biopipen 0.31.5__py3-none-any.whl → 0.31.7__py3-none-any.whl

biopipen/scripts/regulatory/motifBreakR.R

@@ -1,1594 +0,0 @@
-# Patch motifBreakR to avoid getSeq using the bsgenome but a reference fasta file instead
-# This keeps consistent with other non-R processes
-library(stringr)
-library(matrixStats)
-library(TFMPvalue)
-library(motifStack)
-library(Biostrings)
-library(GenomicRanges)
-library(MotifDb)
-
-snpInfo2snpList <- function(snpinfo) {
-    snpinfo$start <- snpinfo$start + 1
-    snpgr <- makeGRangesFromDataFrame(snpinfo)
-    snpgr_meta <- snpinfo[, c("name", "score", "ref", "alt", "ref_seq", "alt_seq")]
-    colnames(snpgr_meta) <- c("SNP_id", "score", "REF", "ALT", "ref_seq", "alt_seq")
-    snpgr_meta$ref_seq <- substring(snpgr_meta$ref_seq, 2)
-    snpgr_meta$alt_seq <- substring(snpgr_meta$alt_seq, 2)
-    elementMetadata(snpgr) <- snpgr_meta
-    snpgr
-}
-
-revcom <- function(ltr) {
-    rclist <- list(A = "T", C = "G", G = "C", T = "A")
-    rclist[[ltr]]
-}
-
-prepareVariants <- function(fsnplist) {
-    # The sequences are already fetched in fsnplist at $ref_seq and $alt_seq
-    ref_len <- nchar(fsnplist$REF)
-    alt_len <- nchar(fsnplist$ALT)
-    is.indel <- ref_len > 1L | alt_len > 1L
-    if (sum(is.indel) < length(is.indel) & sum(is.indel) > 0L) {
-        fsnplist.indel <- fsnplist[is.indel]
-        fsnplist.snv <- fsnplist[!is.indel]
-    } else if (sum(is.indel) == length(is.indel)) {
-        fsnplist.indel <- fsnplist
-        fsnplist.snv <- NULL
-    } else if (sum(is.indel) == 0L) {
-        fsnplist.indel <- NULL
-        fsnplist.snv <- fsnplist
-    }
-    if (!is.null(fsnplist.indel)) {
-        snp.sequence.ref.indel <- fsnplist$ref_seq
-        snp.sequence.alt.indel <- fsnplist$alt_seq
-
-        need.alignment <- !(lengths(fsnplist.indel$REF) == 1 | lengths(fsnplist.indel$ALT) == 1)
-        insertion.var <- lengths(fsnplist.indel$REF) < lengths(fsnplist.indel$ALT)
-        fsnplist.indel$ALT_loc <- 1L
-        fsnplist.indel[insertion.var]$ALT_loc <- Map(seq,
-            from = nchar(fsnplist.indel[insertion.var]$REF) + 1L,
-            to = nchar(fsnplist.indel[insertion.var]$ALT)
-        )
-        fsnplist.indel[!insertion.var]$ALT_loc <- Map(seq,
-            from = nchar(fsnplist.indel[!insertion.var]$ALT) + 1L,
-            to = nchar(fsnplist.indel[!insertion.var]$REF)
-        )
-        ref.len <- nchar(fsnplist.indel[nchar(fsnplist.indel$REF) == nchar(fsnplist.indel$ALT)]$REF)
-        fsnplist.indel[nchar(fsnplist.indel$REF) == nchar(fsnplist.indel$ALT)]$ALT_loc <- lapply(
-            ref.len,
-            function(x) {seq(from = 1L, to = x)}
-        )
-        fsnplist.indel$varType <- "Other"
-        if (sum(insertion.var) > 0) {
-            fsnplist.indel[insertion.var, ]$varType <- "Insertion"
-        }
-        if (sum(lengths(fsnplist.indel$REF) > lengths(fsnplist.indel$ALT)) > 0) {
-            fsnplist.indel[lengths(fsnplist.indel$REF) > lengths(fsnplist.indel$ALT)]$varType <- "Deletion"
-        }
-        if (any(need.alignment)) {
-            need.del <- any(!insertion.var & need.alignment)
-            need.ins <- any(insertion.var & need.alignment)
-            if (need.del) {
-                pattern.del <- Map(matchPattern,
-                    fsnplist.indel[!insertion.var & need.alignment]$ALT,
-                    fsnplist.indel[!insertion.var & need.alignment]$REF,
-                    with.indels = FALSE, max.mismatch = 0
-                )
-                names(pattern.del) <- names(fsnplist.indel[!insertion.var & need.alignment])
-                pattern.del <- sapply(pattern.del, function(x) {
-                    slen <- length(subject(x))
-                    x <- x[start(x) == 1 | end(x) == slen]
-                    if (length(x) > 0) {
-                        x <- x[1]
-                        x <- gaps(x)
-                        x <- as(x, "IRanges")
-                    }
-                })
-                pattern.del.valid <- sapply(pattern.del, function(x) {
-                    length(x) > 0
-                })
-                nr.pattern.del <- lapply(pattern.del[pattern.del.valid], function(x) {
-                    start(x):end(x)
-                })
-                fsnplist.indel[!insertion.var & need.alignment][names(pattern.del[pattern.del.valid])]$ALT_loc <- nr.pattern.del
-                if (any((!insertion.var & need.alignment)[!pattern.del.valid])) {
-                    alignment.del <- Map(pairwiseAlignment,
-                        fsnplist.indel[!insertion.var & need.alignment][!pattern.del.valid]$ALT,
-                        fsnplist.indel[!insertion.var & need.alignment][!pattern.del.valid]$REF,
-                        type = "global"
-                    )
-                    alt.width <- width(fsnplist.indel[!insertion.var & need.alignment][!pattern.del.valid]$ALT)
-                    ref.width <- width(fsnplist.indel[!insertion.var & need.alignment][!pattern.del.valid]$REF)
-                    names(alignment.del) <- names(fsnplist.indel[!insertion.var & need.alignment][!pattern.del.valid])
-                    alignment.ins <- sapply(sapply(alignment.del, insertion), unlist)
-                    alignment.del <- sapply(sapply(alignment.del, deletion), unlist)
-                    alignment.del.valid <- sapply(alignment.del, function(x) {
-                        length(x) > 0
-                    })
-                    alignment.ins.valid <- sapply(alignment.ins, function(x) {
-                        length(x) > 0
-                    })
-                    full.replace <- (alignment.del.valid & alignment.ins.valid & alt.width == ref.width)
-                    alignment.del.valid <- alignment.del.valid & !full.replace
-                    nr.alignment.del <- lapply(alignment.del[alignment.del.valid], function(x) {
-                        start(x):end(x)
-                    })
-                    fsnplist.indel[!insertion.var & need.alignment][names(alignment.del[alignment.del.valid])]$ALT_loc <- nr.alignment.del
-                    rm(alignment.del, nr.alignment.del)
-                }
-                rm(pattern.del, nr.pattern.del, pattern.del.valid, need.del)
-            }
-            if (need.ins) {
-                pattern.ins <- Map(matchPattern,
-                    fsnplist.indel[insertion.var & need.alignment]$REF,
-                    fsnplist.indel[insertion.var & need.alignment]$ALT,
-                    with.indels = FALSE, max.mismatch = 0
-                )
-                names(pattern.ins) <- names(fsnplist.indel[insertion.var & need.alignment])
-                pattern.ins <- sapply(pattern.ins, function(x) {
-                    slen <- length(subject(x))
-                    x <- x[start(x) == 1 | end(x) == slen]
-                    if (length(x) > 0) {
-                        x <- x[1]
-                        x <- gaps(x)
-                        x <- as(x, "IRanges")
-                    }
-                })
-                pattern.ins.valid <- sapply(pattern.ins, function(x) {
-                    length(x) > 0
-                })
-                nr.pattern.ins <- lapply(pattern.ins[pattern.ins.valid], function(x) {
-                    start(x):end(x)
-                })
-                fsnplist.indel[insertion.var & need.alignment][names(pattern.ins[pattern.ins.valid])]$ALT_loc <- nr.pattern.ins
-                if (any((insertion.var & need.alignment)[!pattern.ins.valid])) {
-                    alignment.ins <- Map(pairwiseAlignment,
-                        fsnplist.indel[insertion.var & need.alignment][!pattern.ins.valid]$ALT,
-                        fsnplist.indel[insertion.var & need.alignment][!pattern.ins.valid]$REF,
-                        type = "global"
-                    )
-                    names(alignment.ins) <- names(fsnplist.indel[insertion.var & need.alignment][!pattern.ins.valid])
-                    alignment.ins <- sapply(sapply(alignment.ins, insertion), unlist)
-                    alignment.ins.valid <- sapply(alignment.ins, function(x) {
-                        length(x) > 0
-                    })
-                    nr.alignment.ins <- lapply(alignment.ins[alignment.ins.valid], function(x) {
-                        start(x):end(x)
-                    })
-                    fsnplist.indel[insertion.var & need.alignment][names(alignment.ins[alignment.ins.valid])]$ALT_loc <- nr.alignment.ins
-                    rm(alignment.ins, nr.alignment.ins)
-                }
-                rm(pattern.ins, nr.pattern.ins, pattern.ins.valid, need.ins)
-            }
-            rm(ref.len, insertion.var, need.alignment)
-        }
-    }
-    if (!is.null(fsnplist.snv)) {
-        snp.sequence.ref.snv <- fsnplist$ref_seq
-        snp.sequence.alt.snv <- fsnplist$alt_seq
-        fsnplist.snv$ALT_loc <- 1L
-        fsnplist.snv$varType <- "SNV"
-    }
-    if (sum(is.indel) < length(is.indel) & sum(is.indel) > 0L) {
-        fsnplist <- c(fsnplist.indel, fsnplist.snv)
-        snp.sequence.alt <- strsplit(as.character(c(
-            snp.sequence.alt.indel,
-            snp.sequence.alt.snv
-        )), "")
-        snp.sequence.ref <- strsplit(as.character(c(
-            snp.sequence.ref.indel,
-            snp.sequence.ref.snv
-        )), "")
-        rm(
-            fsnplist.indel, fsnplist.snv,
-            snp.sequence.alt.indel, snp.sequence.ref.indel,
-            snp.sequence.alt.snv, snp.sequence.ref.snv
-        )
-    } else if (sum(is.indel) == length(is.indel)) {
-        fsnplist <- fsnplist.indel
-        snp.sequence.alt <- strsplit(as.character(snp.sequence.alt.indel), "")
-        snp.sequence.ref <- strsplit(as.character(snp.sequence.ref.indel), "")
-        rm(fsnplist.indel, snp.sequence.alt.indel, snp.sequence.ref.indel)
-    } else if (sum(is.indel) == 0L) {
-        fsnplist <- fsnplist.snv
-        snp.sequence.alt <- strsplit(as.character(snp.sequence.alt.snv), "")
