• using R version 4.4.2 Patched (2024-11-18 r87347)
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• checking Rd files ... [0s/0s] NOTE checkRd: (-1) Internals.Rd:65: Lost braces     65 | 01) \code{Import_data(file,type=c('GBS','HapMap','VCF')):}{ This function can be used to import genotypic data in the NAM format, providing a list with a genotypic matrix \code{gen} coded as \code{012} and a vector \code{chr} with count of markers per chromosome. Currently, it helps users to import three types of files: GBS text, HapMap and VCF.}        | ^ checkRd: (-1) Internals.Rd:67: Lost braces     67 | 02) \code{markov(gen,chr):}{ Imputation method based forwards Markov model for SNP data coded as \code{012}. We recommend users to remove non-segregating markers before using this function.}        | ^ checkRd: (-1) Internals.Rd:69: Lost braces     69 | 03) \code{LD(gen):}{ Computes the linkage disequilibrium in terms of r2 for SNP data coded as \code{012}. Missing data is not allowed.}        | ^ checkRd: (-1) Internals.Rd:71: Lost braces     71 | 04) \code{PedMat(ped):}{ Builds a kinship from a pedigree. Input format is provided with \code{PedMat()}.}        | ^ checkRd: (-1) Internals.Rd:73: Lost braces     73 | 05) \code{PedMat2(ped,gen=NULL,IgnoreInbr=FALSE,PureLines=FALSE):}{ Builds a kinship from a genomic data and pedigree. Useful when not all individuals are genotyped. Row names of \code{gen} must indicate the genotype id.}        | ^ checkRd: (-1) Internals.Rd:75: Lost braces     75 | 06) \code{Gdist(gen, method = 1):}{ Computes genetic distance among individuals. Five methods are available: 1) Nei distance; 2) Edwards distance; 3) Reynolds distance; 4) Rogers distance; 5) Provesti's distance. 6) Modified Rogers distance}        | ^ checkRd: (-1) Internals.Rd:77: Lost braces     77 | 07) \code{covar(sp=NULL,rho=3.5,type=1,dist=2.5):}{ Builds a spatial kernel from field plot information. Input format is provided with \code{covar()}. Parameter \code{rho} detemines the decay of relationship among neighbor plots. \code{type} defines if the kernel is exponential (1), Gaussian (2) or some intermediate. \code{dist} informs the distance ratio between range neighbors and row neighbors.}        | ^ checkRd: (-1) Internals.Rd:79: Lost braces     79 | 08) \code{eigX(gen,fam):}{ Computes the input of the argument \code{EIG} of the function \code{gwas2}.}        | ^ checkRd: (-1) Internals.Rd:81: Lost braces     81 | 09) \code{G2A_Kernels(gen):}{ Computes a list of orthogonal kernels containing additive, dominant and first-order epistatic effects, in accordance to the G2A model from ZB Zeng et al. 2005. These kernels can be used for description of genetic architecture through variance components, for that we recommend packages \code{varComp} and \code{BGLR}.}        | ^ checkRd: (-1) Internals.Rd:83: Lost braces     83 | 10) \code{NNsrc(sp=NULL,rho=1,dist=3):}{ Using the same field data input required by the function \code{covar}, this function provides a list of nearest neighbor plots for each entry.}        | ^ checkRd: (-1) Internals.Rd:85: Lost braces     85 | 11) \code{NNcov(NN,y):}{ This function utilizes the output of \code{NNsrc} to generate a numeric vector, averageing the observed values of \code{y}. This function is useful to generate field covariates to control micro-environmental variance without krigging.}        | ^ checkRd: (-1) Internals.Rd:87: Lost braces     87 | 11) \code{emXX(y,gen,...):}{ Fits whole-genome regressions using the expectation-maximization algorithm as opposed to MCMC. Currently avaible methods include BayesA (\code{emBA}), BayesB (\code{emBB}), BayesC (\code{emBC}), BayesD (\code{emBD}), BLASSO (\code{emBL}), FLM (\code{emDE}), Elastic-Net (\code{emEN}), maximum likelihood (\code{emML}) and ridge regression (\code{emRR}). A cross-validation option is also available (\code{emCV}).