X-Git-Url: http://source.jalview.org/gitweb/?a=blobdiff_plain;f=test%2Fjalview%2Fext%2Fensembl%2FEnsemblGeneTest.java;h=33bb189ac8b7dc30f784abd9dc25de77c15a769c;hb=0a9a0c390bce6a5b374f4d559d0b93797e5d36d0;hp=1f1a84e3f1302eb691159d6ec666106d47b1e10d;hpb=e96f5e8ce137e879dd4b4f37fb5c4d134e2778e2;p=jalview.git diff --git a/test/jalview/ext/ensembl/EnsemblGeneTest.java b/test/jalview/ext/ensembl/EnsemblGeneTest.java index 1f1a84e..33bb189 100644 --- a/test/jalview/ext/ensembl/EnsemblGeneTest.java +++ b/test/jalview/ext/ensembl/EnsemblGeneTest.java @@ -1,3 +1,23 @@ +/* + * Jalview - A Sequence Alignment Editor and Viewer ($$Version-Rel$$) + * Copyright (C) $$Year-Rel$$ The Jalview Authors + * + * This file is part of Jalview. + * + * Jalview is free software: you can redistribute it and/or + * modify it under the terms of the GNU General Public License + * as published by the Free Software Foundation, either version 3 + * of the License, or (at your option) any later version. + * + * Jalview is distributed in the hope that it will be useful, but + * WITHOUT ANY WARRANTY; without even the implied warranty + * of MERCHANTABILITY or FITNESS FOR A PARTICULAR + * PURPOSE. See the GNU General Public License for more details. + * + * You should have received a copy of the GNU General Public License + * along with Jalview. If not, see . + * The Jalview Authors are detailed in the 'AUTHORS' file. + */ package jalview.ext.ensembl; import static org.testng.AssertJUnit.assertEquals; @@ -5,6 +25,7 @@ import static org.testng.AssertJUnit.assertFalse; import static org.testng.AssertJUnit.assertSame; import static org.testng.AssertJUnit.assertTrue; +import jalview.api.FeatureSettingsModelI; import jalview.datamodel.SequenceDummy; import jalview.datamodel.SequenceFeature; import jalview.datamodel.SequenceI; @@ -12,6 +33,7 @@ import jalview.io.gff.SequenceOntologyFactory; import jalview.io.gff.SequenceOntologyLite; import jalview.util.MapList; +import java.awt.Color; import java.util.List; import org.testng.annotations.AfterClass; @@ -20,13 +42,13 @@ import org.testng.annotations.Test; public class EnsemblGeneTest { - @BeforeClass + @BeforeClass(alwaysRun = true) public void setUp() { SequenceOntologyFactory.setInstance(new SequenceOntologyLite()); } - @AfterClass + @AfterClass(alwaysRun = true) public void tearDown() { SequenceOntologyFactory.setInstance(null); @@ -129,27 +151,35 @@ public class EnsemblGeneTest SequenceFeature sf1 = new SequenceFeature("transcript", "", 20000, 20500, 0f, null); sf1.setValue("Parent", "gene:" + geneId); + sf1.setValue("transcript_id", "transcript1"); genomic.addSequenceFeature(sf1); // transcript sub-type feature - SequenceFeature sf2 = new SequenceFeature("snRNA", "", 20000, - 20500, 0f, null); + SequenceFeature sf2 = new SequenceFeature("snRNA", "", 20000, 20500, + 0f, null); sf2.setValue("Parent", "gene:" + geneId); + sf2.setValue("transcript_id", "transcript2"); genomic.addSequenceFeature(sf2); // NMD_transcript_variant treated like transcript in Ensembl SequenceFeature sf3 = new SequenceFeature("NMD_transcript_variant", "", 20000, 20500, 0f, null); sf3.setValue("Parent", "gene:" + geneId); + sf3.setValue("transcript_id", "transcript3"); genomic.addSequenceFeature(sf3); // transcript for a different gene - ignored SequenceFeature sf4 = new SequenceFeature("snRNA", "", 20000, 20500, 0f, null); sf4.setValue("Parent", "gene:XYZ"); + sf4.setValue("transcript_id", "transcript4"); genomic.addSequenceFeature(sf4); EnsemblGene testee = new EnsemblGene(); + + /* + * with no filter + */ List features = testee.getTranscriptFeatures(geneId, genomic); assertEquals(3, features.size()); @@ -167,8 +197,8 @@ public class EnsemblGeneTest { String geneId = "ABC123"; EnsemblGene testee = new EnsemblGene(); - SequenceFeature sf = new SequenceFeature("gene", "", 20000, - 20500, 0f, null); + SequenceFeature sf = new SequenceFeature("gene", "", 20000, 20500, 0f, + null); sf.setValue("ID", "gene:" + geneId); assertFalse(testee.retainFeature(sf, geneId)); @@ -200,29 +230,56 @@ public class EnsemblGeneTest { String accId = "ABC123"; EnsemblGene testee = new EnsemblGene(); - + // gene with no ID not valid SequenceFeature sf = new SequenceFeature("gene", "", 1, 2, 0f, null); assertFalse(testee.identifiesSequence(sf, accId)); - + // gene with wrong ID not valid sf.setValue("ID", "gene:XYZ"); assertFalse(testee.identifiesSequence(sf, accId)); - + // gene with right ID is valid sf.setValue("ID", "gene:" + accId); assertTrue(testee.identifiesSequence(sf, accId)); - + // gene sub-type with right ID is valid sf.setType("snRNA_gene"); assertTrue(testee.identifiesSequence(sf, accId)); - + // transcript not valid: sf.setType("transcript"); assertFalse(testee.identifiesSequence(sf, accId)); - + // exon not valid: sf.setType("exon"); assertFalse(testee.identifiesSequence(sf, accId)); } + + /** + * Check behaviour of feature colour scheme for EnsemblGene sequences. + * Currently coded to display exon and sequence_variant (or sub-types) only, + * with sequence_variant in red above exon coloured by label. + */ + @Test(groups = "Functional") + public void testGetFeatureColourScheme() + { + FeatureSettingsModelI fc = new EnsemblGene().getFeatureColourScheme(); + assertTrue(fc.isFeatureDisplayed("exon")); + assertTrue(fc.isFeatureDisplayed("coding_exon")); // subtype of exon + assertTrue(fc.isFeatureDisplayed("sequence_variant")); + assertTrue(fc.isFeatureDisplayed("feature_variant")); // subtype + assertFalse(fc.isFeatureDisplayed("transcript")); + assertEquals(Color.RED, fc.getFeatureColour("sequence_variant") + .getColour()); + assertEquals(Color.RED, fc.getFeatureColour("feature_variant") + .getColour()); + assertTrue(fc.getFeatureColour("exon").isColourByLabel()); + assertTrue(fc.getFeatureColour("coding_exon").isColourByLabel()); + assertEquals(1, fc.compare("sequence_variant", "exon")); + assertEquals(-1, fc.compare("exon", "sequence_variant")); + assertEquals(1, fc.compare("feature_variant", "coding_exon")); + assertEquals(-1, fc.compare("coding_exon", "feature_variant")); + assertEquals(1f, fc.getTransparency()); + } }