-        snp.sequence.ref <- strsplit(as.character(snp.sequence.ref.snv), "")
-        rm(fsnplist.snv, snp.sequence.alt.snv, snp.sequence.ref.snv)
-    }
-    gc()
-    return(list(
-        fsnplist = fsnplist,
-        ref_seq = snp.sequence.ref,
-        alt_seq = snp.sequence.alt
-    ))
-}
-
-## An evaluator function for SNP effect
-
-varEff <- function(allelR, allelA) {
-    score <- allelA - allelR
-    if (abs(score) >= 0.7) {
-        return(list(score = score, effect = "strong"))
-    } else if (abs(score) > 0.4) {
-        return(list(score = score, effect = "weak"))
-    } else {
-        return(list(score = score, effect = "neut"))
-    }
-}
-
-scoreIndel <- function(pwm,
-                       ref.seq, alt.seq,
-                       hit.ref, hit.alt) {
-    ref.windows <- scoreSeqWindows(ppm = pwm, seq = ref.seq)
-    alt.windows <- scoreSeqWindows(ppm = pwm, seq = alt.seq)
-    score <- alt.windows[hit.alt$strand, hit.alt$window] - ref.windows[hit.ref$strand, hit.ref$window]
-    if (abs(score) >= 0.7) {
-        return(list(score = score, effect = "strong"))
-    } else if (abs(score) > 0.4) {
-        return(list(score = score, effect = "weak"))
-    } else {
-        return(list(score = score, effect = "neut"))
-    }
-}
-
-reverseComplementMotif <- function(pwm) {
-    rows <- rownames(pwm)
-    cols <- colnames(pwm)
-    Ns <- pwm["N", ]
-    pwm <- pwm[4:1, length(cols):1]
-    pwm <- rbind(pwm, Ns)
-    rownames(pwm) <- rows
-    colnames(pwm) <- cols
-    return(pwm)
-}
-
-
-scoreSeqWindows <- function(ppm, seq) {
-    ppm.width <- ncol(ppm)
-    seq.len <- length(seq)
-    diag.ind <- rep.int(ppm.width, seq.len - ppm.width)
-    ranges <- vapply(
-        c(0L, cumsum(diag.ind)),
-        function(x,
-                 range = (1L + 0L:(ppm.width - 1L) * (ppm.width + 1L))) {
-            x + range
-        },
-        integer(ppm.width)
-    )
-    scores <- t(ppm[seq, ])[ranges]
-    scores_rc <- t(reverseComplementMotif(ppm)[seq, ])[ranges]
-    scores <- split(scores, ceiling(seq_along(scores) / ppm.width))
-    scores_rc <- split(scores_rc, ceiling(seq_along(scores_rc) / ppm.width))
-    res <- vapply(
-        Map(
-            function(x, y) {
-                matrix(
-                    data = c(x, y), nrow = 2,
-                    byrow = TRUE, dimnames = list(c(1, 2))
-                )
-            },
-            scores, scores_rc
-        ),
-        rowSums,
-        numeric(2)
-    )
-    return(res)
-}
-
-maxThresholdWindows <- function(window.frame) {
-    start.ind <- as.integer(colnames(window.frame)[1]) - 1L
-    max.win <- arrayInd(which.max(window.frame), dim(window.frame))
-    return(list(
-        window = as.integer(colnames(window.frame)[max.win[, 2] + start.ind]),
-        strand = c(1, 2)[max.win[, 1]]
-    ))
-}
-
-
-#' @import methods
-#' @import GenomicRanges
-#' @import S4Vectors
-#' @import BiocGenerics
-#' @import IRanges
-#' @importFrom Biostrings getSeq replaceLetterAt reverseComplement complement replaceAt pairwiseAlignment insertion deletion matchPattern
-#' @importFrom TFMPvalue TFMpv2sc
-#' @importFrom stringr str_locate_all str_sub
-scoreSnpList <- function(fsnplist, pwmList, method = "default", bkg = NULL,
-                         threshold = 1e-3, show.neutral = FALSE, verbose = FALSE,
-                         pwmList.pc = NULL, pwmRanges = NULL, filterp = TRUE) {
-    k <- max(sapply(pwmList, ncol))
-    snp.sequence.alt <- fsnplist$alt_seq
-    snp.sequence.ref <- fsnplist$ref_seq
-    fsnplist <- fsnplist$fsnplist
-
-    res.el.e <- new.env()
-    for (snp.map.i in seq_along(snp.sequence.alt)) {
-        snp.ref <- snp.sequence.ref[[snp.map.i]]
-        snp.alt <- snp.sequence.alt[[snp.map.i]]
-        ref.len <- nchar(fsnplist[snp.map.i]$REF)
-        alt.len <- nchar(fsnplist[snp.map.i]$ALT)
-        alt.loc <- fsnplist[snp.map.i]$ALT_loc[[1]]
-        res.el <- rep(fsnplist[snp.map.i], length(pwmList))
-        res.el$motifPos <- as.integer(NA)
-        res.el$motifID <- mcols(pwmList)$providerID
-        res.el$geneSymbol <- mcols(pwmList)$geneSymbol
-        res.el$dataSource <- mcols(pwmList)$dataSource
-        res.el$providerName <- mcols(pwmList)$providerName
-        res.el$providerId <- mcols(pwmList)$providerId
-        res.el$seqMatch <- as.character(NA)
-        res.el$pctRef <- as.numeric(NA)
-        res.el$pctAlt <- as.numeric(NA)
-        res.el$scoreRef <- as.numeric(NA)
-        res.el$scoreAlt <- as.numeric(NA)
-        if (filterp) {
-            res.el$Refpvalue <- as.numeric(NA)
-            res.el$Altpvalue <- as.numeric(NA)
-        }
-        if (ref.len > 1 | alt.len > 1) {
-            res.el$altPos <- as.numeric(NA)
-            res.el$alleleDiff <- as.numeric(NA)
-            res.el$alleleEffectSize <- as.numeric(NA)
-        } else {
-            res.el$snpPos <- as.integer(NA)
-            res.el$alleleRef <- as.numeric(NA)
-            res.el$alleleAlt <- as.numeric(NA)
-        }
-        res.el$effect <- as.character(NA)
-        for (pwm.i in seq_along(pwmList)) {
-            pwm.basic <- pwmList[[pwm.i]]
-            pwm <- pwmList.pc[[pwm.i]]
-            len <- ncol(pwm)
-            thresh <- threshold[[pwm.i]]
-            seq.start <- min(alt.loc)
-            seq.len <- length(alt.loc)
-            alt.range <- ref.range <- (k - (ncol(pwm) - seq.start)):(k + ncol(pwm) + seq.start + seq.len - 2)
-            if (!show.neutral & identical(snp.ref[ref.range], snp.alt[alt.range])) next()
-            seq.remove <- ref.len - alt.len
-            if (seq.remove < 0) {
-                ref.range <- ref.range[1:(length(ref.range) + seq.remove)]
-            } else {
-                alt.range <- alt.range[1:(length(alt.range) - seq.remove)]
-            }
-            ref.windows <- scoreSeqWindows(ppm = pwm, seq = snp.ref[ref.range])
-            alt.windows <- scoreSeqWindows(ppm = pwm, seq = snp.alt[alt.range])
-            pass.effect <- ifelse(filterp,
-                any(alt.windows > thresh) | any(ref.windows > thresh),
-                any(((alt.windows - pwmRanges[[pwm.i]][1]) / (pwmRanges[[pwm.i]][2] - pwmRanges[[pwm.i]][1]) > thresh)) |
-                    any((ref.windows - pwmRanges[[pwm.i]][1]) / (pwmRanges[[pwm.i]][2] - pwmRanges[[pwm.i]][1]) > thresh)
-            )
-            if (pass.effect) {
-                hit.alt <- maxThresholdWindows(alt.windows)
-                hit.ref <- maxThresholdWindows(ref.windows)
-                bigger <- ref.windows[hit.ref$strand, hit.ref$window] >= alt.windows[hit.alt$strand, hit.alt$window]
-                if (bigger) {
-                    hit <- hit.ref
-                } else {
-                    hit <- hit.alt
-                }
-            } else {
-                hit.alt <- list(window = 0L, strand = 0L)
-                hit.ref <- list(window = 0L, strand = 0L)
-                hit <- NULL
-            }
-            if (!show.neutral) {
-                if (identical(
-                    alt.windows[hit.alt$strand, hit.alt$window],
-                    ref.windows[hit.ref$strand, hit.ref$window]
-                )) {
-                    next()
-                }
-            }
-            if (!is.null(hit)) {
-                result <- res.el[pwm.i]
-                uniquename <- paste(names(result), result$dataSource, result$providerName, result$providerId, sep = "%%")
-                if (nchar(result$REF) > 1 | nchar(result$ALT) > 1) {
-                    allelR <- ref.windows[hit.ref$strand, hit.ref$window]
-                    allelA <- alt.windows[hit.alt$strand, hit.alt$window]
-                    scorediff <- varEff(allelR, allelA)
-                    effect <- scorediff$effect
-                    score <- scorediff$score
-                    # ref.pos <- ref.range[(ncol(pwm) - (seq.start - 1)):((ncol(pwm) + ref.len - seq.start))]
-                    ref.pos <- k:(k + nchar(result$REF) - 1L)
-                    # alt.pos <- alt.range[(ncol(pwm) - (seq.start - 1)):((ncol(pwm) + alt.len - seq.start))]
-                    alt.pos <- k:(k + nchar(result$ALT) - 1L)
-                    if ((effect == "neut" & show.neutral) | effect != "neut") {
-                        res.el.e[[uniquename]] <- updateResultsIndel(result,
-                            snp.ref, snp.alt,
-                            ref.pos, alt.pos,
-                            hit.ref, hit.alt,
-                            ref.windows, alt.windows,
-                            score, effect, len,
-                            k, pwm,
-                            calcp = filterp
-                        )
-                    }
-                } else {
-                    snp.pos <- k:(k + nchar(result$REF) - 1L)
-                    allelR <- ref.windows[hit.ref$strand, hit.ref$window]
-                    allelA <- alt.windows[hit.alt$strand, hit.alt$window]
-                    scorediff <- varEff(allelR, allelA)
-                    effect <- scorediff$effect
-                    score <- scorediff$score
-                    if ((effect == "neut" & show.neutral) | effect != "neut") {
-                        res.el.e[[uniquename]] <- updateResultsIndel(result,
-                            snp.ref, snp.alt,
-                            snp.pos, snp.pos,
-                            hit.ref, hit.alt,
-                            ref.windows, alt.windows,
-                            score, effect, len,
-                            k, pwm,
-                            calcp = filterp
-                        )
-                    }
-                }
-            }
-        }
-    }
-    resultSet <- unlist(GRangesList(as.list.environment(res.el.e)), use.names = FALSE)
-    if (length(resultSet) < 1) {
-        if (verbose) {
-            message(paste(
-                "reached end of SNPs list length =", length(fsnplist),
-                "with 0 potentially disruptive matches to", length(unique(resultSet$geneSymbol)),
-                "of", length(pwmList), "motifs."
