makeSummary returns a dataframe with the number of rows corresponding to the number of genes in the list and columns: gene, Number of eQTL SNPs, Number of GWAS Catalog SNPs, Number of GRASP SNPs.
Object of class 'mgl'; see
Logical flag indicating whether a csv ('Summary.csv') should be saved in the current directory
Provides a brief summary of variants that have been associated with expression and clinical traits. Of interest maybe genes that have evidence of regulatory variants but have not yet been tied to a clinical phenotype or those genes that have evidence of a clinical phenotype but have not yet been shown to have regulatory variants
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