@sjcrh/proteinpaint-client 2.181.0 → 2.182.0

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.
Files changed (950) hide show
  1. package/dist/2dmaf-SLBAWGPG.js +1371 -0
  2. package/dist/AIProjectAdmin-6SH5X3AF.js +830 -0
  3. package/dist/AppHeader-MVYNRMC7.js +833 -0
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@@ -0,0 +1,7 @@
1
+ {
2
+ "version": 3,
3
+ "sources": ["../../shared/utils/src/bulk.sv.js"],
4
+ "sourcesContent": ["import * as bulk from './bulk.js'\nimport * as common from './common.js'\n\n/////////////////////////////////\n//\n// client/server shared\n//\n/////////////////////////////////\n\n// work for both sv/fusion\n// must tell if the data is fusion or sv\n\nexport function parseheader(line, flag, issv) {\n\tconst header = line.toLowerCase().split('\\t')\n\tif (header.length <= 1) return 'invalid file header for fusions'\n\tconst htry = (...lst) => {\n\t\tfor (const a of lst) {\n\t\t\tconst j = header.indexOf(a)\n\t\t\tif (j != -1) return j\n\t\t}\n\t\treturn -1\n\t}\n\tlet i = htry('gene_a', 'gene1', 'genea')\n\tif (i == -1) return 'gene_a missing from header'\n\theader[i] = 'gene1'\n\ti = htry('gene_b', 'gene2', 'geneb')\n\tif (i == -1) return 'gene_b missing from header'\n\theader[i] = 'gene2'\n\ti = htry('chr_a', 'chr1', 'chra')\n\tif (i == -1) return 'chr_a missing from header'\n\theader[i] = 'chr1'\n\ti = htry('chr_b', 'chr2', 'chrb')\n\tif (i == -1) return 'chr_b missing from header'\n\theader[i] = 'chr2'\n\ti = htry('pos_a', 'position_a', 'position1', 'posa')\n\tif (i == -1) return 'pos_a missing from header'\n\theader[i] = 'position1'\n\ti = htry('pos_b', 'position_b', 'position2', 'posb')\n\tif (i == -1) return 'pos_b missing from header'\n\theader[i] = 'position2'\n\ti = htry('isoform_a', 'refseq_a', 'refseq1', 'isoform1', 'sv_refseqa')\n\tif (i == -1) return 'isoform_a missing from header'\n\theader[i] = 'isoform1'\n\ti = htry('isoform_b', 'refseq_b', 'refseq2', 'isoform2', 'sv_refseqb')\n\tif (i == -1) return 'isoform_b missing from header'\n\theader[i] = 'isoform2'\n\ti = htry('strand_a', 'orta')\n\tif (i == -1) return 'strand_a missing from header'\n\theader[i] = 'strand1'\n\ti = htry('strand_b', 'ortb')\n\tif (i == -1) return 'strand_b missing from header'\n\theader[i] = 'strand2'\n\t// optional\n\ti = htry('sample', 'sample_name', 'tumor_sample_barcode')\n\tif (i != -1) header[i] = 'sample'\n\ti = htry('patient', 'donor', 'target_case_id')\n\tif (i != -1) header[i] = 'patient'\n\ti = htry('sampletype', 'sample type', 'sample_type')\n\tif (i != -1) header[i] = 'sampletype'\n\ti = htry('disease')\n\tif (i != -1) header[i] = 'disease'\n\ti = htry('origin')\n\tif (i != -1) header[i] = 'origin'\n\tif (issv) {\n\t\tflag.sv.loaded = true\n\t\tflag.sv.header = header\n\t} else {\n\t\tflag.fusion.loaded = true\n\t\tflag.fusion.header = header\n\t}\n\treturn false\n}\n\nexport function parseline(i, line, flag, issv) {\n\tif (line == '' || line[0] == '#') return\n\tconst lst = line.split('\\t')\n\tconst m = {}\n\tconst header = issv ? flag.sv.header : flag.fusion.header\n\tconst badlines = issv ? flag.sv.badlines : flag.fusion.badlines\n\n\tfor (let j = 0; j < header.length; j++) {\n\t\tm[header[j]] = lst[j]\n\t}\n\tif (!m.chr1) {\n\t\tbadlines.push([i, 'missing chr1', lst])\n\t\treturn\n\t}\n\tif (m.chr1.toLowerCase().indexOf('chr') != 0) {\n\t\tm.chr1 = 'chr' + m.chr1\n\t}\n\tif (!m.chr2) {\n\t\tbadlines.push([i, 'missing chr2', lst])\n\t\treturn\n\t}\n\tif (m.chr2.toLowerCase().indexOf('chr') != 0) {\n\t\tm.chr2 = 'chr' + m.chr2\n\t}\n\tlet v = m.position1\n\tif (!v) {\n\t\tbadlines.push([i, 'missing position1', lst])\n\t\treturn\n\t}\n\tlet v2 = Number.parseInt(v)\n\tif (Number.isNaN(v2) || v2 <= 0) {\n\t\tbadlines.push([i, 'invalid value for position1', lst])\n\t\treturn\n\t}\n\tm.position1 = v2\n\tv = m.position2\n\tif (!v) {\n\t\tbadlines.push([i, 'missing position2', lst])\n\t\treturn\n\t}\n\tv2 = Number.parseInt(v)\n\tif (Number.isNaN(v2) || v2 <= 0) {\n\t\tbadlines.push([i, 'invalid value for position2', lst])\n\t\treturn\n\t}\n\tm.position2 = v2\n\tif (bulk.parsesample(m, flag, i, lst, badlines)) {\n\t\treturn\n\t}\n\tif (m.isoform1 && m.isoform1.indexOf(',') != -1) {\n\t\tconst lst2 = m.isoform1.split(',')\n\t\tm.isoform1 = undefined\n\t\tfor (const t of lst2) {\n\t\t\tif (t != '') m.isoform1 = t\n\t\t}\n\t}\n\tif (m.isoform2 && m.isoform2.indexOf(',') != -1) {\n\t\tconst lst2 = m.isoform2.split(',')\n\t\tm.isoform2 = undefined\n\t\tfor (const t of lst2) {\n\t\t\tif (t != '') m.isoform2 = t\n\t\t}\n\t}\n\tif (!m.gene1) {\n\t\tm.isoform1 = undefined\n\t}\n\tif (!m.gene2) {\n\t\tm.isoform2 = undefined\n\t}\n\tif (m.gene1) {\n\t\t// put data under gene1\n\t\tflag.good++\n\t\tconst m2 = {\n\t\t\tdt: issv ? common.dtsv : common.dtfusionrna,\n\t\t\tclass: issv ? common.mclasssv : common.mclassfusionrna,\n\t\t\tisoform: m.isoform1,\n\t\t\tmname: m.gene2 || m.chr2,\n\t\t\tsample: m.sample,\n\t\t\tpatient: m.patient,\n\t\t\tsampletype: m.sampletype,\n\t\t\torigin: m.origin,\n\t\t\tdisease: m.disease,\n\t\t\tpairlst: [\n\t\t\t\t{\n\t\t\t\t\ta: {\n\t\t\t\t\t\tname: m.gene1,\n\t\t\t\t\t\tisoform: m.isoform1,\n\t\t\t\t\t\tstrand: m.strand1,\n\t\t\t\t\t\tchr: m.chr1,\n\t\t\t\t\t\tposition: m.position1\n\t\t\t\t\t},\n\t\t\t\t\tb: {\n\t\t\t\t\t\tname: m.gene2,\n\t\t\t\t\t\tisoform: m.isoform2,\n\t\t\t\t\t\tstrand: m.strand2,\n\t\t\t\t\t\tchr: m.chr2,\n\t\t\t\t\t\tposition: m.position2\n\t\t\t\t\t}\n\t\t\t\t}\n\t\t\t]\n\t\t}\n\t\tconst n = flag.geneToUpper ? m.gene1.toUpperCase() : m.gene1\n\t\tif (!flag.data[n]) {\n\t\t\tflag.data[n] = []\n\t\t}\n\t\tflag.data[n].push(m2)\n\t}\n\tif (m.gene2 && m.gene2 != m.gene1) {\n\t\t// put data under gene2\n\t\tflag.good++\n\t\tconst m2 = {\n\t\t\tdt: issv ? common.dtsv : common.dtfusionrna,\n\t\t\tclass: issv ? 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