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  • Showing docs for version 3.7-0


    HaplotypeResolver

    Haplotype-based resolution of variants in separate callsets.

    Category Variant Manipulation Tools

    Traversal LocusWalker

    PartitionBy LOCUS


    Overview

    HaplotypeResolver is a tool that takes two VCF files and constructs haplotypes based on the variants inside them. From that, it can resolve potential differences in variant calls that are inherently the same (or similar) variants. Records are annotated with the set and status attributes.

    Input

    Two variant files to resolve.

    Output

    A single consensus VCF.

    Usage example

     java -jar GenomeAnalysisTK.jar \
       -T HaplotypeResolver \
       -R reference.fasta \
       -V:v1 input1.vcf \
       -V:v2 input2.vcf \
       -o output.vcf
     

    Additional Information

    Read filters

    These Read Filters are automatically applied to the data by the Engine before processing by HaplotypeResolver.

    Window size

    This tool uses a sliding window on the reference.


    Command-line Arguments

    Engine arguments

    All tools inherit arguments from the GATK Engine' "CommandLineGATK" argument collection, which can be used to modify various aspects of the tool's function. For example, the -L argument directs the GATK engine to restrict processing to specific genomic intervals; or the -rf argument allows you to apply certain read filters to exclude some of the data from the analysis.

    HaplotypeResolver 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 Inputs
    --variant
     -V
    NA Input VCF file
    Optional Outputs
    --out
     -o
    stdout File to which variants should be written
    Optional Parameters
    --setKey
    set Key used in the INFO key=value tag emitted describing which set the combined VCF record came from
    --statusKey
    status Key used in the INFO key=value tag emitted describing the extent to which records match

    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.


    --out / -o

    File to which variants should be written

    VariantContextWriter  stdout


    --setKey / -setKey

    Key used in the INFO key=value tag emitted describing which set the combined VCF record came from
    Set to 'null' if you don't want the set field emitted.

    String  set


    --statusKey / -statusKey

    Key used in the INFO key=value tag emitted describing the extent to which records match
    Set to 'null' if you don't want the status field emitted.

    String  status


    --variant / -V

    Input VCF file

    This argument supports reference-ordered data (ROD) files in the following formats: BCF2, VCF, VCF3

    R List[RodBinding[VariantContext]]  NA