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Developed in the Data Sciences Platform at the Broad Institute, the toolkit offers a wide variety of tools with a primary focus on variant discovery and genotyping. Its powerful processing engine and high-performance computing features make it capable of taking on projects of any size. Learn more

BaseRecalibratorSparkSharded (EXPERIMENTAL) Follow

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  • BaseRecalibrator on Spark (experimental sharded implementation)

    Category Read Data Manipulation


    Overview

    Experimental sharded spark implementation of the first pass of the base quality score recalibration. Generates a recalibration table based on various covariates. The default covariates are read group, reported quality score, machine cycle, and nucleotide context.

    Input

    The input read data whose base quality scores need to be assessed.

    A database of known polymorphic sites to skip over.

    Output

    A GATK Report file with many tables:

    1. The list of arguments
    2. The quantized qualities table
    3. The recalibration table by read group
    4. The recalibration table by quality score
    5. The recalibration table for all the optional covariates

    The GATK Report is intended to be easy to read by humans or computers. Check out the documentation of the GATKReport to learn how to manipulate this table.

    Examples

     gatk BaseRecalibratorSparkSharded \
       -I gs://my-gcs-bucket/my_reads.bam \
       -R gs://my-gcs-bucket/reference.fasta \
       --known-sites gs://my-gcs-bucket/sites_of_variation.vcf \
       --known-sites gs://my-gcs-bucket/another/optional/setOfSitesToMask.vcf \
       -O gs://my-gcs-bucket/recal_data.table \
       -- \
       --sparkRunner GCS \
       --cluster my-dataproc-cluster
     

    BaseRecalibratorSparkSharded 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
    --input
     -I
    [] BAM/SAM/CRAM file containing reads
    --known-sites
    [] the known variants. Must be local.
    --output
     -O
    null Path to save the final recalibration tables to.
    --reference
     -R
    null Reference sequence file
    Optional Tool Arguments
    --arguments_file
    [] read one or more arguments files and add them to the command line
    --binary-tag-name
    null the binary tag covariate name if using it
    --bqsr-baq-gap-open-penalty
    40.0 BQSR BAQ gap open penalty (Phred Scaled). Default value is 40. 30 is perhaps better for whole genome call sets
    --conf
    [] spark properties to set on the spark context in the format =
    --default-base-qualities
    -1 Assign a default base quality
    --deletions-default-quality
    45 default quality for the base deletions covariate
    --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
    --indels-context-size
     -ics
    3 Size of the k-mer context to be used for base insertions and deletions
    --insertions-default-quality
    45 default quality for the base insertions covariate
    --interval-merging-rule
     -imr
    ALL Interval merging rule for abutting intervals
    --intervals
     -L
    [] One or more genomic intervals over which to operate
    --low-quality-tail
    2 minimum quality for the bases in the tail of the reads to be considered
    --maximum-cycle-value
     -max-cycle
    500 The maximum cycle value permitted for the Cycle covariate
    --mismatches-context-size
     -mcs
    2 Size of the k-mer context to be used for base mismatches
    --mismatches-default-quality
    -1 default quality for the base mismatches covariate
    --preserve-qscores-less-than
    6 Don't recalibrate bases with quality scores less than this threshold (with -bqsr)
    --program-name
    null Name of the program running
    --quantizing-levels
    16 number of distinct quality scores in the quantized output
    --spark-master
    local[*] URL of the Spark Master to submit jobs to when using the Spark pipeline runner.
    --use-original-qualities
     -OQ
    false Use the base quality scores from the OQ tag
    --version
    false display the version number for this tool
    Optional Common Arguments
    --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-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
    --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.


