diff --git a/cypress/e2e/iva/variant-interpreter-grid-cancer-cnv.cy.js b/cypress/e2e/iva/variant-interpreter-grid-cancer-cnv.cy.js index 9e849e7587..5f641ec015 100644 --- a/cypress/e2e/iva/variant-interpreter-grid-cancer-cnv.cy.js +++ b/cypress/e2e/iva/variant-interpreter-grid-cancer-cnv.cy.js @@ -168,7 +168,7 @@ context("Variant Interpreter Grid Cancer CNV", () => { it("should display Cohort Stats (Population Frequencies) tooltip", () => { cy.get("tbody tr:first > td") - .eq(8) + .eq(10) .within(() => { cy.get("a") .trigger("mouseover"); @@ -177,7 +177,7 @@ context("Variant Interpreter Grid Cancer CNV", () => { .should("be.visible"); }); - it("should display reference population frequencies tooltip", () => { + it.skip("should display reference population frequencies tooltip", () => { cy.get("tbody tr:first > td") .eq(9) .within(() => { diff --git a/cypress/e2e/iva/variant-interpreter-grid-cancer.cy.js b/cypress/e2e/iva/variant-interpreter-grid-cancer.cy.js index 8b0b8dd009..fcacff7031 100644 --- a/cypress/e2e/iva/variant-interpreter-grid-cancer.cy.js +++ b/cypress/e2e/iva/variant-interpreter-grid-cancer.cy.js @@ -210,7 +210,7 @@ context("Variant Interpreter Grid Cancer", () => { it("should display cohort stats (population frequencies) tooltip", () => { cy.get("tbody tr:first > td") - .eq(8) + .eq(10) .within(() => { cy.get("a").trigger("mouseover"); }); @@ -220,7 +220,7 @@ context("Variant Interpreter Grid Cancer", () => { it("should reference population frequencies tooltip", () => { cy.get("tbody tr:first > td") - .eq(9) + .eq(11) .within(() => { cy.get("a") .trigger("mouseover"); diff --git a/cypress/e2e/iva/variant-interpreter-grid-germline.cy.js b/cypress/e2e/iva/variant-interpreter-grid-germline.cy.js index 3b21ca27e5..8ff4d37102 100644 --- a/cypress/e2e/iva/variant-interpreter-grid-germline.cy.js +++ b/cypress/e2e/iva/variant-interpreter-grid-germline.cy.js @@ -174,7 +174,7 @@ context("Variant Interpreter Grid Germiline", () => { it("should display cohort stats (Population Frequencies) tooltip", () => { cy.get("tbody tr:first > td") - .eq(8) + .eq(9) .within(() => { cy.get("a") .trigger("mouseover"); @@ -185,7 +185,7 @@ context("Variant Interpreter Grid Germiline", () => { it("should display reference population frequencies tooltip", () => { cy.get("tbody tr:first > td") - .eq(9) + .eq(10) .within(() => { cy.get("a") .trigger("mouseover"); @@ -196,7 +196,7 @@ context("Variant Interpreter Grid Germiline", () => { it("should display ACMG Prediction (Classification) tooltip", () => { cy.get("tbody tr:first > td") - .eq(14) + .eq(15) .within(() => { cy.get("a") .trigger("mouseover"); diff --git a/src/sites/iva/conf/browsers.settings.js b/src/sites/iva/conf/browsers.settings.js index 924664f245..dfaab64cb5 100644 --- a/src/sites/iva/conf/browsers.settings.js +++ b/src/sites/iva/conf/browsers.settings.js @@ -718,7 +718,25 @@ const INTERPRETER_SETTINGS = { ], }, { - id: "methods" + id: "methods", + items: [ + { + type: "SINGLE", + methods: [ + {id: "exomiser"}, + ], + }, + { + type: "FAMILY", + methods: [ + {id: "exomiser"}, + ], + }, + { + type: "CANCER", + methods: [], + }, + ], }, { id: "variant-browser", diff --git a/src/webcomponents/commons/grid-commons.js b/src/webcomponents/commons/grid-commons.js index dd562c9b98..27a7ba4493 100644 --- a/src/webcomponents/commons/grid-commons.js +++ b/src/webcomponents/commons/grid-commons.js @@ -272,9 +272,9 @@ export default class GridCommons { } } - isColumnVisible(colName) { + isColumnVisible(colName, parentName) { if (this.config.columns?.length > 0) { - return this.config.columns.includes(colName); + return this.config.columns.includes(colName) || this.config.columns.includes(parentName); } else { // Columns are visible by default. return true; diff --git a/src/webcomponents/deprecated/select-field-token.js b/src/webcomponents/deprecated/select-field-token.js deleted file mode 100644 index e69de29bb2..0000000000 diff --git a/src/webcomponents/study/deprecated/variable-manager.js b/src/webcomponents/study/deprecated/variable-manager.js deleted file mode 100644 index e69de29bb2..0000000000 diff --git a/src/webcomponents/variant/analysis/deprecated/test/knockout.20201029141213.SChLEA.js b/src/webcomponents/variant/analysis/deprecated/test/knockout.20201029141213.SChLEA.js deleted file mode 100644 index b8f24cfb2c..0000000000 --- a/src/webcomponents/variant/analysis/deprecated/test/knockout.20201029141213.SChLEA.js +++ /dev/null @@ -1,378 +0,0 @@ -export default [ - { - "sampleId": "ISDBM322015", - "sex": "MALE", - "phenotypes": [ - { - "id": "HP:0000519", - "name": "Developmental cataract", - "source": "HPO", - "status": "OBSERVED" - }, - { - "id": "HP:0000545", - "name": "Myopia", - "source": "HPO", - "status": "OBSERVED" - } - ], - "disorders": [ - { - "id": "OMIM:611597", - "name": "Cataract, Autosomal Dominant, Multiple Types 1", - "source": "OMIM" - } - ], - "stats": { - "numGenes": 1, - "numTranscripts": 1, - "byType": { - "HOM_ALT": 1, - "COMP_HET": 0, - "HET_ALT": 0, - "DELETION_OVERLAP": 0 - } - }, - "genes": [ - { - "name": "BRCA2", - "transcripts": [ - { - "id": "ENST00000470094", - "biotype": "nonsense_mediated_decay", - "variants": [ - { - "id": "13:32959534:A:G", - "genotype": "1/1", - "filter": "PASS", - "qual": "1579.7800000000002", - "knockoutType": "HOM_ALT", - "sequenceOntologyTerms": [ - { - "accession": "SO:0001621", - "name": "NMD_transcript_variant" - }, - { - "accession": "SO:0001627", - "name": "intron_variant" - } - ] - } - ] - } - ] - } - ] - }, - { - "sampleId": "ISDBM322016", - "sex": "MALE", - "phenotypes": [ - { - "id": "HP:0000545", - "name": "Myopia", - "source": "HPO", - "status": "OBSERVED" - }, - { - "id": "HP:0000519", - "name": "Developmental cataract", - "source": "HPO", - "status": "OBSERVED" - } - ], - "disorders": [ - { - "id": "OMIM:611597", - "name": "Cataract, Autosomal Dominant, Multiple Types 1", - "source": "OMIM" - } - ], - "stats": { - "numGenes": 1, - "numTranscripts": 2, - "byType": { - "HOM_ALT": 3, - "COMP_HET": 0, - "HET_ALT": 0, - "DELETION_OVERLAP": 0 - } - }, - "genes": [ - { - "name": "BRCA2", - "transcripts": [ - { - "id": "ENST00000470094", - "biotype": "nonsense_mediated_decay", - "variants": [ - { - "id": "13:32959199:C:T", - "genotype": "1/1", - "filter": "PASS", - "qual": "161.63", - "knockoutType": "HOM_ALT", - "sequenceOntologyTerms": [ - { - "accession": "SO:0001621", - "name": "NMD_transcript_variant" - }, - { - "accession": "SO:0001627", - "name": "intron_variant" - } - ] - }, - { - "id": "13:32971425:T:C", - "genotype": "1/1", - "filter": "PASS", - "qual": "162.35", - "knockoutType": "HOM_ALT", - "sequenceOntologyTerms": [ - { - "accession": "SO:0001621", - "name": "NMD_transcript_variant" - }, - { - "accession": "SO:0001627", - "name": "intron_variant" - } - ] - } - ] - }, - { - "id": "ENST00000533776", - "biotype": "retained_intron", - "variants": [ - { - "id": "13:32971425:T:C", - "genotype": "1/1", - "filter": "PASS", - "qual": "162.35", - "knockoutType": "HOM_ALT", - "sequenceOntologyTerms": [ - { - "accession": "SO:0001619", - "name": "non_coding_transcript_variant" - }, - { - "accession": "SO:0001627", - "name": "intron_variant" - } - ] - }, - { - "id": "13:32977496:C:A", - "genotype": "1/1", - "filter": "PASS", - "qual": "121.58", - "knockoutType": "HOM_ALT", - "sequenceOntologyTerms": [ - { - "accession": "SO:0001632", - "name": "downstream_gene_variant" - } - ] - } - ] - } - ] - } - ] - }, - { - "sampleId": "ISDBM322017", - "sex": "FEMALE", - "phenotypes": [ - { - "id": "HP:0000545", - "name": "Myopia", - "source": "HPO", - "status": "OBSERVED" - }, - { - "id": "HP:0002077", - "name": "Migraine with aura", - "source": "HPO", - "status": "OBSERVED" - } - ], - "disorders": [ - { - "id": "OMIM:300125", - "name": "Migraine, Familial Typical, Susceptibility To, 2", - "source": "OMIM" - } - ], - "stats": { - "numGenes": 1, - "numTranscripts": 2, - "byType": { - "HOM_ALT": 1, - "COMP_HET": 0, - "HET_ALT": 0, - "DELETION_OVERLAP": 0 - } - }, - "genes": [ - { - "name": "BRCA2", - "transcripts": [ - { - "id": "ENST00000470094", - "biotype": "nonsense_mediated_decay", - "variants": [ - { - "id": "13:32971425:T:C", - "genotype": "1/1", - "filter": "PASS", - "qual": "162.35", - "knockoutType": "HOM_ALT", - "sequenceOntologyTerms": [ - { - "accession": "SO:0001621", - "name": "NMD_transcript_variant" - }, - { - "accession": "SO:0001627", - "name": "intron_variant" - } - ] - } - ] - }, - { - "id": "ENST00000533776", - "biotype": "retained_intron", - "variants": [ - { - "id": "13:32971425:T:C", - "genotype": "1/1", - "filter": "PASS", - "qual": "162.35", - "knockoutType": "HOM_ALT", - "sequenceOntologyTerms": [ - { - "accession": "SO:0001619", - "name": "non_coding_transcript_variant" - }, - { - "accession": "SO:0001627", - "name": "intron_variant" - } - ] - } - ] - } - ] - } - ] - }, - { - "sampleId": "ISDBM322018", - "sex": "FEMALE", - "phenotypes": [ - { - "id": "HP:0002077", - "name": "Migraine with aura", - "source": "HPO", - "status": "OBSERVED" - }, - { - "id": "HP:0000958", - "name": "Dry skin", - "source": "HPO", - "status": "OBSERVED" - } - ], - "disorders": [ - { - "id": "OMIM:300125", - "name": "Migraine, Familial Typical, Susceptibility To, 2", - "source": "OMIM" - } - ], - "stats": { - "numGenes": 1, - "numTranscripts": 2, - "byType": { - "HOM_ALT": 2, - "COMP_HET": 0, - "HET_ALT": 0, - "DELETION_OVERLAP": 0 - } - }, - "genes": [ - { - "name": "BRCA2", - "transcripts": [ - { - "id": "ENST00000470094", - "biotype": "nonsense_mediated_decay", - "variants": [ - { - "id": "13:32959534:A:G", - "genotype": "1/1", - "filter": "PASS", - "qual": "1579.7800000000002", - "knockoutType": "HOM_ALT", - "sequenceOntologyTerms": [ - { - "accession": "SO:0001621", - "name": "NMD_transcript_variant" - }, - { - "accession": "SO:0001627", - "name": "intron_variant" - } - ] - }, - { - "id": "13:32971425:T:C", - "genotype": "1/1", - "filter": "PASS", - "qual": "162.35", - "knockoutType": "HOM_ALT", - "sequenceOntologyTerms": [ - { - "accession": "SO:0001621", - "name": "NMD_transcript_variant" - }, - { - "accession": "SO:0001627", - "name": "intron_variant" - } - ] - } - ] - }, - { - "id": "ENST00000533776", - "biotype": "retained_intron", - "variants": [ - { - "id": "13:32971425:T:C", - "genotype": "1/1", - "filter": "PASS", - "qual": "162.35", - "knockoutType": "HOM_ALT", - "sequenceOntologyTerms": [ - { - "accession": "SO:0001619", - "name": "non_coding_transcript_variant" - }, - { - "accession": "SO:0001627", - "name": "intron_variant" - } - ] - } - ] - } - ] - } - ] - } -]; diff --git a/src/webcomponents/variant/analysis/deprecated/test/knockout.20201103172343.kFIvpr.gene.js b/src/webcomponents/variant/analysis/deprecated/test/knockout.20201103172343.kFIvpr.gene.js deleted file mode 100644 index 9de6c81aff..0000000000 --- a/src/webcomponents/variant/analysis/deprecated/test/knockout.20201103172343.kFIvpr.gene.js +++ /dev/null @@ -1,521 +0,0 @@ -export default [{ - "id": "ENSG00000105737", - "name": "GRIK5", - "chromosome": "19", - "start": 42502473, - "end": 42573650, - "strand": "-", - "biotype": "protein_coding", - "annotation": { - "diseases": [ - { - "id": "umls:C0036341", - "name": "Schizophrenia", - "score": 0.21548465, - "numberOfPubmeds": 5, - "associationTypes": [ - "Biomarker, GeneticVariation" - ], - "sources": [ - "BeFree", - "CTD_human", - "GAD" - ], - "source": "disgenet" - }, - { - "id": "umls:C0035126", - "name": "Reperfusion Injury", - "score": 0.1, - "numberOfPubmeds": 1, - "associationTypes": [ - "Biomarker" - ], - "sources": [ - "RGD" - ], - "source": "disgenet" - }, - { - "id": "umls:C0036572", - "name": "Seizures", - "score": 0.1, - "numberOfPubmeds": 1, - "associationTypes": [ - "Biomarker" - ], - "sources": [ - "RGD" - ], - "source": "disgenet" - }, - { - "id": "umls:C0014556", - "name": "Epilepsy, Temporal Lobe", - "score": 0.1, - "numberOfPubmeds": 1, - "associationTypes": [ - "Biomarker" - ], - "sources": [ - "RGD" - ], - "source": "disgenet" - }, - { - "id": "umls:C0005586", - "name": "Bipolar Disorder", - "score": 0.002600572, - "numberOfPubmeds": 2, - "associationTypes": [ - "Biomarker, GeneticVariation" - ], - "sources": [ - "BeFree", - "GAD" - ], - "source": "disgenet" - }, - { - "id": "umls:C0004352", - "name": "Autistic Disorder", - "score": 0.0017010274, - "numberOfPubmeds": 6, - "associationTypes": [ - "Biomarker" - ], - "sources": [ - "BeFree" - ], - "source": "disgenet" - }, - { - "id": "umls:C0011581", - "name": "Depressive Disorder", - "score": 0.00056700915, - "numberOfPubmeds": 2, - "associationTypes": [ - "Biomarker" - ], - "sources": [ - "BeFree" - ], - "source": "disgenet" - }, - { - "id": "umls:C0162872", - "name": "Aortic Aneurysm, Thoracic", - "score": 0.00056700915, - "numberOfPubmeds": 2, - "associationTypes": [ - "Biomarker" - ], - "sources": [ - "BeFree" - ], - "source": "disgenet" - }, - { - "id": "umls:C1510586", - "name": "Autism spectrum disorders", - "score": 0.00056700915, - "numberOfPubmeds": 2, - "associationTypes": [ - "Biomarker" - ], - "sources": [ - "BeFree" - ], - "source": "disgenet" - }, - { - "id": "umls:C0812393", - "name": "depression", - "score": 0.00056700915, - "numberOfPubmeds": 2, - "associationTypes": [ - "Biomarker" - ], - "sources": [ - "BeFree" - ], - "source": "disgenet" - }, - { - "id": "umls:C0011570", - "name": "Depression", - "score": 0.00056700915, - "numberOfPubmeds": 2, - "associationTypes": [ - "Biomarker" - ], - "sources": [ - "BeFree" - ], - "source": "disgenet" - }, - { - "id": "umls:C0028768", - "name": "Obsessive-Compulsive Disorder", - "score": 0.00056700915, - "numberOfPubmeds": 2, - "associationTypes": [ - "Biomarker" - ], - "sources": [ - "BeFree" - ], - "source": "disgenet" - }, - { - "id": "umls:C0011124", - "name": "Decreased Libido", - "score": 0.00028350457, - "numberOfPubmeds": 1, - "associationTypes": [ - "Biomarker" - ], - "sources": [ - "BeFree" - ], - "source": "disgenet" - }, - { - "id": "umls:C0549622", - "name": "Sexual Dysfunction", - "score": 0.00028350457, - "numberOfPubmeds": 1, - "associationTypes": [ - "Biomarker" - ], - "sources": [ - "BeFree" - ], - "source": "disgenet" - }, - { - "id": "umls:C0023448", - "name": "Leukemia, Lymphoid", - "score": 0.00028350457, - "numberOfPubmeds": 1, - "associationTypes": [ - "Biomarker" - ], - "sources": [ - "BeFree" - ], - "source": "disgenet" - }, - { - "id": "umls:C1292769", - "name": "Precursor B-cell lymphoblastic leukemia", - "score": 0.00028350457, - "numberOfPubmeds": 1, - "associationTypes": [ - "Biomarker" - ], - "sources": [ - "BeFree" - ], - "source": "disgenet" - }, - { - "id": "umls:C0003469", - "name": "Anxiety Disorders", - "score": 0.00028350457, - "numberOfPubmeds": 1, - "associationTypes": [ - "Biomarker" - ], - "sources": [ - "BeFree" - ], - "source": "disgenet" - }, - { - "id": "umls:C0006012", - "name": "Borderline Personality Disorder", - "score": 0.00028350457, - "numberOfPubmeds": 1, - "associationTypes": [ - "Biomarker" - ], - "sources": [ - "BeFree" - ], - "source": "disgenet" - }, - { - "id": "umls:C0036877", - "name": "sexual dysfunction", - "score": 0.00028350457, - "numberOfPubmeds": 1, - "associationTypes": [ - "Biomarker" - ], - "sources": [ - "BeFree" - ], - "source": "disgenet" - }, - { - "id": "umls:C0023449", - "name": "ACUTE LYMPHOCYTIC LEUKEMIA", - "score": 0.00028350457, - "numberOfPubmeds": 1, - "associationTypes": [ - "Biomarker" - ], - "sources": [ - "BeFree" - ], - "source": "disgenet" - }, - { - "id": "umls:C0525045", - "name": "Mood Disorders", - "score": 0.00028350457, - "numberOfPubmeds": 1, - "associationTypes": [ - "Biomarker" - ], - "sources": [ - "BeFree" - ], - "source": "disgenet" - }, - { - "id": "umls:C0006287", - "name": "Bronchopulmonary Dysplasia", - "score": 0.00028350457, - "numberOfPubmeds": 1, - "associationTypes": [ - "Biomarker" - ], - "sources": [ - "BeFree" - ], - "source": "disgenet" - }, - { - "id": "umls:C0007137", - "name": "Carcinoma, Squamous Cell", - "score": 0.00028350457, - "numberOfPubmeds": 1, - "associationTypes": [ - "Biomarker" - ], - "sources": [ - "BeFree" - ], - "source": "disgenet" - }, - { - "id": "umls:C0014548", - "name": "Epilepsy, Generalized", - "score": 0.00028350457, - "numberOfPubmeds": 1, - "associationTypes": [ - "Biomarker" - ], - "sources": [ - "BeFree" - ], - "source": "disgenet" - } - ], - "drugs": [ - { - "geneName": "GRIK5", - "drugName": "4185", - "source": "dgidb", - "studyType": "GuideToPharmacologyInteractions", - "type": "n/a" - }, - { - "geneName": "GRIK5", - "drugName": "4231", - "source": "dgidb", - "studyType": "GuideToPharmacologyInteractions", - "type": "n/a" - }, - { - "geneName": "GRIK5", - "drugName": "4075", - "source": "dgidb", - "studyType": "GuideToPharmacologyInteractions", - "type": "n/a" - }, - { - "geneName": "GRIK5", - "drugName": "4085", - "source": "dgidb", - "studyType": "GuideToPharmacologyInteractions", - "type": "n/a" - }, - { - "geneName": "GRIK5", - "drugName": "4317", - "source": "dgidb", - "studyType": "GuideToPharmacologyInteractions", - "type": "n/a" - }, - { - "geneName": "GRIK5", - "drugName": "4181", - "source": "dgidb", - "studyType": "GuideToPharmacologyInteractions", - "type": "n/a" - }, - { - "geneName": "GRIK5", - "drugName": "TEZAMPANEL", - "source": "dgidb", - "studyType": "TdgClinicalTrial", - "type": "n/a" - }, - { - "geneName": "GRIK5", - "drugName": "DB00142", - "source": "dgidb", - "studyType": "DrugBank", - "type": "n/a" - } - ] - }, - "individuals": [ - { - "id": "ISDBM322016", - "sampleId": "ISDBM322016", - "transcripts": [ - { - "id": "ENST00000602210", - "biotype": "retained_intron", - "variants": [ - { - "id": "19:42506044:C:G", - "genotype": "1/1", - "filter": "PASS", - "qual": "34.02", - "knockoutType": "HOM_ALT", - "sequenceOntologyTerms": [ - { - "accession": "SO:0001619", - "name": "non_coding_transcript_variant" - }, - { - "accession": "SO:0001627", - "name": "intron_variant" - } - ] - } - ] - }, - { - "id": "ENST00000454993", - "biotype": "retained_intron", - "variants": [ - { - "id": "19:42506044:C:G", - "genotype": "1/1", - "filter": "PASS", - "qual": "34.02", - "knockoutType": "HOM_ALT", - "sequenceOntologyTerms": [ - { - "accession": "SO:0001619", - "name": "non_coding_transcript_variant" - }, - { - "accession": "SO:0001627", - "name": "intron_variant" - } - ] - } - ] - } - ] - }, - { - "id": "ISDBM322018", - "sampleId": "ISDBM322018", - "transcripts": [ - { - "id": "ENST00000602210", - "biotype": "retained_intron", - "variants": [ - { - "id": "19:42506044:C:G", - "genotype": "1/1", - "filter": "PASS", - "qual": "34.02", - "knockoutType": "HOM_ALT", - "sequenceOntologyTerms": [ - { - "accession": "SO:0001619", - "name": "non_coding_transcript_variant" - }, - { - "accession": "SO:0001627", - "name": "intron_variant" - } - ] - } - ] - }, - { - "id": "ENST00000454993", - "biotype": "retained_intron", - "variants": [ - { - "id": "19:42506044:C:G", - "genotype": "1/1", - "filter": "PASS", - "qual": "34.02", - "knockoutType": "HOM_ALT", - "sequenceOntologyTerms": [ - { - "accession": "SO:0001619", - "name": "non_coding_transcript_variant" - }, - { - "accession": "SO:0001627", - "name": "intron_variant" - } - ] - } - ] - } - ] - }, - { - "id": "ISDBM322015", - "sampleId": "ISDBM322015", - "transcripts": [ - { - "id": "ENST00000594528", - "biotype": "nonsense_mediated_decay", - "variants": [ - { - "id": "19:42554437:C:A", - "genotype": "1/1", - "filter": "PASS", - "qual": "45.769999999999996", - "knockoutType": "HOM_ALT", - "sequenceOntologyTerms": [ - { - "accession": "SO:0001621", - "name": "NMD_transcript_variant" - }, - { - "accession": "SO:0001627", - "name": "intron_variant" - } - ] - } - ] - } - ] - } - ] -}]; diff --git a/src/webcomponents/variant/analysis/deprecated/test/knockout.20201103172343.kFIvpr.individuals.js b/src/webcomponents/variant/analysis/deprecated/test/knockout.20201103172343.kFIvpr.individuals.js deleted file mode 100644 index 6760254f79..0000000000 --- a/src/webcomponents/variant/analysis/deprecated/test/knockout.20201103172343.kFIvpr.individuals.js +++ /dev/null @@ -1,243 +0,0 @@ -export default [ - { - "sampleId": "ISDBM322015", - "sex": "MALE", - "phenotypes": [ - { - "id": "HP:0000519", - "name": "Developmental cataract", - "source": "HPO", - "status": "OBSERVED" - }, - { - "id": "HP:0000545", - "name": "Myopia", - "source": "HPO", - "status": "OBSERVED" - } - ], - "disorders": [ - { - "id": "OMIM:611597", - "name": "Cataract, Autosomal Dominant, Multiple Types 1", - "source": "OMIM" - } - ], - "stats": { - "numGenes": 1, - "numTranscripts": 1, - "byType": { - "HOM_ALT": 1, - "COMP_HET": 0, - "HET_ALT": 0, - "DELETION_OVERLAP": 0 - } - }, - "genes": [ - { - "name": "GRIK5", - "transcripts": [ - { - "id": "ENST00000594528", - "biotype": "nonsense_mediated_decay", - "variants": [ - { - "id": "19:42554437:C:A", - "genotype": "1/1", - "filter": "PASS", - "qual": "45.769999999999996", - "knockoutType": "HOM_ALT", - "sequenceOntologyTerms": [ - { - "accession": "SO:0001621", - "name": "NMD_transcript_variant" - }, - { - "accession": "SO:0001627", - "name": "intron_variant" - } - ] - } - ] - } - ] - } - ] - }, - { - "sampleId": "ISDBM322016", - "sex": "MALE", - "phenotypes": [ - { - "id": "HP:0000545", - "name": "Myopia", - "source": "HPO", - "status": "OBSERVED" - }, - { - "id": "HP:0000519", - "name": "Developmental cataract", - "source": "HPO", - "status": "OBSERVED" - } - ], - "disorders": [ - { - "id": "OMIM:611597", - "name": "Cataract, Autosomal Dominant, Multiple Types 1", - "source": "OMIM" - } - ], - "stats": { - "numGenes": 1, - "numTranscripts": 2, - "byType": { - "HOM_ALT": 1, - "COMP_HET": 0, - "HET_ALT": 0, - "DELETION_OVERLAP": 0 - } - }, - "genes": [ - { - "name": "GRIK5", - "transcripts": [ - { - "id": "ENST00000602210", - "biotype": "retained_intron", - "variants": [ - { - "id": "19:42506044:C:G", - "genotype": "1/1", - "filter": "PASS", - "qual": "34.02", - "knockoutType": "HOM_ALT", - "sequenceOntologyTerms": [ - { - "accession": "SO:0001619", - "name": "non_coding_transcript_variant" - }, - { - "accession": "SO:0001627", - "name": "intron_variant" - } - ] - } - ] - }, - { - "id": "ENST00000454993", - "biotype": "retained_intron", - "variants": [ - { - "id": "19:42506044:C:G", - "genotype": "1/1", - "filter": "PASS", - "qual": "34.02", - "knockoutType": "HOM_ALT", - "sequenceOntologyTerms": [ - { - "accession": "SO:0001619", - "name": "non_coding_transcript_variant" - }, - { - "accession": "SO:0001627", - "name": "intron_variant" - } - ] - } - ] - } - ] - } - ] - }, - { - "sampleId": "ISDBM322018", - "sex": "FEMALE", - "phenotypes": [ - { - "id": "HP:0002077", - "name": "Migraine with aura", - "source": "HPO", - "status": "OBSERVED" - }, - { - "id": "HP:0000958", - "name": "Dry skin", - "source": "HPO", - "status": "OBSERVED" - } - ], - "disorders": [ - { - "id": "OMIM:300125", - "name": "Migraine, Familial Typical, Susceptibility To, 2", - "source": "OMIM" - } - ], - "stats": { - "numGenes": 1, - "numTranscripts": 2, - "byType": { - "HOM_ALT": 1, - "COMP_HET": 0, - "HET_ALT": 0, - "DELETION_OVERLAP": 0 - } - }, - "genes": [ - { - "name": "GRIK5", - "transcripts": [ - { - "id": "ENST00000602210", - "biotype": "retained_intron", - "variants": [ - { - "id": "19:42506044:C:G", - "genotype": "1/1", - "filter": "PASS", - "qual": "34.02", - "knockoutType": "HOM_ALT", - "sequenceOntologyTerms": [ - { - "accession": "SO:0001619", - "name": "non_coding_transcript_variant" - }, - { - "accession": "SO:0001627", - "name": "intron_variant" - } - ] - } - ] - }, - { - "id": "ENST00000454993", - "biotype": "retained_intron", - "variants": [ - { - "id": "19:42506044:C:G", - "genotype": "1/1", - "filter": "PASS", - "qual": "34.02", - "knockoutType": "HOM_ALT", - "sequenceOntologyTerms": [ - { - "accession": "SO:0001619", - "name": "non_coding_transcript_variant" - }, - { - "accession": "SO:0001627", - "name": "intron_variant" - } - ] - } - ] - } - ] - } - ] - } -]; diff --git a/src/webcomponents/variant/analysis/deprecated/test/opencga-knockout-analysis-result.html b/src/webcomponents/variant/analysis/deprecated/test/opencga-knockout-analysis-result.html deleted file mode 100644 index 29fc1ebb52..0000000000 --- a/src/webcomponents/variant/analysis/deprecated/test/opencga-knockout-analysis-result.html +++ /dev/null @@ -1,152 +0,0 @@ - - - - - -
- - - - - - -