mclass[key]) mclass[key] = {}\n\t\t\tfor (const subkey in overrides.mclass[key]) {\n\t\t\t\tmclass[key][subkey] = overrides.mclass[key][subkey]\n\t\t\t}\n\t\t}\n\t}\n}\n\n/* legacy function. input is comma-joined multiple consequences\nperforms case insensitive match and returns severity rank\nTODO share data with SOterms\n*/\nexport const vepinfo = function (s) {\n\tconst l = s.toLowerCase().split(',')\n\tlet rank = 1\n\tif (l.indexOf('transcript_ablation') != -1) {\n\t\t// FIXME no class for whole gene deletion\n\t\treturn [dtdel, mclassdel, rank]\n\t}\n\trank++\n\tif (l.indexOf('splice_acceptor_variant') != -1) return [dtsnvindel, 'L', rank]\n\trank++\n\tif (l.indexOf('splice_donor_variant') != -1) return [dtsnvindel, 'L', rank]\n\trank++\n\tif (l.indexOf('stop_gained') != -1) return [dtsnvindel, 'N', rank]\n\trank++\n\tif (l.indexOf('frameshift_variant') != -1) return [dtsnvindel, 'F', rank]\n\trank++\n\tif (l.indexOf('stop_lost') != -1) return [dtsnvindel, 'N', rank]\n\trank++\n\tif (l.indexOf('start_lost') != -1) return [dtsnvindel, 'N', rank]\n\trank++\n\tif (l.indexOf('transcript_amplification') != -1) {\n\t\t// FIXME no class for whole gene amp\n\t\treturn [dtsnvindel, mclassnonstandard, rank]\n\t}\n\trank++\n\tif (\n\t\tl.indexOf('inframe_insertion') != -1 ||\n\t\tl.indexOf('conservative_inframe_insertion') != -1 ||\n\t\tl.indexOf('disruptive_inframe_insertion') != -1\n\t)\n\t\treturn [dtsnvindel, 'I', rank]\n\trank++\n\tif (\n\t\tl.indexOf('inframe_deletion') != -1 ||\n\t\tl.indexOf('conservative_inframe_deletion') != -1 ||\n\t\tl.indexOf('disruptive_inframe_deletion') != -1\n\t)\n\t\treturn [dtsnvindel, 'D', rank]\n\trank++\n\tif (l.indexOf('missense_variant') != -1) return [dtsnvindel, 'M', rank]\n\trank++\n\tif (l.indexOf('protein_altering_variant') != -1) return [dtsnvindel, 'ProteinAltering', rank]\n\trank++\n\tif (l.indexOf('splice_region_variant') != -1) return [dtsnvindel, 'P', rank]\n\trank++\n\tif (l.indexOf('incomplete_terminal_codon_variant') != -1) return [dtsnvindel, 'N', rank]\n\trank++\n\tif (l.indexOf('stop_retained_variant') != -1) return [dtsnvindel, 'S', rank]\n\trank++\n\tif (l.indexOf('synonymous_variant') != -1) return [dtsnvindel, 'S', rank]\n\trank++\n\tif (l.indexOf('coding_sequence_variant') != -1) return [dtsnvindel, mclassnonstandard, rank]\n\trank++\n\tif (l.indexOf('mature_mirna_variant') != -1) return [dtsnvindel, 'E', rank]\n\trank++\n\tif (l.indexOf('5_prime_utr_variant') != -1) return [dtsnvindel, mclassutr5, rank]\n\trank++\n\tif (l.indexOf('3_prime_utr_variant') != -1) return [dtsnvindel, mclassutr3, rank]\n\trank++\n\tif (l.indexOf('non_coding_transcript_exon_variant') != -1) return [dtsnvindel, 'E', rank]\n\trank++\n\tif (l.indexOf('intron_variant') != -1) return [dtsnvindel, 'Intron', rank]\n\trank++\n\tif (l.indexOf('nmd_transcript_variant') != -1) return [dtsnvindel, 'S', rank]\n\trank++\n\tif (l.indexOf('non_coding_transcript_variant') != -1) return [dtsnvindel, 'E', rank]\n\trank++\n\tif (l.indexOf('upstream_gene_variant') != -1) return [dtsnvindel, mclassnoncoding, rank]\n\trank++\n\tif (l.indexOf('downstream_gene_variant') != -1) return [dtsnvindel, mclassnoncoding, rank]\n\trank++\n\tif (l.indexOf('tfbs_ablation') != -1) return [dtsnvindel, mclassnoncoding, rank]\n\trank++\n\tif (l.indexOf('tfbs_amplification') != -1) return [dtsnvindel, mclassnoncoding, rank]\n\trank++\n\tif (l.indexOf('tf_binding_site_variant') != -1) return [dtsnvindel, mclassnoncoding, rank]\n\trank++\n\tif (l.indexOf('regulatory_region_ablation') != -1) return [dtsnvindel, mclassnoncoding, rank]\n\trank++\n\tif (l.indexOf('regulatory_region_amplification') != -1) return [dtsnvindel, mclassnoncoding, rank]\n\trank++\n\tif (l.indexOf('feature_elongation') != -1) return [dtsnvindel, mclassnoncoding, rank]\n\trank++\n\tif (l.indexOf('regulatory_region_variant') != -1) return [dtsnvindel, mclassnoncoding, rank]\n\trank++\n\tif (l.indexOf('feature_truncation') != -1) return [dtsnvindel, mclassnoncoding, rank]\n\trank++\n\tif (l.indexOf('intergenic_variant') != -1) return [dtsnvindel, mclassnoncoding, rank]\n\trank++\n\treturn [dtsnvindel, mclassnonstandard, rank]\n}\n\n// m orgin\nexport const germlinelegend =\n\t'<circle cx=\"7\" cy=\"12\" r=\"7\" fill=\"#b1b1b1\"></circle><path d=\"M6.735557395310443e-16,-11A11,11 0 0,1 11,0L9,0A9,9 0 0,0 5.51091059616309e-16,-9Z\" transform=\"translate(7,12)\" fill=\"#858585\" stroke=\"none\"></path>'\n\nexport const morigin: Record<string, any> = {}\n\nexport const moriginsomatic = 'S'\nmorigin[moriginsomatic] = {\n\tlabel: 'Somatic',\n\tdesc: 'A variant found only in a tumor sample. The proportion is indicated by lack of any arc.',\n\tlegend: '<circle cx=\"7\" cy=\"12\" r=\"7\" fill=\"#b1b1b1\"></circle>'\n}\nexport const morigingermline = 'G'\nmorigin[morigingermline] = {\n\tlabel: 'Germline',\n\tdesc: 'A constitutional variant found in a normal sample. The proportion is indicated by the span of the solid arc within the whole circle.',\n\tlegend: germlinelegend\n}\n\nmorigin.germline = morigin[morigingermline]\nmorigin.somatic = morigin[moriginsomatic]\n\nexport const moriginrelapse = 'R'\nmorigin[moriginrelapse] = {\n\tlabel: 'Relapse',\n\tdesc: 'A somatic variant found only in a relapse sample. The proportion is indicated by the span of the hollow arc within the whole circle.',\n\tlegend:\n\t\t'<circle cx=\"7\" cy=\"12\" r=\"7\" fill=\"#b1b1b1\"></circle><path d=\"M6.735557395310443e-16,-11A11,11 0 0,1 11,0L9,0A9,9 0 0,0 