{
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  "Type": "Package",
  "Title": "GWAS-to-CRISPR Data Pipeline for High-Throughput SNP Target\nExtraction",
  "Version": "0.1.5",
  "Authors@R": "c(person(given = \"Othman S. I.\", family = \"Mohammed\", email = \"admin@leopard.ly\", role = c(\"aut\", \"cre\")), person(given = \"LEOPARD.LY LTD\", role = \"cph\"))",
  "Description": "Provides a reproducible pipeline to conduct genome-wide\nassociation studies (GWAS) and extract single-nucleotide\npolymorphisms (SNPs) for a human trait or disease. Given\naggregated GWAS dataset(s) and a user-defined significance\nthreshold, the package retrieves significant SNPs from the GWAS\nCatalog using supported trait identifiers, annotates their gene\ncontext, and can write a harmonised metadata table in\ncomma-separated values (CSV) format, genomic intervals in the\nBrowser Extensible Data (BED) format, and sequences in the\nFASTA (text-based sequence) format with user-defined flanking\nregions for clustered regularly interspaced short palindromic\nrepeats (CRISPR) guide design. The existing efo_id argument is\nretained for backward compatibility. The package prepares\ncomputational artifacts for downstream workflows; it does not\nperform biological causality testing, clinical interpretation,\ntherapeutic design, or wet-lab validation. For details on the\nresources and methods see: Buniello et al. (2019)\n<doi:10.1093/nar/gky1120>; Sollis et al. (2023)\n<doi:10.1093/nar/gkac1010>; Jinek et al. (2012)\n<doi:10.1126/science.1225829>.",
  "License": "MIT + file LICENSE",
  "URL": "https://github.com/leopard0ly/gwas2crispr",
  "BugReports": "https://github.com/leopard0ly/gwas2crispr/issues",
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  "Repository": "https://leopard0ly.r-universe.dev",
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