-            ))
-        }
-        return(NULL)
-    } else {
-        if ("ALT_loc" %in% names(mcols(resultSet))) mcols(resultSet)$ALT_loc <- NULL
-        max.match <- max(vapply(str_locate_all(resultSet$seqMatch, "\\w"), max, integer(1)))
-        min.match <- min(vapply(str_locate_all(resultSet$seqMatch, "\\w"), min, integer(1)))
-        resultSet$seqMatch <- str_sub(resultSet$seqMatch,
-            start = min.match + 1,
-            end = max.match + 1
-        )
-        if (verbose) {
-            message(paste(
-                "reached end of SNPs list length =", length(fsnplist),
-                "with", length(resultSet), "potentially disruptive matches to", length(unique(resultSet$geneSymbol)),
-                "of", length(pwmList), "motifs."
-            ))
-        }
-        return(resultSet)
-    }
-}
-
-#' @importFrom matrixStats colRanges
-#' @importFrom stringr str_pad
-#' @importFrom TFMPvalue TFMsc2pv
-updateResultsSnv <- function(result, snp.seq, snp.pos, hit, ref.windows, alt.windows,
-                             allelR, allelA, effect, len, k, pwm, calcp) {
-    strand.opt <- c("+", "-")
-    strand(result) <- strand.opt[[hit$strand]]
-    hit$window <- as.integer(hit$window)
-    mresult <- mcols(result)
-    mresult[["snpPos"]] <- start(result)
-    mresult[["motifPos"]] <- as.integer(snp.pos)
-    matchs <- snp.seq
-    seq.pos <- snp.pos + hit$window - 1
-    matchs[-(seq.pos)] <- tolower(matchs[-(seq.pos)])
-    matchs <- paste(matchs, collapse = "")
-    mresult[["seqMatch"]] <- str_pad(matchs, width = k * 2, side = "both")
-    start(result) <- start(result) - snp.pos + 1
-    end(result) <- end(result) - snp.pos + len
-    if (calcp) {
-        mresult[["scoreRef"]] <- ref.windows[hit$strand, hit$window]
-        mresult[["scoreAlt"]] <- alt.windows[hit$strand, hit$window]
-        mresult[["Refpvalue"]] <- NA
-        mresult[["Altpvalue"]] <- NA
-        pwmrange <- colSums(colRanges(pwm))
-        mresult[["pctRef"]] <- (mresult[["scoreRef"]] - pwmrange[[1]]) / (pwmrange[[2]] - pwmrange[[1]])
-        mresult[["pctAlt"]] <- (mresult[["scoreAlt"]] - pwmrange[[1]]) / (pwmrange[[2]] - pwmrange[[1]])
-    } else {
-        mresult[["pctRef"]] <- ref.windows[hit$strand, hit$window]
-        mresult[["pctAlt"]] <- alt.windows[hit$strand, hit$window]
-    }
-    mresult[["alleleRef"]] <- allelR
-    mresult[["alleleAlt"]] <- allelA
-    mresult[["effect"]] <- effect
-    mcols(result) <- mresult
-    return(result)
-}
-
-
-updateResultsIndel <- function(result,
-                               ref.seq, alt.seq,
-                               ref.pos, alt.pos,
-                               hit.ref, hit.alt,
-                               ref.windows, alt.windows,
-                               score, effect, len, k, pwm, calcp) {
-    strand.opt <- c("+", "-")
-    if (score > 0L) {
-        best.hit <- hit.alt
-        matchs <- alt.seq
-        snp.pos <- alt.pos
-    } else {
-        best.hit <- hit.ref
-        matchs <- ref.seq
-        snp.pos <- ref.pos
-    }
-
-    strand(result) <- strand.opt[[best.hit$strand]]
-    best.hit$window <- as.integer(best.hit$window)
-    mresult <- mcols(result)
-    alt_loc <- range(mresult$ALT_loc)
-    ref_start <- (1 - alt_loc[[1]])
-    ref_start <- ifelse(ref_start <= 0, ref_start - 1, ref_start)
-    motif.start <- (alt_loc[[1]]) + (-len) + (best.hit$window) + ref_start
-    motif.start <- ifelse(motif.start >= 0, motif.start + 1, motif.start)
-    if ((mresult$varType == "Insertion" & score < 0) |
-        (mresult$varType == "Deletion" & score > 0)) {
-        motif.end <- motif.start + len
-    } else {
-        if (motif.start > 0) {
-            motif.end <- len - length(motif.start:length(alt_loc[1]:alt_loc[2]))
-        } else {
-            motif.end <- motif.start + len - length(alt_loc[1]:alt_loc[2])
-        }
-    }
-    motif.end <- ifelse(motif.end <= 0, motif.end - 1, motif.end)
-    mresult$motifPos <- list(c(motif.start, motif.end))
-    mresult$altPos <- mresult$ALT_loc
-    seq.range <- (k - (len - alt_loc[[1]])):(k + len + alt_loc[[2]] - 2)
-    matchs[-(snp.pos)] <- tolower(matchs[-(snp.pos)])
-    matchs <- paste(matchs[seq.range], collapse = "")
-    mresult[["seqMatch"]] <- str_pad(matchs, width = (k * 2) + alt_loc[[2]], side = "both")
-    pwmrange <- colSums(colRanges(pwm[-5, ]))
-    mresult[["scoreRef"]] <- ref.windows[hit.ref$strand, hit.ref$window]
-    mresult[["scoreAlt"]] <- alt.windows[hit.alt$strand, hit.alt$window]
-    mresult[["pctRef"]] <- (mresult[["scoreRef"]] - pwmrange[[1]]) / (pwmrange[[2]] - pwmrange[[1]])
-    mresult[["pctAlt"]] <- (mresult[["scoreAlt"]] - pwmrange[[1]]) / (pwmrange[[2]] - pwmrange[[1]])
-    if (calcp) {
-        mresult[["Refpvalue"]] <- NA
-        mresult[["Altpvalue"]] <- NA
-    }
-    mresult[["alleleDiff"]] <- score
-    mresult[["effect"]] <- effect
-    mresult[["alleleEffectSize"]] <- score / pwmrange[[2]]
-    mcols(result) <- mresult
-    return(result)
-}
-
-#' @importFrom matrixStats colMaxs colMins
-preparePWM <- function(pwmList,
-                       filterp,
-                       bkg,
-                       scoreThresh,
-                       method = "default") {
-    bkg <- bkg[c("A", "C", "G", "T")]
-
-    scounts <- as.integer(mcols(pwmList)$sequenceCount)
-    scounts[is.na(scounts)] <- 20L
-    pwmList.pc <- Map(function(pwm, scount) {
-        pwm <- (pwm * scount + 0.25) / (scount + 1)
-    }, pwmList, scounts)
-    if (method == "ic") {
-        pwmOmegas <- lapply(pwmList.pc, function(pwm, b = bkg) {
-            omegaic <- colSums(pwm * log2(pwm / b))
-        })
-    }
-    if (method == "default") {
-        pwmOmegas <- lapply(pwmList.pc, function(pwm) {
-            omegadefault <- colMaxs(pwm) - colMins(pwm)
-        })
-    }
-    if (method == "log") {
-        pwmList.pc <- lapply(pwmList.pc, function(pwm, b) {
-            pwm <- log(pwm) - log(b)
-        }, b = bkg)
-        pwmOmegas <- 1
-    }
-    if (method == "notrans") {
-        pwmOmegas <- 1
-    }
-    pwmList.pc <- Map(function(pwm, omega) {
-        if (length(omega) == 1 && omega == 1) {
-            return(pwm)
-        } else {
-            omegamatrix <- matrix(rep(omega, 4), nrow = 4, byrow = TRUE)
-            pwm <- pwm * omegamatrix
-        }
-    }, pwmList.pc, pwmOmegas)
-    pwmRanges <- Map(function(pwm, omega) {
-        x <- colSums(colRanges(pwm))
-        return(x)
-    }, pwmList.pc, pwmOmegas)
-    if (filterp) {
-        pwmList.pc2 <- lapply(pwmList.pc, round, digits = 2)
-        pwmThresh <- lapply(pwmList.pc2, TFMpv2sc, pvalue = scoreThresh, bg = bkg, type = "PWM")
-        pwmThresh <- Map("+", pwmThresh, -0.02)
-    } else {
-        pwmThresh <- rep.int(scoreThresh, times = length(pwmRanges))
-    }
-    pwmList@listData <- lapply(pwmList, function(pwm) {
-        pwm <- pwm[c("A", "C", "G", "T"), ]
-        pwm <- rbind(pwm, N = 0)
-        colnames(pwm) <- as.character(1:ncol(pwm))
-        return(pwm)
-    })
-    pwmList.pc <- lapply(pwmList.pc, function(pwm) {
-        pwm <- pwm[c("A", "C", "G", "T"), ]
-        pwm <- rbind(pwm, N = 0)
-        colnames(pwm) <- as.character(1:ncol(pwm))
-        return(pwm)
-    })
-    return(list(
-        pwmList = pwmList,
-        pwmListPseudoCount = pwmList.pc,
-        pwmRange = pwmRanges,
-        pwmThreshold = pwmThresh
-    ))
-}
-
-
-#' Predict The Disruptiveness Of Single Nucleotide Polymorphisms On
-#' Transcription Factor Binding Sites.