5.51091059616309e-16,-9Z\" transform=\"translate(7,12)\" fill=\"none\" stroke=\"#858585\"></path>'\n}\nexport const morigingermlinepathogenic = 'GP'\nmorigin[morigingermlinepathogenic] = {\n\tlabel: 'Germline pathogenic',\n\tdesc: 'A constitutional variant with pathogenic allele.',\n\tlegend: germlinelegend\n}\nexport const morigingermlinenonpathogenic = 'GNP'\nmorigin[morigingermlinenonpathogenic] = {\n\tlabel: 'Germline non-pathogenic',\n\tdesc: 'A constitutional variant with non-pathogenic allele.',\n\tlegend: germlinelegend,\n\thidden: true\n}\n\nexport const tkt = {\n\tusegm: 'usegm',\n\tds: 'dataset',\n\tbigwig: 'bigwig',\n\tbigwigstranded: 'bigwigstranded',\n\tjunction: 'junction',\n\tmdsjunction: 'mdsjunction',\n\tmdssvcnv: 'mdssvcnv', // replaced by mds3\n\tmdsexpressionrank: 'mdsexpressionrank',\n\tmdsvcf: 'mdsvcf', // for snv/indels, currently vcf, may include MAF\n\t//mdsgeneral:'mdsgeneral', // replaces mdssvcnv ****** not ready yet\n\tbedj: 'bedj',\n\tpgv: 'profilegenevalue',\n\tbampile: 'bampile',\n\thicstraw: 'hicstraw',\n\texpressionrank: 'expressionrank',\n\taicheck: 'aicheck',\n\tase: 'ase',\n\tmds3: 'mds3', //\n\tbedgraphdot: 'bedgraphdot',\n\tbam: 'bam',\n\tld: 'ld'\n}\n\nexport function validtkt(what) {\n\tfor (const k in tkt) {\n\t\tif (what == tkt[k]) {\n\t\t\treturn true\n\t\t}\n\t}\n\treturn false\n}\n\n/*\nmember track types from mdsvcf\nto get rid of hardcoded strings\nin future may include MAF format files\n*/\nexport const mdsvcftype = {\n\tvcf: 'vcf'\n}\n\n/*\nfor custom mdssvcnv track\nor general track\nto avoid using hard-coded string\n*/\nexport const custommdstktype = {\n\tvcf: 'vcf',\n\tsvcnvitd: 'svcnvitd',\n\tgeneexpression: 'geneexpression'\n}\n\n// codons that are not here are stop codon!!\nexport const codon = {\n\tGCT: 'A',\n\tGCC: 'A',\n\tGCA: 'A',\n\tGCG: 'A',\n\tCGT: 'R',\n\tCGC: 'R',\n\tCGA: 'R',\n\tCGG: 'R',\n\tAGA: 'R',\n\tAGG: 'R',\n\tAAT: 'N',\n\tAAC: 'N',\n\tGAT: 'D',\n\tGAC: 'D',\n\tTGT: 'C',\n\tTGC: 'C',\n\tCAA: 'Q',\n\tCAG: 'Q',\n\tGAA: 'E',\n\tGAG: 'E',\n\tGGT: 'G',\n\tGGC: 'G',\n\tGGA: 'G',\n\tGGG: 'G',\n\tCAT: 'H',\n\tCAC: 'H',\n\tATT: 'I',\n\tATC: 'I',\n\tATA: 'I',\n\tTTA: 'L',\n\tTTG: 'L',\n\tCTT: 'L',\n\tCTC: 'L',\n\tCTA: 'L',\n\tCTG: 'L',\n\tAAA: 'K',\n\tAAG: 'K',\n\tATG: 'M',\n\tTTT: 'F',\n\tTTC: 'F',\n\tCCT: 'P',\n\tCCC: 'P',\n\tCCA: 'P',\n\tCCG: 'P',\n\tTCT: 'S',\n\tTCC: 'S',\n\tTCA: 'S',\n\tTCG: 'S',\n\tAGT: 'S',\n\tAGC: 'S',\n\tACT: 'T',\n\tACC: 'T',\n\tACA: 'T',\n\tACG: 'T',\n\tTGG: 'W',\n\tTAT: 'Y',\n\tTAC: 'Y',\n\tGTT: 'V',\n\tGTC: 'V',\n\tGTA: 'V',\n\tGTG: 'V'\n}\n\nexport const codon_stop = '*'\n\nexport function nt2aa(gm) {\n\t// must convert genome seq to upper case!!!\n\tif (!gm.genomicseq) return undefined\n\tconst enlst: string[] = []\n\tif (gm.coding) {\n\t\tfor (const e of gm.coding.values()) {\n\t\t\tconst s = gm.genomicseq.substr(e[0] - gm.start, e[1] - e[0])\n\t\t\tif (gm.strand == '-') {\n\t\t\t\tenlst.push(reversecompliment(s))\n\t\t\t} else {\n\t\t\t\tenlst.push(s)\n\t\t\t}\n\t\t}\n\t}\n\tconst nt = enlst.join('')\n\tconst pep: string[] = []\n\n\t/*\n\tif startCodonFrame is set, will not begin translation from first nt, but will skip 1 or 2 nt at the beginning\n\tin case of IGKC, frame=1 means it will borrow 1 nt from the previous IGKJ exons\n\tso the first two nucleotides from the current exon will have to be skipped when translating IGKC alone\n\t*/\n\tconst startntidx = gm.startCodonFrame ? 3 - gm.startCodonFrame : 0\n\tfor (let i = startntidx; i < nt.length; i += 3) {\n\t\tconst a = codon[nt.substr(i, 3)]\n\t\tpep.push(a || codon_stop)\n\t}\n\tgm.cdseq = nt\n\treturn pep.join('')\n}\n\nexport function bplen(len, isfile?: boolean) {\n\t// if \"isfile\" is true, to measure file size instead of basepair len\n\tif (len >= 1000000000) return (len / 1000000000).toFixed(1) + ' Gb'\n\tif (len >= 10000000) return Math.ceil(len / 1000000) + ' Mb'\n\tif (len >= 1000000) return (len / 1000000).toFixed(1) + ' Mb'\n\tif (len >= 10000) return Math.ceil(len / 1000) + ' Kb'\n\tif (len >= 1000) return (len / 1000).toFixed(1) + ' Kb'\n\treturn len + (isfile ? 'bytes' : ' bp')\n}\n\nexport const basecolor = {\n\tA: '#ca0020',\n\tT: '#f4a582',\n\tC: '#92c5de',\n\tG: '#0571b0'\n}\n\nexport function basecompliment(nt) {\n\tswitch (nt) {\n\t\tcase 'A':\n\t\t\treturn 'T'\n\t\tcase 'T':\n\t\t\treturn 'A'\n\t\tcase 'C':\n\t\t\treturn 'G'\n\t\tcase 'G':\n\t\t\treturn 'C'\n\t\tcase 'a':\n\t\t\treturn 't'\n\t\tcase 't':\n\t\t\treturn 'a'\n\t\tcase 'c':\n\t\t\treturn 'g'\n\t\tcase 'g':\n\t\t\treturn 'c'\n\t\tdefault:\n\t\t\treturn nt\n\t}\n}\n\nexport function reversecompliment(s) {\n\tconst tmp: string[] = []\n\tfor (let i = s.length - 1; i >= 0; i--) {\n\t\ttmp.push(basecompliment(s[i]))\n\t}\n\treturn tmp.join('')\n}\n\nexport function spliceeventchangegmexon(gm, evt) {\n\t/*\n\talter gm.coding[], by exon-skip/alt events\n\tfor frame checking\n\tgm must have coding\n\t*/\n\tconst gm2 = {\n\t\tchr: gm.chr,\n\t\tstart: gm.start,\n\t\tstop: gm.stop,\n\t\tstrand: gm.strand,\n\t\tcoding: [] as number[][]\n\t}\n\tif (evt.isskipexon || evt.isaltexon) {\n\t\tfor (let i = 0; i < gm.exon.length; i++) {\n\t\t\tconst codingstart = Math.max(gm.codingstart, gm.exon[i][0])\n\t\t\tconst codingstop = Math.min(gm.codingstop, gm.exon[i][1])\n\t\t\tif (codingstart > codingstop) {\n\t\t\t\t// not coding exon\n\t\t\t\tcontinue\n\t\t\t}\n\t\t\tif (evt.skippedexon.indexOf(i) == -1) {\n\t\t\t\t// not skipped\n\t\t\t\tgm2.coding.push([codingstart, codingstop])\n\t\t\t} else {\n\t\t\t\t// skipped\n\t\t\t}\n\t\t}\n\t} else