Error checks and plotting speedups for dive_phe2mash function
This commit is contained in:
@@ -20,7 +20,8 @@ dive_phe2mash(
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scale.phe = TRUE,
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roll.size = 50,
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U.ed = NA,
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U.hyp = NA
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U.hyp = NA,
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verbose = TRUE
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)
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}
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\arguments{
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@@ -73,6 +74,8 @@ generating these once and reusing them for multiple mash runs can save time.}
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\item{U.hyp}{Other covariance matrices for mash. Specify these as a list. These
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matrices must have dimensions that match the number of phenotypes where
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univariate GWAS ran successfully.}
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\item{verbose}{Output some information on the iterations? Default is \code{TRUE}.}
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}
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\value{
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A mash object made up of all phenotypes where univariate GWAS ran
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29
man/expand_cov.Rd
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29
man/expand_cov.Rd
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@@ -0,0 +1,29 @@
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% Generated by roxygen2: do not edit by hand
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% Please edit documentation in R/mash-evaluation.R
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\name{expand_cov}
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\alias{expand_cov}
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\title{Create expanded list of covariance matrices expanded by
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grid, Sigma_{lk} = omega_l U_k}
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\usage{
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expand_cov(Ulist, grid, usepointmass = TRUE)
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}
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\arguments{
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\item{Ulist}{a list of covarance matrices}
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\item{grid}{a grid of scalar values by which the covariance
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matrices are to be sc}
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\item{usepointmass}{if TRUE adds a point mass at 0 (null component)
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to the list}
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}
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\value{
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This takes the covariance matrices in Ulist and multiplies
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them by the grid values If usepointmass is TRUE then it adds a null
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component.
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}
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\description{
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This is an internal (non-exported) function. This help
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page provides additional documentation mainly intended for
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developers and expert users.
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}
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\keyword{internal}
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39
man/get_GxE.Rd
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39
man/get_GxE.Rd
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@@ -0,0 +1,39 @@
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% Generated by roxygen2: do not edit by hand
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% Please edit documentation in R/mash-evaluation.R
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\name{get_GxE}
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\alias{get_GxE}
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\title{Get data frames of types of GxE from a mash object}
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\usage{
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get_GxE(m, factor = 0.4, thresh = 0.05)
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}
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\arguments{
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\item{m}{An object of type mash}
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\item{factor}{a number between 0 and 1. The factor within which effects are
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considered to be shared.}
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\item{thresh}{Numeric. The threshold for including an effect in the assessment}
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}
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\value{
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A list containing eight data frames. Those with names that start
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"S_" contain significant effects of different types between pairs of
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named rows and columns. S_all_pairwise contains all significant effects;
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NS_pairwise contains all non-significant effects. S_CN contains effects
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significant in only one condition, and effects with a significantly
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different magnitude (differential sensitivity). This dataframe is not
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conservative using the local false sign rate test - we can't determine
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the sign of one of the effects for effects significant in only one
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condition - so it's not recommended to use this, but included. S_2_no
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contains effects significant in both conditions that do not differ
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significantly in magnitude. These effects do not have GxE. S_AP contains
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effects significant in both conditions that differ in their sign - and
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have antagonistic pleiotropy. S_DS contains effects significant in both
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conditions that differ in the magnitude of their effect, but not their
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sign - differentially sensitive alleles. S_1_row and S_1_col contain
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effects that are significant in just one of the two conditions - the row
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or the column, respectively.
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}
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\description{
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Performs set operations to determine pairwise GxE for effects
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from a mash object.
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}
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18
man/get_U_by_mass.Rd
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18
man/get_U_by_mass.Rd
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% Generated by roxygen2: do not edit by hand
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% Please edit documentation in R/mash-evaluation.R
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\name{get_U_by_mass}
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\alias{get_U_by_mass}
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\title{Get the positions of objects in a mash object Ulist that are above
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some mass threshold.}
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\usage{
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get_U_by_mass(m, thresh = 0.05)
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}
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\arguments{
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\item{m}{An object of type mash}
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\item{thresh}{Numeric. The mass threshold for including a covariance matrix}
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}
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\description{
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Get the positions of objects in a mash object Ulist that are
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above some mass threshold.
