use of org.molgenis.data.annotation.core.entity.impl.framework.AbstractAnnotator in project molgenis by molgenis.
the class OmimAnnotator method init.
@Override
public void init() {
List<Attribute> attributes = createOmimOutputAttributes();
AnnotatorInfo omimInfo = AnnotatorInfo.create(AnnotatorInfo.Status.READY, AnnotatorInfo.Type.PHENOTYPE_ASSOCIATION, NAME, "OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is " + "freely available and updated daily. The full-text, referenced overviews in OMIM contain information on all " + "known mendelian disorders and over 15,000 genes. OMIM focuses on the relationship between phenotype and genotype.", attributes);
EntityAnnotator entityAnnotator = new AbstractAnnotator(OMIM_RESOURCE, omimInfo, geneNameQueryCreator, new OmimResultFilter(entityTypeFactory, this), dataService, resources, new SingleFileLocationCmdLineAnnotatorSettingsConfigurer(OMIM_LOCATION, omimAnnotatorSettings)) {
@Override
public List<Attribute> createAnnotatorAttributes(AttributeFactory attributeFactory) {
return createOmimOutputAttributes();
}
};
annotator.init(entityAnnotator);
}
use of org.molgenis.data.annotation.core.entity.impl.framework.AbstractAnnotator in project molgenis by molgenis.
the class DannAnnotator method init.
@Override
public void init() {
List<Attribute> attributes = createDannOutputAttributes();
AnnotatorInfo dannInfo = AnnotatorInfo.create(AnnotatorInfo.Status.READY, AnnotatorInfo.Type.PATHOGENICITY_ESTIMATE, NAME, "Annotating genetic variants, especially non-coding variants, " + "for the purpose of identifying pathogenic variants remains a challenge." + " Combined annotation-dependent depletion (CADD) is an al- gorithm designed " + "to annotate both coding and non-coding variants, and has been shown to outper- form " + "other annotation algorithms. CADD trains a linear kernel support vector machine (SVM) " + "to dif- ferentiate evolutionarily derived, likely benign, alleles from simulated, " + "likely deleterious, variants. However, SVMs cannot capture non-linear relationships" + " among the features, which can limit performance. To address this issue, we have" + " developed DANN. DANN uses the same feature set and training data as CADD to train" + " a deep neural network (DNN). DNNs can capture non-linear relation- ships among " + "features and are better suited than SVMs for problems with a large number of samples " + "and features. We exploit Compute Unified Device Architecture-compatible " + "graphics processing units and deep learning techniques such as dropout and momentum " + "training to accelerate the DNN training. DANN achieves about a 19%relative reduction " + "in the error rate and about a 14%relative increase in the area under the curve (AUC) metric " + "over CADD’s SVM methodology. " + "All data and source code are available at https://cbcl.ics.uci.edu/ public_data/DANN/.", attributes);
EntityAnnotator entityAnnotator = new AbstractAnnotator(DANN_TABIX_RESOURCE, dannInfo, new LocusQueryCreator(vcfAttributes), new MultiAllelicResultFilter(attributes, vcfAttributes), dataService, resources, new SingleFileLocationCmdLineAnnotatorSettingsConfigurer(DANN_LOCATION, dannAnnotatorSettings)) {
@Override
public List<Attribute> createAnnotatorAttributes(AttributeFactory attributeFactory) {
return createDannOutputAttributes();
}
};
annotator.init(entityAnnotator);
}
use of org.molgenis.data.annotation.core.entity.impl.framework.AbstractAnnotator in project molgenis by molgenis.
the class ThousandGenomesAnnotator method init.
@Override
public void init() {
List<Attribute> attributes = createThousandGenomesOutputAttributes();
AnnotatorInfo thousandGenomeInfo = AnnotatorInfo.create(Status.READY, AnnotatorInfo.Type.POPULATION_REFERENCE, NAME, "The 1000 Genomes Project is an international collaboration to produce an " + "extensive public catalog of human genetic variation, including SNPs and structural variants, " + "and their haplotype contexts. This resource will support genome-wide association studies and other " + "medical research studies. " + "The genomes of about 2500 unidentified people from about 25 populations around the world will be" + "sequenced using next-generation sequencing technologies. " + "The results of the study will be freely and publicly accessible to researchers worldwide. " + "Further information about the project is available in the About tab. Information about downloading, " + "browsing or using the 1000 Genomes data is available at: http://www.1000genomes.org/ ", attributes);
LocusQueryCreator locusQueryCreator = new LocusQueryCreator(vcfAttributes);
MultiAllelicResultFilter multiAllelicResultFilter = new MultiAllelicResultFilter(singletonList(attributeFactory.create().setName(THOUSAND_GENOME_AF_RESOURCE_ATTRIBUTE_NAME).setDataType(DECIMAL)), vcfAttributes);
EntityAnnotator entityAnnotator = new AbstractAnnotator(THOUSAND_GENOME_MULTI_FILE_RESOURCE, thousandGenomeInfo, locusQueryCreator, multiAllelicResultFilter, dataService, resources, (annotationSourceFileName) -> {
thousendGenomesAnnotatorSettings.set(ROOT_DIRECTORY, annotationSourceFileName);
thousendGenomesAnnotatorSettings.set(FILEPATTERN, "ALL.chr%s.phase3_shapeit2_mvncall_integrated_v5.20130502.genotypes.vcf.gz");
thousendGenomesAnnotatorSettings.set(CHROMOSOMES, "1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22");
}) {
@Override
public List<Attribute> createAnnotatorAttributes(AttributeFactory attributeFactory) {
return createThousandGenomesOutputAttributes();
}
@Override
protected Object getResourceAttributeValue(Attribute attr, Entity entityType) {
String attrName = THOUSAND_GENOME_AF.equals(attr.getName()) ? THOUSAND_GENOME_AF_RESOURCE_ATTRIBUTE_NAME : attr.getName();
return entityType.get(attrName);
}
};
annotator.init(entityAnnotator);
}
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