(Internal) Extracts evidence of structural variations from reads
Category Structural Variant Discovery
Overview
(Internal) Extracts evidence of structural variations from readsThis tool is used in development and should not be of interest to most researchers. It repackages the first two steps of the structural variation workflow as a separate tool for the convenience of developers.
This tool examines a SAM/BAM/CRAM for reads, or groups of reads, that demonstrate evidence of a structural variation in the vicinity. It records this evidence as a group of text files in a specified output directory on Spark's HDFS file system.
Inputs
- A file of paired-end, aligned and coordinate-sorted reads.
Output
- A directory of text files describing the evidence for structural variation discovered.
Usage example
gatk ExtractSVEvidenceSpark \ -I input_reads.bam \ -O hdfs://my_cluster-m:8020/output_directory --aligner-index-image ignored --kmers-to-ignore ignored
This tool can be run without explicitly specifying Spark options. That is to say, the given example command without Spark options will run locally. See Tutorial#10060 for an example of how to set up and run a Spark tool on a cloud Spark cluster.
ExtractSVEvidenceSpark specific arguments
This table summarizes the command-line arguments that are specific to this tool. For more details on each argument, see the list further down below the table or click on an argument name to jump directly to that entry in the list.
Argument name(s) | Default value | Summary | |
---|---|---|---|
Required Arguments | |||
--aligner-index-image |
null | bwa-mem index image file | |
--input -I |
[] | BAM/SAM/CRAM file containing reads | |
--kmers-to-ignore |
null | file containing ubiquitous kmer list. see FindBadGenomicKmersSpark to generate it. | |
--output -O |
null | HDFS path for output | |
Optional Tool Arguments | |||
--adapter-sequence |
null | Adapter sequence. | |
--allowed-short-fragment-overhang |
10 | Proper pairs have the positive strand read upstream of the negative strand read, but we allow this much slop for short fragments. | |
--arguments_file |
[] | read one or more arguments files and add them to the command line | |
--assembled-contigs-output-order -sort |
coordinate | sorting order to be used for the output assembly alignments SAM/BAM file | |
--assembly-to-mapped-size-ratio-guess |
7 | Guess at the ratio of reads in the final assembly to the number reads mapped to the interval. | |
--bam-partition-size |
0 | maximum number of bytes to read from a file into each partition of reads. Setting this higher will result in fewer partitions. Note that this will not be equal to the size of the partition in memory. Defaults to 0, which uses the default split size (determined by the Hadoop input format, typically the size of one HDFS block). | |
--breakpoint-evidence-dir |
null | directory for evidence output | |
--breakpoint-intervals |
null | file for breakpoint intervals output | |
--cleaner-max-copy-number |
4 | KmerCleaner maximum copy number (not count, but copy number) for a kmer. Kmers observed too frequently are probably mismapped or ubiquitous. | |
--cleaner-max-intervals |
3 | KmerCleaner maximum number of intervals for a localizing kmer. If a kmer occurs in too many intervals, it isn't sufficiently local. | |
--cleaner-min-kmer-count |
4 | KmerCleaner minimum kmer count for a localizing kmer. If we see it less often than this many times, we're guessing it's erroneous. | |
--conf |
[] | spark properties to set on the spark context in the format = | |
--cross-contigs-to-ignore |
null | file containing alt contig names that will be ignored when looking for inter-contig pairs | |
--disable-sequence-dictionary-validation |
false | If specified, do not check the sequence dictionaries from our inputs for compatibility. Use at your own risk! | |
--exclusion-interval-padding |
0 | Exclusion interval padding. | |
--exclusion-intervals |
null | file of reference intervals to exclude | |
--external-evidence |
null | external evidence input file | |
--external-evidence-uncertainty |
150 | Uncertainty in location of external evidence. | |
--external-evidence-weight |
10 | Weight to give external evidence. | |
--fastq-dir |
null | output dir for assembled fastqs | |
--gcs-max-retries -gcs-retries |
20 | If the GCS bucket channel errors out, how many times it will attempt to re-initiate the connection | |
--help -h |
false | display the help message | |
--high-coverage-intervals |
null | file for high-coverage intervals output | |
--high-depth-coverage-factor |
3 | We filter out contiguous regions of the genome that have coverage of at least high-depth-coverage-factor * avg-coverage and a peak coverage of high-depth-coverage-peak-factor * avg-coverage, because the reads mapped to those regions tend to be non-local and high depth prevents accurate assembly. | |
--high-depth-coverage-peak-factor |