    --arguments_file / NA

    read one or more arguments files and add them to the command line

    List[File]  []


    --binary-tag-name / NA

    the binary tag covariate name if using it
    The tag name for the binary tag covariate (if using it)

    String  null


    --bqsr-baq-gap-open-penalty / NA

    BQSR BAQ gap open penalty (Phred Scaled). Default value is 40. 30 is perhaps better for whole genome call sets

    double  40.0  [ [ -∞  ∞ ] ]


    --conf / -conf

    spark properties to set on the spark context in the format =

    List[String]  []


    --default-base-qualities / NA

    Assign a default base quality
    If reads are missing some or all base quality scores, this value will be used for all base quality scores. By default this is set to -1 to disable default base quality assignment.

    byte  -1  [ [ -∞  ∞ ] ]


    --deletions-default-quality / NA

    default quality for the base deletions covariate
    A default base qualities to use as a prior (reported quality) in the mismatch covariate model. This value will replace all base qualities in the read for this default value. Negative value turns it off. [default is on]

    byte  45  [ [ -∞  ∞ ] ]


    --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]  []


    --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


    --indels-context-size / -ics

    Size of the k-mer context to be used for base insertions and deletions
    The context covariate will use a context of this size to calculate its covariate value for base insertions and deletions. Must be between 1 and 13 (inclusive). Note that higher values will increase runtime and required java heap size.

    int  3  [ [ -∞  ∞ ] ]


    --input / -I

    BAM/SAM/CRAM file containing reads

    R List[String]  []


    --insertions-default-quality / NA

    default quality for the base insertions covariate
    A default base qualities to use as a prior (reported quality) in the insertion covariate model. This parameter is used for all reads without insertion quality scores for each base. [default is on]

    byte  45  [ [ -∞  ∞ ] ]


    --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-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]  []


    --known-sites / NA

    the known variants. Must be local.

    R List[String]  []


    --low-quality-tail / NA

    minimum quality for the bases in the tail of the reads to be considered
    Reads with low quality bases on either tail (beginning or end) will not be considered in the context. This parameter defines the quality below which (inclusive) a tail is considered low quality

    byte  2  [ [ -∞  ∞ ] ]


    --maximum-cycle-value / -max-cycle

    The maximum cycle value permitted for the Cycle covariate
    The cycle covariate will generate an error if it encounters a cycle greater than this value. This argument is ignored if the Cycle covariate is not used.

    int  500  [ [ -∞  ∞ ] ]


    --mismatches-context-size / -mcs

    Size of the k-mer context to be used for base mismatches
    The context covariate will use a context of this size to calculate its covariate value for base mismatches. Must be between 1 and 13 (inclusive). Note that higher values will increase runtime and required java heap size.

    int  2  [ [ -∞  ∞ ] ]


    --mismatches-default-quality / NA

    default quality for the base mismatches covariate
    A default base qualities to use as a prior (reported quality) in the mismatch covariate model. This value will replace all base qualities in the read for this default value. Negative value turns it off. [default is off]

    byte  -1  [ [ -∞  ∞ ] ]


    --output / -O

    Path to save the final recalibration tables to.

    R String  null


    --preserve-qscores-less-than / NA

    Don't recalibrate bases with quality scores less than this threshold (with -bqsr)
    This flag tells GATK not to modify quality scores less than this value. Instead they will be written out unmodified in the recalibrated BAM file. In general it's unsafe to change qualities scores below < 6, since base callers use these values to indicate random or bad bases. For example, Illumina writes Q2 bases when the machine has really gone wrong. This would be fine in and of itself, but when you select a subset of these reads based on their ability to align to the reference and their dinucleotide effect, your Q2 bin can be elevated to Q8 or Q10, leading to issues downstream.

    int  6  [ [ -∞  ∞ ] ]


    --program-name / NA

    Name of the program running

    String  null


    --quantizing-levels / NA

    number of distinct quality scores in the quantized output
    BQSR generates a quantization table for quick quantization later by subsequent tools. BQSR does not quantize the base qualities, this is done by the engine with the -qq or -bqsr options. This parameter tells BQSR the number of levels of quantization to use to build the quantization table.

    int  16  [ [ -∞  ∞ ] ]


    --QUIET / NA

    Whether to suppress job-summary info on System.err.

    Boolean  false


    --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-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 file

    R String  null


    --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[*]


    --TMP_DIR / NA

    Undocumented option

    List[File]  []


    --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


    --use-original-qualities / -OQ

    Use the base quality scores from the OQ tag
    This flag tells GATK to use the original base qualities (that were in the data before BQSR/recalibration) which are stored in the OQ tag, if they are present, rather than use the post-recalibration quality scores. If no OQ tag is present for a read, the standard qual score will be used.

    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


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    GATK version 4.0.2.0 built at 25-48-2019 02:48:40.

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