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}
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@@ -2,8 +2,7 @@
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% Please edit documentation in R/wrapper.R
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\name{get_best_PC_df}
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\alias{get_best_PC_df}
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\title{Return best number of PCs in terms of lambda_GC for Panicum virgatum.
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Return best number of PCs in terms of lambda_GC for the CDBN.}
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\title{Return best number of PCs in terms of lambda_GC}
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\usage{
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get_best_PC_df(df)
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}
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@@ -16,7 +15,7 @@ A dataframe containing the best lambda_GC value and number of PCs
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for each phenotype in the data frame.
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}
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\description{
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Given a dataframe created using pvdiv_lambda_GC, this function
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Given a dataframe created using div_lambda_GC, this function
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returns the first lambda_GC less than 1.05, or the smallest lambda_GC,
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for each column in the dataframe.
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}
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24
man/get_colnames.Rd
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24
man/get_colnames.Rd
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% Generated by roxygen2: do not edit by hand
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% Please edit documentation in R/mash-evaluation.R
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\name{get_colnames}
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\alias{get_colnames}
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\title{Get column names from a mash object}
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\usage{
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get_colnames(m)
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}
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\arguments{
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\item{m}{An object of type mash}
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}
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\value{
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A vector of phenotype names
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}
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\description{
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This function extracts the column names from the local false
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sign rate table of a mash object's results. This can tell you the condition
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names or phenotype names used in the mash object. That can be useful for
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looking at a subset of these columns, say.
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}
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\examples{
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\dontrun{get_colnames(m = mash_obj)}
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}
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17
man/get_date_filename.Rd
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17
man/get_date_filename.Rd
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% Generated by roxygen2: do not edit by hand
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% Please edit documentation in R/mash-evaluation.R
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\name{get_date_filename}
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\alias{get_date_filename}
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\title{Get current date-time in a filename-appropriate format.}
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\usage{
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get_date_filename()
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}
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\value{
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A string containing the current date-time with spaces and colons
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replaced with underscores and periods, respectively.
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}
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\description{
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Converts the current \code{Sys.time()} system time to a format
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that is acceptable to include in a filename. Changes punctuation that
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won't work in a filename.
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}
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38
man/get_estimated_pi.Rd
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38
man/get_estimated_pi.Rd
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% Generated by roxygen2: do not edit by hand
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% Please edit documentation in R/mash-evaluation.R
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\name{get_estimated_pi}
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\alias{get_estimated_pi}
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\title{Return the estimated mixture proportions. Use get_estimated_pi to
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extract the estimates of the mixture proportions for different types of
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covariance matrix. This tells you which covariance matrices have most of
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the mass.}
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\usage{
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get_estimated_pi(m, dimension = c("cov", "grid", "all"))
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}
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\arguments{
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\item{m}{the mash result}
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\item{dimension}{indicates whether you want the mixture proportions for the
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covariances, grid, or all}
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}
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\value{
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a named vector containing the estimated mixture proportions.
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}
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\description{
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Return the estimated mixture proportions. Use get_estimated_pi to
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extract the estimates of the mixture proportions for different types of
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covariance matrix. This tells you which covariance matrices have most of
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the mass.
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}
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\details{
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If the fit was done with \code{usepointmass=TRUE} then the first
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element of the returned vector will correspond to the null, and the
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remaining elements to the non-null covariance matrices. Suppose the fit
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was done with $K$ covariances and a grid of length $L$. If
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\code{dimension=cov} then the returned vector will be of length $K$
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(or $K+1$ if \code{usepointmass=TRUE}). If \code{dimension=grid} then
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the returned vector will be of length $L$ (or $L+1$). If
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\code{dimension=all} then the returned vector will be of length $LK$ (or
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$LK+1$). The names of the vector will be informative for which
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combination each element corresponds to.