if (evt.a5ss || evt.a3ss) {\n\t\t// still equal number of exons\n\t\t// adjust the affected exon first, then figure out coding[]\n\t\tconst exons = gm.exon.map(e => [e[0], e[1]])\n\t\tconst forward = gm.strand == '+'\n\t\tif (evt.a5ss) {\n\t\t\tif (forward) {\n\t\t\t\texons[evt.exon5idx][1] = evt.junctionB.start\n\t\t\t} else {\n\t\t\t\texons[evt.exon5idx + 1][0] = evt.junctionB.stop\n\t\t\t}\n\t\t} else {\n\t\t\tif (forward) {\n\t\t\t\texons[evt.exon5idx + 1][0] = evt.junctionB.stop\n\t\t\t} else {\n\t\t\t\texons[evt.exon5idx][1] = evt.junctionB.start\n\t\t\t}\n\t\t}\n\t\t// from new exons, figure out coding exons\n\t\tfor (const e of exons) {\n\t\t\tconst codingstart = Math.max(gm.codingstart, e[0])\n\t\t\tconst codingstop = Math.min(gm.codingstop, e[1])\n\t\t\tif (codingstart > codingstop) {\n\t\t\t\t// not coding exon\n\t\t\t\tcontinue\n\t\t\t}\n\t\t\tgm2.coding.push([codingstart, codingstop])\n\t\t}\n\t}\n\treturn gm2\n}\n\nexport function fasta2gmframecheck(gm, str) {\n\t/*\n\tgm{}\n\t\t.chr\n\t\t.start\n\t\t.stop\n\t\t\tstart/stop is transcript position\n\t\t.strand\n\t\t.coding[]\n\tstr\n\t\tsamtools faidx output\n\t*/\n\tconst lines = str.split('\\n')\n\t// remove fasta header\n\tlines.shift()\n\tgm.genomicseq = lines.join('').toUpperCase()\n\n\tconst aaseq = nt2aa(gm)\n\tif (!aaseq) return OUT_frame\n\n\tlet thisframe = OUT_frame\n\tconst stopcodonidx = aaseq.indexOf(codon_stop)\n\tif (stopcodonidx == aaseq.length - 1) {\n\t\t// the first appearance of stop codon is at the last of translation\n\t\tthisframe = IN_frame\n\t}\n\treturn thisframe\n}\n\nexport function validate_vcfinfofilter(obj) {\n\t/*\n\tvalidate vcfinfofilter as from embedding api or dataset\n\t*/\n\n\tif (!obj.lst) return '.lst missing'\n\n\tif (!Array.isArray(obj.lst)) return 'input is not an array'\n\n\tfor (const set of obj.lst) {\n\t\tif (!set.name) return 'name missing from a set of .vcfinfofilter.lst'\n\n\t\tif (set.autocategory || set.categories) {\n\t\t\t// categorical info, auto or defined\n\n\t\t\tif (!set.autocategory) {\n\t\t\t\tfor (const k in set.categories) {\n\t\t\t\t\tconst v = set.categories[k]\n\t\t\t\t\tif (!set.autocolor && !v.color)\n\t\t\t\t\t\treturn '.color missing for class ' + k + ' from .categories of set ' + set.name\n\t\t\t\t\tif (!v.label) {\n\t\t\t\t\t\tv.label = k\n\t\t\t\t\t}\n\t\t\t\t}\n\t\t\t}\n\n\t\t\tif (set.categoryhidden) {\n\t\t\t\tfor (const k in set.categoryhidden) {\n\t\t\t\t\tif (!set.categories[k]) return 'unknown hidden-by-default category ' + k + ' from set ' + set.name\n\t\t\t\t}\n\t\t\t} else {\n\t\t\t\tset.categoryhidden = {}\n\t\t\t}\n\t\t} else if (set.numericfilter) {\n\t\t\t// otherwise, numerical value, the style of population frequency filter\n\t\t\tconst lst: any[] = []\n\t\t\tfor (const v of set.numericfilter) {\n\t\t\t\tif (typeof v == 'number') {\n\t\t\t\t\t/*\n\t\t\t\t\tjust a number, defaults to 'lower-than'\n\t\t\t\t\t*/\n\t\t\t\t\tlst.push({ side: '<', value: v })\n\t\t\t\t} else {\n\t\t\t\t\tlst.push({\n\t\t\t\t\t\tside: v.side || '<',\n\t\t\t\t\t\tvalue: v.value\n\t\t\t\t\t})\n\t\t\t\t}\n\t\t\t}\n\t\t\tset.numericfilter = lst\n\n\t\t\t//return 'no .categories or .numericfilter from set '+set.name\n\t\t}\n\n\t\tif (set.altalleleinfo) {\n\t\t\tif (!set.altalleleinfo.key) {\n\t\t\t\treturn '.key missing from .altalleleinfo from set ' + set.name\n\t\t\t}\n\t\t} else if (set.locusinfo) {\n\t\t\tif (!set.locusinfo.key) {\n\t\t\t\treturn '.key missing from .locusinfo from set ' + set.name\n\t\t\t}\n\t\t} else {\n\t\t\treturn 'neither .altalleleinfo or .locusinfo is available from set ' + set.name\n\t\t}\n\t}\n}\n\nexport function contigNameNoChr(genome, chrlst) {\n\t/*\n\tFIXME hard-coded for human genome styled chromosome names\n\t*/\n\tfor (const n in genome.majorchr) {\n\t\tif (chrlst.indexOf(n.replace('chr', '')) != -1) {\n\t\t\treturn true\n\t\t}\n\t}\n\tif (genome.minorchr) {\n\t\tfor (const n in genome.minorchr) {\n\t\t\tif (chrlst.indexOf(n.replace('chr', '')) != -1) {\n\t\t\t\treturn true\n\t\t\t}\n\t\t}\n\t}\n\treturn false\n}\nexport function contigNameNoChr2(genome, chrlst) {\n\t// returns number of matching chr names that either includes \"chr\" or not\n\t// for detecting if chrlst entirely mismatch with what's in the genome build\n\t// TODO replace contigNameNoChr\n\tlet nochrcount = 0,\n\t\thaschrcount = 0\n\tfor (const n in genome.majorchr) {\n\t\tif (chrlst.includes(n)) {\n\t\t\thaschrcount++\n\t\t} else if (chrlst.includes(n.replace('chr', ''))) {\n\t\t\tnochrcount++\n\t\t}\n\t}\n\tif (genome.minorchr) {\n\t\tfor (const n in genome.minorchr) {\n\t\t\tif (chrlst.includes(n)) {\n\t\t\t\thaschrcount++\n\t\t\t} else if (chrlst.includes(n.replace('chr', ''))) {\n\t\t\t\tnochrcount++\n\t\t\t}\n\t\t}\n\t}\n\treturn [nochrcount, haschrcount]\n}\n\nexport function getMax_byiqr(lst, novaluemax) {\n\t/*\n\tlst: array of numbers\n\tnovaluemax: when lst is empty, return this value\n\tcutoff value based on IQR to exclude outlier values\n\t*/\n\tif (lst.length == 0) return novaluemax\n\tlst.sort((i, j) => i - j)\n\tconst max = lst[lst.length - 1]\n\tif (lst.length <= 5) return max\n\tconst q1 = lst[Math.floor(lst.length / 4)]\n\tconst q2 = lst[Math.floor((lst.length * 3) / 4)]\n\treturn Math.min(q2 + (q2 - q1) * 1.5, max)\n}\n\nexport function alleleInGenotypeStr(genotype, allele) {\n\tif (!genotype) return false\n\tif (genotype.indexOf('/') != -1) {\n\t\treturn genotype.split('/').indexOf(allele) != -1\n\t}\n\treturn genotype.split('|').indexOf(allele) != -1\n}\n\nexport const gmmode = {\n\tgenomic: 'genomic',\n\tsplicingrna: 'splicing RNA', // if just 1 exon, use \"RNA\" as label\n\texononly: 'exon only',\n\tprotein: 'protein',\n\tgmsum: 'aggregated exons'\n}\n\n/*\ninput:\n\nm={}\n\tm.csq=[]\n\t\telement: {\n\t\t\tAllele: str,\n\t\t\tConsequence: str,\n\t\t\tCANONICAL: str, // true if _isoform is canonical\n\t\t\t...