binmod: binmod

Description Usage Arguments Details Value References Examples

View source: R/binmod.R

Description

This is the main function for bin model analysis.

Usage

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binmod(x, y, map, beta0=NA, binsizelist=-1, full.search=FALSE, foldid=NA, ...)

Arguments

x

input matrix, of dimensions nobs*nvars; each row is a observation vector of an individual and each column is a genotypic indicator vector for a molecular marker.

y

a matrix of response variable (phenotypic observations), of dimensions nobs*1.

map

A data frame for linkage map or physical map.

beta0

Estimated SNP effects obtained by univariate analysis. By default, the glm function in R will be called by the binmod to calculate the estimates of effects.

binsizelist

A list of binsizes to be considered in the analysis. A default list will be generated if the option was ignored or an invalid list has been specified.

full.search

A logic indicator selecting search strategies. If FALSE was assigned, the binmod will complete the running as soon as the optimal binsize was found. Otherwise, analysis will be conducted for all binsizes on the list.

foldid

An optional vector of values between 1 and nfold identifying what fold each observation is in. If not supplied, a random vector is generated under nfold=10.

...

Other parameters need to be passed to glmnet/r and glm/r.

Details

The function invokes binmod analysis for genomic value prediction. The default settings are strongly suggested for new users.

Value

grid

information of all searched binsizes

grid$mselist

a 'data.frame': nbinsizes of 4 variables # A list of mean square errors

grid$mselist$binsize

size settings of the bins, eight in bp or cM.

grid$mselist$mse

mean square error

grid$mselist$mse_std

the standard deviation of MSEs

grid$mselist$nbin

number of bins under the binsize setting

grid$optbinsize

optimal binsize

grid$optid

order of the optimal binsize in the grid

optimal

result obtained under the optimal binsize

optimal$predict

phentypic values and its' predicted values under the optimal model.

optimal$predict$y

original phenotypic observations

optimal$predict$yp_cv

predictions by 10-fold cross-validation.

optimal$beta

estimated bin parameters

optimal$beta$beta

bin effect

optimal$beta$SSx

sum of square of bin indicator

optimal$beta$Se

residual error

optimal$beta$Sb

estimating error of bin effect

optimal$beta$Wald

Wald-test statistics

optimal$beta$LOD

LOD-test statistics

optimal$xbin

indicator matrix of the bins under the optimal binsize

optimal$map

'data.frame': of 5 variables: #bin map

optimal$map$chr

chromosome id

optimal$map$pos

bin position

optimal$map$pos_id

mean of the orders of markers in the bin

optimal$map$start_id

the order the first maker in a bin

optimal$map$end_id

the order the last maker in a bin

optimal$binsize

optimal binsize

optimal$cv

cross-validation results

optimal$cv$binsize

binsize

optimal$cv$nbin

number of bins under the binsize setting

optimal$cv$mse

mean squared error obtained from cross-validation

optimal$cv$r

Pearson's correlation coefficient obtained from cross-validation

snp

SNP information

snp$map

linkage map or physical map

snp$map$chr

chromosome id

snp$map$pos

marker position

snp$map$pos_id

marker order

snp$effect

single marker analysis result

snp$effect$beta

SNP effect

snp$effect$SSx

sum of square of genotypic indicator

snp$effect$Se

residual variance

snp$effect$Sb

estimating error of marker effect

snp$effect$Wald

Wald-test statistics

snp$effect$LOD

LOD test statistics

snp$mapinfo

a brief summary of the map

snp$mapinfo$chr

chromosome id

snp$mapinfo$start

the position of the first marker on the chromosome

snp$mapinfo$end

the position of the last marker on the chromosome

snp$mapinfo$length

length of the chromosome

snp$mapinfo$nmark

number of markers on the chromosome

snp$mapinfo$aver

average interval of the chromosome

snp$mapinfo$min.interval

the smallest interval size on the chromosome

cvfit

A cv.glmnet project. See manual of glmnet for details.

References

Zhiqiu Hu, Zhiquan Wang, and Shizhong Xu (2012) An infinitesimal model for quantitative trait genomic value prediction. PloS ONE

Examples

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#load PAS library
library (PAS)
#load the demo data
data (beef)
#perform binmod analysis under the default settings.
binmod.result=binmod (x , y , map)
#plot binmod result
plot(binmod.result)
str(binmod.result)
#Output the predicted phenotypic values that was obtained
#by 10-fold cross validation .
predict(binmod.result)
#predict the phenotypic values for new individuals
x1=x[sample(1:NROW(x) , 20), ]
bin.pred.x1=predict(binmod.result, newx=x1)
str(bin.pred.x1)

PAS documentation built on May 2, 2019, 11:11 a.m.