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}
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21
man/get_log10bf.Rd
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21
man/get_log10bf.Rd
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% Generated by roxygen2: do not edit by hand
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% Please edit documentation in R/mash-evaluation.R
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\name{get_log10bf}
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\alias{get_log10bf}
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\title{Return the Bayes Factor for each effect}
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\usage{
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get_log10bf(m)
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}
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\arguments{
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\item{m}{the mash result (from joint or 1by1 analysis); must have been
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computed using usepointmass = TRUE}
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}
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\value{
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if m was fitted using usepointmass=TRUE then returns a vector of
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the log10(bf) values for each effect. That is, the jth element
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lbf_j is log10(Pr(Bj | g = ghat-nonnull)/Pr(Bj | g = 0)) where gha
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t-nonnull is the non-null part of ghat. Otherwise returns NULL.
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}
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\description{
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Return the Bayes Factor for each effect
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}
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18
man/get_marker_df.Rd
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18
man/get_marker_df.Rd
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% Generated by roxygen2: do not edit by hand
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% Please edit documentation in R/mash-evaluation.R
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\name{get_marker_df}
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\alias{get_marker_df}
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\title{Get mash marker_df}
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\usage{
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get_marker_df(m, snp)
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}
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\arguments{
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\item{m}{An object of type mash}
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\item{snp}{A bigSNP object, produced by the bigsnpr package. Here, the WAMI
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SNP information.}
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}
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\description{
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Pulls SNP markers information in the mash object from a bigsnp
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object.
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}
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28
man/get_n_significant_conditions.Rd
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28
man/get_n_significant_conditions.Rd
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% Generated by roxygen2: do not edit by hand
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% Please edit documentation in R/mash-evaluation.R
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\name{get_n_significant_conditions}
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\alias{get_n_significant_conditions}
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\title{Count number of conditions each effect is significant in}
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\usage{
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get_n_significant_conditions(
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m,
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thresh = 0.05,
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conditions = NULL,
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sig_fn = get_lfsr
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)
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}
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\arguments{
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\item{m}{the mash result (from joint or 1by1 analysis)}
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\item{thresh}{indicates the threshold below which to call signals significant}
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\item{conditions}{which conditions to include in check (default to all)}
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\item{sig_fn}{the significance function used to extract significance from mash object; eg could be ashr::get_lfsr or ashr::get_lfdr}
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}
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\value{
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a vector containing the number of significant conditions
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}
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\description{
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Count number of conditions each effect is significant in
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}
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14
man/get_ncond.Rd
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14
man/get_ncond.Rd
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% Generated by roxygen2: do not edit by hand
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% Please edit documentation in R/mash-evaluation.R
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\name{get_ncond}
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\alias{get_ncond}
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\title{Get number of conditions}
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\usage{
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get_ncond(m)
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}
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\arguments{
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\item{m}{The mash result}
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}
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\description{
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Get number of conditions
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}
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40
man/get_pairwise_sharing.Rd
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40
man/get_pairwise_sharing.Rd
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% Generated by roxygen2: do not edit by hand
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% Please edit documentation in R/mash-evaluation.R
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\name{get_pairwise_sharing}
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\alias{get_pairwise_sharing}
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\title{Compute the proportion of (significant) signals shared by magnitude in each pair of conditions, based on the poterior mean}
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\usage{
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get_pairwise_sharing(m, factor = 0.5, lfsr_thresh = 0.05, FUN = identity)
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}
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\arguments{
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\item{m}{the mash fit}
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\item{factor}{a number between 0 and 1 - the factor within which effects are
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considered to be shared.}
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\item{lfsr_thresh}{the lfsr threshold for including an effect in the
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assessment}
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\item{FUN}{a function to be applied to the estimated effect sizes before
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assessing sharing. The most obvious choice beside the default
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'FUN=identity' would be 'FUN=abs' if you want to ignore the sign of the
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effects when assesing sharing.}
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}
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\description{
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Compute the proportion of (significant) signals shared by magnitude in each pair of conditions, based on the poterior mean
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}
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\details{
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For each pair of tissues, first identify the effects that are
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significant (by lfsr<lfsr_thresh) in at least one of the two tissues.