\n\t\t\t_isoform: str,\n\t\t\t_class: str,\n\t\t\t_csqrank: int\n\t\t}\n\tm.ann=[]\n\t\tannovar output. may be derelict\nblock={}\n\tblock.usegm={ isoform }\n\tcan be a mock object when running this function in node!\n\ndoes:\n\tfind an annotation from m.csq[] that's fitting the circumstance\n\t- current gm isoform displayed in block gene mode\n\t- any canonical isoform from m.csq[] (can be missing if vep is not instructed to do it)\n\t- one with highest _csqrank\n\tthen, copy its class/mname to m{}\n\thas many fall-back and always try to assign class/mname\n\nno return\n*/\nexport function vcfcopymclass(m, block) {\n\tif (m.csq) {\n\t\tlet useone // point to the element of m.csq[], from this class/mname is copied to m{}\n\n\t\tif (block.usegm) {\n\t\t\t// block is in gm mode, find a csq matching with the genemodel isoform\n\t\t\tuseone = m.csq.find(i => i._isoform == block.usegm.isoform)\n\t\t}\n\n\t\tif (!useone) {\n\t\t\t// no match to usegm isoform; can be due to in genomic mode and zoomed out, where this variant is from a neighboring gene near block.usegm\n\t\t\t// find one using canonical isoform\n\t\t\tuseone = m.csq.find(i => i.CANONICAL)\n\n\t\t\tif (!useone) {\n\t\t\t\t// none of the elements in m.csq[] is using a canonical isoform, as that's a vep optional output\n\t\t\t\t// last method: choose *colorful* annotation based on if is canonical, _csqrank\n\t\t\t\tuseone = m.csq[0]\n\t\t\t\tfor (const q of m.csq) {\n\t\t\t\t\tif (q._csqrank < useone._csqrank) {\n\t\t\t\t\t\tuseone = q\n\t\t\t\t\t}\n\t\t\t\t}\n\t\t\t}\n\t\t}\n\n\t\tif (useone) {\n\t\t\tm.gene = useone._gene\n\t\t\tm.isoform = useone._isoform\n\t\t\tm.class = useone._class\n\t\t\tm.dt = useone._dt\n\t\t\tm.mname = useone._mname\n\n\t\t\tif (m.class == mclassnoncoding) {\n\t\t\t\t// noncoding converted from csq is not a meaningful, drab color, has no mname label, delete so later will be converted to non-protein class\n\t\t\t\tdelete m.class\n\t\t\t}\n\t\t}\n\t} else if (m.ann) {\n\t\t// there could be many applicable annotations, the first one not always desirable\n\t\t// choose *colorful* annotation based on _csqrank\n\t\tlet useone: any = null\n\t\tif (block.usegm) {\n\t\t\tfor (const q of m.ann) {\n\t\t\t\tif (q._isoform != block.usegm.isoform) continue\n\t\t\t\tif (useone) {\n\t\t\t\t\tif (q._csqrank < useone._csqrank) {\n\t\t\t\t\t\tuseone = q\n\t\t\t\t\t}\n\t\t\t\t} else {\n\t\t\t\t\tuseone = q\n\t\t\t\t}\n\t\t\t}\n\t\t\tif (!useone && block.gmmode == gmmode.genomic) {\n\t\t\t\t// no match to this gene, but in genomic mode, maybe from other genes?\n\t\t\t\tuseone = m.ann[0]\n\t\t\t}\n\t\t} else {\n\t\t\tuseone = m.ann[0]\n\t\t\tfor (const q of m.ann) {\n\t\t\t\tif (q._csqrank < useone._csqrank) {\n\t\t\t\t\tuseone = q\n\t\t\t\t}\n\t\t\t}\n\t\t}\n\t\tif (useone) {\n\t\t\tm.gene = useone._gene\n\t\t\tm.isoform = useone._isoform\n\t\t\tm.class = useone._class\n\t\t\tm.dt = useone._dt\n\t\t\tm.mname = useone._mname\n\n\t\t\tif (m.class == mclassnoncoding) {\n\t\t\t\tdelete m.class\n\t\t\t}\n\t\t}\n\t}\n\n\tif (m.class == undefined) {\n\t\t// infer class from m.type, which was assigned by vcf.js\n\t\tif (mclass[m.type]) {\n\t\t\tm.class = m.type\n\t\t\tm.dt = mclass[m.type].dt\n\t\t\tm.mname = m.id && m.id != '.' ? m.id : m.ref + '>' + m.alt\n\t\t\tif (m.mname.length > 15) {\n\t\t\t\t// avoid long indel\n\t\t\t\tm.mname = m.type\n\t\t\t}\n\t\t} else {\n\t\t\tm.class = mclassnonstandard\n\t\t\tm.dt = dtsnvindel\n\t\t\tm.mname = m.type\n\t\t}\n\t}\n\n\tdelete m.type\n}\n\n/*\nused in:\n\tmdssvcnv track, mutation attributes, items that are not annotated by an attribute for showing in legend, and server-side filtering\n*/\nexport const not_annotated = 'Unannotated'\n\n// kernal density estimator as from https://www.d3-graph-gallery.com/graph/density_basic.html\n\nexport function kernelDensityEstimator(kernel, X) {\n\treturn function (V) {\n\t\treturn X.map(x => {\n\t\t\treturn [x, V.map(v => kernel(x - v)).reduce((i, j) => i + j, 0) / V.length]\n\t\t})\n\t}\n}\n\nexport function kernelEpanechnikov(k) {\n\treturn function (v) {\n\t\treturn Math.abs((v /= k)) <= 1 ? (0.75 * (1 - v * v)) / k : 0\n\t}\n}\n\n/////////////////////// color sets /////////////////////////\n\nexport const schemeCategory20 = [\n\t'#1f77b4',\n\t'#aec7e8',\n\t'#ff7f0e',\n\t'#ffbb78',\n\t'#2ca02c',\n\t'#98df8a',\n\t'#d62728',\n\t'#ff9896',\n\t'#9467bd',\n\t'#c5b0d5',\n\t'#8c564b',\n\t'#c49c94',\n\t'#e377c2',\n\t'#f7b6d2',\n\t'#7f7f7f',\n\t'#c7c7c7',\n\t'#bcbd22',\n\t'#dbdb8d',\n\t'#17becf',\n\t'#9edae5'\n]\nexport const schemeCategory2 = ['#e75480', 'blue']\n\nexport function getColorScheme(number) {\n\tif (number > 20) {\n\t\tconst scheme: string[] = []\n\t\tfor (let i = 0; i < number; i++) scheme.push(d3.interpolateRainbow(i / number))\n\t\treturn scheme\n\t}\n\tif (number > 12) return schemeCategory20\n\telse if (number > 8) return d3.schemePaired\n\telse if (number > 2) return d3.schemeDark2\n\telse return schemeCategory2\n}\nexport function getColors(number) {\n\tconst scheme = getColorScheme(number)\n\treturn d3scale.scaleOrdinal(scheme)\n}\n\n// for now not using getColorScheme() for protein domains, because this color list have been in use since 2015...