bamreadcounts: extract nucleotide counts for targeted variants from the BAM...

View source: R/ntcounts.R

bamreadcountsR Documentation

extract nucleotide counts for targeted variants from the BAM file.

Description

Given a BAM file and target loci, 'bamreadcounts' fetches redcounts for A, T, G, C, Ins, and Del. Function name is an homage to https://github.com/genome/bam-readcount

Usage

bamreadcounts(
  bam = NULL,
  loci = NULL,
  zerobased = FALSE,
  mapq = 10,
  sam_flag = 1024,
  op = NULL,
  fa = NULL,
  nthreads = 4
)

Arguments

bam

Input bam file(s). Required.

loci

Loci file. Can be a tsv file or a data.frame. First two columns should contain chromosome and position (by default assumes coordinates are 1-based)

zerobased

are coordinates zero-based. Default FALSE.

mapq

Map quality. Default 10

sam_flag

SAM FLAG to filter reads. Default 1024

op

Output file basename. Default parses from BAM file

fa

Indexed fasta file. If provided, extracts and adds reference base to the output tsv.

nthreads

Number of threads to use. Each BAM file will be launched on a separate thread. Works only on Unix and macOS.


PoisonAlien/maftools documentation built on Nov. 5, 2024, 4:12 p.m.