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Then compute what fraction of these have an estimated (posterior mean)
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effect size within a factor \code{factor} of one another. The results are
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returned as an R by R matrix.
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}
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\examples{
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\dontrun{
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get_pairwise_sharing(m) # sharing by magnitude (same sign)
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get_pairwise_sharing(m, factor=0) # sharing by sign
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get_pairwise_sharing(m, FUN=abs) # sharing by magnitude when sign is ignored
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}
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}
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42
man/get_significant_results.Rd
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42
man/get_significant_results.Rd
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@@ -0,0 +1,42 @@
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% Generated by roxygen2: do not edit by hand
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% Please edit documentation in R/mash-evaluation.R
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\name{get_significant_results}
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\alias{get_significant_results}
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\title{From a mash result, get effects that are significant in at least
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one condition.}
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\usage{
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get_significant_results(
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m,
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thresh = 0.05,
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conditions = NULL,
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sig_fn = ashr::get_lfsr
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)
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get_significant_results(
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m,
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thresh = 0.05,
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conditions = NULL,
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sig_fn = ashr::get_lfsr
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)
|
||||
}
|
||||
\arguments{
|
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\item{m}{the mash result (from joint or 1by1 analysis)}
|
||||
|
||||
\item{thresh}{indicates the threshold below which to call signals significant}
|
||||
|
||||
\item{conditions}{which conditions to include in check (default to all)}
|
||||
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\item{sig_fn}{the significance function used to extract significance from mash object; eg could be ashr::get_lfsr or ashr::get_lfdr. (Small values must indicate significant.)}
|
||||
}
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\value{
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a vector containing the indices of the significant effects, by
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order of most significant to least
|
||||
|
||||
a vector containing the indices of the significant effects, by order of most significant to least
|
||||
}
|
||||
\description{
|
||||
From a mash result, get effects that are significant in at least
|
||||
one condition.
|
||||
|
||||
From a mash result, get effects that are significant in at least one condition
|
||||
}
|
||||
35
man/mash_plot_Ulist.Rd
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35
man/mash_plot_Ulist.Rd
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@@ -0,0 +1,35 @@
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||||
% Generated by roxygen2: do not edit by hand
|
||||
% Please edit documentation in R/mash-evaluation.R
|
||||
\name{mash_plot_Ulist}
|
||||
\alias{mash_plot_Ulist}
|
||||
\title{ggplot of specific covariance matrix patterns}
|
||||
\usage{
|
||||
mash_plot_Ulist(
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||||
m,
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||||
range = NA,
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||||
saveoutput = FALSE,
|
||||
suffix = "",
|
||||
limits = TRUE,
|
||||
labels = TRUE
|
||||
)
|
||||
}
|
||||
\arguments{
|
||||
\item{m}{An object of type mash}
|
||||
|
||||
\item{range}{Numeric vector. Which covariance matrices should be plotted?}
|
||||
|
||||
\item{saveoutput}{Logical. Should the output be saved to the path?}
|
||||
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||||
\item{suffix}{Character. Optional. A unique suffix used to save the files,
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||||
instead of the current date & time.}
|
||||
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||||
\item{limits}{should there be plot limits of -1 and 1? Default is true.}
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||||
}
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||||
\value{
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||||
A list of dataframes used to make the tile plots and the plots
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||||
themselves.
