[Genabel-commits] r2079 - pkg/MultiABEL/man
noreply at r-forge.r-project.org
noreply at r-forge.r-project.org
Sat Feb 9 04:33:00 CET 2019
Author: shenxia
Date: 2019-02-09 04:33:00 +0100 (Sat, 09 Feb 2019)
New Revision: 2079
Modified:
pkg/MultiABEL/man/MultiABEL.Rd
pkg/MultiABEL/man/MultiLoad.Rd
pkg/MultiABEL/man/MultiRep.Rd
pkg/MultiABEL/man/MultiSummary.Rd
pkg/MultiABEL/man/Multivariate.Rd
pkg/MultiABEL/man/load.summary.Rd
Log:
update manuals
Modified: pkg/MultiABEL/man/MultiABEL.Rd
===================================================================
--- pkg/MultiABEL/man/MultiABEL.Rd 2019-02-09 03:32:22 UTC (rev 2078)
+++ pkg/MultiABEL/man/MultiABEL.Rd 2019-02-09 03:33:00 UTC (rev 2079)
@@ -5,7 +5,6 @@
\alias{MultiABEL}
\alias{multiabel}
\alias{MultiABEL-package}
-\alias{MultiABEL-package}
\title{Multivariate GWAS in R}
\description{
MultiABEL: Multivariate Genome-Wide Association Analyses
Modified: pkg/MultiABEL/man/MultiLoad.Rd
===================================================================
--- pkg/MultiABEL/man/MultiLoad.Rd 2019-02-09 03:32:22 UTC (rev 2078)
+++ pkg/MultiABEL/man/MultiLoad.Rd 2019-02-09 03:33:00 UTC (rev 2079)
@@ -6,9 +6,9 @@
\alias{multiload}
\title{Load individual-level data for multivariate GWA analysis}
\usage{
-MultiLoad(gwaa.data = NULL, phenofile = NULL, genofile = NULL, trait.cols,
- covariate.cols = NULL, cuts = 20, impute = TRUE, gaussianize = TRUE,
- ...)
+MultiLoad(gwaa.data = NULL, phenofile = NULL, genofile = NULL,
+ trait.cols, covariate.cols = NULL, cuts = 20, impute = TRUE,
+ gaussianize = TRUE, ...)
}
\arguments{
\item{gwaa.data}{An (optional) object of \code{{gwaa.data-class}}.}
Modified: pkg/MultiABEL/man/MultiRep.Rd
===================================================================
--- pkg/MultiABEL/man/MultiRep.Rd 2019-02-09 03:32:22 UTC (rev 2078)
+++ pkg/MultiABEL/man/MultiRep.Rd 2019-02-09 03:33:00 UTC (rev 2079)
@@ -76,9 +76,12 @@
}
}
\references{
-Xia Shen, ..., Gordan Lauc, Jim Wilson, Yurii Aulchenko (2014).
-Multi-omic-variate analysis identified the association between 14q32.33 and
-compound N-Glycosylation of human Immunoglobulin G \emph{Submitted}.
+Shen X, Klaric L, Sharapov S, Mangino M, Ning Z, Wu D,
+Trbojevic-Akmacic I, Pucic-Bakovic M, Rudan I, Polasek O,
+Hayward C, Spector TD, Wilson JF, Lauc G, Aulchenko YS (2017):
+Multivariate discovery and replication of five novel loci
+associated with Immunoglobulin G N-glycosylation.
+\emph{Nature Communications}, 8, 447; doi: 10.1038/s41467-017-00453-3.
}
\seealso{
\code{\link{Multivariate}}
Modified: pkg/MultiABEL/man/MultiSummary.Rd
===================================================================
--- pkg/MultiABEL/man/MultiSummary.Rd 2019-02-09 03:32:22 UTC (rev 2078)
+++ pkg/MultiABEL/man/MultiSummary.Rd 2019-02-09 03:33:00 UTC (rev 2079)
@@ -6,7 +6,8 @@
\alias{multi.summary}
\title{Multivariate genome-wide association scan using summary statistics}
\usage{
-MultiSummary(x, index = NULL, type = "direct", vars = NULL)
+MultiSummary(x, index = NULL, type = "direct", vars = NULL,
+ high.dim = FALSE)
}
\arguments{
\item{x}{A data object of class \code{multi.summary} loaded by the function \code{load.summary}.}
@@ -23,11 +24,15 @@
\item{vars}{A numeric vector gives the variance of the genotypes at each SNP, e.g. coded as 0, 1 and 2.
