#' Fit Cox survival to all variants in a .vcf.gz file from
#' Michigan imputation server
#'
#' Performs survival analysis using Cox proportional hazard models on imputed
#' genetic data stored in compressed VCF files
#'
#' @param vcf.file character(1) path to VCF file. This file needs to accompanied
#' with an index file (.csi file).
#' @param covariate.file matrix(1) comprising phenotype (time, event) and
#' additional covariate data.
#' @param id.column character(1) providing exact match to sample ID column
#' from \code{covariate.file}
#' @param time.to.event character(1) string that matches time column name
#' in pheno.file
#' @param event character(1) string that matches event column name in
#' pheno.file
#' @param covariates character vector with matching column names in
#' pheno.file of covariates of interest
#' @param inter.term character(1) string giving the column name of the
#' covariate that will be added to the interaction term with
#' SNP (e.g. \code{term*SNP}). See details.
#' @param print.covs character(1) string of either \code{"only"},
#' \code{"all"} or \code{"some"},
#' defining which covariate statistics should be printed to the output.
#' See details.
#' @param sample.ids character vector with sample ids to include in analysis
#' @param r2.filter integer(1) of imputation quality
#' score filter (i.e. 0.7 will filter r2 > 0.7)
#' @param maf.filter integer(1) filter out minor allele frequency below
#' threshold (i.e. 0.005 will filter MAF > 0.005)
#' @param chunk.size integer(1) number of variants to process per thread
#' @param out.file character(1) string with output name
#' @param verbose logical(1) for messages that describe which part of the
#' analysis is currently being run
#' @param clusterObj A cluster object that can be used with the
#' \code{parApply} function. See details.
#'
#' @details
#' Testing for SNP-covariate interactions:
#' User can define the column name of the covariate that will be included in
#' the interaction term.
#' For example, for given covariates \code{a} and \code{b}, where \code{c} is
#' defined as the \code{inter.term} the model will be:
#' \code{~ a + b + c + SNP + c*SNP}.
#'
#' Printing results of other covariates:
#' \code{print.covs} argument controls the number of covariates will be printed
#' as output. The function is set to \code{only} by default and will only print
#' the SNP or if an interaction term is given, the results of the interaction
#' term (e.g. \code{SNP*covariate}). Whereas, \code{all} will print results
#' (coef, se.coef, p.value etc) of all covariates included in the model.
#' \code{some} is only applicable if an interaction term is given and will
#' print the results for SNP, covariate tested for interaction
#' and the interaction term.
#' User should be mindful about using the \code{all} option, as it will likely
#' slow down the analysis and will increase the output file size.
#'
#' User defined parallelization:
#' This function uses \code{parApply} from \code{parallel} package to fit
#' models to SNPs in parallel.
#' User is not required to set any options for the parallelization.
#' However, advanced users who wish to optimize it, can provide a cluster
#' object generated by \code{makeCluster} family of functions that suits
#' their need and platform.
#
#' @return
#' Saves two text files directly to disk:
#' \code{.coxph} extension containing CoxPH survival analysis results.
#' \code{.snps_removed} extension containing SNPs that were removed
#' due to low variance or user-defined thresholds.
#'
#' @examples
#' vcf.file <- system.file(package="gwasurvivr",
#' "extdata",
#' "michigan.chr14.dose.vcf.gz")
#' pheno.fl <- system.file(package="gwasurvivr",
#' "extdata",
#' "simulated_pheno.txt")
#' pheno.file <- read.table(pheno.fl,
#' sep=" ",
#' header=TRUE,
#' stringsAsFactors = FALSE)
#' pheno.file$SexFemale <- ifelse(pheno.file$sex=="female", 1L, 0L)
#' sample.ids <- pheno.file[pheno.file$group=="experimental",]$ID_2
#' michiganCoxSurv(vcf.file=vcf.file,
#' covariate.file=pheno.file,
#' id.column="ID_2",
#' sample.ids=sample.ids,
#' time.to.event="time",
#' event="event",
#' covariates=c("age", "SexFemale", "DrugTxYes"),
#' inter.term=NULL,
#' print.covs="only",
#' out.file="michigan_example",
#' r2.filter=0.3,
#' maf.filter=0.005,
#' chunk.size=50,
#' verbose=TRUE,
#' clusterObj=NULL)
#'
#' @importFrom survival Surv coxph.fit
#' @importFrom utils write.table
#' @importFrom matrixStats rowMeans2
#' @importFrom SummarizedExperiment rowRanges
#' @importFrom stats pnorm complete.cases
#' @import parallel
#' @import VariantAnnotation
#'
#' @export
michiganCoxSurv <- function(vcf.file,
covariate.file,
id.column,
sample.ids=NULL,
time.to.event,
event,
covariates,
inter.term=NULL,
print.covs="only",
out.file,
maf.filter=0.05,
r2.filter=NULL,
chunk.size=5000,
verbose=TRUE,
clusterObj=NULL){
coxSurv(createMichiganCoxSurv(vcf.file = vcf.file,
covariate.file = covariate.file,
id.column = id.column,
sample.ids=sample.ids,
time.to.event = time.to.event,
event = event,
covariates = covariates,
inter.term=inter.term,
print.covs=print.covs,
out.file = out.file,
maf.filter=maf.filter,
r2.filter=r2.filter,
chunk.size=chunk.size,
verbose=verbose,
clusterObj=clusterObj))
}
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