7 | We filter out contiguous regions of the genome that have coverage of at least high-depth-coverage-factor * avg-coverage and a peak coverage of high-depth-coverage-peak-factor * avg-coverage, because the reads mapped to those regions tend to be non-local and high depth prevents accurate assembly. | |
--include-mapping-location |
true | Include read mapping location in FASTQ files. | |
--interval-merging-rule -imr |
ALL | Interval merging rule for abutting intervals | |
--interval-only-assembly |
false | Don't look for extra reads mapped outside the interval. | |
--intervals -L |
[] | One or more genomic intervals over which to operate | |
--k-size |
51 | Kmer size. | |
--kmer-intervals |
null | file for kmer intervals output | |
--kmer-max-dust-score |
49 | Maximum kmer DUST score. | |
--max-fastq-size |
3000000 | Maximum total bases in FASTQs that can be assembled. | |
--max-tracked-fragment-length |
2000 | Largest fragment size that will be explicitly counted in determining fragment size statistics. | |
--min-coherent-evidence-count |
7 | Minimum weight of the evidence that shares a distal target locus to validate the evidence. | |
--min-evidence-count |
15 | Minimum weight of the corroborating read evidence to validate some single piece of evidence. | |
--min-evidence-mapq |
20 | The minimum mapping quality for reads used to gather evidence of breakpoints. | |
--min-evidence-match-length |
45 | The minimum length of the matched portion of an interesting alignment. Reads that don't match at least this many reference bases won't be used in gathering evidence. | |
--min-kmers-per-interval |
5 | Minimum number of localizing kmers in a valid interval. | |
--num-reducers |
0 | For tools that shuffle data or write an output, sets the number of reducers. Defaults to 0, which gives one partition per 10MB of input. | |
--program-name |
null | Name of the program running | |
--qname-intervals-for-assembly |
null | file for mapped qname intervals output | |
--qname-intervals-mapped |
null | file for mapped qname intervals output | |
--read-metadata |
null | output file for read metadata | |
--reference -R |
null | Reference sequence | |
--sharded-output |
false | For tools that write an output, write the output in multiple pieces (shards) | |
--spark-master |
local[*] | URL of the Spark Master to submit jobs to when using the Spark pipeline runner. | |
--target-link-file |
null | output file for non-assembled breakpoints in bedpe format | |
--unfiltered-breakpoint-evidence-dir |
null | directory for evidence output | |
--version |
false | display the version number for this tool | |
--write-gfas |
false | Write GFA representation of assemblies in fastq-dir. | |
Optional Common Arguments | |||
--disable-read-filter -DF |
[] | Read filters to be disabled before analysis | |
--disable-tool-default-read-filters |
false | Disable all tool default read filters (WARNING: many tools will not function correctly without their default read filters on) | |
--exclude-intervals -XL |
[] | One or more genomic intervals to exclude from processing | |
--gatk-config-file |
null | A configuration file to use with the GATK. | |
--interval-exclusion-padding -ixp |
0 | Amount of padding (in bp) to add to each interval you are excluding. | |
--interval-padding -ip |
0 | Amount of padding (in bp) to add to each interval you are including. | |
--interval-set-rule -isr |
UNION | Set merging approach to use for combining interval inputs | |
--QUIET |
false | Whether to suppress job-summary info on System.err. | |
--read-filter -RF |
[] | Read filters to be applied before analysis | |
--read-index |
[] | Indices to use for the read inputs. If specified, an index must be provided for every read input and in the same order as the read inputs. If this argument is not specified, the path to the index for each input will be inferred automatically. | |
--read-validation-stringency -VS |
SILENT | Validation stringency for all SAM/BAM/CRAM/SRA files read by this program. The default stringency value SILENT can improve performance when processing a BAM file in which variable-length data (read, qualities, tags) do not otherwise need to be decoded. | |
--TMP_DIR |
[] | Undocumented option | |
--use-jdk-deflater -jdk-deflater |
false | Whether to use the JdkDeflater (as opposed to IntelDeflater) | |
--use-jdk-inflater -jdk-inflater |
false | Whether to use the JdkInflater (as opposed to IntelInflater) | |
--verbosity |
INFO | Control verbosity of logging. | |
Advanced Arguments | |||
--expand-assembly-graph |
true | Traverse assembly graph and produce contigs for all paths. | |
--pop-variant-bubbles |
false | Aggressively simplify local assemblies, ignoring small variants. | |
--remove-shadowed-contigs |
true | Simplify local assemblies by removing contigs shadowed by similar contigs. | |
--showHidden |
false | display hidden arguments |
Argument details
Arguments in this list are specific to this tool. Keep in mind that other arguments are available that are shared with other tools (e.g. command-line GATK arguments); see Inherited arguments above.
