Description Usage Arguments Value Examples
Regress one phenotype on the given genes at a single marker.
1 2  | 
pheno: | 
 numeric matrix with one column. Sample IDs must be in rownames and must match rownames in genoprobs.  | 
chr: | 
 character containing a single chromosome ID.  | 
pos: | 
 numeric value indicating the position in Mb at which to mediate.  | 
type: | 
 character value that is either 'haplo' or 'snp', indicating which type of genotype values to mediate upon.  | 
expr: | 
 numeric matrix containing the gene expression values. Sample names in rownames and Ensembl IDs in colnames.  | 
ensembl: | 
 data.frame containing gene annotation as obtained from   | 
genoprobs: | 
 list containing 3-dimensional arrays of allele probs, one for each chromosome. In qtl2 format. Samples in rows, 8 founders in columns, markers in slices.  | 
addcovar: | 
 numeric matrix of additive covariates *without* the intercept. Sample IDs must be in rownames. Typically creates using model.matrix(~covar1 + covar2, data = data).  | 
cc_dbfile: | 
 full path to the CC_SNP database file created by Karl Broman.  | 
data.frame containing the mediation results.
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17  | data(pheno)
data(genoprobs)
data(map)
data(addcovar)
data(expr)
chr = 13
pos = 112.205823
build = 90
ensembl = get_ensembl_genes(chr = chr, build = build)
          med = mediate(pheno = pheno,
          chr = chr,
          pos = pos,
          type = "haplo",
          expr = dataset.islet.rnaseq$expr,
          ensembl = ensembl,
          genoprobs = genoprobs,
          addcovar = addcovar)
 | 
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