R/globals.R

In otargen: Access Open Target Genetics

utils::globalVariables(c("BP","BPcum","CHR","EFO_ID","Gene_name","L2G_score","Lead_variant",
"Molecular_trait","P","Source","Study","Tissue","Trait_reported","Trait_reported_trimmed",
"Traits","bestColocGenes","bestGenes","bestLocus2Genes","best_locus2genes_gene_symbol",
"best_locus2genes_score","beta_shape","chr_len","distances","distances.tissues","distinctA","distinctB",
"functionalPredictions","functionalPredictions.tissues","gene.id","gene.symbol",
"gene_id","gene_symbol","h3","h4","head","ind","intervals","intervals.tissues",
"leftVariant.id","log2(H4/H3)","log2h4h3","overallScore","overlapAB",
"overlappedVariantsForStudies","overlaps","place","pval","qtlStudyId",
"qtls","qtls.tissues","reorder","setNames","stack","study.hasSumstats",
"study.nCases","study.nInitial","study.nReplication","study.numAssocLoci",
"study.pmid","study.pubAuthor","study.pubDate","study.pubJournal",
"study.pubTitle","study.source","study.studyId","study.traitCategory",
"study.traitReported","study.traitReported_trimmed","tissue.name","tot",".",
"values","variant","variant.chromosome","variant.id","variant_id",
"variant.mostSevereConsequence","variant.position","variantIdA",
"variantIdB","yProbaModel","yProbaDistance","study.traitEfos",
"yProbaInteraction","variant_chromosome","variant_position","yProbaMolecularQTL","yProbaPathogenicity","where",""))