-#'
-#' @param snpList The output of \code{snps.from.rsid} or \code{snps.from.file}
-#' @param pwmList An object of class \code{MotifList} containing the motifs that
-#'   you wish to interrogate
-#' @param threshold Numeric; the maximum p-value for a match to be called or a minimum score threshold
-#' @param method Character; one of \code{default}, \code{log}, \code{ic}, or \code{notrans}; see
-#'   details.
-#' @param bkg Numeric Vector; the background probabilites of the nucleotides
-#'   used with method=\code{log} method=\code{ic}
-#' @param filterp Logical; filter by p-value instead of by pct score.
-#' @param show.neutral Logical; include neutral changes in the output
-#' @param verbose Logical; if running serially, show verbose messages
-#' @param BPPARAM a BiocParallel object see \code{\link[BiocParallel]{register}}
-#'   and see \code{getClass("BiocParallelParam")} for additional parameter
-#'   classes.  Try \code{BiocParallel::registered()} to see what's availible and
-#'   for example \code{BiocParallel::bpparam("SerialParam")} would allow serial
-#'   evaluation.
-#' @seealso See \code{\link{snps.from.rsid}} and \code{\link{snps.from.file}} for
-#'   information about how to generate the input to this function and
-#'   \code{\link{plotMB}} for information on how to visualize it's output
-#' @details \pkg{motifbreakR} works with position probability matrices (PPM). PPM
-#' are derived as the fractional occurrence of nucleotides A,C,G, and T at
-#' each position of a position frequency matrix (PFM). PFM are simply the
-#' tally of each nucleotide at each position across a set of aligned
-#' sequences. With a PPM, one can generate probabilities based on the
-#' genome, or more practically, create any number of position specific
-#' scoring matrices (PSSM) based on the principle that the PPM contains
-#' information about the likelihood of observing a particular nucleotide at
-#' a particular position of a true transcription factor binding site. What
-#' follows is a discussion of the three different algorithms that may be
-#' employed in calls to the \pkg{motifbreakR} function via the \code{method}
-#' argument.
-#'
-#' Suppose we have a frequency matrix \eqn{M} of width \eqn{n} (\emph{i.e.} a
-#' PPM as described above). Furthermore, we have a sequence \eqn{s} also of
-#' length \eqn{n}, such that
-#' \eqn{s_{i} \in \{ A,T,C,G \}, i = 1,\ldots n}{s_i in {A,T,G,C}, i = 1 \ldots n}.
-#' Each column of
-#' \eqn{M} contains the frequencies of each letter in each position.
-#'
-#' Commonly in the literature sequences are scored as the sum of log
-#' probabilities:
-#'
-#' \strong{Equation 1}
-#'
-#' \deqn{F( s,M ) = \sum_{i = 1}^{n}{\log( \frac{M_{s_{i},i}}{b_{s_{i}}} )}}{
-#' F( s,M ) = \sum_(i = 1)^n log ((M_s_i,_i)/b_s_i)}
-#'
-#' where \eqn{b_{s_{i}}}{b_s_i} is the background frequency of letter \eqn{s_{i}}{s_i} in
-#' the genome of interest. This method can be specified by the user as
-#' \code{method='log'}.
-#'
-#' As an alternative to this method, we introduced a scoring method to
-#' directly weight the score by the importance of the position within the
-#' match sequence. This method of weighting is accessed by specifying
-#' \code{method='ic'} (information content). A general representation
-#' of this scoring method is given by:
-#'
-#' \strong{Equation 2}
-#'
-#' \deqn{F( s,M ) = p_{s} \cdot \omega_{M}}{F( s,M ) = p_s . \omega_M}
-#'
-#' where \eqn{p_{s}}{p_s} is the scoring vector derived from sequence \eqn{s} and matrix
-#' \eqn{M}, and \eqn{w_{M}}{w_M} is a weight vector derived from \eqn{M}. First, we
-#' compute the scoring vector of position scores \eqn{p}
-#'
-#' \strong{Equation 3}
-#'
-#' \deqn{p_{s} = ( M_{s_{i},i} ) \textrm{\ \ \ where\ \ \ } \frac{i = 1,\ldots n}{s_{i} \in \{ A,C,G,T \}}}{
-#' p_s = ( M_s_i,_i ) where (i = 1 \ldots n)/(s_i in {A,C,G,T})}
-#'
-#' and second, for each \eqn{M} a constant vector of weights
-#' \eqn{\omega_{M} = ( \omega_{1},\omega_{2},\ldots,\omega_{n} )}{\omega_M = ( \omega_1, \omega_2, \ldots, \omega_n)}.
-#'
-#' There are two methods for producing \eqn{\omega_{M}}{\omega_M}. The first, which we
-#' call weighted sum, is the difference in the probabilities for the two
-#' letters of the polymorphism (or variant), \emph{i.e.}
-#' \eqn{\Delta p_{s_{i}}}{\Delta p_s_i}, or the difference of the maximum and minimum
-#' values for each column of \eqn{M}:
-#'
-#' \strong{Equation 4.1}
-#'
-#' \deqn{\omega_{i} = \max \{ M_{i} \} - \min \{ M_{i} \}\textrm{\ \ \ \ where\ \ \ \ \ \ }i = 1,\ldots n}{
-#' \omega_i = max{M_i} - min{M_i} where i = 1 \ldots n}
-#'
-#' The second variation of this theme is to weight by relative entropy.
-#' Thus the relative entropy weight for each column \eqn{i} of the matrix is
-#' given by:
-#'
-#' \strong{Equation 4.2}
-#'
-#' \deqn{\omega_{i} = \sum_{j \in \{ A,C,G,T \}}^{}{M_{j,i}\log_2( \frac{M_{j,i}}{b_{i}} )}\textrm{\ \ \ \ \ where\ \ \ \ \ }i = 1,\ldots n}{
-#' \omega_i = \sum_{j in {A,C,G,T}} {M_(j,i)} log2(M_(j,i)/b_i) where i = 1 \ldots n}
-#'
-#' where \eqn{b_{i}}{b_i} is again the background frequency of the letter \eqn{i}.
-#'
-#' Thus, there are 3 possible algorithms to apply via the \code{method}
-#' argument. The first is the standard summation of log probabilities
-#' (\code{method='log'}). The second and third are the weighted sum and
-#' information content methods (\code{method='default'} and \code{method='ic'}) specified by
-#' equations 4.1 and 4.2, respectively. \pkg{motifbreakR} assumes a
-#' uniform background nucleotide distribution (\eqn{b}) in equations 1 and
-#' 4.2 unless otherwise specified by the user. Since we are primarily
-#' interested in the difference between alleles, background frequency is
-#' not a major factor, although it can change the results. Additionally,
-#' inclusion of background frequency introduces potential bias when
-#' collections of motifs are employed, since motifs are themselves
-#' unbalanced with respect to nucleotide composition. With these cautions
-#' in mind, users may override the uniform distribution if so desired. For
-#' all three methods, \pkg{motifbreakR} scores and reports the reference
-#' and alternate alleles of the sequence
-#' (\eqn{F( s_{\textsc{ref}},M )}{F( s_ref,M )} and
-#' \eqn{F( s_{\textsc{alt}},M )}{F( s_alt,M )}), and provides the matrix scores
-#' \eqn{p_{s_{\textsc{ref}}}}{p_s_ref} and \eqn{p_{s_{\textsc{alt}}}}{p_s_alt} of the SNP (or
-#' variant). The scores are scaled as a fraction of scoring range 0-1 of
-#' the motif matrix, \eqn{M}. If either of
-#' \eqn{F( s_{\textsc{ref}},M )}{F( s_ref,M )} and
-#' \eqn{F( s_{\textsc{alt}},M )}{F( s_alt,M )} is greater than a user-specified
-#' threshold (default value of 0.85) the SNP is reported. By default
-#' \pkg{motifbreakR} does not display neutral effects,
-#' (\eqn{\Delta p_{i} < 0.4}{\Delta p_i < 0.4}) but this behaviour can be
-#' overridden.
-#'
-#' Additionally, now, with the use of \code{\link{TFMPvalue-package}}, we may filter by p-value of the match.
-#' This is unfortunately a two step process. First, by invoking \code{filterp=TRUE} and setting a threshold at
-#' a desired p-value e.g 1e-4, we perform a rough filter on the results by rounding all values in the PWM to two
-#' decimal place, and calculating a scoring threshold based upon that. The second step is to use the function \code{\link{calculatePvalue}()}
-#' on a selection of results which will change the \code{Refpvalue} and \code{Altpvalue} columns in the output from \code{NA} to the p-value
-#' calculated by \code{\link{TFMsc2pv}}.  This can be (although not always) a very memory and time intensive process if the algorithm doesn't converge rapidly.