\nconst proteinDomainColors = [\n\t'#8dd3c7',\n\t'#bebada',\n\t'#fb8072',\n\t'#80b1d3',\n\t'#E8E89E',\n\t'#a6d854',\n\t'#fdb462',\n\t'#ffd92f',\n\t'#e5c494',\n\t'#b3b3b3'\n]\nexport function proteinDomainColorScale() {\n\treturn d3scale.scaleOrdinal().range(proteinDomainColors)\n}\n\n/////////////////////// end of color sets /////////////////////////\n\nexport const truncatingMutations = ['F', 'N', 'L', 'P']\nexport const proteinChangingMutations = ['F', 'N', 'L', 'P', 'D', 'I', 'ProteinAltering', 'M']\nexport const synonymousMutations = ['S', 'Intron', 'Utr3', 'Utr5', 'noncoding', 'E']\nexport const mutationClasses = Object.values(mclass)\n\t.filter(m => m.dt == dtsnvindel)\n\t.map(m => m.key)\nexport const CNVClasses = Object.values(mclass)\n\t.filter(m => m.dt == dtcnv)\n\t.map(m => m.key)\n\n// dt terms used for filtering variants for geneVariant term\nconst dtTerms_temp = [\n\t{\n\t\tid: 'snvindel',\n\t\tquery: 'snvindel',\n\t\tname: dt2label[dtsnvindel],\n\t\tparent_id: null,\n\t\tisleaf: true,\n\t\ttype: 'dtsnvindel',\n\t\tdt: dtsnvindel,\n\t\tvalues: {}\n\t},\n\t{\n\t\tid: 'cnv',\n\t\tquery: 'cnv',\n\t\tname: dt2label[dtcnv],\n\t\tparent_id: null,\n\t\tisleaf: true,\n\t\ttype: 'dtcnv',\n\t\tdt: dtcnv,\n\t\tvalues: {}\n\t},\n\t{\n\t\tid: 'fusion',\n\t\tquery: 'svfusion',\n\t\tname: dt2label[dtfusionrna],\n\t\tparent_id: null,\n\t\tisleaf: true,\n\t\ttype: 'dtfusion',\n\t\tdt: dtfusionrna,\n\t\tvalues: {}\n\t},\n\t{\n\t\tid: 'sv',\n\t\tquery: 'svfusion',\n\t\tname: dt2label[dtsv],\n\t\tparent_id: null,\n\t\tisleaf: true,\n\t\ttype: 'dtsv',\n\t\tdt: dtsv,\n\t\tvalues: {}\n\t}\n]\n// add origin annotations to dt terms\nconst dtTerms_temp2: any[] = []\nfor (const dtTerm of dtTerms_temp as any[]) {\n\tdtTerm.name_noOrigin = dtTerm.name // for labeling groups in groupsetting\n\tdtTerms_temp2.push(dtTerm) // no origin\n\tfor (const origin of ['somatic', 'germline']) {\n\t\t// add origins\n\t\tconst addOrigin = {\n\t\t\tid: `${dtTerm.id}_${origin}`,\n\t\t\tname: `${dtTerm.name} (${origin})`,\n\t\t\torigin\n\t\t}\n\t\tdtTerms_temp2.push(Object.assign({}, dtTerm, addOrigin))\n\t}\n}\nexport const dtTerms = dtTerms_temp2\n\nexport const colorScaleMap = {\n\tblueWhiteRed: { domain: [0, 0.5, 1], range: ['blue', 'white', 'red'] },\n\tgreenWhiteRed: { domain: [0, 0.5, 1], range: ['green', 'white', 'red'] },\n\tblueYellowRed: {\n\t\tdomain: [0, 0.17, 0.33, 0.5, 0.67, 0.83, 1],\n\t\trange: ['#313695', '#649AC7', '#BCE1ED', '#FFFFBF', '#FDBE70', '#EA5839', '#A50026']\n\t},\n\tgreenBlackRed: {\n\t\tdomain: [0, 0.17, 0.33, 0.5, 0.67, 0.83, 1],\n\t\trange: ['#00FF00', '#14E10C', '#1AAF10', '#000000', '#B01205', '#E20E03', '#FF0000']\n\t},\n\tblueBlackYellow: {\n\t\tdomain: [0, 0.17, 0.33, 0.5, 0.67, 0.83, 1],\n\t\trange: ['#0000FF', '#0000CC', '#000099', '#202020', '#999900', '#CCCC00', '#FFFF00']\n\t},\n\t// when hierCluster z-score transformation is not 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Math.max(0, Math.ceil(chr.len / 2) - 10000),\n\t\t\tstop: Math.min(chr.len, Math.ceil(chr.len / 2) + 10000)\n\t\t}\n\t}\n\t{\n\t\t// special handling for snv4\n\t\tconst tmp = s.split('.')\n\t\tif (tmp.length >= 2) {\n\t\t\tconst chr = genome.chrlookup[tmp[0].toUpperCase()]\n\t\t\tconst pos = Number.parseInt(tmp[1])\n\t\t\tconst e = invalidcoord(genome, tmp[0], pos, pos + 1)\n\t\t\tif (!e) {\n\t\t\t\t// valid snv4\n\t\t\t\tconst bpspan = 400\n\t\t\t\treturn {\n\t\t\t\t\tchr: chr.name,\n\t\t\t\t\tchrlen: chr.len,\n\t\t\t\t\tstart: Math.max(0, pos - Math.ceil(bpspan / 2)),\n\t\t\t\t\tstop: Math.min(chr.len, pos + Math.ceil(bpspan / 2)),\n\t\t\t\t\tactualposition: { position: pos, len: 1 }\n\t\t\t\t}\n\t\t\t}\n\t\t}\n\t}\n\tconst tmp = s.split(/[-:\\s]+/)\n\tif (tmp.length == 2) {\n\t\t// must be chr - pos\n\t\tconst pos = Number.parseInt(tmp[1])\n\t\tconst e = invalidcoord(genome, tmp[0], pos, pos + 1)\n\t\tif (e) {\n\t\t\treturn null\n\t\t}\n\t\tconst chr = genome.chrlookup[tmp[0].toUpperCase()]\n\t\tconst bpspan = 400\n\t\treturn {\n\t\t\tchr: chr.name,\n\t\t\tchrlen: chr.len,\n\t\t\tstart: Math.max(0, pos - Math.ceil(bpspan / 2)),\n\t\t\tstop: Math.min(chr.len, pos + Math.ceil(bpspan / 2)),\n\t\t\tactualposition: { position: pos, len: 1 }\n\t\t}\n\t}\n\tif (tmp.length == 3) {\n\t\t// must be chr - start - stop\n\t\tlet start = Number.parseInt(tmp[1]),\n\t\t\tstop = Number.parseInt(tmp[2])\n\t\tconst e = invalidcoord(genome, tmp[0], start, stop)\n\t\tif (e) {\n\t\t\treturn null\n\t\t}\n\t\tconst actualposition = { position: start, len: stop - start }\n\t\tconst chr = genome.chrlookup[tmp[0].toUpperCase()]\n\n\t\tif (!donotextend) {\n\t\t\tconst minspan = 400\n\t\t\tif (stop - start < minspan) {\n\t\t\t\tlet center = Math.ceil((start + stop) / 2)\n\t\t\t\tif (center + minspan / 2 >= chr.len) {\n\t\t\t\t\tcenter = chr.len - Math.ceil(minspan / 2)\n\t\t\t\t}\n\t\t\t\tstart = Math.max(0, center - Math.ceil(minspan / 2))\n\t\t\t\tstop = start 