--adapter-sequence / NA
Adapter sequence.
String null
--aligner-index-image / NA
bwa-mem index image file
R String null
--allowed-short-fragment-overhang / NA
Proper pairs have the positive strand read upstream of the negative strand read, but we allow this much slop for short fragments.
int 10 [ [ -∞ ∞ ] ]
--arguments_file / NA
read one or more arguments files and add them to the command line
List[File] []
--assembled-contigs-output-order / -sort
sorting order to be used for the output assembly alignments SAM/BAM file
The --assembled-contigs-output-order argument is an enumerated type (SortOrder), which can have one of the following values:
- unsorted
- queryname
- coordinate
- duplicate
- unknown
SortOrder coordinate
--assembly-to-mapped-size-ratio-guess / NA
Guess at the ratio of reads in the final assembly to the number reads mapped to the interval.
int 7 [ [ -∞ ∞ ] ]
--bam-partition-size / NA
maximum number of bytes to read from a file into each partition of reads. Setting this higher will result in fewer partitions. Note that this will not be equal to the size of the partition in memory. Defaults to 0, which uses the default split size (determined by the Hadoop input format, typically the size of one HDFS block).
long 0 [ [ -∞ ∞ ] ]
--breakpoint-evidence-dir / NA
directory for evidence output
String null
--breakpoint-intervals / NA
file for breakpoint intervals output
String null
--cleaner-max-copy-number / NA
KmerCleaner maximum copy number (not count, but copy number) for a kmer. Kmers observed too frequently are probably mismapped or ubiquitous.
int 4 [ [ -∞ ∞ ] ]
--cleaner-max-intervals / NA
KmerCleaner maximum number of intervals for a localizing kmer. If a kmer occurs in too many intervals, it isn't sufficiently local.
int 3 [ [ -∞ ∞ ] ]
--cleaner-min-kmer-count / NA
KmerCleaner minimum kmer count for a localizing kmer. If we see it less often than this many times, we're guessing it's erroneous.
int 4 [ [ -∞ ∞ ] ]
--conf / -conf
spark properties to set on the spark context in the format =
List[String] []
--cross-contigs-to-ignore / NA
file containing alt contig names that will be ignored when looking for inter-contig pairs
This is a path to a text file of contig names (one per line) that will be ignored when looking for inter-contig pairs.
String null
--disable-read-filter / -DF
Read filters to be disabled before analysis
List[String] []
--disable-sequence-dictionary-validation / -disable-sequence-dictionary-validation
If specified, do not check the sequence dictionaries from our inputs for compatibility. Use at your own risk!
boolean false
--disable-tool-default-read-filters / -disable-tool-default-read-filters
Disable all tool default read filters (WARNING: many tools will not function correctly without their default read filters on)
boolean false
--exclude-intervals / -XL
One or more genomic intervals to exclude from processing
Use this argument to exclude certain parts of the genome from the analysis (like -L, but the opposite).
This argument can be specified multiple times. You can use samtools-style intervals either explicitly on the
command line (e.g. -XL 1 or -XL 1:100-200) or by loading in a file containing a list of intervals
(e.g. -XL myFile.intervals).
List[String] []
--exclusion-interval-padding / NA
Exclusion interval padding.
int 0 [ [ -∞ ∞ ] ]
--exclusion-intervals / NA
file of reference intervals to exclude
This is a file that calls out the coordinates of intervals in the reference assembly to exclude from
consideration when calling putative breakpoints.