-#'
-#' @return a GRanges object containing:
-#'  \item{REF}{the reference allele for the variant}
-#'  \item{ALT}{the alternate allele for the variant}
-#'  \item{snpPos}{the coordinates of the variant}
-#'  \item{motifPos}{The position of the motif relative the the variant}
-#'  \item{geneSymbol}{the geneSymbol corresponding to the TF of the TF binding motif}
-#'  \item{dataSource}{the source of the TF binding motif}
-#'  \item{providerName, providerId}{the name and id provided by the source}
-#'  \item{seqMatch}{the sequence on the 5' -> 3' direction of the "+" strand
-#'  that corresponds to DNA at the position that the TF binding motif was found.}
-#'  \item{pctRef}{The score as determined by the scoring method, when the sequence contains the reference variant allele, normalized to a scale from 0 - 1. If \code{filterp = FALSE},
-#'  this is the value that is thresholded.}
-#'  \item{pctAlt}{The score as determined by the scoring method, when the sequence contains the alternate variant allele, normalized to a scale from 0 - 1. If \code{filterp = FALSE},
-#'  this is the value that is thresholded.}
-#'  \item{scoreRef}{The score as determined by the scoring method, when the sequence contains the reference variant allele}
-#'  \item{scoreAlt}{The score as determined by the scoring method, when the sequence contains the alternate variant allele}
-#'  \item{Refpvalue}{p-value for the match for the pctRef score, initially set to \code{NA}. see \code{\link{calculatePvalue}} for more information}
-#'  \item{Altpvalue}{p-value for the match for the pctAlt score, initially set to \code{NA}. see \code{\link{calculatePvalue}} for more information}
-#'  \item{alleleRef}{The proportional frequency of the reference allele at position \code{motifPos} in the motif}
-#'  \item{alleleAlt}{The proportional frequency of the alternate allele at position \code{motifPos} in the motif}
-#'  \item{altPos}{the position, relative to the reference allele, of the alternate allele}
-#'  \item{alleleDiff}{The difference between the score on the reference allele and the score on the alternate allele}
-#'  \item{alleleEffectSize}{The ratio of the \code{alleleDiff} and the maximal score of a sequence under the PWM}
-#'  \item{effect}{one of weak, strong, or neutral indicating the strength of the effect.}
-#'  each SNP in this object may be plotted with \code{\link{plotMB}}
-#' @examples
-#' library(BSgenome.Hsapiens.UCSC.hg19)
-#' # prepare variants
-#' load(system.file("extdata",
-#'     "pca.enhancer.snps.rda",
-#'     package = "motifbreakR"
-#' )) # loads snps.mb
-#' pca.enhancer.snps <- sample(snps.mb, 20)
-#' # Get motifs to interrogate
-#' data(hocomoco)
-#' motifs <- sample(hocomoco, 50)
-#' # run motifbreakR
-#' results <- motifbreakR(pca.enhancer.snps,
-#'     motifs,
-#'     threshold = 0.85,
-#'     method = "ic",
-#'     BPPARAM = BiocParallel::SerialParam()
-#' )
-#' @import BiocParallel
-#' @import parallel
-#' @importFrom parallel clusterEvalQ
-#' @importFrom BiocParallel bplapply
-#' @importFrom stringr str_length str_trim
-#' @export
-motifbreakR <- function(snpList, pwmList, threshold = 0.85, filterp = FALSE,
-                        method = "default", show.neutral = FALSE, verbose = FALSE,
-                        bkg = c(A = 0.25, C = 0.25, G = 0.25, T = 0.25),
-                        BPPARAM = bpparam()) {
-    ## Cluster / MC setup
-    if (.Platform$OS.type == "windows" && inherits(BPPARAM, "MulticoreParam")) {
-        warning(paste0(
-            "Serial evaluation under effect, to achive parallel evaluation under\n",
-            "Windows, please supply an alternative BPPARAM"
-        ))
-    }
-    cores <- bpnworkers(BPPARAM)
-    num.snps <- length(snpList)
-    if (num.snps < cores) {
-        cores <- num.snps
-    }
-    if (!(is(BPPARAM, "MulticoreParam") | is(BPPARAM, "SerialParam"))) {
-        bpstart(BPPARAM)
-        cl <- bpbackend(BPPARAM)
-        clusterEvalQ(cl, library("MotifDb"))
-    }
-
-    pwms <- preparePWM(
-        pwmList = pwmList, filterp = filterp,
-        scoreThresh = threshold, bkg = bkg,
-        method = method
-    )
-    snpList <- prepareVariants(fsnplist = snpList)
-
-    snpList_cores <- split(as.list(rep(names(snpList), times = cores)), 1:cores)
-    for (splitr in seq_along(snpList)) {
-        splitcores <- sapply(suppressWarnings(split(snpList[[splitr]], 1:cores)), list)
-        for (splitcore in seq_along(snpList_cores)) {
-            snpList_cores[[splitcore]][[splitr]] <- splitcores[[splitcore]]
-            names(snpList_cores[[splitcore]])[splitr] <- names(snpList)[splitr]
-        }
-    }
-    snpList <- snpList_cores
-    rm(snpList_cores)
-
-    x <- bplapply(snpList, scoreSnpList,
-        pwmList = pwms$pwmList, threshold = pwms$pwmThreshold,
-        pwmList.pc = pwms$pwmListPseudoCount, pwmRanges = pwms$pwmRange,
-        method = method, bkg = bkg, show.neutral = show.neutral,
-        verbose = ifelse(cores == 1, verbose, FALSE),
-        filterp = filterp, BPPARAM = BPPARAM
-    )
-
-    ## Cluster / MC cleanup
-    if (inherits(x, "try-error")) {
-        if (is(BPPARAM, "SnowParam")) {
-            bpstop(BPPARAM)
-        }
-        stop(attributes(x)$condition)
-    }
-    if (is(BPPARAM, "SnowParam")) {
-        bpstop(BPPARAM)
-    }
-
-    drops <- sapply(x, is.null)
-    x <- x[!drops]
-    pwmList <- pwms$pwmList
-    pwmList@listData <- lapply(pwms$pwmList, function(pwm) {
-        pwm <- pwm[c("A", "C", "G", "T"), ]
-        return(pwm)
-    })
-    pwmList.pc <- lapply(pwms$pwmListPseudoCount, function(pwm) {
-        pwm <- pwm[c("A", "C", "G", "T"), ]
-        return(pwm)
-    })
-
-    if (length(x) > 1) {
-        x <- unlist(GRangesList(unname(x)))
-        snpList <- unlist(GRangesList(lapply(snpList, `[[`, "fsnplist")), use.names = FALSE)
-        x <- x[order(match(x$SNP_id, snpList$SNP_id)), , drop = FALSE]
-        # attributes(x)$genome.package <- genome.package
-        attributes(x)$motifs <- pwmList[mcols(pwmList)$providerId %in% unique(x$providerId) &
-            mcols(pwmList)$providerName %in% unique(x$providerName), ]
-        attributes(x)$scoremotifs <- pwmList.pc[names(attributes(x)$motifs)]
-    } else {
-        if (length(x) == 1L) {
-            x <- x[[1]]
-            # attributes(x)$genome.package <- genome.package
-            attributes(x)$motifs <- pwmList[mcols(pwmList)$providerId %in% unique(x$providerId) &
-                mcols(pwmList)$providerName %in% unique(x$providerName), ]
-            attributes(x)$scoremotifs <- pwmList.pc[names(attributes(x)$motifs)]
-        } else {
-            warning("No SNP/Motif Interactions reached threshold")
-            x <- NULL
-        }
-    }
-    if (verbose && cores > 1) {
-        if (is.null(x)) {
-            message(paste(
-                "reached end of SNPs list length =", num.snps, "with 0 potentially disruptive matches to",
-                length(unique(x$geneSymbol)), "of", length(pwmList), "motifs."
-            ))
-        } else {
-            message(paste(
-                "reached end of SNPs list length =", num.snps, "with",
-                length(x), "potentially disruptive matches to", length(unique(x$geneSymbol)),
-                "of", length(pwmList), "motifs."
-            ))
-        }
-    }
-    return(x)
-}
-
-
-#' Calculate the significance of the matches for the reference and alternate alleles for the for their PWM
-#'
-#' @param results The output of \code{motifbreakR} that was run with \code{filterp=TRUE}
-#' @param background Numeric Vector; the background probabilities of the nucleotides
-#' @param granularity Numeric Vector; the granularity to which to round the PWM,
-#'  larger values compromise full accuracy for speed of calculation. A value of
-#'  \code{NULL} does no rounding.
-#' @param BPPARAM a BiocParallel object see \code{\link[BiocParallel]{register}}
-#'   and see \code{getClass("BiocParallelParam")} for additional parameter
-#'   classes.  Try \code{BiocParallel::registered()} to see what's available and
-#'   for example \code{BiocParallel::bpparam("SerialParam")} would allow serial
-#'   evaluation.
-#' @return a GRanges object. The same Granges object that was input as \code{results}, but with
-#'  \code{Refpvalue} and \code{Altpvalue} columns in the output modified from \code{NA} to the p-value
-#'  calculated by \code{\link{TFMsc2pv}}.
-#' @seealso See \code{\link{TFMsc2pv}} from the \pkg{TFMPvalue} package for
-#'   information about how the p-values are calculated.
-#' @details This function is intended to be used on a selection of results produced by \code{\link{motifbreakR}}, and
-#' this can be (although not always) a very memory and time intensive process if the algorithm doesn't converge rapidly.
-#' @source H{\'e}l{\`e}ne Touzet and Jean-St{\'e}phane Varr{\'e} (2007) Efficient and accurate P-value computation for Position Weight Matrices.
-#'  Algorithms for Molecular Biology, \bold{2: 15}.
