R/reads.R

Defines functions getReadsPage streamReads getReads getCigar getPosition getReferenceName getFlags readsToGAlignments

Documented in getReads getReadsPage readsToGAlignments

# Copyright 2014 Google Inc. All rights reserved.
#
# Licensed under the Apache License, Version 2.0 (the 'License');
# you may not use this file except in compliance with the License.
# You may obtain a copy of the License at
#
#     http://www.apache.org/licenses/LICENSE-2.0
#
# Unless required by applicable law or agreed to in writing, software
# distributed under the License is distributed on an 'AS IS' BASIS,
# WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied.
# See the License for the specific language governing permissions and
# limitations under the License.

#' Get one page of reads from Google Genomics.
#'
#' In general, use the getReads method instead.  It calls this method,
#' returning reads from all of the pages that comprise the requested
#' genomic range.
#'
#' By default, this function gets reads for a small genomic region for one
#' sample in 1,000 Genomes.
#'
#' Note that the Global Alliance for Genomics and Health API uses a 0-based
#' coordinate system.  For more detail, please see GA4GH discussions such
#' as the following:
#' \itemize{
#'    \item\url{https://github.com/ga4gh/schemas/issues/168}
#'    \item\url{https://github.com/ga4gh/schemas/issues/121}
#'}
#'
#' @param readGroupSetId The read group set ID.
#' @param chromosome The chromosome.
#' @param start Start position on the chromosome in 0-based coordinates.
#' @param end End position on the chromosome in 0-based coordinates.
#' @param fields A subset of fields to retrieve.  The default (NULL) will
#'   return all fields.
#' @param pageToken The page token. This can be NULL (default) for the first
#'   page.
#' @return A two-element list is returned by the function.
#'
#'     reads: A list of R objects corresponding to the JSON objects returned
#'               by the Google Genomics Reads API.
#'
#'     nextPageToken: The token to be used to retrieve the next page of
#'                    results, if applicable.
#' @family page fetch functions
#' @examples
#' # Authenticated on package load from the env variable GOOGLE_API_KEY.
#' readsPage <- getReadsPage()
#' summary(readsPage)
#' summary(readsPage$reads[[1]])
getReadsPage <- function(readGroupSetId="CMvnhpKTFhDnk4_9zcKO3_YB",
                         chromosome="22",
                         start=16051400,
                         end=16051500,
                         fields=NULL,
                         pageToken=NULL) {

  body <- list(readGroupSetIds=list(readGroupSetId), referenceName=chromosome,
               start=start, end=end, pageToken=pageToken)

  results <- getSearchPage("reads", body, fields, pageToken)

  list(reads=results$alignments, nextPageToken=results$nextPageToken)
}

streamReads <- function(readGroupSetId, chromosome, start, end) {
  if (missing(readGroupSetId) || missing(chromosome) ||
      missing(start) || missing(end)) {
    stop("All arguments need to be provided to streamReads.")
  }

  body <- list(readGroupSetId = readGroupSetId, referenceName = chromosome,
               start = start, end = end)

  callGRPCMethod("StreamReads", toJSON(body))
}

#' Get reads from Google Genomics.
#'
#' This function will return all of the reads that comprise the requested
#' genomic range, iterating over paginated results as necessary.
#'
#' By default, this function gets reads for a small genomic region for one
#' sample in 1,000 Genomes.
#'
#' Optionally pass a converter as appropriate for your use case.  By passing it
#' to this method, only the converted objects will be accumulated in memory.
#' The converter function should return an empty container of the desired type
#' if called without any arguments.
#'
#' @param readGroupSetId The read group set ID.
#' @param chromosome The chromosome.
#' @param start Start position on the chromosome in 0-based coordinates.
#' @param end End position on the chromosome in 0-based coordinates.
#' @param fields A subset of fields to retrieve.  The default (NULL) will
#'               return all fields.
#' @param converter A function that takes a list of read R objects and returns
#'                  them converted to the desired type.
#' @param useGRPC Whether to use GRPC mechanism to query.
#' @return By default, the return value is a list of R objects
#' corresponding to the JSON objects returned by the Google Genomics
#' Reads API.  If a converter is passed, object(s) of the type
#' returned by the converter will be returned by this function.
#' @seealso \code{\link{getVariants}}
#' @examples
#' # Authenticated on package load from the env variable GOOGLE_API_KEY.
#' reads <- getReads()
#' summary(reads)
#' summary(reads[[1]])
getReads <- function(readGroupSetId="CMvnhpKTFhDnk4_9zcKO3_YB",
                     chromosome="22",
                     start=16051400,
                     end=16051500,
                     fields=NULL,
                     converter=c,
                     useGRPC = getOption("google_genomics_use_grpc")) {
  if (isTRUE(useGRPC)) {
    stopifnot(isGRPCAvailable())
    result <- streamReads(readGroupSetId, chromosome, start, end)
    if (is.null(result)) {
      stop("Something went wrong. Check printed messages above.")
    }
    return(converter(fromJSON(result)$alignments))
  }

