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Meta | ||
doc | ||
.idea | ||
.Rproj.user | ||
.Rhistory | ||
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language: r | ||
r: bioc-release | ||
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before_install: | ||
- sudo apt-get update | ||
- sudo apt-get install r-cran-rjags | ||
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# r_build_args: --no-build-vignettes --no-manual --no-resave-data | ||
r_check_args: --no-build-vignettes # --no-manual | ||
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#script: | ||
#- travis_wait R CMD build . | ||
#- R CMD check --no-build-vignettes *tar.gz |
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Package: infercnv | ||
Type: Package | ||
Title: Infer Copy Number Variation from Single-Cell RNA-Seq Data | ||
Version: 0.8.2 | ||
Version: 0.99.0 | ||
Date: 2018-11-08 | ||
Authors@R: c( person("Timothy", "Tickle", email = "ttickle@broadinstitute.org", role = c("aut", "cre")), person("Itay", "Tirosh", email = "tirosh@broadinstitute.org", role = "aut"), person("Christophe", "Georgescu", email = "cgeorges@broadinstitute.org", role = "aut"), person("Maxwell", "Brown", email = "mbrown@broadinstitute.org", role = "aut"), person("Brian", "Haas", email = "bhaas@broadinstitute.org", role = "aut")) | ||
Author: Timothy Tickle [aut, cre], Itay Tirosh [aut], Christophe Georgescu [aut], Maxwell Brown [aut], Brian Haas [aut] | ||
Maintainer: Christophe Georgescu <cgeorges@broadinstitute.org> | ||
BugReports: https://github.com/broadinstitute/inferCNV/issues | ||
Description: Using single-cell RNA-Seq expression to visualize CNV in cells. | ||
Depends: R(>= 3.2.1) | ||
biocViews: Software, CopyNumberVariation, VariantDetection, StructuralVariation, GenomicVariation, Genetics, Transcriptomics, StatisticalMethod, Bayesian, HiddenMarkovModel, SingleCell | ||
Depends: R(>= 3.5) | ||
License: BSD_3_clause + file LICENSE | ||
LazyData: TRUE | ||
VignetteBuilder: knitr | ||
Suggests: BiocStyle, knitr, rmarkdown, testthat | ||
Enhances: NGCHM | ||
RoxygenNote: 6.1.0 | ||
RoxygenNote: 6.1.1 | ||
NeedsCompilation: no | ||
Imports: RColorBrewer, gplots, futile.logger, stats, utils, methods, ape, Matrix, binhf, fastcluster, dplyr, coin | ||
SystemRequirements: JAGS 4.x.y | ||
Imports: graphics, grDevices, RColorBrewer, gplots, futile.logger, stats, utils, methods, ape, Matrix, fastcluster, dplyr, HiddenMarkov, ggplot2, edgeR, coin, caTools, reshape, rjags, fitdistrplus, future, foreach, doParallel, BiocGenerics, SummarizedExperiment, SingleCellExperiment, tidyr, parallel, coda, gridExtra, argparse | ||
BugReports: https://github.com/broadinstitute/inferCNV/issues | ||
URL: https://github.com/broadinstitute/inferCNV/wiki | ||
Collate: | ||
'NextGenHeatMap.R' | ||
'SplatterScrape.R' | ||
'inferCNV.R' | ||
'inferCNV_BayesNet.R' | ||
'inferCNV_HMM.R' | ||
'inferCNV_constants.R' | ||
'inferCNV_heatmap.R' | ||
'inferCNV_hidden_spike.R' | ||
'inferCNV_i3HMM.R' | ||
'inferCNV_mask_non_DE.R' | ||
'inferCNV_meanVarSim.R' | ||
'inferCNV_ops.R' | ||
'inferCNV_spike.R' | ||
'inferCNV_simple_sim.R' | ||
'inferCNV_tumor_subclusters.R' | ||
'inferCNV_tumor_subclusters.random_smoothed_trees.R' | ||
'noise_reduction.R' |
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