-#' @examples
-#' data(example.results)
-#' rs1006140 <- example.results[example.results$SNP_id %in% "rs1006140"]
-#' # low granularity for speed; 1e-6 or 1e-7 recommended for accuracy
-#' rs1006140 <- calculatePvalue(rs1006140, BPPARAM = BiocParallel::SerialParam(), granularity = 1e-4)
-#'
-#' ##' @importFrom qvalue qvalue
-#'
-#' @export
-calculatePvalue <- function(results,
-                            background = c(A = 0.25, C = 0.25, G = 0.25, T = 0.25),
-                            granularity = NULL,
-                            BPPARAM = BiocParallel::SerialParam()) {
-
-    ## Cluster / MC setup
-    if (.Platform$OS.type == "windows" && inherits(BPPARAM, "MulticoreParam")) {
-        warning(paste0(
-            "Serial evaluation under effect, to achive parallel evaluation under\n",
-            "Windows, please supply an alternative BPPARAM"
-        ))
-    }
-    cores <- bpnworkers(BPPARAM)
-    num.res <- length(results)
-    if (num.res < cores) {
-        cores <- num.res
-    }
-    if (!(is(BPPARAM, "MulticoreParam") | is(BPPARAM, "SerialParam"))) {
-        bpstart(BPPARAM)
-        cl <- bpbackend(BPPARAM)
-        clusterEvalQ(cl, library("MotifDb"))
-    }
-    if (!("scoreRef" %in% names(mcols(results)))) {
-        stop("incorrect results format; please rerun analysis with filterp=TRUE")
-    } else {
-        pwmListmeta <- mcols(attributes(results)$motifs, use.names = TRUE)
-        pwmList <- attributes(results)$scoremotifs
-        if (!is.null(granularity)) {
-            pwmList <- lapply(pwmList, function(x, g) {
-                x <- floor(x / g) * g
-                return(x)
-            }, g = granularity)
-        }
-        results_sp <- split(results, 1:length(results))
-        pvalues <- bplapply(results_sp, function(i, pwmList, pwmListmeta, bkg) {
-            result <- i
-            pwm.id <- result$providerId
-            pwm.name.f <- result$providerName
-            pwmmeta <- pwmListmeta[pwmListmeta$providerId == pwm.id & pwmListmeta$providerName == pwm.name.f, ]
-            pwm <- pwmList[[rownames(pwmmeta)[1]]]
-            ref <- TFMsc2pv(pwm, mcols(result)[["scoreRef"]], bg = bkg, type = "PWM")
-            alt <- TFMsc2pv(pwm, mcols(result)[["scoreAlt"]], bg = bkg, type = "PWM")
-            # gc()
-            return(data.frame(ref = ref, alt = alt))
-        }, pwmList = pwmList, pwmListmeta = pwmListmeta, bkg = background, BPPARAM = BPPARAM)
-        ## Cluster / MC cleanup
-        if (inherits(pvalues, "try-error")) {
-            if (is(BPPARAM, "SnowParam")) {
-                bpstop(BPPARAM)
-            }
-            stop(attributes(pvalues)$condition)
-        }
-        pvalues.df <- base::do.call("rbind", c(pvalues, make.row.names = FALSE))
-        results$Refpvalue <- pvalues.df[, "ref"]
-        results$Altpvalue <- pvalues.df[, "alt"]
-
-        if (is(BPPARAM, "SnowParam")) {
-            bpstop(BPPARAM)
-        }
-
-        return(results)
-    }
-}
-
-addPWM.stack <- function(identifier, index, GdObject, pwm_stack, ...) {
-    plotMotifLogoStack.3(pwm_stack)
-}
-
-selcor <- function(identifier, index, GdObject, ...) {
-    if (identical(index, 1L)) {
-        return(TRUE)
-    } else {
-        return(FALSE)
-    }
-}
-
-selall <- function(identifier, GdObject, ...) {
-    return(TRUE)
-}
-
-#' @importFrom grid grid.newpage pushViewport viewport popViewport
-plotMotifLogoStack.3 <- function(pfms, ...) {
-    n <- length(pfms)
-    lapply(pfms, function(.ele) {
-        # if (class(.ele) != "pfm")
-        if (!is(.ele, "pfm")) {
-            stop("pfms must be a list of class pfm")
-        }
-    })
-    assign("tmp_motifStack_symbolsCache", list(), pos = ".GlobalEnv")
-    # grid.newpage()
-    ht <- 1 / n
-    y0 <- 0.5 * ht
-    for (i in rev(seq.int(n))) {
-        pushViewport(viewport(y = y0, height = ht))
-        plotMotifLogo(pfms[[i]],
-            motifName = pfms[[i]]@name, ncex = 1,
-            p = pfms[[i]]@background, colset = pfms[[i]]@color,
-            xlab = NA, newpage = FALSE, margins = c(
-                1.5, 4.1,
-                1.1, 0.1
-            ), ...
-        )
-        popViewport()
-        y0 <- y0 + ht
-    }
-    rm(list = "tmp_motifStack_symbolsCache", pos = ".GlobalEnv")
-    return()
-}
-
-#' @importFrom stringr str_replace
-#' @importFrom motifStack addBlank
-DNAmotifAlignment.2snp <- function(pwms, result) {
-    from <- min(sapply(result$motifPos, `[`, 1))
-    to <- max(sapply(result$motifPos, `[`, 2))
-    #  pos <- mcols(result)$motifPos
-    #  pos <- pos[as.logical(strand(result) == "+")][1]
-    for (pwm.i in seq_along(pwms)) {
-        # pwm <- pwms[[pwm.i]]@mat
-        ## get pwm info from result data
-        pwm.name <- pwms[[pwm.i]]@name
-        pwm.name <- str_replace(pwm.name, pattern = "-:rc$", replacement = "")
-        pwm.name <- str_replace(pwm.name, pattern = "-:r$", replacement = "")
-        pwm.info <- attributes(result)$motifs
-        pwm.id <- mcols(pwm.info[pwm.name, ])$providerId
-        pwm.name <- mcols(pwm.info[pwm.name, ])$providerName
-        mresult <- result[result$providerId == pwm.id & result$providerName == pwm.name, ]
-        mstart <- mresult$motifPos[[1]][1]
-        mend <- mresult$motifPos[[1]][2]
-        if ((mcols(mresult)$varType == "Insertion" & mcols(mresult)$alleleDiff < 0) |
-            (mcols(mresult)$varType == "Deletion" & mcols(mresult)$alleleDiff > 0)) {
-            new.mat <- cbind(
-                pwms[[pwm.i]]@mat[, 1:abs(mresult$motifPos[[1]][1])],
-                matrix(c(0.25, 0.25, 0.25, 0.25), ncol = length(mcols(mresult)$altPos[[1]]), nrow = 4),
-                pwms[[pwm.i]]@mat[, (abs(mresult$motifPos[[1]][1]) + 1):ncol(pwms[[pwm.i]]@mat)]
-            )
-            pwms[[pwm.i]]@mat <- new.mat
-            start.offset <- mstart - from
-            end.offset <- to - mend
-        } else {
-            if (mstart < 0 | from > 0) {
-                start.offset <- mstart - from
-            } else {
-                start.offset <- (mstart - 1) - from
-            }
-            if (mend > 0 | to < 0) {
-                end.offset <- to - mend
-            } else {
-                end.offset <- to - (mend + 1)
-            }
-        }
-        if (start.offset > 0) {
-            pwms[[pwm.i]] <- addBlank(x = pwms[[pwm.i]], n = start.offset, b = FALSE)
-        }
-        if (end.offset > 0) {
-            pwms[[pwm.i]] <- addBlank(x = pwms[[pwm.i]], n = end.offset, b = TRUE)
-        }
-    }
-    return(pwms)
-}
-
-
-
-#' Plot a genomic region surrounding a genomic variant, and potentially disrupted
-#' motifs
-#'
-#' @param results The output of \code{motifbreakR}
-#' @param rsid Character; the identifier of the variant to be visualized
-#' @param reverseMotif Logical; if the motif is on the "-" strand show the
-#'   the motifs as reversed \code{FALSE} or reverse complement \code{TRUE}
-#' @param effect Character; show motifs that are strongly effected \code{c("strong")},
-#'   weakly effected \code{c("weak")}, or both \code{c("strong", "weak")}
-#' @param altAllele Character; The default value of \code{NULL} uses the first (or only)
-#'   alternative allele for the SNP to be plotted.
-#' @seealso See \code{\link{motifbreakR}} for the function that produces output to be
-#'   visualized here, also \code{\link{snps.from.rsid}} and \code{\link{snps.from.file}}
-#'   for information about how to generate the input to \code{\link{motifbreakR}}
-#'   function.
-#' @details \code{plotMB} produces output showing the location of the SNP on the
-#'   chromosome, the surrounding sequence of the + strand, the footprint of any
-#'   motif that is disrupted by the SNP or SNV, and the DNA sequence motif(s).
-#'   The \code{altAllele} argument is included for variants like rs1006140 where
-#'   multiple alternate alleles exist, the reference allele is A, and the alternate
-#'   can be G,T, or C. \code{plotMB} only plots one alternate allele at a time.
-#' @return plots a figure representing the results of \code{motifbreakR} at the
-#'   location of a single SNP, returns invisible \code{NULL}.
