getUniqueCleavageEvents {GUIDEseq} | R Documentation

## Using UMI sequence to obtain the starting sequence library

### Description

PCR amplification often leads to biased representation of the starting sequence population. To track the sequence tags present in the initial sequence library, a unique molecular identifier (UMI) is added to the 5 prime of each sequence in the staring library. This function uses the UMI sequence plus the first few sequence from R1 reads to obtain the starting sequence library.

### Usage

    getUniqueCleavageEvents(alignment.inputfile, umi.inputfile,
     alignment.format = c("auto", "bam", "bed"),
     umi.header = FALSE, read.ID.col = 1,
    umi.col = 2, umi.sep = "\t", keep.chrM = FALSE,
    keep.R1only = TRUE, keep.R2only = TRUE,
    concordant.strand = TRUE, max.paired.distance = 1000,
    min.mapping.quality = 30, max.R1.len = 130, max.R2.len = 130,
    apply.both.max.len = FALSE, same.chromosome = TRUE,
    distance.inter.chrom = -1, min.R1.mapped = 20, min.R2.mapped = 20,
    apply.both.min.mapped = FALSE, max.duplicate.distance = 0,
    umi.plus.R1start.unique = TRUE, umi.plus.R2start.unique = TRUE,
    n.cores.max = 6)

### Arguments

`alignment.inputfile` | The alignment file. Currently supports bed output file with CIGAR information. Suggest run the workflow binReads.sh, which sequentially runs barcode binning, adaptor removal, alignment to genome, alignment quality filtering, and bed file conversion. Please download the workflow function and its helper scripts at http://mccb.umassmed.edu/GUIDE-seq/binReads/
`umi.inputfile` | A text file containing at least two columns, one is the read identifier and the other is the UMI or UMI plus the first few bases of R1 reads. Suggest use getUMI.sh to generate this file. Please download the script and its helper scripts at http://mccb.umassmed.edu/GUIDE-seq/getUMI/
`alignment.format` | The format of the alignment input file. Currently only bam and bed file format is supported. BED format will be deprecated soon.
`umi.header` | Indicates whether the umi input file contains a header line or not. Default to FALSE
`read.ID.col` | The index of the column containing the read identifier in the umi input file, default to 1
`umi.col` | The index of the column containing the umi or umi plus the first few bases of sequence from the R1 reads, default to 2
`umi.sep` | column separator in the umi input file, default to tab
`keep.chrM` | Specify whether to include alignment from chrM. Default FALSE
`keep.R1only` | Specify whether to include alignment with only R1 without paired R2. Default TRUE
`keep.R2only` | Specify whether to include alignment with only R2 without paired R1. Default TRUE
`concordant.strand` | Specify whether the R1 and R2 should be aligned to the same strand or opposite strand. Default opposite.strand (TRUE)
`max.paired.distance` | Specify the maximum distance allowed between paired R1 and R2 reads. Default 1000 bp
`min.mapping.quality` | Specify min.mapping.quality of acceptable alignments
`max.R1.len` | The maximum retained R1 length to be considered for downstream analysis, default 130 bp. Please note that default of 130 works well when the read length 150 bp. Please also note that retained R1 length is not necessarily equal to the mapped R1 length
`max.R2.len` | The maximum retained R2 length to be considered for downstream analysis, default 130 bp. Please note that default of 130 works well when the read length 150 bp. Please also note that retained R2 length is not necessarily equal to the mapped R2 length
`apply.both.max.len` | Specify whether to apply maximum length requirement to both R1 and R2 reads, default FALSE
`same.chromosome` | Specify whether the paired reads are required to align to the same chromosome, default TRUE
`distance.inter.chrom` | Specify the distance value to assign to the paired reads that are aligned to different chromosome, default -1
`min.R1.mapped` | The maximum mapped R1 length to be considered for downstream analysis, default 30 bp.
`min.R2.mapped` | The maximum mapped R2 length to be considered for downstream analysis, default 30 bp.
`apply.both.min.mapped` | Specify whether to apply minimum mapped length requirement to both R1 and R2 reads, default FALSE
`max.duplicate.distance` | Specify the maximum distance apart for two reads to be considered as duplicates, default 0. Currently only 0 is supported
`umi.plus.R1start.unique` | To specify whether two mapped reads are considered as unique if both containing the same UMI and same alignment start for R1 read, default TRUE.
`umi.plus.R2start.unique` | To specify whether two mapped reads are considered as unique if both containing the same UMI and same alignment start for R2 read, default TRUE.
`n.cores.max` | Indicating maximum number of cores to use in multi core mode, i.e., parallel processing, default 6. Please set it to 1 to disable multicore processing for small dataset.

