getFragmentOverlaps: getFragmentOverlaps

View source: R/getFragmentOverlaps.R

getFragmentOverlapsR Documentation

getFragmentOverlaps

Description

Count the number of overlapping fragments.

Usage

getFragmentOverlaps(
  x,
  barcodes = NULL,
  regionsToExclude = GRanges(c("M", "chrM", "MT", "X", "Y", "chrX", "chrY"), IRanges(1L,
    width = 10^8)),
  minFrags = 500L,
  uniqueFrags = TRUE,
  maxFragSize = 1000L,
  removeHighOverlapSites = TRUE,
  fullInMemory = FALSE,
  BPPARAM = NULL,
  verbose = TRUE,
  ret = c("stats", "loci", "coverages")
)

Arguments

x

The path to a fragments file, or a GRanges object containing the fragments (with the 'name' column containing the barcode, and optionally the 'score' column containing the count).

barcodes

Optional character vector of cell barcodes to consider

regionsToExclude

A GRanges of regions to exclude. As per the original Amulet method, we recommend excluding repeats, as well as sex and mitochondrial chromosomes.

minFrags

Minimum number of fragments for a barcode to be considered. If 'uniqueFrags=TRUE', this is the minimum number of unique fragments. Ignored if 'barcodes' is given.

uniqueFrags

Logical; whether to use only unique fragments.

maxFragSize

Integer indicating the maximum fragment size to consider

removeHighOverlapSites

Logical; whether to remove sites that have more than two reads in unexpectedly many cells.

fullInMemory

Logical; whether to process all chromosomes together. This will speed up the process but at the cost of a very high memory consumption (as all fragments will be loaded in memory). This is anyway the default mode when 'x' is not Tabix-indexed.

BPPARAM

A 'BiocParallel' parameter object for multithreading. Note that multithreading will increase the memory usage.

verbose

Logical; whether to print progress messages.

ret

What to return, either barcode 'stats' (default), 'loci', or 'coverages'.

Details

When used on normal (or compressed) fragment files, this implementation is relatively fast (except for reading in the data) but it has a large memory footprint since the overlaps are performed in memory. It is therefore recommended to compress the fragment files using bgzip and index them with Tabix; in this case each chromosome will be read and processed separately, leading to a considerably lower memory footprint.

Value

A data.frame with counts and overlap statistics for each barcode.


plger/scDblFinder documentation built on Oct. 19, 2024, 6:26 a.m.