-#' @examples
-#' data(example.results)
-#' example.results
-#' \donttest{
-#' library(BSgenome.Hsapiens.UCSC.hg19)
-#' plotMB(results = example.results, rsid = "rs1006140", effect = "strong", altAllele = "C")
-#' }
-#' @importFrom motifStack DNAmotifAlignment colorset motifStack plotMotifLogo plotMotifLogoStack
-#' @importClassesFrom motifStack pfm marker
-#' @import grDevices
-#' @importFrom grid gpar
-#' @importFrom Gviz IdeogramTrack SequenceTrack GenomeAxisTrack HighlightTrack
-#'   AnnotationTrack plotTracks
-#' @export
-plotMB <- function(results, rsid, reverseMotif = TRUE, effect = c("strong", "weak"), altAllele = NULL) {
-    motif.starts <- sapply(results$motifPos, `[`, 1)
-    motif.starts <- start(results) + motif.starts
-    motif.starts <- order(motif.starts)
-    results <- results[motif.starts]
-    g <- genome(results)[[1]]
-    result <- results[results$SNP_id %in% rsid]
-    if (is.null(altAllele)) {
-        altAllele <- result$ALT[[1]]
-    }
-    result <- result[result$ALT == altAllele]
-    result <- result[order(sapply(result$motifPos, min), sapply(result$motifPos, max)), ]
-    result <- result[result$effect %in% effect]
-    chromosome <- as.character(seqnames(result))[[1]]
-    genome.package <- attributes(result)$genome.package
-    genome.bsgenome <- eval(parse(text = genome.package))
-    seq.len <- max(length(result$REF[[1]]), length(result$ALT[[1]]))
-    distance.to.edge <- max(abs(c(
-        sapply(result$motifPos, min),
-        sapply(result$motifPos, max)
-    ))) + 4
-    from <- start(result)[[1]] - distance.to.edge + 1
-    to <- end(result)[[1]] + distance.to.edge
-    pwmList <- attributes(result)$motifs
-    pwm.names <- result$providerId
-    results_motifs <- paste0(result$providerId, result$providerName)
-    list_motifs <- paste0(mcols(pwmList)$providerId, mcols(pwmList)$providerName)
-    pwms <- pwmList <- pwmList[match(results_motifs, list_motifs)]
-    if (reverseMotif) {
-        for (pwm.i in seq_along(pwms)) {
-            pwm.name <- names(pwms[pwm.i])
-            pwm.id <- mcols(pwms[pwm.name, ])$providerId
-            pwm.name.f <- mcols(pwms[pwm.name, ])$providerName
-            doRev <- as.logical(strand(result[result$providerId == pwm.id & result$providerName == pwm.name.f, ]) == "-")
-            if (doRev) {
-                pwm <- pwms[[pwm.i]]
-                pwm <- pwm[, rev(1:ncol(pwm))]
-                rownames(pwm) <- c("T", "G", "C", "A")
-                pwm <- pwm[c("A", "C", "G", "T"), ]
-                pwms[[pwm.i]] <- pwm
-                names(pwms)[pwm.i] <- paste0(names(pwms)[pwm.i], "-:rc")
-            }
-        }
-    } else {
-        for (pwm.i in seq_along(pwms)) {
-            pwm.name <- names(pwms[pwm.i])
-            pwm.id <- mcols(pwms[pwm.name, ])$providerId
-            pwm.name.f <- mcols(pwms[pwm.name, ])$providerName
-            doRev <- as.logical(strand(result[result$providerId == pwm.id & result$providerName == pwm.name.f, ]) == "-")
-            if (doRev) {
-                pwm <- pwms[[pwm.i]]
-                pwm <- pwm[, rev(1:ncol(pwm))]
-                pwms[[pwm.i]] <- pwm
-                names(pwms)[pwm.i] <- paste0(names(pwms)[pwm.i], "-:r")
-            }
-        }
-    }
-    pwms <- lapply(names(pwms), function(x, pwms = pwms) {
-        new("pfm",
-            mat = pwms[[x]],
-            name = x
-        )
-    }, pwms)
-    pwms <- DNAmotifAlignment.2snp(pwms, result)
-    pwmwide <- max(sapply(pwms, function(x) {
-        ncol(x@mat)
-    }))
-
-    markerStart <- result$motifPos[[1]][1]
-    if (markerStart > 0) {
-        markerEnd <- length(result$altPos[[1]]) + 1
-        markerEnd <- markerEnd - markerStart
-        markerStart <- 1
-    } else {
-        markerStart <- -1 * markerStart
-        markerEnd <- markerStart + length(result$altPos[[1]])
-        if (result$varType[[1]] %in% c("Other", "SNV")) {
-            markerStart <- markerStart + 1
-        }
-    }
-    varType <- result$varType[[1]]
-    varType <- switch(varType,
-        Deletion = "firebrick",
-        Insertion = "springgreen4",
-        Other = "gray13"
-    )
-    markerRect <- new("marker",
-        type = "rect",
-        start = markerStart,
-        stop = markerEnd,
-        gp = gpar(
-            lty = 2,
-            fill = NA,
-            lwd = 3,
-            col = varType
-        )
-    )
-    for (pwm.i in seq_along(pwms)) {
-        pwms[[pwm.i]]@markers <- list(markerRect)
-    }
-    ideoT <- try(IdeogramTrack(genome = g, chromosome = chromosome), silent = TRUE)
-    if (inherits(ideoT, "try-error")) {
-        backup.band <- data.frame(
-            chrom = chromosome, chromStart = 0,
-            chromEnd = length(genome.bsgenome[[chromosome]]),
-            name = chromosome, gieStain = "gneg"
-        )
-        ideoT <- IdeogramTrack(genome = g, chromosome = chromosome, bands = backup.band)
-    }
-
-    ### blank alt sequence
-    altseq <- genome.bsgenome[[chromosome]]
-
-    ### Replace longer sections
-    at <- IRanges(start = start(result[1]), width = width(result[1]))
-    if (result$varType[[1]] == "Deletion") {
-        reflen <- length(result$REF[[1]])
-        addedN <- DNAString(paste0(rep.int(".", reflen), collapse = ""))
-        addedN <- replaceLetterAt(addedN, at = (1:reflen)[-result$altPos[[1]]], result$ALT[[1]])
-        axisT <- GenomeAxisTrack(exponent = 0)
-        seqT <- SequenceTrack(genome.bsgenome, fontcolor = colorset("DNA", "auto"))
-        altseq <- replaceAt(x = altseq, at = at, addedN)
-    } else if (result$varType[[1]] == "Insertion") {
-        altlen <- length(result$ALT[[1]])
-        addedN <- DNAString(paste0(rep.int(".", altlen), collapse = ""))
-        addedN <- replaceLetterAt(addedN, at = (1:altlen)[-result$altPos[[1]]], result$REF[[1]])
-        refseq <- genome.bsgenome[[chromosome]]
-        refseq <- DNAStringSet(replaceAt(x = refseq, at = at, addedN))
-        altseq <- replaceAt(x = altseq, at = at, result$ALT[[1]])
-        names(refseq) <- chromosome
-        seqT <- SequenceTrack(refseq,
-            fontcolor = c(colorset("DNA", "auto"), N = "#FFFFFF", . = "#FFE3E6"),
-            chromosome = chromosome
-        )
-    } else {
-        axisT <- GenomeAxisTrack(exponent = 0)
-        altseq <- replaceAt(x = altseq, at = at, result$ALT[[1]])
-        seqT <- SequenceTrack(genome.bsgenome, fontcolor = colorset("DNA", "auto"))
-    }
-    altseq <- DNAStringSet(altseq)
-    names(altseq) <- chromosome
-    seqAltT <- SequenceTrack(altseq,
-        fontcolor = c(colorset("DNA", "auto"), N = "#FFFFFF", . = "#FFE3E6"),
-        chromosome = chromosome
-    )
-
-    # altseq <- replaceLetterAt(altseq, at = wherereplace, letter = rep.int("N", sum(wherereplace)))
-    # altseq <- replaceLetterAt(altseq, at = !wherereplace, letter = result$ALT[[1]])
-    histart <- start(result[1]) + min(result[1]$altPos[[1]]) - 2
-    histart <- ifelse(result[1]$varType %in% c("Other", "SNV"), histart + 1, histart)
-    hiend <- start(result[1]) + min(result[1]$altPos[[1]]) - 2 + length(result[1]$altPos[[1]])
-    hiT <- HighlightTrack(
-        trackList = list(seqT, seqAltT),
-        start = histart,
-        end = hiend,
-        chromosome = chromosome
-    )
-
-    selectingfun <- selcor
-    detailfun <- addPWM.stack
-
-    motif_ids <- names(pwmList)
-    names(motif_ids) <- mcols(pwmList)$providerName
-
-    for (mymotif_i in seq_along(result)) {
-        mymotif <- result[mymotif_i]
-        start(mymotif) <- start(mymotif) + min(mymotif$altPos[[1]]) - 1
-        width(mymotif) <- length(mymotif$altPos[[1]])
-        variant.start <- start(mymotif)
-        variant.end <- end(mymotif)
-        if (mymotif$motifPos[[1]][1] < 0) {
-            start(mymotif) <- start(mymotif) + (mymotif$motifPos[[1]][1])
-        } else {
-            start(mymotif) <- start(mymotif) + (mymotif$motifPos[[1]][1] - 1)
-        }
-        if (mymotif$motifPos[[1]][2] < 0) {
-            end(mymotif) <- end(mymotif) + (mymotif$motifPos[[1]][2] + 1)
-        } else {
-            end(mymotif) <- end(mymotif) + (mymotif$motifPos[[1]][2])
-        }
-        if ((result[mymotif_i]$varType == "Deletion" & result[mymotif_i]$alleleDiff > 0) |
-            (result[mymotif_i]$varType == "Insertion" & result[mymotif_i]$alleleDiff < 0)) {
-            mymotif <- c(mymotif, mymotif)
-            end(mymotif)[1] <- variant.start - 1
-            start(mymotif)[2] <- variant.end + 1
-            mymotif[which.min(width(mymotif))]$motifPos <- NA
-        }
-        if (exists("mres")) {
-            mres <- c(mres, mymotif)
-        } else {
-            mres <- mymotif
-        }
-    }
-    result <- mres
-    rm(mres)
-    motif_ids <- motif_ids[result$providerName]
-    presult <- result
-    strand(presult) <- "*"
-    pres_cols <- DataFrame(
-        feature = ifelse(!is.na(result$motifPos),
-            paste(result$geneSymbol, "motif", sep = "_"), ""
-        ),
-        group = result$providerName,
-        id = motif_ids
-    )
-    presult <- GRanges(
-        seqnames = seqnames(result[1]),
-        ranges = ranges(result)
-    )
-    mcols(presult) <- pres_cols
-
-    motifT <- AnnotationTrack(presult,
-        fun = detailfun,
-        detailsFunArgs = list(pwm_stack = pwms),
-        name = names(result)[[1]],
-        selectFun = selectingfun,
-        reverseStacking = FALSE,
-        stacking = "squish"
-    )
-
-    if (exists("axisT")) {
-        track_list <- list(ideoT, motifT, hiT, axisT)
-    } else {
-        track_list <- list(ideoT, motifT, hiT)
-    }
-    plotTracks(track_list,
-        from = from, to = to, showBandId = TRUE,
-        cex.main = 0.8, col.main = "darkgrey",
-        add53 = TRUE, labelpos = "below", chromosome = chromosome, # groupAnnotation = "id",
-        fontcolor.item = "black",
-        collapse = FALSE, min.width = 1, featureAnnotation = "feature", cex.feature = 0.8,
-        details.size = 0.85, detailsConnector.pch = NA, detailsConnector.lty = 0,
-        shape = "box", cex.group = 0.8, fonts = c("sans", "Helvetica")
-    )
-    return(invisible(NULL))
-}
-
-#' Export motifbreakR results to csv or tsv
-#'
-#' @param results The output of \code{motifbreakR}
-#' @param file Character; the file name of the destination file
-#' @param format Character; one of tsv (tab separated values) or csv (comma separated values)
-#' @return \code{exportMBresults} produces an output file containing the output
-#' of the motifbreakR function.