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||||
}
|
||||
\description{
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||||
Creates a tile plot using ggplot of the covariance matrices
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||||
specified in the mash model.
|
||||
}
|
||||
27
man/mash_plot_covar.Rd
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27
man/mash_plot_covar.Rd
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||||
% Generated by roxygen2: do not edit by hand
|
||||
% Please edit documentation in R/mash-evaluation.R
|
||||
\name{mash_plot_covar}
|
||||
\alias{mash_plot_covar}
|
||||
\title{ggplot of covariance matrix masses}
|
||||
\usage{
|
||||
mash_plot_covar(m, saveoutput = FALSE, suffix = "")
|
||||
}
|
||||
\arguments{
|
||||
\item{m}{An object of type mash}
|
||||
|
||||
\item{saveoutput}{Logical. Should the output be saved to the path?}
|
||||
|
||||
\item{suffix}{Character. Optional. A unique suffix used to save the files,
|
||||
instead of the current date & time.}
|
||||
}
|
||||
\description{
|
||||
Creates a bar plot using ggplot of the masses that are on each
|
||||
covariance matrix specified in the mash model.
|
||||
}
|
||||
\note{
|
||||
This plot can be useful for seeing the overall patterns of effects in
|
||||
the data used in mash. Non-significant effects will add mass to the
|
||||
"no_effects" covariance matrix, while significant effects will add mass
|
||||
to one of the other covariance matrices. You can use mash_plot_Ulist()
|
||||
to plot the covariance matrix patterns themselves.
|
||||
}
|
||||
47
man/mash_plot_manhattan_by_condition.Rd
Normal file
47
man/mash_plot_manhattan_by_condition.Rd
Normal file
@@ -0,0 +1,47 @@
|
||||
% Generated by roxygen2: do not edit by hand
|
||||
% Please edit documentation in R/mash-evaluation.R
|
||||
\name{mash_plot_manhattan_by_condition}
|
||||
\alias{mash_plot_manhattan_by_condition}
|
||||
\title{Manhattan plot in ggplot colored by significant conditions}
|
||||
\usage{
|
||||
mash_plot_manhattan_by_condition(
|
||||
m,
|
||||
snp,
|
||||
cond = NA,
|
||||
saveoutput = FALSE,
|
||||
suffix = "",
|
||||
thresh = 0.05
|
||||
)
|
||||
}
|
||||
\arguments{
|
||||
\item{m}{A mash object (outputted by mash).}
|
||||
|
||||
\item{snp}{A bigSNP object, produced by the bigsnpr package. Here,
|
||||
the WAMI SNP information.}
|
||||
|
||||
\item{cond}{A vector of phenotypes. Defaults to the names of each
|
||||
column in the mash object.}
|
||||
|
||||
\item{saveoutput}{Logical. Should the output be saved to the path?}
|
||||
|
||||
\item{suffix}{Character. Optional. A unique suffix used to save the files,
|
||||
instead of the current date & time.}
|
||||
|
||||
\item{thresh}{Numeric. The threshold used for the local false sign rate to
|
||||
call significance in a condition.}
|
||||
}
|
||||
\value{
|
||||
A \code{tbl_df()} of the data used to make the Manhattan plot, and a
|
||||
ggplot object containing the Manhattan.
|
||||
}
|
||||
\description{
|
||||
Takes a mash object and, for some vector of phenotypes, returns
|
||||
a Manhattan plot ggplot object (and its dataframe). Each SNP in the plot
|
||||
is colored by the number of phenotypes it is significant for. Even and
|
||||
odd chromosomes have different shapes for their SNPs, so that
|
||||
chromosome identity can be determined.
