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  "Description": "A streamlined tool for eplet analysis of donor and\nrecipient HLA (human leukocyte antigen) mismatch. Messy,\nlow-resolution HLA typing data is cleaned, and imputed to\nhigh-resolution using the NMDP (National Marrow Donor Program)\nhaplotype reference database\n<https://haplostats.org/haplostats>. High resolution data is\nanalyzed for overall or single antigen eplet mismatch using a\nreference table (currently supporting 'HLAMatchMaker'\n<http://www.epitopes.net> versions 2 and 3). Data can enter or\nexit the workflow at different points depending on the user's\naims and initial data quality.",
  "Authors@R": "c(person(\"Joan\",\"Zhang\",email = \"joan.zhang@emory.edu\", role = c(\"aut\", \"cre\")),\nperson(\"Aileen\",\"Johnson\",email = \"aileen.johnson@emory.edu \", role = c(\"aut\")),\nperson(\"Christian P\",\"Larsen\",email = \"clarsen@emory.edu\", role = c(\"cph\", \"aut\")))",
  "License": "MIT + file LICENSE",
  "Encoding": "UTF-8",
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  "URL": "https://pubmed.ncbi.nlm.nih.gov/35101308/,\nhttps://emory-larsenlab.shinyapps.io/hlar_shiny/",
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  "Repository": "https://larsenlab.r-universe.dev",
  "Date/Publication": "2023-03-02 21:38:22 UTC",
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    "CalAlleleTopN",
    "CalEpletMHCI",
    "CalEpletMHCII",
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    "CountAlleleMism",
    "EvalAlleleMism",
    "ImputeHaplo"
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    {
      "page": "CalAlleleMismFreq",
      "title": "Evaluate the frequency of specific allele mismatches",
      "topics": [
        "CalAlleleMismFreq"
      ]
    },
    {
      "page": "CalAlleleTopN",
      "title": "topN most frequent HLA alleles",
      "topics": [
        "CalAlleleTopN"
      ]
    },
    {
      "page": "CalEpletMHCI",
      "title": "Calculate class I HLA eplet mismatch",
      "topics": [
        "CalEpletMHCI"
      ]
    },
    {
      "page": "CalEpletMHCII",
      "title": "Calculate class II HLA eplet mismatch.",
      "topics": [
        "CalEpletMHCII"
      ]
    },
    {
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      "title": "Clean messy HLA typing data",
      "topics": [
        "CleanAllele"
      ]
    },
    {
      "page": "CountAlleleMism",
      "title": "Count HLA mismatch at the allele level",
      "topics": [
        "CountAlleleMism"
      ]
    },
    {
      "page": "EvalAlleleMism",
      "title": "Evaluate mismatched alleles",
      "topics": [
        "EvalAlleleMism"
      ]
    },
    {
      "page": "ImputeHaplo",
      "title": "Imputation",
      "topics": [
        "ImputeHaplo"
      ]
    },
    {
      "page": "utils",
      "title": "Basic functions",
      "topics": [
        "CalRiskScore",
        "FuncForCompHaplo",
        "GenerateLookup",
        "na_to_empty_string",
        "utils"
      ]
    }
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      "title": "Eplet Mismatch",
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      "headings": [
        "Aims",
        "Overview",
        "Use Cases:",
        "Example: Investigate the Importance of Eplet Mismatch in Retrospective Transplant Cohort",
        "Step 1: Import recipient and donor typing data. We have an example cohort that can be loaded into the environment with the following code. This is  A cohort of 14 recipients with donor and recipient high resolution HLA typing data for HLA Class I (A, B, C) and HLA Class II (DRB1, DRB3/4/5, and DQb and DQb).",
        "Step 2: Calculate MHCI mismatch, pull information from result using single and overall outputs.",
        "Example 1 - MHC-I",
        "Step 3: Calculate MHCII mismatch and DRDQ risk score, pull information from result using single and overall outputs.",
        "Step 4: Use visuals to examine the data.",
        "Sources",
        "MatchMaker Logic:"
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        "Load Test Data Set",
        "Generate List of Possible Haplotypes and Sort Most likely Pairs",
        "Impute high-resolution data",
        "Notes:"
      ],
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