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DESCRIPTION
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Package: trellis
Title: Somatic structural variant analysis
Version: 1.0.1
Author: Rob Scharpf, Daniel Bruhm, Dorothy Hallberg, Victor Velculescu
Maintainer: Rob Scharpf <[email protected]>
Description: Analysis of somatic structural variants from whole genome sequencing.
Depends:
R (>= 4.0.0),
GenomicRanges
Imports:
methods,
BiocGenerics,
S4Vectors,
Rsamtools,
GenomeInfoDb,
GenomicAlignments (>= 1.10.0),
IRanges,
SummarizedExperiment,
graph,
stats,
DNAcopy,
matrixStats,
utils,
dplyr (>= 0.8.5),
tidyr,
RBGL,
magrittr,
ggplot2,
RColorBrewer,
AnnotationDbi,
scales,
GenomicFeatures,
BSgenome,
Biostrings,
grid,
gridExtra,
tibble,
purrr,
readr
Suggests:
tidyverse,
knitr,
testthat,
svbams,
BSgenome.Hsapiens.UCSC.hg19,
TxDb.Hsapiens.UCSC.hg19.refGene,
svfilters.hg18,
svfilters.hg19,
BiocStyle,
rmarkdown,
data.table,
org.Hs.eg.db,
ggnet,
network,
sna,
Rgraphviz,
kableExtra
Collate:
'help.R'
'AllGenerics.R'
'Amplicon-class.R'
'DNAcopy-class.R'
'GAlignmentPairs-utils.R'
'Rearrangement-class.R'
'Deletion-class.R'
'DeletionList-class.R'
'DeletionParam-class.R'
'ExonSubset-class.R'
'GRanges-utils.R'
'Preprocess-class.R'
'RearrangementList-class.R'
'RearrangementParams-class.R'
'RearrangmentParams-class.R'
'SegmentParam-class.R'
'Transcripts-class.R'
'acf.R'
'alignment-utils.R'
'amplicon-utils.R'
'baf-utils.R'
'blat-utils.R'
'copynumber-methods.R'
'data-utils.R'
'data.R'
'deletion-utils.R'
'fasta-utils.R'
'functions.R'
'functions_for_CRAM.R'
'fusion-utils.R'
'galignment-utils.R'
'germlineOutliers.R'
'improper-methods.R'
'listCNVs.R'
'listGenomeFilters.R'
'preprocess-utils.R'
'read_pairs.R'
'rear_reads.R'
'rearrangement-utils.R'
'rearlist-utils.R'
'recurrent.R'
'segment.R'
'seqinfo-utils.R'
'uniprot.R'
LazyData: true
VignetteBuilder: knitr
biocViews: Sequencing, HighThroughputSequencing, CopyNumberVariants
Encoding: UTF-8
RoxygenNote: 7.3.2
License: GPL-3