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  "Title": "Variant annotations for structural variants",
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  "Date": "2024-04-23",
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  "Description": "StructuralVariantAnnotation provides a framework for\nanalysis of structural variants within the Bioconductor\necosystem. This package contains contains useful helper\nfunctions for dealing with structural variants in VCF format.\nThe packages contains functions for parsing VCFs from a number\nof popular callers as well as functions for dealing with\nbreakpoints involving two separate genomic loci encoded as\nGRanges objects.",
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  "Author": "Daniel Cameron [aut, cre] (ORCID:\n<https://orcid.org/0000-0002-0951-7116>),\nRuining Dong [aut] (ORCID: <https://orcid.org/0000-0003-1433-0484>)",
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      "title": "Adjusting the nominal position of a pair of partnered breakpoint.",
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      "title": "Extracting unpartnered breakend structural variants as a GRanges",
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        "breakendRanges,VCF-method"
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        "breakpointRanges",
        "breakpointRanges,VCF-method"
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      "title": "Finds duplication events that are reported as inserts. As sequence alignment algorithms do no allow backtracking, long read-based variant callers will frequently report small duplication as insertion events. Whilst both the duplication and insertion representations result in the same sequence, this representational difference is problematic when comparing variant call sets.",
      "topics": [
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    },
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      "title": "Determining whether the variant is a structural variant",
      "topics": [
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        "isStructural,CollapsedVCF-method",
        "isStructural,ExpandedVCF-method",
        "isStructural,VCF-method"
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    },
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      "title": "Determining whether the variant is a symbolic allele.",
      "topics": [
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        "isSymbolic,CollapsedVCF-method",
        "isSymbolic,ExpandedVCF-method"
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      "title": "Detecting nuclear mitochondria fusion events.",
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