### Value

`cleavage.gr` | Cleavage sites with one site per UMI as GRanges with metadata column total set to 1 for each range
`unique.umi.plus.R2` | a data frame containing unique cleavage site from R2 reads mapped to plus strand with the following columns chr.y (chromosome of readSide.y/R2 read) chr.x (chromosome of readSide.x/R1 read) strand.y (strand of readSide.y/R2 read) strand.x (strand of readSide.x/R1 read) start.y (start of readSide.y/R2 read) end.x (start of readSide.x/R1 read) UMI (unique molecular identifier (umi) or umi with the first few bases of R1 read)
`unique.umi.minus.R2` | a data frame containing unique cleavage site from R2 reads mapped to minus strand with the following columns chr.y (chromosome of readSide.y/R2 read) chr.x (chromosome of readSide.x/R1 read) strand.y (strand of readSide.y/R2 read) strand.x (strand of readSide.x/R1 read) end.y (end of readSide.y/R2 read) start.x (start of readSide.x/R1 read) UMI (unique molecular identifier (umi) or umi with the first few bases of R1 read)
`unique.umi.plus.R1` | a data frame containing unique cleavage site from R1 reads mapped to minus strand without corresponding R2 reads mapped to the plus strand, with the following columns chr.y (chromosome of readSide.y/R2 read) chr.x (chromosome of readSide.x/R1 read) strand.y (strand of readSide.y/R2 read) strand.x (strand of readSide.x/R1 read) start.x (start of readSide.x/R1 read) start.y (start of readSide.y/R2 read) UMI (unique molecular identifier (umi) or umi with the first few bases of R1 read)
`unique.umi.minus.R1` | a data frame containing unique cleavage site from R1 reads mapped to plus strand without corresponding R2 reads mapped to the minus strand, with the following columns chr.y (chromosome of readSide.y/R2 read) chr.x (chromosome of readSide.x/R1 read) strand.y (strand of readSide.y/R2 read) strand.x (strand of readSide.x/R1 read) end.x (end of readSide.x/R1 read) end.y (end of readSide.y/R2 read) UMI (unique molecular identifier (umi) or umi with the first few bases of R1 read)
`all.umi` | a data frame containing all the mapped reads with the following columns. readName (read ID), chr.x (chromosome of readSide.x/R1 read), start.x (start of eadSide.x/R1 read), end.x (end of eadSide.x/R1 read), mapping.qual.x (mapping quality of readSide.x/R1 read), strand.x (strand of readSide.x/R1 read), cigar.x (CIGAR of readSide.x/R1 read) , readSide.x (1/R1), chr.y (chromosome of readSide.y/R2 read) start.y (start of readSide.y/R2 read), end.y (end of readSide.y/R2 read), mapping.qual.y (mapping quality of readSide.y/R2 read), strand.y (strand of readSide.y/R2 read), cigar.y (CIGAR of readSide.y/R2 read), readSide.y (2/R2) R1.base.kept (retained R1 length), R2.base.kept (retained R2 length), distance (distance between mapped R1 and R2), UMI (unique molecular identifier (umi) or umi with the first few bases of R1 read)

### Author(s)

Lihua Julie Zhu

### References

Shengdar Q Tsai and J Keith Joung et al. GUIDE-seq enables genome-wide profiling of off-target cleavage by CRISPR-Cas nucleases. Nature Biotechnology 33, 187 to 197 (2015)

### See Also

getPeaks

### Examples

        if(interactive())
        {
            umiFile <- system.file("extdata", "UMI-HEK293_site4_chr13.txt",
               package = "GUIDEseq")
            alignFile <- system.file("extdata","bowtie2.HEK293_site4_chr13.sort.bam" ,
                package = "GUIDEseq")
            cleavages <- getUniqueCleavageEvents(
                alignment.inputfile = alignFile , umi.inputfile = umiFile,
                n.cores.max = 1)
            names(cleavages)
            #output a summary of duplicate counts for sequencing saturation assessment
            table(cleavages$umi.count.summary$n)
        }

[Package GUIDEseq version 1.18.0 Index]