alignSTAR: STAR alignment

View source: R/core_in_WEXAC.R

alignSTARR Documentation

STAR alignment

Description

Wrapper to perform alignment of sequencing reads to a reference genome using STAR (Dobin) and sorting and indexing using Samtools.

Usage

alignSTAR(
  read1Files,
  STARgenomeDir,
  pairedEnd = TRUE,
  zipped = TRUE,
  nCores = 4,
  alignEndsType = "Local",
  alignIntronMax = 0,
  outFilterMultimapNmax = 10,
  outDir,
  otherSTARparams = "",
  dry = FALSE
)

Arguments

read1Files

character. Path to R1 FASTQ files

STARgenomeDir

character. Path to STAR genome to map to

pairedEnd

logical. Indicating if to expect a Read2 FASTQ file File will be automatically looked for but both need to include "_R1", and "_R2" in their respective file names.

zipped

logical. TRUE as default for zipped FASTQ files, will be read with zcat. If set to FALSE FASTQ files will be read with cat, as not zipped.

nCores

numeric. Number of cores used for alignment and sorting processes.

alignEndsType

character. type of read ends alignment (See STAR manual for more info)

alignIntronMax

numeric. maximum intron size, if 0, max intron size will be determined by default as (2ˆwinBinNbits)*winAnchorDistNbins (See STAR manual for more info)

outFilterMultimapNmax

numeric. Threshold for which a read will have multiple mappings. Default is 10. For unique alignment change the value to 1.

outDir

character. Path to output directory

otherSTARparams

character. Additional parameters not covered by the arguments of this function can be added here, separated by spaces.

dry

logical. If set to TRUE the alignment is not performed, only output are the paths to expected output files.


SchwartzLab/brainSTORM documentation built on May 14, 2022, 5:14 p.m.