  pageToken <- NULL
  reads <- converter()
  repeat {
    result <- getReadsPage(readGroupSetId=readGroupSetId,
                           chromosome=chromosome,
                           start=start,
                           end=end,
                           fields=fields,
                           pageToken=pageToken)
    pageToken <- result$nextPageToken
    # TODO improve performance,
    # see https://github.com/Bioconductor/GoogleGenomics/issues/17
    reads <- c(reads, converter(result$reads))
    if (is.null(pageToken) || pageToken == "") {
      break
    }
    message(paste("Continuing read query with the nextPageToken:", pageToken))
  }

  message("Reads are now available.")
  reads
}

# Transformation helpers
cigar_enum_map <- list(
    ALIGNMENT_MATCH="M",
    CLIP_HARD="H",
    CLIP_SOFT="S",
    DELETE="D",
    INSERT="I",
    PAD="P",
    SEQUENCE_MATCH="=",
    SEQUENCE_MISMATCH="X",
    SKIP="N")

getCigar <- function(read) {
  paste(
      sapply(
          read$alignment$cigar,
          function(cigarPiece) {
            paste0(cigarPiece$operationLength,
                   cigar_enum_map[cigarPiece$operation])
          }),
      collapse="")
}

getPosition <- function(read) {
  as.integer(read$alignment$position$position)
}

getReferenceName <- function(read) {
  read$alignment$position$referenceName
}

getFlags <- function(read) {
  flags <- 0

  if (isTRUE(read$numberReads == 2)) {
    flags <- flags + 1  # read_paired
  }
  if (isTRUE(read$properPlacement)) {
    flags <- flags + 2  # read_proper_pair
  }
  if (is.null(getPosition(read))) {
    flags <- flags + 4  # read_unmapped
  }
  if (is.null(read$nextMatePosition$position)) {
    flags <- flags + 8  # mate_unmapped
  }
  if (isTRUE(read$alignment$position$reverseStrand)) {
    flags <- flags + 16  # read_reverse_strand
  }
  if (isTRUE(read$nextMatePosition$reverseStrand)) {
    flags <- flags + 32  # mate_reverse_strand
  }
  if (isTRUE(read$readNumber == 0)) {
    flags <- flags + 64  # first_in_pair
  }
  if (isTRUE(read$readNumber == 1)) {
    flags <- flags + 128  # second_in_pair
  }
  if (isTRUE(read$secondaryAlignment)) {
    flags <- flags + 256  # secondary_alignment
  }
  if (isTRUE(read$failedVendorQualityChecks)) {
    flags <- flags + 512  # failed_quality_check
  }
  if (isTRUE(read$duplicateFragment)) {
    flags <- flags + 1024  # duplicate_read
  }
  if (isTRUE(read$supplementaryAlignment)) {
    flags <- flags + 2048  # supplementary_alignment
  }
  flags
}

#' Convert reads to GAlignments.
#'
#' Note that the Global Alliance for Genomics and Health API uses a 0-based
#' coordinate system.  For more detail, please see GA4GH discussions such
#' as the following:
#' \itemize{
#'    \item\url{https://github.com/ga4gh/schemas/issues/168}
#'    \item\url{https://github.com/ga4gh/schemas/issues/121}
#' }
#'
#' @param reads A list of R objects corresponding to the JSON objects
#'  returned by the Google Genomics Reads API.
#' @param oneBasedCoord Convert genomic positions to 1-based coordinates.
#' @param slStyle The style for seqnames (chrN or N or...).  Default is UCSC.
#' @return \link[GenomicAlignments]{GAlignments}
#' @family reads converter functions
#' @examples
#' # Authenticated on package load from the env variable GOOGLE_API_KEY.
#' alignments1 <- getReads(converter=readsToGAlignments)
#' summary(alignments1)
#' alignments2 <- readsToGAlignments(getReads())
#' print(identical(alignments1, alignments2))
readsToGAlignments <- function(reads, oneBasedCoord=TRUE, slStyle="UCSC") {

  if (missing(reads)) {
    return(GAlignments())
  }

  # Transform the Genomics API data into a GAlignments object
  names <- sapply(reads, "[[", "fragmentName")
  cigars <- sapply(reads, getCigar)
  positions <- sapply(reads, getPosition)
  if (oneBasedCoord) {
    positions <- as.integer(positions + 1)
  }
  flags <- sapply(reads, getFlags)
  chromosomes <- sapply(reads, getReferenceName)

  isMinusStrand <- bamFlagAsBitMatrix(as.integer(flags),
                                      bitnames="isMinusStrand")
  alignments <- GAlignments(
      seqnames=Rle(chromosomes),
      strand=strand(as.vector(ifelse(isMinusStrand, "-", "+"))),
      pos=positions, cigar=cigars, names=names, flag=flags)

  seqlevelsStyle(alignments) <- slStyle
  alignments
}

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GoogleGenomics documentation built on May 2, 2019, 12:54 a.m.