|
||||
}
|
||||
\examples{
|
||||
\dontrun{manhattan_out <- mash_ggman_by_condition(m = m, saveoutput = TRUE)}
|
||||
|
||||
}
|
||||
44
man/mash_plot_marker_effect.Rd
Normal file
44
man/mash_plot_marker_effect.Rd
Normal file
@@ -0,0 +1,44 @@
|
||||
% Generated by roxygen2: do not edit by hand
|
||||
% Please edit documentation in R/mash-evaluation.R
|
||||
\name{mash_plot_marker_effect}
|
||||
\alias{mash_plot_marker_effect}
|
||||
\title{ggplot of single mash effect}
|
||||
\usage{
|
||||
mash_plot_marker_effect(
|
||||
m,
|
||||
snp = snp,
|
||||
n = NA,
|
||||
i = NA,
|
||||
marker = TRUE,
|
||||
saveoutput = FALSE,
|
||||
suffix = ""
|
||||
)
|
||||
}
|
||||
\arguments{
|
||||
\item{m}{An object of type mash}
|
||||
|
||||
\item{snp}{A bigSNP object, produced by the bigsnpr package. Here,
|
||||
the WAMI SNP information.}
|
||||
|
||||
\item{n}{Optional. Integer or integer vector. The result number to plot, in
|
||||
order of significance. 1 would be the top result, for example. Find
|
||||
these with \code{\link{get_significant_results}}.}
|
||||
|
||||
\item{i}{Optional. Integer or integer vector. The result number to plot, in
|
||||
the order of the mash object. 1 would be the first marker in the mash
|
||||
object, for example. Find these with \code{\link{get_marker_df}}.}
|
||||
|
||||
\item{marker}{Optional. Print the marker name on the plot?}
|
||||
|
||||
\item{saveoutput}{Logical. Should the output be saved to the path?}
|
||||
|
||||
\item{suffix}{Character. Optional. A unique suffix used to save the files,
|
||||
instead of the current date & time.}
|
||||
}
|
||||
\description{
|
||||
Creates a plot with point estimates and standard errors for
|
||||
effects of a single SNP in multiple conditions.
|
||||
}
|
||||
\note{
|
||||
Specify only one of n or i.
|
||||
}
|
||||
45
man/mash_plot_pairwise_sharing.Rd
Normal file
45
man/mash_plot_pairwise_sharing.Rd
Normal file
@@ -0,0 +1,45 @@
|
||||
% Generated by roxygen2: do not edit by hand
|
||||
% Please edit documentation in R/mash-evaluation.R
|
||||
\name{mash_plot_pairwise_sharing}
|
||||
\alias{mash_plot_pairwise_sharing}
|
||||
\title{Create a ggplot of pairwise sharing of mash effects}
|
||||
\usage{
|
||||
mash_plot_pairwise_sharing(
|
||||
m = NULL,
|
||||
effectRDS = NULL,
|
||||
corrmatrix = NULL,
|
||||
reorder = TRUE,
|
||||
saveoutput = FALSE,
|
||||
filename = NA,
|
||||
suffix = "",
|
||||
...
|
||||
)
|
||||
}
|
||||
\arguments{
|
||||
\item{m}{An object of type mash}
|
||||
|
||||
\item{effectRDS}{An RDS containing a correlation matrix.}
|
||||
|
||||
\item{corrmatrix}{A correlation matrix}
|
||||
|
||||
\item{reorder}{Logical. Should the columns be reordered by similarity?}
|
||||
|
||||
\item{saveoutput}{Logical. Should the output be saved to the path?}
|
||||
|
||||
\item{filename}{Character string with an output filename. Optional.}
|
||||
|
||||
\item{suffix}{Character. Optional. A unique suffix used to save the files,
|
||||
instead of the current date & time.}
|
||||
|
||||
\item{...}{Other arguments to \code{\link{get_pairwise_sharing}} or
|
||||
\code{\link{ggcorr}}.}
|
||||
}
|
||||
\value{
|
||||
A list containing a dataframe containing the correlations and a
|
||||
ggplot2 object containing the correlation plot.
|
||||
}
|
||||
\description{
|
||||
Given a correlation matrix, an RDS with a correlation matrix, or
|
||||
a mash object, create a ggplot of pairwise sharing of mash effects using
|
||||
\code{\link{get_pairwise_sharing}} and \code{\link{ggcorr}}.