Only used when \code{type = "precise"}.}
+
+\item{high.dim}{Are the phenotypes high-dimensional or not? This is particularly important when the ratio
+of the number of individuals (n) to the number of phenotypes being analyzed (p) is not big enough, e.g when
+analyzing a big number of omics phenotypes in a small cohort. Default = \code{FALSE}.}
}
\value{
The function returns a data frame containing the multi-trait GWAS results, where the row names are
the variants names. The column names are: variant name (\code{Marker}), allele frequency (\code{Freq}),
-the smallest sample size of the traits (\code{N}), effect on the phenotype score (\code{Beta.S}, see reference),
+the effective sample size of the multiple traits (\code{N}), effect on the phenotype score (\code{Beta.S}, see reference),
standard error (\code{SE}), p-value (\code{P}), and the rest the coefficients to construct the phenotype score
(see reference).
}
@@ -59,9 +64,11 @@
}
}
\references{
-Xia Shen, Zheng Ning, Yakov Tsepilov, Peter K. Joshi,
-James F. Wilson, Yudi Pawitan, Chris S. Haley, Yurii S. Aulchenko (2016).
-Fast pleiotropic meta-analysis for genetic studies. \emph{Submitted}.
+Zheng Ning, Yakov Tsepilov, Peter K. Joshi,
+James F. Wilson, Yudi Pawitan, Chris S. Haley,
+Yurii S. Aulchenko, Xia Shen (2018).
+Pleiotropic meta-analysis for genomic studies: discovery, replication,
+and interpretation. \emph{Submitted}.
}
\seealso{
\code{load.summary}
Modified: pkg/MultiABEL/man/Multivariate.Rd
===================================================================
--- pkg/MultiABEL/man/Multivariate.Rd 2019-02-09 03:32:22 UTC (rev 2078)
+++ pkg/MultiABEL/man/Multivariate.Rd 2019-02-09 03:33:00 UTC (rev 2079)
@@ -48,9 +48,12 @@
}
\references{
-Xia Shen, ..., Jim Wilson, Gordan Lauc, Yurii Aulchenko (2015).
-Multi-omic-variate analysis identified novel loci associated with
-compound N-Glycosylation of human Immunoglobulin G. \emph{Submitted}.
+Shen X, Klaric L, Sharapov S, Mangino M, Ning Z, Wu D,
+Trbojevic-Akmacic I, Pucic-Bakovic M, Rudan I, Polasek O,
+Hayward C, Spector TD, Wilson JF, Lauc G, Aulchenko YS (2017):
+Multivariate discovery and replication of five novel loci
+associated with Immunoglobulin G N-glycosylation.
+\emph{Nature Communications}, 8, 447; doi: 10.1038/s41467-017-00453-3.
}
\seealso{
\code{\link{MultiLoad}}
Modified: pkg/MultiABEL/man/load.summary.Rd
===================================================================
--- pkg/MultiABEL/man/load.summary.Rd 2019-02-09 03:32:22 UTC (rev 2078)
+++ pkg/MultiABEL/man/load.summary.Rd 2019-02-09 03:33:00 UTC (rev 2079)
@@ -4,9 +4,9 @@
\alias{load.summary}
\title{Loading multiple summary statistics from genome-wide association studies}
\usage{
-load.summary(files, cor.pheno = NULL, indep.snps = NULL, est.var = FALSE,
- columnNames = c("snp", "a1", "a2", "freq", "beta", "se", "n"),
- fixedN = NULL)
+load.summary(files, cor.pheno = NULL, indep.snps = NULL,
+ est.var = FALSE, columnNames = c("snp", "a1", "a2", "freq", "beta",
+ "se", "n"), fixedN = NULL, data.table = TRUE)
}
\arguments{
\item{files}{A vector of file names as strings. Each file name should contain summary statistics of
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