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AK,EAAE;AACrD;AAEO,SAAS,aAAa,YAAY,OAAO,OAAO,MAAM;AAC5D,MAAI,CAAC,WAAY,QAAO;AACxB,MAAI,CAAC,MAAO,QAAO;AACnB,QAAM,MAAM,WAAW,UAAU,MAAM,YAAY,CAAC;AACpD,MAAI,CAAC,IAAK,QAAO,8BAA8B;AAC/C,MAAI,CAAC,OAAO,UAAU,KAAK,EAAG,QAAO,6BAA6B;AAClE,MAAI,QAAQ,KAAK,SAAS,IAAI,IAAK,QAAO,4BAA4B;AACtE,MAAI,CAAC,OAAO,UAAU,IAAI,EAAG,QAAO,6BAA6B;AACjE,MAAI,OAAO,KAAK,OAAO,IAAI,IAAK,QAAO,4BAA4B;AACnE,MAAI,QAAQ,KAAM,QAAO;AACzB,SAAO;AACR;AAEO,SAAS,WAAW,GAAG,QAAQ,aAAa;AAClD,MAAI,EAAE,QAAQ,MAAM,EAAE;AACtB,QAAM,MAAM,OAAO,UAAU,EAAE,YAAY,CAAC;AAC5C,MAAI,KAAK;AAER,WAAO;MACN,KAAK,IAAI;MACT,QAAQ,IAAI;MACZ,OAAO,KAAK,IAAI,GAAG,KAAK,KAAK,IAAI,MAAM,CAAC,IAAI,GAAK;MACjD,MAAM,KAAK,IAAI,IAAI,KAAK,KAAK,KAAK,IAAI,MAAM,CAAC,IAAI,GAAK;IACvD;EACD;AACA;AAEC,UAAMA,OAAM,EAAE,MAAM,GAAG;AACvB,QAAIA,KAAI,UAAU,GAAG;AACpB,YAAMC,OAAM,OAAO,UAAUD,KAAI,CAAC,EAAE,YAAY,CAAC;AACjD,YAAM,MAAM,OAAO,SAASA,KAAI,CAAC,CAAC;AAClC,YAAM,IAAI,aAAa,QAAQA,KAAI,CAAC,GAAG,KAAK,MAAM,CAAC;AACnD,UAAI,CAAC,GAAG;AAEP,cAAM,SAAS;AACf,eAAO;UACN,KAAKC,KAAI;UACT,QAAQA,KAAI;UACZ,OAAO,KAAK,IAAI,GAAG,MAAM,KAAK,KAAK,SAAS,CAAC,CAAC;UAC9C,MAAM,KAAK,IAAIA,KAAI,KAAK,MAAM,KAAK,KAAK,SAAS,CAAC,CAAC;UACnD,gBAAgB,EAAE,UAAU,KAAK,KAAK,EAAE;QACzC;MACD;IACD;EACD;AACA,QAAM,MAAM,EAAE,MAAM,SAAS;AAC7B,MAAI,IAAI,UAAU,GAAG;AAEpB,UAAM,MAAM,OAAO,SAAS,IAAI,CAAC,CAAC;AAClC,UAAM,IAAI,aAAa,QAAQ,IAAI,CAAC,GAAG,KAAK,MAAM,CAAC;AACnD,QAAI,GAAG;AACN,aAAO;IACR;AACA,UAAMA,OAAM,OAAO,UAAU,IAAI,CAAC,EAAE,YAAY,CAAC;AACjD,UAAM,SAAS;AACf,WAAO;MACN,KAAKA,KAAI;MACT,QAAQA,KAAI;MACZ,OAAO,KAAK,IAAI,GAAG,MAAM,KAAK,KAAK,SAAS,CAAC,CAAC;MAC9C,MAAM,KAAK,IAAIA,KAAI,KAAK,MAAM,KAAK,KAAK,SAAS,CAAC,CAAC;MACnD,gBAAgB,EAAE,UAAU,KAAK,KAAK,EAAE;IACzC;EACD;AACA,MAAI,IAAI,UAAU,GAAG;AAEpB,QAAI,QAAQ,OAAO,SAAS,IAAI,CAAC,CAAC,GACjC,OAAO,OAAO,SAAS,IAAI,CAAC,CAAC;AAC9B,UAAM,IAAI,aAAa,QAAQ,IAAI,CAAC,GAAG,OAAO,IAAI;AAClD,QAAI,GAAG;AACN,aAAO;IACR;AACA,UAAM,iBAAiB,EAAE,UAAU,OAAO,KAAK,OAAO,MAAM;AAC5D,UAAMA,OAAM,OAAO,UAAU,IAAI,CAAC,EAAE,YAAY,CAAC;AAEjD,QAAI,CAAC,aAAa;AACjB,YAAM,UAAU;AAChB,UAAI,OAAO,QAAQ,SAAS;AAC3B,YAAI,SAAS,KAAK,MAAM,QAAQ,QAAQ,CAAC;AACzC,YAAI,SAAS,UAAU,KAAKA,KAAI,KAAK;AACpC,mBAASA,KAAI,MAAM,KAAK,KAAK,UAAU,CAAC;QACzC;AACA,gBAAQ,KAAK,IAAI,GAAG,SAAS,KAAK,KAAK,UAAU,CAAC,CAAC;AACnD,eAAO,QAAQ;MAChB;IACD;AAEA,WAAO;MACN,KAAKA,KAAI;MACT,QAAQA,KAAI;MACZ;MACA;MACA;IACD;EACD;AACA,SAAO;AACR;",
6
+ "names": ["tmp", "chr"]
7
+ }
@@ -0,0 +1,102 @@
1
+ import {
2
+ renderTable
3
+ } from "./chunk-SA7APTJR.js";
4
+
5
+ // termdb/handlers/termCollection.ts
6
+ var SearchHandler = class {
7
+ async init(opts) {
8
+ this.callback = opts.callback;
9
+ this.app = opts.app;
10
+ opts.holder.style("display", "");
11
+ const tableDiv = opts.holder.append("div");
12
+ const termlst = opts.details.termlst ?? [];
13
+ renderTable({
14
+ columns: [{ label: "VARIABLES" }],
15
+ rows: termlst.map((t) => {
16
+ return [{ value: t.name }];
17
+ }),
18
+ div: tableDiv,
19
+ maxWidth: "30vw",
20
+ maxHeight: "40vh",
21
+ noButtonCallback: () => {
22
+ },
23
+ // FIXME to supply a real callback
24
+ striped: false,
25
+ showHeader: true,
26
+ //false,
27
+ selectAll: true,
28
+ columnButtons: void 0,
29
+ //Leave until table.js is typed
30
+ buttons: void 0
31
+ });
32
+ let categoryTable;
33
+ let ckSource = [];
34
+ if (opts.details.categoryKeys) {
35
+ ckSource = opts.details.categoryKeys;
36
+ const categoryDiv = opts.holder.append("div").style("margin-top", "15px");
37
+ const values = opts.details.termlst[0].values || {};
38
+ categoryTable = categoryDiv.append("div");
39
+ renderTable({
40
+ columns: [{ label: "CATEGORIES" }],
41
+ rows: ckSource.map((ck) => {
42
+ return [{ value: values[ck.key]?.label ?? ck.key, checked: ck.shown }];
43
+ }),
44
+ div: categoryTable,
45
+ maxWidth: "30vw",
46
+ maxHeight: "40vh",
47
+ noButtonCallback: () => {
48
+ },
49
+ // FIXME to supply a real callback
50
+ striped: false,
51
+ showHeader: true,
52
+ //false,
53
+ selectAll: true,
54
+ columnButtons: void 0,
55
+ //Leave until table.js is typed
56
+ buttons: void 0
57
+ });
58
+ }
59
+ opts.holder.append("div").style("float", "right").style("padding", "6px 20px").append("button").attr("class", "sjpp_apply_btn sja_filter_tag_btn").text("Select").on("click", () => {
60
+ const trs = tableDiv.select("table").select("tbody").node().querySelectorAll("tr");
61
+ const selectedTermlst = termlst.filter((term, i) => {
62
+ const checked = trs[i]?.querySelectorAll("td")[1]?.querySelector("input")?.checked;
63
+ return checked === true;
64
+ });
65
+ if (selectedTermlst.length === 0) {
66
+ alert("Please select at least one term");
67
+ return;
68
+ }
69
+ const propsByTermId = {};
70
+ if (opts.details.propsByTermId) {
71
+ for (const t of selectedTermlst) {
72
+ if (opts.details.propsByTermId[t.id]) propsByTermId[t.id] = opts.details.propsByTermId[t.id];
73
+ }
74
+ }
75
+ let categoryKeys;
76
+ if (categoryTable) {
77
+ const trs2 = categoryTable.select("table").select("tbody").node().querySelectorAll("tr");
78
+ categoryKeys = ckSource.map((ck, i) => {
79
+ const checked = trs2[i].querySelectorAll("td")[1].querySelector("input")?.checked;
80
+ return { key: ck.key, shown: !!checked };
81
+ });
82
+ }
83
+ opts.callback({
84
+ type: "termCollection",
85
+ termIds: selectedTermlst.map((i) => i.id),
86
+ termlst: selectedTermlst,
87
+ name: opts.details.name,
88
+ valueTransform: opts.details.valueTransformByPlots?.[opts.usecase.target],
89
+ // memberType = ds.cohort.termdb.termCollections[].type for client code
90
+ memberType: opts.details.memberType || opts.details.type,
91
+ categoryKeys,
92
+ isleaf: true,
93
+ propsByTermId
94
+ });
95
+ });
96
+ }
97
+ };
98
+
99
+ export {
100
+ SearchHandler
101
+ };
102
+ //# sourceMappingURL=chunk-54EMVNPW.js.map
@@ -0,0 +1,302 @@
1
+ import {
2
+ appear2 as appear,
3
+ axisstyle,
4
+ bwSetting,
5
+ disappear2 as disappear,
6
+ makeNumericAxisConfig,
7
+ rgb2hex
8
+ } from "./chunk-SA7APTJR.js";
9
+ import {
10
+ dofetch3
11
+ } from "./chunk-7EMWHCVW.js";
12
+ import {
13
+ axisLeft
14
+ } from "./chunk-LOZEKOES.js";
15
+ import {
16
+ format,
17
+ linear
18
+ } from "./chunk-OAWQ6LOO.js";
