{
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  "Package": "famSKATRC",
  "Type": "Package",
  "Title": "Family Sequence Kernel Association Test for Rare and Common\nVariants",
  "Version": "1.1.0",
  "Author": "Khalid B. Kunji [aut, cre], Mohamad Saad [aut]",
  "Authors@R": "c(person(given = \"Khalid B.\", family = \"Kunji\", role = c(\"aut\",\n\"cre\"), email = \"kkunji@hbku.edu.qa\"), person(given = \"Mohamad\",\nfamily = \"Saad\", role = c(\"aut\"), email = \"msaad@hbku.edu.qa\"))",
  "Maintainer": "Khalid B. Kunji <kkunji@hbku.edu.qa>",
  "Description": "FamSKAT-RC is a family-based association kernel test for\nboth rare and common variants. This test is general and several\nspecial cases are known as other methods: famSKAT, which only\nfocuses on rare variants in family-based data, SKAT, which\nfocuses on rare variants in population-based data (unrelated\nindividuals), and SKAT-RC, which focuses on both rare and\ncommon variants in population-based data. When one applies\nfamSKAT-RC and sets the value of phi to 1, famSKAT-RC becomes\nfamSKAT. When one applies famSKAT-RC and set the value of phi\nto 1 and the kinship matrix to the identity matrix, famSKAT-RC\nbecomes SKAT. When one applies famSKAT-RC and set the kinship\nmatrix (fullkins) to the identity matrix (and phi is not equal\nto 1), famSKAT-RC becomes SKAT-RC. We also include a small\nsample synthetic pedigree to demonstrate the method with. For\nmore details see Saad M and Wijsman EM (2014)\n<doi:10.1002/gepi.21844>.",
  "License": "GPL (>= 3)",
  "URL": "https://www.r-project.org,\nhttps://www.ncbi.nlm.nih.gov/pubmed/25132070",
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  "Packaged": {
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    "User": "root"
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  "Repository": "https://kkunji.r-universe.dev",
  "Date/Publication": "2017-11-09 14:01:06 UTC",
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