highlod(scans, lod.thr =0, drop.lod =1.5, extend =TRUE, restrict.lod =FALSE,...)pull.highlod(object, chr, pos,...)## S3 method for class 'highlod'print(x,...)## S3 method for class 'highlod'summary(object,...)## S3 method for class 'highlod'plot(x,..., quant.level =NULL, sliding =FALSE)## S3 method for class 'highlod'max(x, lod.thr =NULL, window =NULL, quant.level =NULL,...)## S3 method for class 'highlod'quantile(x, probs =NULL, lod.thr =NULL, n.quant, n.pheno, max.quantile =TRUE,...)
Arguments
scans: object of class scanone
lod.thr: LOD threshold
drop.lod: LOD drop from max to keep for support intervals
extend: extend support interval just past drop.lod; matches behavior of lodint when TRUE
restrict.lod: restrict to loci above LOD threshold if TRUE; matches behavior of lodint when FALSE (default)
chr: chromosome identifier
pos: position, or range of positions, in cM
x,object: object of class highlod
probs: probability levels for quantiles (should be > 0.5)
n.quant: maximum of s.quant
n.pheno: number of phenotypes considered
max.quantile: return only quantiles of max LOD across genome if TRUE
window: size of window for smoothing hotspot size
quant.level: vector of LOD levels for 1 up to length(quant.level) size hotspots
sliding: plot as sliding hotspot if TRUE
...: arguments passed along
See Also
highlod, hotperm
Returns
Data frame with - row: row number in scanone object
phenos: phenotype column number
lod: LOD score for phenotype at locus indicated by row
Details
The highlod condenses a scanone object to the peaks above a lod.thr and/or within drop.lod of such peaks. The pull.highlod pulls out the entries at a particular genomic location or interval of locations. Summary, print, plot, max and quantile methods provide ways to examine a highlod object.