}        | ^ checkRd: (-1) Internals.Rd:89: Lost braces     89 | 12) \code{CNT(X):}{ Centralizes parameters from matrix \code{X}.}        | ^ checkRd: (-1) Internals.Rd:91: Lost braces     91 | 13) \code{IMP(X):}{ Imputes missing points from matrix \code{X} with the average value of the column.}        | ^ checkRd: (-1) Internals.Rd:93: Lost braces     93 | 14) \code{GAU(X):}{ Creates a Gaussian kernel from matrix \code{X}.}        | ^ checkRd: (-1) Internals.Rd:95: Lost braces     95 | 15) \code{GRM(X, Code012=FALSE):}{ Creates genomic relationship matrix as linear kernel from matrix \code{X}. If genotypes are coded as 012 and Code012=TRUE, the kinship is the same as proposed by VanRaden (2008), otherwise the outcome is an additive G2A kernel.}        | ^ checkRd: (-1) Internals.Rd:97: Lost braces     97 | 16) \code{MSX(X):}{ Computes the cross-product of each column of \code{X} and the sum of variances of each column of \code{X}.}        | ^ checkRd: (-1) Internals.Rd:99: Lost braces     99 | 17) \code{NOR(y,X,cxx,xx,maxit=50,tol=10e-6):}{ Solves a ridge regression using GSRU, where \code{y} corresponds to the response variable, \code{X} is the set of parameters, \code{cxx} and \code{xx} are the output from the MSX function, \code{maxit} and \code{tol} are the convergence criteria.}        | ^ checkRd: (-1) Internals.Rd:101: Lost braces    101 | 18) \code{SPC(y,blk,row,col,rN=3,cN=1):}{ Computes a spatial covariate, similar to what could be obtained using NNsrc and NNcov but in a single step. It often is faster than NNsrc/NNcov.}        | ^ checkRd: (-1) Internals.Rd:103: Lost braces    103 | 19) \code{SPM(blk,row,col,rN=3,cN=1):}{ Computes a spatial matrix that capture nearest neighbots, to be used as design matrix of random effects. The least-square solution gives the same as SPC.}        | ^ checkRd: (-1) Internals.Rd:105: Lost braces    105 | 20) \code{BRR2(y,X1,X2,it=1500,bi=500,df=5,R2=0.5):}{ A simple C++ implementation of a Bayesian Ridge Regression that accomodates two random effects.}        | ^ checkRd: (-1) Internals.Rd:107: Lost braces    107 | 21) \code{emML2(y,X1,X2,D1=NULL,D2=NULL):}{ A simple C++ implementation of emML that accomodates two random effects.}        | ^ checkRd: (-1) Internals.Rd:109: Lost braces    109 | 22) \code{press(y,K,MaxIt=10):}{Solves a PRESS-regularized GBLUP. You can provide K as a matrix or as the output of the functin eigen. MaxIt the maximum number of iterations to for updating missing values (if any) if H*y does not converge.}        | ^ checkRd: (-1) Internals.Rd:111: Lost braces    111 | 23) \code{emGWA(y,gen):}{ A vanilla algorithm written in C++ for GWAS (very simple, but very efficient). It fits a snpBLUP via EM-REML based GSRU, then run an additional round checkinkg the likelihood of treating each marker as fixed effect instead of random, thus avoiding double-fitting. It returns the marker p-values, snpBLUP marker effects for genomic prediction, LS marker effects from the GWAS, variance components, heritability, and GEBVs (fitted values).}        | ^ checkRd: (-1) Internals.Rd:113: Lost braces    113 | 24) \code{BCpi(y,X,it=3000,bi=500,df=5,R2=0.5):}{ A vanilla implementation in C++ of BayesCpi for GWAS or GWP. It returns the marker p-values (as the minus log probability of marker excluded), marker effects for genomic prediction, probability of marker included, variance components, heritability, and GEBVs (fitted values). }        | ^ checkRd: (-1) Internals.Rd:115: Lost braces    115 | 25) \code{mrr(Y,X)/mkr(Y,K)/mrrV2(Y,X)/mrr2X(Y,X1,X2)/mkr2X(Y,K1,K2):}{A C++ implementation for multivariate regression.}        | ^
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