|
||||
}
|
||||
40
man/mash_plot_sig_by_condition.Rd
Normal file
40
man/mash_plot_sig_by_condition.Rd
Normal file
@@ -0,0 +1,40 @@
|
||||
% Generated by roxygen2: do not edit by hand
|
||||
% Please edit documentation in R/mash-evaluation.R
|
||||
\name{mash_plot_sig_by_condition}
|
||||
\alias{mash_plot_sig_by_condition}
|
||||
\title{Significant SNPs per number of conditions}
|
||||
\usage{
|
||||
mash_plot_sig_by_condition(
|
||||
m,
|
||||
conditions = NA,
|
||||
saveoutput = FALSE,
|
||||
suffix = "",
|
||||
thresh = 0.05
|
||||
)
|
||||
}
|
||||
\arguments{
|
||||
\item{m}{An object of type mash}
|
||||
|
||||
\item{conditions}{A vector of conditions. Get these with get_colnames(m).}
|
||||
|
||||
\item{saveoutput}{Logical. Save plot output to a file? Default is FALSE.}
|
||||
|
||||
\item{suffix}{Character. Optional. A unique suffix used to save the files,
|
||||
instead of the current date & time.}
|
||||
|
||||
\item{thresh}{What is the threshold to call an effect significant? Default
|
||||
is 0.05.}
|
||||
}
|
||||
\value{
|
||||
A list containing a dataframe of the number of SNPs significant per
|
||||
number of conditions, and a ggplot object using that dataframe.
|
||||
}
|
||||
\description{
|
||||
For some number of columns in a mash object that correspond to
|
||||
conditions, find the number of SNPs that are significant for that number
|
||||
of conditions.
|
||||
}
|
||||
\examples{
|
||||
\dontrun{mash_plot_sig_by_condition(m = mash_obj, saveoutput = TRUE)}
|
||||
|
||||
}
|
||||
11
man/printf2.Rd
Normal file
11
man/printf2.Rd
Normal file
@@ -0,0 +1,11 @@
|
||||
% Generated by roxygen2: do not edit by hand
|
||||
% Please edit documentation in R/wrapper.R
|
||||
\name{printf2}
|
||||
\alias{printf2}
|
||||
\title{Verbose?}
|
||||
\usage{
|
||||
printf2(verbose, ...)
|
||||
}
|
||||
\description{
|
||||
Verbose?
|
||||
}
|
||||
15
man/reorder_cormat.Rd
Normal file
15
man/reorder_cormat.Rd
Normal file
@@ -0,0 +1,15 @@
|
||||
% Generated by roxygen2: do not edit by hand
|
||||
% Please edit documentation in R/mash-evaluation.R
|
||||
\name{reorder_cormat}
|
||||
\alias{reorder_cormat}
|
||||
\title{Reorder correlation matrix}
|
||||
\usage{
|
||||
reorder_cormat(cormat)
|
||||
}
|
||||
\arguments{
|
||||
\item{cormat}{A correlation matrix}
|
||||
}
|
||||
\description{
|
||||
Reorder correlation coefficients from a matrix of things
|
||||
(including NA's) and hierarchically cluster them
|
||||
}
|
||||
23
man/scale_cov.Rd
Normal file
23
man/scale_cov.Rd
Normal file
@@ -0,0 +1,23 @@
|
||||
% Generated by roxygen2: do not edit by hand
|
||||
% Please edit documentation in R/mash-evaluation.R
|
||||
\name{scale_cov}
|
||||
\alias{scale_cov}
|
||||
\title{Scale each covariance matrix in list Ulist by a scalar in
|
||||
vector grid}
|
||||
\usage{
|
||||
scale_cov(Ulist, grid)
|
||||
}
|
||||
\arguments{
|
||||
\item{Ulist}{a list of matrices}
|
||||
|
||||
\item{grid}{a vector of scaling factors (standard deviaions)}
|
||||
}
|
||||
\value{
|
||||
a list with length length(Ulist)*length(grid)
|
||||
}
|
||||
\description{
|
||||
This is an internal (non-exported) function. This help
|
||||
page provides additional documentation mainly intended for
|
||||
developers and expert users.
|
||||
}
|
||||
\keyword{internal}
|
||||
Reference in New Issue
Block a user