Get genetic information on candidate regulators and co-mapping traits.
Get chromosome (phys.chr) and physical position in cM (phys.pos), along with the LOD score (peak.lod) at the peak position (peak.pos), and the chromosome where the peak is located (peak.chr). Some candidates may map to the same chromosome where they are physically located.
GetCandReg(highobj, annot, traits) GetCisCandReg(highobj, cand.reg, lod.thr = NULL) GetCoMappingTraits(highobj, cand.reg)
highobj: data frame from highlod, which is sparse summary of high LODs in large scanone objectannot: data frame with annotation information; must have first column as unique identifier, third column as chromosome, and fifth column as position in cM; typically column 2 has gene name, and column 4 has position in Mbtraits: names of traits to examine as candidate regulators; names must correspond to phenotypes in cross objectcand.reg: data frame with candidate regulator; see value section belowlod.thr: LOD threshold; restrict to intervals above this value if not NULLTraits that map to positions close to their physical locations are said to map in cis (local linkages). Traits that map to positions away from their physical locations are said to map in trans (distal linkages). There is no unambiguous way to determine how close a trait needs to map to its physical location in order to be classified as cis. Our choice is to classify a trait as cis if the 1.5-LOD support interval (Manichaikul et al. 2006) around the LOD peak contains the trait's physical location, and if the LOD score at its physical location is higher the the LOD threshold. The function GetCisCandReg determines which of the candidate regulators map in cis. The function GetCoMappingTraits returns a list with the putative targets of each trait. A trait is included in the putative target list of a trait when its LOD peak is greater than lod.thr and the drop LOD support interval around the peak contains the location of the trait's QTL. The function JoinTestOutputs currently relies on external files that contain results of FitAllTests. It needs to be rewritten to save space.
GetCoMappingTraits returns a list with each element being the names of co-mapping traits for a particular name in traits. GetCandReg returns a data frame while GetCisCandReg
returns a list with a similar candidate regulator data frame as the element cis.reg, and the index of trait names as the element cis.index. The elements of the candidate regulator data frame are as follows (peak.pos.lower and peak.pos.upper only for GetCisCandReg): - gene: name of trait, which might be a gene name
phys.chr: chromosome on which gene physically resides
phys.pos: physical position (in cM)
peak.chr: chromosome where peak LOD is located
peak.pos: position of peak (in cM)
peak.lod: LOD value at peak
peak.pos.lower,peak.pos.upper: lower and upper bounds of the 1.5-LOD support interval around peak.pos
Manichaikul et al. (2006) Genetics
Elias Chaibub Neto
highlod, FitAllTests, scanone
## data(CMSTCross) is loaded lazily. CMSTscan <- scanone(CMSTCross, pheno.col = 1:3, method = "hk") CMSThigh <- highlod(CMSTscan) traits <- names(CMSTCross$pheno) annot <- data.frame(name = traits, traits = traits, chr = rep(1, 3), Mb.pos = c(55,10,100)) annot$cM.pos <- annot$Mb.pos cand.reg <- GetCandReg(CMSThigh, annot, traits) cis.cand.reg <- GetCisCandReg(CMSThigh, cand.reg) comap.targets <- GetCoMappingTraits(CMSThigh, cand.reg)