Each line is a tab-delimited interval with 1-based inclusive coordinates like this:
chr1 124535434 142535434
String null
--expand-assembly-graph / NA
Traverse assembly graph and produce contigs for all paths.
boolean true
--external-evidence / NA
external evidence input file
String null
--external-evidence-uncertainty / NA
Uncertainty in location of external evidence.
int 150 [ [ -∞ ∞ ] ]
--external-evidence-weight / NA
Weight to give external evidence.
int 10 [ [ -∞ ∞ ] ]
--fastq-dir / NA
output dir for assembled fastqs
String null
--gatk-config-file / NA
A configuration file to use with the GATK.
String null
--gcs-max-retries / -gcs-retries
If the GCS bucket channel errors out, how many times it will attempt to re-initiate the connection
int 20 [ [ -∞ ∞ ] ]
--help / -h
display the help message
boolean false
--high-coverage-intervals / NA
file for high-coverage intervals output
String null
--high-depth-coverage-factor / NA
We filter out contiguous regions of the genome that have coverage of at least high-depth-coverage-factor * avg-coverage and a peak coverage of high-depth-coverage-peak-factor * avg-coverage, because the reads mapped to those regions tend to be non-local and high depth prevents accurate assembly.
int 3 [ [ -∞ ∞ ] ]
--high-depth-coverage-peak-factor / NA
We filter out contiguous regions of the genome that have coverage of at least high-depth-coverage-factor * avg-coverage and a peak coverage of high-depth-coverage-peak-factor * avg-coverage, because the reads mapped to those regions tend to be non-local and high depth prevents accurate assembly.
int 7 [ [ -∞ ∞ ] ]
--include-mapping-location / NA
Include read mapping location in FASTQ files.
boolean true
--input / -I
BAM/SAM/CRAM file containing reads
R List[String] []
--interval-exclusion-padding / -ixp
Amount of padding (in bp) to add to each interval you are excluding.
Use this to add padding to the intervals specified using -XL. For example, '-XL 1:100' with a
padding value of 20 would turn into '-XL 1:80-120'. This is typically used to add padding around targets when
analyzing exomes.
int 0 [ [ -∞ ∞ ] ]
--interval-merging-rule / -imr
Interval merging rule for abutting intervals
By default, the program merges abutting intervals (i.e. intervals that are directly side-by-side but do not
actually overlap) into a single continuous interval. However you can change this behavior if you want them to be
treated as separate intervals instead.
The --interval-merging-rule argument is an enumerated type (IntervalMergingRule), which can have one of the following values:
- ALL
- OVERLAPPING_ONLY
IntervalMergingRule ALL
--interval-only-assembly / NA
Don't look for extra reads mapped outside the interval.
boolean false
--interval-padding / -ip
Amount of padding (in bp) to add to each interval you are including.
Use this to add padding to the intervals specified using -L. For example, '-L 1:100' with a
padding value of 20 would turn into '-L 1:80-120'. This is typically used to add padding around targets when
analyzing exomes.
int 0 [ [ -∞ ∞ ] ]
--interval-set-rule / -isr
Set merging approach to use for combining interval inputs
By default, the program will take the UNION of all intervals specified using -L and/or -XL. However, you can
change this setting for -L, for example if you want to take the INTERSECTION of the sets instead. E.g. to
perform the analysis only on chromosome 1 exomes, you could specify -L exomes.intervals -L 1 --interval-set-rule
INTERSECTION. However, it is not possible to modify the merging approach for intervals passed using -XL (they will
always be merged using UNION).
Note that if you specify both -L and -XL, the -XL interval set will be subtracted from the -L interval set.
The --interval-set-rule argument is an enumerated type (IntervalSetRule), which can have one of the following values:
- UNION
- Take the union of all intervals
- INTERSECTION
- Take the intersection of intervals (the subset that overlaps all intervals specified)
IntervalSetRule UNION
--intervals / -L
One or more genomic intervals over which to operate
List[String] []
--k-size / NA
Kmer size.
int 51 [ [ -∞ ∞ ] ]
--kmer-intervals / NA
file for kmer intervals output
String null
--kmer-max-dust-score / NA
Maximum kmer DUST score.
int 49 [ [ -∞ ∞ ] ]
--kmers-to-ignore / NA
file containing ubiquitous kmer list. see FindBadGenomicKmersSpark to generate it.
