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#' @keywords internal
#' @aliases tigger-package
"_PACKAGE"
# Project documentation for tigger
#' tigger
#'
#' Here we provide a \strong{T}ool for \strong{I}mmuno\strong{g}lobulin
#' \strong{G}enotype \strong{E}lucidation via \strong{R}ep-Seq (TIgGER).
#' TIgGER inferrs the set of Ig alleles carried by an
#' individual (including any novel alleles) and then uses this set of alleles to
#' correct the initial assignments given to sample sequences by existing tools.
#'
#' @details
#' Immunoglobulin repertoire sequencing (AIRR-Seq, Rep-Seq) data is currently the
#' subject of much study. A key step in analyzing these data involves assigning
#' the closest known V(D)J germline alleles to the (often somatically mutated)
#' sample sequences using a tool such as IMGT/HighV-QUEST. However, if the
#' sample utilizes alleles not in the germline database used for alignment, this
#' step will fail. Additionally, this alignment has an associated error rate of
#' ~5%, notably among sequences carrying a large number of somatic
#' mutations. The purpose of TIgGER is to address these issues.
#'
#' @section Allele detection and genotyping:
#' \itemize{
#' \item \link{findNovelAlleles}: Detect novel alleles.
#' \item \link{plotNovel}: Plot evidence of novel alleles.
#' \item \link{inferGenotype}: Infer an Ig genotype using a frequency approach.
#' \item \link{inferGenotypeBayesian}: Infer an Ig genotype using a Bayesian approach.
#' \item \link{plotGenotype}: A colorful genotype visualization.
#' \item \link{genotypeFasta}: Convert a genotype to sequences.
#' \item \link{reassignAlleles}: Correct allele calls.
#' \item \link{generateEvidence}: Generate evidence for the genotype and
#' allele detection inferrence.
#' }
#'
#' @section Mutation handling:
#' \itemize{
#' \item \link{getMutatedPositions}: Find mutation locations.
#' \item \link{getMutCount}: Find distance from germline.
#' \item \link{findUnmutatedCalls}: Subset unmutated sequences.
#' \item \link{getPopularMutationCount}: Find most common sequence's
#' mutation count.
#' \item \link{insertPolymorphisms}: Insert SNPs into a sequence.
#' }
#'
#' @section Input, output and formatting:
#' \itemize{
#' \item \link{readIgFasta}: Read a fasta file of Ig sequences.
#' \item \link{updateAlleleNames}: Correct outdated allele names.
#' \item \link{sortAlleles}: Sort allele names intelligently.
#' \item \link{cleanSeqs}: Standardize sequence format.
#' }
#'
#' @name tigger
#' @docType package
#' @references
#' \enumerate{
#' \item Gadala-Maria, et al. (2015) Automated analysis of high-throughput B cell
#' sequencing data reveals a high frequency of novel immunoglobulin V gene
#' segment alleles. PNAS. 112(8):E862-70.
#' }
#'
#' @import ggplot2
#' @importFrom alakazam getAllele getGene getFamily translateDNA DNA_COLORS checkColumns
#' @importFrom doParallel registerDoParallel
#' @importFrom dplyr do n desc %>%
#' glimpse distinct group_indices
#' as_data_frame data_frame
#' bind_cols bind_rows combine inner_join
#' filter select arrange
#' group_by ungroup
#' mutate pull rename slice
#' summarise transmute
#' @importFrom foreach foreach %dopar% registerDoSEQ
#' @importFrom graphics plot
#' @importFrom gridExtra arrangeGrob
#' @importFrom gtools ddirichlet
#' @importFrom iterators icount
#' @importFrom lazyeval interp
#' @importFrom parallel clusterEvalQ clusterExport makeCluster stopCluster
#' @importFrom rlang .data := sym syms
#' @importFrom stats na.omit setNames ecdf sd cor cov median mad
#' confint lm
#' @importFrom stringi stri_length stri_detect_fixed stri_replace_all_regex
#' stri_sub stri_sub<- stri_trans_toupper
#' @importFrom tidyr gather spread unnest
#' @importFrom utils citation
NULL
# Package loading actions
.onAttach <- function(libname, pkgname) {
msg <- citation(pkgname)
msg <-paste(c(format(msg,"citation")),collapse="\n\n")
packageStartupMessage(msg)
}
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