19
+
20
+ // src/block.tk.bigwig.js
21
+ function bigwigfromtemplate(tk, template) {
22
+ tk.scale = {};
23
+ if (template.scale) {
24
+ for (const k in template.scale) {
25
+ tk.scale[k] = template.scale[k];
26
+ }
27
+ } else {
28
+ tk.scale.auto = 1;
29
+ }
30
+ if (tk.normalize) {
31
+ } else {
32
+ tk.normalize = {
33
+ dividefactor: 1,
34
+ disable: 1
35
+ };
36
+ }
37
+ tk.barheight = template.height || 50;
38
+ tk.height_main = tk.toppad + tk.barheight + tk.bottompad;
39
+ if (!tk.ncolor) tk.ncolor = "#BD005E";
40
+ if (!tk.ncolor2) tk.ncolor2 = "#5E00BD";
41
+ if (!tk.pcolor) tk.pcolor = "#005EBD";
42
+ if (!tk.pcolor2) tk.pcolor2 = "#FA7D00";
43
+ }
44
+ function bigwigmaketk(tk, block) {
45
+ tk.img = tk.glider.append("image");
46
+ tk.tklabel.attr("y", tk.barheight / 2);
47
+ tk.leftaxis = tk.gleft.append("g");
48
+ tk.config_handle = block.maketkconfighandle(tk).on("click", () => {
49
+ tk.tkconfigtip.clear().showunder(tk.config_handle.node());
50
+ bigwigconfigpanel(tk, block, tk.tkconfigtip.d, () => bigwigload(tk, block));
51
+ });
52
+ }
53
+ async function bigwigload(tk, block) {
54
+ block.tkcloakon(tk);
55
+ const par = block.tkarg_q(tk);
56
+ if (tk.dotplotfactor) par.dotplotfactor = tk.dotplotfactor;
57
+ if (tk.bgcolor) par.bgcolor = tk.bgcolor;
58
+ tk.height_main = tk.toppad + tk.barheight + tk.bottompad;
59
+ tk.img.attr("width", block.width).attr("height", tk.barheight);
60
+ let errtext;
61
+ try {
62
+ let data;
63
+ if (tk.imgData) {
64
+ data = tk.imgData;
65
+ } else {
66
+ data = await dofetch3("tkbigwig", { method: "POST", body: JSON.stringify(par) });
67
+ }
68
+ if (data.error) throw data.error;
69
+ if (!data.src) throw "data.src missing";
70
+ tk.tklabel.transition().attr("y", tk.barheight / 2);
71
+ tk.img.attr("xlink:href", data.src);
72
+ if (data.minv != void 0) {
73
+ tk.scale.min = data.minv;
74
+ }
75
+ if (data.maxv != void 0) {
76
+ tk.scale.max = data.maxv;
77
+ }
78
+ tk.leftaxis.selectAll("*").remove();
79
+ if (data.nodata) {
80
+ throw "No data in view range";
81
+ }
82
+ const scale = linear().domain([tk.scale.min, tk.scale.max]).range([tk.barheight, 0]);
83
+ const axis = axisLeft().scale(scale).tickValues([tk.scale.min, tk.scale.max]);
84
+ if (tk.integer4axis) {
85
+ axis.tickFormat(format("d"));
86
+ }
87
+ axisstyle({
88
+ axis: tk.leftaxis.call(axis),
89
+ color: "black",
90
+ showline: true
91
+ });
92
+ } catch (err) {
93
+ tk.img.attr("width", 0).attr("height", 0);
94
+ if (err.stack) {
95
+ console.log(err.stack);
96
+ }
97
+ errtext = typeof err == "string" ? err : err.message;
98
+ } finally {
99
+ block.tkcloakoff(tk, { error: errtext });
100
+ block.block_setheight();
101
+ for (const panel of tk.subpanels) {
102
+ bigwigloadsubpanel(tk, block, panel);
103
+ }
104
+ }
105
+ }
106
+ async function bigwigloadsubpanel(tk, block, panel) {
107
+ block.tkcloakon_subpanel(panel);
108
+ const par = block.tkarg_q(tk);
109
+ if (tk.dotplotfactor) {
110
+ par.dotplotfactor = tk.dotplotfactor;
111
+ }
112
+ par.width = panel.width;
113
+ par.rglst = [
114
+ {
115
+ chr: panel.chr,
116
+ start: panel.start,
117
+ stop: panel.stop,
118
+ width: panel.width
119
+ }
120
+ ];
121
+ delete par.percentile;
122
+ delete par.autoscale;
123
+ panel.img.attr("width", panel.width).attr("height", tk.barheight);
124
+ let errtext;
125
+ try {
126
+ if (tk.imgData) throw "subpanel not supported by imgData yet";
127
+ const data = await dofetch3("tkbigwig", { method: "POST", body: JSON.stringify(par) });
128
+ if (data.error) throw data.error;
129
+ panel.img.attr("xlink:href", data.src);
130
+ } catch (err) {
131
+ panel.img.attr("width", 0).attr("height", 0);
132
+ if (err.stack) {
133
+ console.log(err.stack);
134
+ }
135
+ errtext = typeof err == "string" ? err : err.message;
136
+ } finally {
137
+ block.tkcloakoff_subpanel(panel, { error: errtext });
138
+ }
139
+ }
140
+ function bigwigconfigpanel(tk, block, holder, loader) {
141
+ const config = {
142
+ pcolor: {},
143
+ ncolor: {},
144
+ pcolor2: {},
145
+ ncolor2: {},
146
+ // .row
147
+ // .lab
148
+ dotplot: {},
149
+ // .row
150
+ dividefactor: {}
151
+ };
152
+ {
153
+ const row = holder.append("div").style("margin-bottom", "15px");
154
+ row.append("span").html("Height&nbsp;&nbsp;");
155
+ row.append("input").attr("size", 5).property("value", tk.barheight).on("keyup", (event) => {
156
+ if (event.code != "Enter") return;
157
+ const s = event.target.value;
158
+ if (s == "") return;
159
+ const v = Number.parseInt(s);
160
+ if (Number.isNaN(v) || v <= 1) {
161
+ alert("track height must be positive integer");
162
+ return;
163
+ }
164
+ tk.barheight = v;
165
+ loader(bwSetting.height);
166
+ });
167
+ }
168
+ config.pcolor.row = holder.append("div").style("margin-bottom", "15px");
169
+ config.pcolor.lab = config.pcolor.row.append("span").text("Positive value color").style("padding-right", "10px");
170
+ config.pcolor.row.append("input").attr("type", "color").property("value", rgb2hex(tk.pcolor)).on("change", (event) => {
171
+ tk.pcolor = event.target.value;
172
+ loader(bwSetting.pcolor);
173
+ });
174
+ config.ncolor.row = holder.append("div").style("margin-bottom", "15px");
175
+ config.ncolor.lab = config.ncolor.row.append("span").text("Negative value color").style("padding-right", "10px");
176
+ config.ncolor.row.append("input").attr("type", "color").property("value", rgb2hex(tk.ncolor)).on("change", (event) => {
177
+ tk.ncolor = event.target.value;
178
+ loader(bwSetting.ncolor);
179
+ });
180