-#' @examples
-#' data(example.results)
-#' example.results
-#' \donttest{
-#' exportMBresults(example.results, file = "output.tsv", format = "tsv")
-#' }
-#' @export
-exportMBresults <- function(results, file, format = c("tsv")) {
-    if (missing(file)) {
-        stop("select output file location")
-    }
-    if (!(format %in% c("csv", "tsv"))) {
-        stop("format must be one of csv or tsv")
-    }
-    sep <- switch(format,
-        csv = ",",
-        tsv = "\t"
-    )
-    names(results) <- NULL
-    results <- as.data.frame(results)
-    results <- results[, !colnames(results) %in% "width"]
-    results$start <- results$start - 1
-    results$motifPos <- vapply(results$motifPos, function(x) {
-        paste0(x[1], ";", x[2])
-    }, FUN.VALUE = character(1))
-    if (format == "tsv") {
-        write.table(x = results, file = file, quote = FALSE, sep = sep, row.names = FALSE, col.names = TRUE)
-    } else {
-        write.csv(x = results, file = file, row.names = FALSE, col.names = TRUE)
-    }
-}
-
-#' Find Corresponding TF Binding From The ReMap2022 Project
-#'
-#' @param remap_data Character; either the path to a local copy of the non-redundant
-#'   peak set, or one of \code{hg38} for Homo sapiens, \code{mm10} for Mus musculus,
-#'   \code{dm6} for Drosophila melanogaster, or \code{TAIR10} for Arabidopsis thaliana,
-#'   to be queried (slowly) online.
-#' @details \code{snps.from.file} takes a character vector describing the file path
-#'  to a bed file that contains the necissary information to generate the input for
-#'  \code{motifbreakR} see \url{http://www.genome.ucsc.edu/FAQ/FAQformat.html#format1}
-#'  for a complete description of the BED format.  Our convention deviates in that there
-#'  is a required format for the name field.  \code{name} is defined as chromosome:start:REF:ALT
-#'  or the rsid from dbSNP (if you've included the optional SNPlocs argument).
-#'  For example if you were to include rs123 in it's alternate
-#'  format it would be entered as chr7:24966446:C:A
-#' @return a GRanges object containing:
-#'  \item{SNP_id}{The rsid of the snp with the "rs" portion stripped}
-#'  \item{alleles_as_ambig}{THE IUPAC ambiguity code between the reference and
-#'  alternate allele for this SNP}
-#'  \item{REF}{The reference allele for the SNP}
-#'  \item{ALT}{The alternate allele for the SNP}
-#' @examples
-#' library(BSgenome.Drerio.UCSC.danRer7)
-#'
-#' @importFrom rtracklayer import
-#' @importFrom Biostrings IUPAC_CODE_MAP uniqueLetters BStringSetList DNA_ALPHABET
-#' @importFrom VariantAnnotation readVcf ref alt isSNV VcfFile ScanVcfParam
-#' @importFrom SummarizedExperiment rowRanges
-#' @importFrom stringr str_sort str_split
-#' @export
-
-findSupportingRemapPeaks <- function(results, genome) {
-    genome <- match.arg(genome, c("hg38", "mm10", "dm6", "TAIR10_TF", "TAIR10_HISTONE"))
-
-    remap_links <- list(
-        hg38 = "https://remap.univ-amu.fr/storage/remap2022/hg38/MACS2/remap2022_nr_macs2_hg38_v1_0.bed.gz",
-        mm10 = "https://remap.univ-amu.fr/storage/remap2022/mm10/MACS2/remap2022_nr_macs2_mm10_v1_0.bed.gz",
-        dm6 = "https://remap.univ-amu.fr/storage/remap2022/dm6/MACS2/remap2022_nr_macs2_dm6_v1_0.bed.gz",
-        TAIR10_TF = "https://remap.univ-amu.fr/storage/remap2022/tair10/tf/MACS2/remap2022_nr_macs2_TAIR10_v1_0.bed.gz",
-        TAIR10_HISTONE = "https://remap.univ-amu.fr/storage/remap2022/tair10/histones/MACS2/remap2022_histone_nr_macs2_TAIR10_v1_0.bed.gz"
-    )
-
-    results$matchingBindingEvent <- NA
-    results$matchingCelltype <- NA
-
-    uniqmb <- results
-    mcols(uniqmb) <- NULL
-    names(uniqmb) <- NULL
-    uniqmb <- sort(unique(uniqmb))
-
-    remap_binding <- loadPeakFile(remap_links, genome)
-    remap_binding <- subsetByOverlaps(remap_binding, uniqmb)
-
-    if (length(remap_binding) < 1) {
-        return(results)
-    }
-
-    mb_overlaps <- findOverlaps(results, remap_binding)
-    variant_to_peak <- unique(data.frame(variant = names(results[queryHits(mb_overlaps), ]), tf.binding = remap_binding[subjectHits(mb_overlaps), ]$name))
-    tf_ct <- stringr::str_split(variant_to_peak$tf.binding, ":")
-    variant_to_peak$tf.binding <- vapply(tf_ct, FUN = `[`, character(1), 1)
-    variant_to_peak$tf.celltype <- vapply(tf_ct, FUN = `[`, character(1), 2)
-    variant_to_peak$tf.celltype <- lapply(variant_to_peak$tf.celltype, function(x) {
-        stringr::str_split(x, ",", simplify = T)[1, ]
-    })
-    mcol_variant_to_gene <- data.frame(variant = names(results), tf.gene = results$geneSymbol, motif = results$providerId)
-
-    if ("manuallyCuratedGeneMotifAssociationTable" %in% slotNames(attributes(results)$motifs)) {
-        mb_genelist <- attributes(results)$motifs@manuallyCuratedGeneMotifAssociationTable
-        mb_genelist <- unique(mb_genelist[mb_genelist$motif %in% results$providerId, c("motif", "tf.gene")])
-        mb_genelist_aug <- unique(data.frame(motif = results$providerId, tf.gene = results$geneSymbol))
-        mb_genelist <- unique(rbind(mb_genelist, mb_genelist_aug))
-        variant_to_gene <- data.frame(variant = names(results), motif = results$providerId)
-        variant_to_gene_master <- merge(variant_to_gene, mb_genelist, all.x = TRUE, sort = FALSE)
-        variant_to_gene <- unique(variant_to_gene_master[, c("variant", "tf.gene")])
-    } else {
-        variant_to_gene_master <- mcol_variant_to_gene
-        variant_to_gene <- unique(variant_to_gene_master[, c("variant", "tf.gene")])
-    }
-
-    variant_mb_peak <- merge(variant_to_gene_master, variant_to_peak, all.x = TRUE, sort = FALSE)
-    variant_mb_peak <- unique(variant_mb_peak[variant_mb_peak$tf.gene == variant_mb_peak$tf.binding, ])
-    variant_mb_peak <- variant_mb_peak[!is.na(variant_mb_peak$variant), c("variant", "tf.binding", "tf.celltype", "motif")]
-
-    split_vmbp <- split(variant_mb_peak, as.factor(variant_mb_peak$variant))
-
-    for (variant in seq_along(split_vmbp)) {
-        pvariant <- names(split_vmbp[variant])
-        vgm <- split_vmbp[[variant]]
-        mbv_sel <- which(mcol_variant_to_gene$variant == pvariant)
-        vgm$motif <- factor(vgm$motif, levels = mcol_variant_to_gene[mbv_sel, "motif"])
-        names(vgm$tf.celltype) <- vgm$tf.binding
-        vgmm <- vgm[which(vgm$motif %in% mcol_variant_to_gene$motif), ]
-        vgmm <- split(vgmm, vgmm$motif)
-        vgmg <- vgm[which(vgm$tf.gene %in% mcol_variant_to_gene$tf.gene), ]
-        vgmg <- split(vgmg, vgmg$motif)
-        vgm <- mapply(rbind, vgmm, vgmg, SIMPLIFY = F)
-
-        results[mbv_sel]$matchingBindingEvent <- lapply(vgm, function(x) {
-            unique(x$tf.binding)
-        })[results[mbv_sel]$providerId]
-        results[mbv_sel]$matchingCelltype <- lapply(vgm, function(x) {
-            x$tf.celltype
-        })[results[mbv_sel]$providerId]
-        if (any(lengths(results[mbv_sel]$matchingBindingEvent) == 0)) {
-            results[mbv_sel][lengths(results[mbv_sel]$matchingBindingEvent) == 0]$matchingBindingEvent <- NA
-            results[mbv_sel][lengths(results[mbv_sel]$matchingCelltype) == 0]$matchingCelltype <- NA
-        }
-    }
-    attributes(results)$peaks <- remap_binding
-    return(results)
-}
-
-#' @importFrom tools R_user_dir
-#' @importFrom BiocFileCache BiocFileCache
-.get_cache <- function() {
-    cache <- R_user_dir("motifbreakR", which = "cache")
-    BiocFileCache(cache = cache, ask = F)
-}
-
-cachePeakFile <- function(fileURL, genome) {
-    bfc <- .get_cache()
-    rname <- paste("remap2022", genome, sep = "_")
-    rid <- bfcquery(bfc, genome, "rname")$rid
-    if (!length(rid)) {
-        rid <- names(bfcadd(bfc, rname, fileURL, ext = ".Rdata", download = FALSE))
-    }
-    if (!isFALSE(bfcneedsupdate(bfc, rid))) {
-        message("downloading peak file")
-        bfcdownload(bfc, rid, ask = FALSE, FUN = convertPeakFile)
-        message("peak download complete")
-    }
-    bfcrpath(bfc, rids = rid)
-}
-
-#' @importFrom vroom vroom
-loadPeakFile2 <- function(url_list, genome) {
-    peak_path <- cachePeakFile(url_list[[genome]], genome)
-    remap_peaks <- GRanges(vroom(peak_path,
-        delim = "\t",
-        col_names = c(
-            "chr", "start", "end", "name",
-            "score", "strand", "tstart",
-            "tend", "color"
-        ),
-        col_types = c("ciiciciic"),
-        col_select = c(chr, start, end, name),
-        progress = FALSE
-    ))
-    return(remap_peaks)
-}
-
-loadPeakFile <- function(url_list, genome) {
-    peak_path <- cachePeakFile(url_list[[genome]], genome)
-    remap_peaks <- readRDS(peak_path)
-    return(remap_peaks)
-}
-
-convertPeakFile <- function(from, to) {
-    message("processing peak file")
-    remap_peaks <- GRanges(vroom(from,
-        delim = "\t",
-        col_names = c(
-            "chr", "start", "end", "name",
-            "score", "strand", "tstart",
-            "tend", "color"
-        ),
-        col_types = c("ciiciciic"),
-        col_select = c(chr, start, end, name),
-        progress = FALSE
-    ))
-    saveRDS(remap_peaks, file = to)
-    message("processing peak file")
-    TRUE
-}