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.
Version: |
1.99.0 |
Depends: |
R (≥ 3.6), GenomicRanges, GenomeInfoDb |
Imports: |
methods, e1071, reshape2, ggplot2, TailRank, JuliaCall, IRanges, qpdf, grDevices, graphics, stats, utils |
Suggests: |
knitr, rmarkdown, markdown, Gviz, rtracklayer |
Published: |
2022-03-28 |
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 results |