This is a path to a file of kmers that appear too frequently in the reference to be usable as probes to localize
reads. We don't calculate it here, because it depends only on the reference.
The program FindBadGenomicKmersSpark can produce such a list for you.
R String null
--max-fastq-size / NA
Maximum total bases in FASTQs that can be assembled.
int 3000000 [ [ -∞ ∞ ] ]
--max-tracked-fragment-length / NA
Largest fragment size that will be explicitly counted in determining fragment size statistics.
int 2000 [ [ -∞ ∞ ] ]
--min-coherent-evidence-count / NA
Minimum weight of the evidence that shares a distal target locus to validate the evidence.
int 7 [ [ -∞ ∞ ] ]
--min-evidence-count / NA
Minimum weight of the corroborating read evidence to validate some single piece of evidence.
int 15 [ [ -∞ ∞ ] ]
--min-evidence-mapq / NA
The minimum mapping quality for reads used to gather evidence of breakpoints.
int 20 [ [ -∞ ∞ ] ]
--min-evidence-match-length / NA
The minimum length of the matched portion of an interesting alignment. Reads that don't match at least this many reference bases won't be used in gathering evidence.
int 45 [ [ -∞ ∞ ] ]
--min-kmers-per-interval / NA
Minimum number of localizing kmers in a valid interval.
int 5 [ [ -∞ ∞ ] ]
--num-reducers / NA
For tools that shuffle data or write an output, sets the number of reducers. Defaults to 0, which gives one partition per 10MB of input.
int 0 [ [ -∞ ∞ ] ]
--output / -O
HDFS path for output
R String null
--pop-variant-bubbles / NA
Aggressively simplify local assemblies, ignoring small variants.
boolean false
--program-name / NA
Name of the program running
String null
--qname-intervals-for-assembly / NA
file for mapped qname intervals output
String null
--qname-intervals-mapped / NA
file for mapped qname intervals output
String null
--QUIET / NA
Whether to suppress job-summary info on System.err.
Boolean false
--read-filter / -RF
Read filters to be applied before analysis
List[String] []
--read-index / -read-index
Indices to use for the read inputs. If specified, an index must be provided for every read input and in the same order as the read inputs. If this argument is not specified, the path to the index for each input will be inferred automatically.
List[String] []
--read-metadata / NA
output file for read metadata
String null
--read-validation-stringency / -VS
Validation stringency for all SAM/BAM/CRAM/SRA files read by this program. The default stringency value SILENT can improve performance when processing a BAM file in which variable-length data (read, qualities, tags) do not otherwise need to be decoded.
The --read-validation-stringency argument is an enumerated type (ValidationStringency), which can have one of the following values:
- STRICT
- LENIENT
- SILENT
ValidationStringency SILENT
--reference / -R
Reference sequence
String null
--remove-shadowed-contigs / NA
Simplify local assemblies by removing contigs shadowed by similar contigs.
boolean true
--sharded-output / NA
For tools that write an output, write the output in multiple pieces (shards)
boolean false
--showHidden / -showHidden
display hidden arguments
boolean false
--spark-master / NA
URL of the Spark Master to submit jobs to when using the Spark pipeline runner.
String local[*]
--target-link-file / NA
output file for non-assembled breakpoints in bedpe format
String null
--TMP_DIR / NA
Undocumented option
List[File] []
--unfiltered-breakpoint-evidence-dir / NA
directory for evidence output
String null
--use-jdk-deflater / -jdk-deflater
Whether to use the JdkDeflater (as opposed to IntelDeflater)
boolean false
--use-jdk-inflater / -jdk-inflater
Whether to use the JdkInflater (as opposed to IntelInflater)
boolean false
--verbosity / -verbosity
Control verbosity of logging.
The --verbosity argument is an enumerated type (LogLevel), which can have one of the following values:
- ERROR
- WARNING
- INFO
- DEBUG
LogLevel INFO
--version / NA
display the version number for this tool
boolean false
--write-gfas / NA
Write GFA representation of assemblies in fastq-dir.
boolean false
GATK version 4.0.4.0 built at 02-47-2019 02:47:54.
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