Our method integrates information from all sequenced samples, thus avoiding loss of alleles due to low coverage. Moreover, it increases the statistical power to uncover sequencing or alignment errors <doi:10.1093/plphys/kiad191>.
Version: 2.1.0 Depends: R (≥ 3.6), GenomicRanges, GenomeInfoDb Imports: methods, e1071, extraDistr, reshape2, ggplot2, TailRank, JuliaCall, IRanges, qpdf, grDevices, graphics, stats, utils Suggests: knitr, rmarkdown, markdown, Gviz, rtracklayer Published: 2023-03-29 DOI: 10.32614/CRAN.package.RTIGER Author: Rafael Campos-Martin [cre], Sophia Schmickler [aut], Manish Goel [ctb], Korbinian Schneeberger [aut], Achim Tresch [aut] Maintainer: Rafael Campos-Martin <rfael.mpi at gmail.com> License: GPL-2 | GPL-3 [expanded from: GPL (≥ 2)] NeedsCompilation: no Materials: README CRAN checks: RTIGER resultsRetroSearch is an open source project built by @garambo | Open a GitHub Issue
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