R/liftover_grlist.R

In serachoi1230/EpiCompare: Comparison, Benchmarking & QC of Epigenomic Datasets

#' Liftover peak list
#' 
#' Perform genome build liftover to one or more
#'  \link[GenomicRanges]{GRanges} objects at once.
#' @param grlist A named list of \link[GenomicRanges]{GRanges} objects,
#'  or simply a single unlisted \link[GenomicRanges]{GRanges} object.
#'  Can perform liftover within species or across species.
#' @param input_build The genome build of \code{grlist}.
#' @param output_build Desired genome build for
#'  \code{grlist} to be lifted over to.
#' @param as_grangeslist Return as a \link[GenomicRanges]{GRangesList}. 
#' @param merge_all Merge all \link[GenomicRanges]{GRanges} into a single
#'  \link[GenomicRanges]{GRanges} object.
#' @param style Chromosome style,
#'  set by \link[GenomeInfoDb]{seqlevelsStyle}.
#'  \itemize{
#'  \item{"UCSC" : }{Uses the chromosome style "chr1".}
#'  \item{"NCBI" : }{Uses the chromosome style "1"}
#'  }
#' @param verbose Print messages.
#' @inheritParams remove_nonstandard_chrom
#' 
#' @returns Named list of lifted \link[GenomicRanges]{GRanges} objects.
#' @export
#' @importFrom AnnotationHub AnnotationHub
#' @importFrom rtracklayer liftOver
#' @importFrom GenomicRanges GRangesList
#' @examples 
#' grlist <- list("gr1"=GenomicRanges::GRanges("4:1-100000"),
#'                "gr2"=GenomicRanges::GRanges("6:1-100000"),
#'                "gr3"=GenomicRanges::GRanges("8:1-100000"))
#'
#' grlist_lifted <- liftover_grlist(grlist = grlist,
#'                                  input_build = "hg19",
#'                                  output_build="hg38")
liftover_grlist <- function(grlist,
                            input_build,
                            output_build="hg19",
                            style="UCSC",
                            keep_chr = paste0(
                                "chr",c(seq_len(22),"X","Y")
                            ),
                            as_grangeslist=FALSE,
                            merge_all=FALSE,
                            verbose=TRUE){ 
    
    input_build <- translate_genome(genome = input_build, 
                                    style = "UCSC")
    output_build <- translate_genome(genome = output_build, 
                                     style = "UCSC")
    #### No liftover necessary ####
    if(input_build==output_build){
        messager("grlist is already in the output_build format.",
                 "Skipping liftover.",v=verbose)
      if(isTRUE(as_grangeslist)){
        messager("Converting to GRangesList.",v=verbose)
        grlist <- GenomicRanges::GRangesList(grlist,
                                             compress = FALSE) 
      }
        return(grlist)
    } 
    #### Check if it's a single element ####
    tmp_list <- FALSE
    if(is_granges(grlist)){
        grlist <- list(gr1=grlist)
        tmp_list <- TRUE
    }
    #### Chain files ####
    grlist_chain <- get_chain_file(grlist = grlist,
                                   input_build = input_build, 
                                   output_build = output_build, 
                                   verbose = verbose)
    grlist <- grlist_chain$grlist
    chain <- grlist_chain$chain
    #### Liftover iteratively ####
    grlist_lifted <- mapply(grlist, FUN = function(gr){
        gr <- clean_granges(gr = gr)
        suppressMessages(suppressWarnings(
            GenomeInfoDb::seqlevelsStyle(gr) <- "UCSC"
        ))
        gr2 <- rtracklayer::liftOver(x = gr, 
                                     chain = chain) 
        suppressMessages(suppressWarnings(
            GenomeInfoDb::seqlevelsStyle(gr) <- style
        ))
        return(unlist(gr2))
    })    
    #### Clean up chroms ####
    grlist_lifted <- remove_nonstandard_chrom(grlist = grlist_lifted, 
                                              keep_chr = keep_chr,
                                              verbose = verbose)
    #### Merge list into one ####
    if(isTRUE(merge_all)) as_grangeslist <- TRUE
    if(isTRUE(as_grangeslist)){
        messager("Converting to GRangesList.",v=verbose)
        grlist_lifted <- GenomicRanges::GRangesList(grlist_lifted, 
                                                    compress = FALSE) 
    }
    if(isTRUE(merge_all)){
        messager("Merging all GRanges into one.",v=verbose)
        grlist_lifted <- unlist(grlist_lifted)
    }
    if(isTRUE(tmp_list)) grlist_lifted <- grlist_lifted[[1]]
    return(grlist_lifted)
}