count_normalize_chip: Counts and normalizes (and transforms) ChIP-seq read coverage

In kevinlkx/TOP: Predict transcription factor occupancy using DNase- or ATAC-seq data

Counts and normalizes (and transforms) ChIP-seq read coverage

Description

Counts ChIP-seq read coverage for each BAM file using the coverage function from bedtools. Then normalizes the read counts by scaling to the reference ChIP-seq library size, and transforms the ChIP-seq read counts.

Usage

count_normalize_chip(
  sites,
  chip_bam_files,
  chip_idxstats_files,
  chrom_size_file,
  ref_size = 2e+07,
  transform = c("none", "asinh", "log2", "sqrt"),
  bedtools_path = "bedtools"
)

Arguments

sites	A data frame containing the candidate sites.
chip_bam_files	ChIP-seq BAM files (may include multiple replicates).
chip_idxstats_files	ChIP-seq idxstats files (may include multiple replicates). (Default: uses the corresponding .idxstats.txt files in the same directory of the BAM files).
chrom_size_file	Chromosome size file.
ref_size	Scales to ChIP-seq reference library size (Default: 2e7)
transform	Transformation for ChIP-seq read counts. Options are ‘none’ (no transformation), ‘asinh’, ‘log2’, and ‘'sqrt'’.
bedtools_path	Path to bedtools executable.

Value

A data frame of candidate sites and normalized (and transformed) ChIP-seq read counts around each candidate site.

Examples

## Not run: 
sites_chip <- count_normalize_chip(sites,
                                   chip_bam_files=c('ChIPseq.rep1.bam', 'ChIPseq.rep2.bam'),
                                   chrom_size_file='hg38.chrom.sizes',
                                   ref_size=2e7)

## End(Not run)

kevinlkx/TOP documentation built on May 4, 2022, 6:30 p.m.