+ if (!tk.scale.auto) {
181
+ config.pcolor2.row = holder.append("div").style("margin-bottom", "15px");
182
+ config.pcolor2.lab = config.pcolor2.row.append("span").html("&ge;Max color").style("padding-right", "10px");
183
+ config.pcolor2.row.append("input").attr("type", "color").property("value", rgb2hex(tk.pcolor2)).on("change", (event) => {
184
+ tk.pcolor2 = event.target.value;
185
+ loader(bwSetting.pcolor2);
186
+ });
187
+ config.ncolor2.row = holder.append("div").style("margin-bottom", "15px");
188
+ config.ncolor2.lab = config.ncolor2.row.append("span").html("&le;Min color").style("padding-right", "10px");
189
+ config.ncolor2.row.append("input").attr("type", "color").property("value", rgb2hex(tk.ncolor2)).on("change", (event) => {
190
+ tk.ncolor2 = event.target.value;
191
+ loader(bwSetting.ncolor2);
192
+ });
193
+ }
194
+ {
195
+ const setting = {};
196
+ if (tk.scale.auto) {
197
+ setting.auto = 1;
198
+ } else if (tk.scale.percentile) {
199
+ setting.percentile = tk.scale.percentile;
200
+ } else {
201
+ setting.fixed = { min: tk.scale.min, max: tk.scale.max };
202
+ }
203
+ makeNumericAxisConfig({
204
+ holder: holder.append("div").style("margin-bottom", "15px"),
205
+ setting,
206
+ callback: (s) => {
207
+ if (s.auto) {
208
+ tk.scale.auto = 1;
209
+ loader(bwSetting.autoscale);
210
+ return;
211
+ }
212
+ if (s.fixed) {
213
+ delete tk.scale.auto;
214
+ delete tk.scale.percentile;
215
+ tk.scale.max = s.fixed.max;
216
+ tk.scale.min = s.fixed.min;
217
+ loader(bwSetting.fixedscale);
218
+ return;
219
+ }
220
+ delete tk.scale.auto;
221
+ tk.scale.percentile = s.percentile;
222
+ loader(bwSetting.percentilescale);
223
+ }
224
+ });
225
+ }
226
+ {
227
+ config.dotplot.row = holder.append("div").style("margin-bottom", "15px");
228
+ config.dotplot.row.append("span").html("Dot plot&nbsp;&nbsp;");
229
+ const s = config.dotplot.row.append("select").on("change", (event) => {
230
+ const i = event.target.selectedIndex;
231
+ if (i == 0) {
232
+ delete tk.dotplotfactor;
233
+ } else {
234
+ tk.dotplotfactor = Number.parseInt(event.target.options[i].innerHTML);
235
+ }
236
+ loader(i == 0 ? bwSetting.nodotplot : bwSetting.usedotplot);
237
+ });
238
+ let o = s.append("option").text("no");
239
+ if (!tk.dotplotfactor) {
240
+ o.property("selected", 1);
241
+ }
242
+ o = s.append("option").text("5");
243
+ if (tk.dotplotfactor == 5) {
244
+ o.property("selected", 1);
245
+ }
246
+ o = s.append("option").text("10");
247
+ if (tk.dotplotfactor == 10) {
248
+ o.property("selected", 1);
249
+ }
250
+ o = s.append("option").text("15");
251
+ if (tk.dotplotfactor == 15) {
252
+ o.property("selected", 1);
253
+ }
254
+ o = s.append("option").text("20");
255
+ if (tk.dotplotfactor == 20) {
256
+ o.property("selected", 1);
257
+ }
258
+ }
259
+ config.dividefactor.row = holder.append("div");
260
+ {
261
+ const id = Math.random().toString();
262
+ const input = config.dividefactor.row.append("input").attr("type", "checkbox").attr("id", id);
263
+ if (!tk.normalize.disable) {
264
+ input.property("checked", 1);
265
+ }
266
+ config.dividefactor.row.append("label").html("&nbsp;Apply normalization").attr("for", id);
267
+ const folder = config.dividefactor.row.append("div").style("margin", "5px 10px 0px 20px").style("display", tk.normalize.disable ? "none" : "block");
268
+ folder.append("span").html("Divide raw value by&nbsp;");
269
+ const factorinput = folder.append("input").attr("type", "number").style("width", "60px").property("value", tk.normalize.dividefactor).on("keyup", (event) => {
270
+ if (event.code != "Enter" && event.code != "NumpadEnter") return;
271
+ const v = event.target.value;
272
+ if (v <= 0) {
273
+ return;
274
+ }
275
+ tk.normalize.dividefactor = v;
276
+ loader(bwSetting.usedividefactor);
277
+ });
278
+ folder.append("div").text("Enter a value above zero").style("font-size", ".7em").style("color", "#858585");
279
+ input.on("change", (event) => {
280
+ if (event.target.checked) {
281
+ appear(folder);
282
+ delete tk.normalize.disable;
283
+ factorinput.property("value", tk.normalize.dividefactor);
284
+ loader(bwSetting.usedividefactor);
285
+ return;
286
+ }
287
+ disappear(folder);
288
+ tk.normalize.disable = 1;
289
+ loader(bwSetting.nodividefactor);
290
+ });
291
+ }
292
+ return config;
293
+ }
294
+
295
+ export {
296
+ bigwigfromtemplate,
297
+ bigwigmaketk,
298
+ bigwigload,
299
+ bigwigloadsubpanel,
300
+ bigwigconfigpanel
301
+ };
302
+ //# sourceMappingURL=chunk-57RBC6IZ.js.map
@@ -0,0 +1,37 @@
1
+ import {
2
+ addGeneSearchbox,
3
+ getGEunit
4
+ } from "./chunk-SA7APTJR.js";
5
+ import {
6
+ Menu
7
+ } from "./chunk-HYOEWQ5P.js";
8
+ import {
9
+ TermTypes
10
+ } from "./chunk-NOEAT6CX.js";
11
+
12
+ // termdb/handlers/geneExpression.ts
13
+ var SearchHandler = class {
14
+ init(opts) {
15
+ this.callback = opts.callback;
16
+ this.app = opts.app;
17
+ const holder = opts.holder.append("div").style("padding", "10px 0px");
18
+ const geneSearch = addGeneSearchbox({
19
+ tip: new Menu({ padding: "0px" }),
20
+ genome: opts.genomeObj,
21
+ row: holder,
22
+ searchOnly: "gene",
23
+ callback: () => this.selectGene(geneSearch.geneSymbol)
24
+ });
25
+ }
26
+ async selectGene(gene) {
27
+ const unit = getGEunit(this.app.vocabApi);
28
+ const name = `${gene} ${unit}`;
29
+ if (!gene) throw new Error("No gene selected");
30
+ this.callback({ gene, name, type: TermTypes.GENE_EXPRESSION });
31
+ }
32
+ };
33
+
34
+ export {
35
+ SearchHandler
36
+ };
37
+ //# sourceMappingURL=chunk-5OUTR67M.js.map