BamUtil: dedup

Overview of the dedup function of bamUtil

The dedup option of bamUtil determines duplicates in a coordinate sorted SAM/BAM file. It either marks or removes the lower quality duplicates.

This tool also contains the option to perform recalibration.

NOTE: This tool does not properly work on templates that have more than 2 segments. It does not properly match reads when more than 2 reads have the same read name.

Potential future features:

• Soft clip overlapping reads (for now, use: BamUtil: clipOverlap

Handling Duplicates

The deduper reads all the alignments in a coordinate-sorted SAM/BAM looking for duplicates.

The deduper assumes that duplicates in the input BAM file are not marked.

When the deduper detects a marked duplicate in the input BAM file, it will throw an error and stop. To override this behavior, use the --force option; in this mode, alignments that are marked as duplicates in the input file are unmarked before the deduper begins its detection algorithm. The result is that only duplicates detected by the deduper will be marked in or removed from the output file.

The handling of paired-end reads assumes that the mate information in the SAM/BAM records is accurate. If a mate is not found at the expected position, an error message is printed (once per file) indicating this error. Paired-end reads whose mate cannot be found are not marked duplicate and are not used for duplicate marking of other paired-end reads. Single-end reads with the same key as paired-end reads whose mate cannot be found are still marked as duplicate. If this error is encountered, you may want to fix the mate information and reprocess the file through the deduper. Use the --oneChrom option to treat reads with a mate on a different chromosome as single-ended. This option is useful if you are running the deduper on just a single chromosome.

Implementation Notes

Duplicates are determined by checking for matching keys.

The Key is comprised of:

1. Chromosome
2. Orientation (forward/reverse)
3. unclipped start(forward)/end(reverse)
4. Library

Rules:

• Skip Unmapped Reads, they are not marked as duplicate
• Mark a Single-End Read Duplicate (or remove it if configured to do so) if:
  1. A paired-end record has the same key (even if the pair is not proper/the mate is unmapped/the mate is not found)
     -OR-
  2. A single-end record has the same key and a higher base quality sum (sum of all base qualities in the record)
• Mark both Paired-End Reads Duplicate if:

1. Another paired-end pair has the same set of keys and has a higher base quality sum.

This code assumes that at most 1000 bases are clipped at the start of a read.

How to use it

When dedup is invoked without any arguments the usage information is displayed as described below under Usage.

The input SAM/BAM file is required, input File (--in), and must be sorted by coordinate.

The output SAM/BAM file is also required, output File (--out).

Usage

./bam dedup (options) --in <InputBamFile> --out <OutputBamFile> [--log <logFile>] [--oneChrom] [--rmDups] [--force] [--verbose] [--noeof] [--params] [--recab] --refFile <ReferenceFile> [--dbsnp <dbsnpFile>] [--blended <weight>] 

Parameters

Required parameters :
	--in <infile>   : input BAM file name (must be sorted)
	--out <outfile> : output BAM file name (same order with original file)
Optional parameters : (see SAM format specification for details)
	--log <logfile> : log and summary statistics (default: [outfile].log)
	--oneChrom      : Treat reads with mates on different chromosomes as single-ended.
	--rmDups        : Remove duplicates (default is to mark duplicates)
	--force         : Allow mark-duplicated BAM file and force unmarking the duplicates
                    Default is to throw errors when trying to run a mark-duplicated BAM
	--verbose       : Turn on verbose mode
	--noeof         : do not expect an EOF block on a bam file.
	--params        : print the parameter settings
	--recab         : Recalibrate in addition to deduping

Recab Specific Required Parameters
	--refFile <reference file>    : reference file name
Recab Specific Optional Parameters : 
	--dbsnp <known variance file> : dbsnp file of positions
	--blended <weight>            : blended model weight

Input File (--in)

Use --in followed by your file name to specify the SAM/BAM input file.

The program automatically determines if your input file is SAM/BAM/uncompressed BAM without any input other than a filename from the user, unless your input file is stdin.

A - is used to indicate to read from stdin and the extension is used to determine the file type (no extension indicates SAM).

SAM/BAM/Uncompressed BAM from file	--in yourFileName
SAM from stdin	--in -
BAM from stdin	--in -.bam
Uncompressed BAM from stdin	--in -.ubam

Note: Uncompressed BAM is compressed using compression level-0 (so it is not an entirely uncompressed file). This matches the samtools implementation so pipes between our tools and samtools are supported.

Note: The input file must be sorted by coordinate.

Output File (--out)

Use --out followed by your file name to specify the SAM/BAM output file.

The file extension is used to determine whether to write SAM/BAM/uncompressed BAM. A - is used to indicate stdout and the extension for file type (no extension is SAM).

SAM to file	--out yourFileName.sam
BAM to file	--out yourFileName.bam
Uncompressed BAM to file	--out yourFileName.ubam
SAM to stdout	--out -
BAM to stdout	--out -.bam
Uncompressed BAM to stdout	--out -.ubam

Note: Uncompressed BAM is compressed using compression level-0 (so it is not an entirely uncompressed file). This matches the samtools implementation so pipes between our tools and samtools are supported.

Do not require BGZF EOF block (--noeof)

Use --noeof if you do not expect a trailing eof block in your bgzf file.

By default, the trailing empty block is expected and checked for.

Print the Program Parameters (--params)

Use --params to print the parameters for your program to stderr.

Return Value

Returns -1 if input parameters are invalid.

Returns the SamStatus for the reads/writes (0 on success).