Package: CNVMotif
Title: Explore, Analyze and Visualize Catalogs and Patterns of
    Copy Number Variation in Cancer Genomics
Version: 0.1.0
Date: 2020-07-16
Authors@R: 
    person(given = "Shixiang",
           family = "Wang",
           role = c("aut", "cre"),
           email = "w_shixiang@163.com",
           comment = c(ORCID = "0000-0001-9855-7357"))
Description: Provides functionality for exploring, analyzing and
    visualizing the copy number variation (CNV) motifs in cancer genomics.
License: MIT + file LICENSE
Imports: 
    Biostrings,
    cluster,
    data.table,
    dplyr,
    factoextra,
    ggplot2,
    ggseqlogo,
    magrittr,
    msa,
    purrr,
    Rcpp,
    tidyr
Suggests: 
    covr,
    doParallel,
    foreach,
    ggmsa,
    ggpubr,
    scales,
    testthat
LinkingTo: 
    Rcpp
biocViews:
Encoding: UTF-8
LazyData: true
Roxygen: list(markdown = TRUE, roclets = c("collate",
    "namespace", "rd", "roxytest::testthat_roclet"))
RoxygenNote: 7.1.1