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{ | ||
// See https://go.microsoft.com/fwlink/?LinkId=733558 | ||
// for the documentation about the tasks.json format | ||
"version": "2.0.0", | ||
"tasks": [ | ||
{ | ||
"label": "build", | ||
"type": "shell", | ||
"command": "make build" | ||
}, | ||
{ | ||
"label": "test", | ||
"type": "shell", | ||
"command": "make test", | ||
"problemMatcher": [] | ||
}, | ||
{ | ||
"label": "pkgdown_build", | ||
"type": "shell", | ||
"command": "Rscript -e 'pkgdown::build_site()'", | ||
"problemMatcher": [] | ||
}, | ||
] | ||
} |
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2018-02-26 Li Jianfeng <[email protected]> | ||
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* initial annovarR shiny App (inst/extdata/tools/shiny) | ||
* initial anor shiny App (inst/extdata/tools/shiny) | ||
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2018-01-19 Li Jianfeng <[email protected]> | ||
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Package: annovarR | ||
Package: anor | ||
Type: Package | ||
Title: Integrated Framework to Annotate Genetic Variants | ||
Version: 1.3 | ||
Authors@R: person("Jianfeng", "Li", email = "[email protected]", role = c("aut", "cre"), comment = c(ORCID = "0000-0003-2349-208X")) | ||
Description: | ||
The 'annovarR' package provides R functions as well as database resources which offer an integrated framework to annotate genetic variants from genome and transcriptome data. The wrapper functions of 'annovarR' unified the interface of many published annotation tools, such as 'VEP' (<http://asia.ensembl.org/info/docs/tools/vep/index.html>), 'ANNOVAR' (<http://annovar.openbioinformatics.org/>), 'vcfanno' (<https://github.com/brentp/vcfanno>) and 'AnnotationDbi' (<http://www.bioconductor.org/packages/release/bioc/html/AnnotationDbi.html>). It also simplified the use of some of the external annotation tools in R. Besides, massive published genetic variants annotation databases were integrated into 'annovarR'. For example, 'annovarR' provides a newly RNA-seq allele frequency database, BRVar, which built from total 1,285 cases public B-progenitor acute lymphoblastic leukemia (B-ALL) transcriptome data. | ||
The 'anor' package provides R functions as well as database resources which offer an integrated framework to annotate genetic variants from genome and transcriptome data. The wrapper functions of 'anor' unified the interface of many published annotation tools, such as 'VEP' (<http://asia.ensembl.org/info/docs/tools/vep/index.html>), 'ANNOVAR' (<http://annovar.openbioinformatics.org/>), 'vcfanno' (<https://github.com/brentp/vcfanno>) and 'AnnotationDbi' (<http://www.bioconductor.org/packages/release/bioc/html/AnnotationDbi.html>). It also simplified the use of some of the external annotation tools in R. Besides, massive published genetic variants annotation databases were integrated into 'anor'. For example, 'anor' provides a newly RNA-seq allele frequency database, BRVar, which built from total 1,285 cases public B-progenitor acute lymphoblastic leukemia (B-ALL) transcriptome data. | ||
Depends: | ||
R (>= 3.3.0) | ||
URL: https://github.com/JhuangLab/annovarR | ||
BugReports: https://github.com/JhuangLab/annovarR/issues | ||
URL: https://github.com/JhuangLab/anor | ||
BugReports: https://github.com/JhuangLab/anor/issues | ||
License: MIT + file LICENSE | ||
Encoding: UTF-8 | ||
LazyData: true | ||
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@@ -29,7 +29,7 @@ Imports: | |
devtools, | ||
AnnotationDbi, | ||
liteq | ||
RoxygenNote: 6.1.1 | ||
RoxygenNote: 7.1.0 | ||
Suggests: testthat, | ||
knitr, | ||
rmarkdown, | ||
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@@ -3,10 +3,10 @@ FROM bioinstaller/ngsjs:latest | |
## This handle reaches Jianfeng | ||
MAINTAINER "Jianfeng Li" [email protected] | ||
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ADD . /tmp/annovarR | ||
ADD . /tmp/anor | ||
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Run runuser -s /bin/bash -l opencpu -c "Rscript -e 'pacman::p_load(maftools, clusterProfiler, CEMiTool, org.Hs.eg.db, DT)'" \ | ||
&& runuser -s /bin/bash -l opencpu -c "Rscript -e 'devtools::install(\"/tmp/annovarR\", dependences = T)'" \ | ||
&& rm -rf /tmp/annovarR \ | ||
&& runuser -s /bin/bash -l opencpu -c "Rscript -e 'devtools::install(\"/tmp/anor\", dependences = T)'" \ | ||
&& rm -rf /tmp/anor \ | ||
&& rm -rf /var/lib/apt/lists/* \ | ||
&& rm -rf /tmp/downloaded_packages/ /tmp/*.rds |
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#' The 'annovarR' package provides R functions as well as database resources which offer an | ||
#' The 'anor' package provides R functions as well as database resources which offer an | ||
#' integrated framework to annotate genetic variants from genome and transcriptome data. | ||
#' The wrapper functions of 'annovarR' unified the interface of many published annotation tools, | ||
#' The wrapper functions of 'anor' unified the interface of many published annotation tools, | ||
#' such as 'VEP' (\url{http://asia.ensembl.org/info/docs/tools/vep/index.html}), | ||
#' 'ANNOVAR' (\url{http://annovar.openbioinformatics.org/}), 'vcfanno' (\url{https://github.com/brentp/vcfanno}) | ||
#' and 'AnnotationDbi' (\url{http://www.bioconductor.org/packages/release/bioc/html/AnnotationDbi.html}). | ||
#' It also simplified the use of some of the external annotation tools in R. | ||
#' Besides, massive published genetic variants annotation databases were integrated into 'annovarR'. | ||
#' For example, 'annovarR' provides a newly RNA-seq allele frequency database, BRVar, | ||
#' Besides, massive published genetic variants annotation databases were integrated into 'anor'. | ||
#' For example, 'anor' provides a newly RNA-seq allele frequency database, BRVar, | ||
#' which built from total 1,285 cases public B-progenitor acute lymphoblastic leukemia (B-ALL) transcriptome data. | ||
#' | ||
#' @author | ||
#' Li Jianfeng \url{[email protected]} | ||
#' @seealso | ||
#' Useful links: | ||
#' | ||
#' \url{https://github.com/JhuangLab/annovarR} | ||
#' \url{https://github.com/JhuangLab/anor} | ||
#' | ||
#' Report bugs at \url{https://github.com/JhuangLab/annovarR/issues} | ||
#' Report bugs at \url{https://github.com/JhuangLab/anor/issues} | ||
#' | ||
#' @docType package | ||
#' @name annovarR | ||
#' @name anor | ||
#' @import stringr DBI data.table futile.logger configr BioInstaller glue liteq | ||
#' @importFrom stringi stri_rand_strings | ||
#' @importFrom utils packageVersion head installed.packages compareVersion install.packages | ||
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.onAttach <- function(libname, pkgname) { | ||
op <- options() | ||
# msg <- sprintf('annovarR %s \n', packageVersion('annovarR')) msg <- | ||
# sprintf('%s Documentation: ?annovarR, example(annovarR) and | ||
# browseVignettes(\'annovarR\')', msg) packageStartupMessage(msg) | ||
# msg <- sprintf('anor %s \n', packageVersion('anor')) msg <- | ||
# sprintf('%s Documentation: ?anor, example(anor) and | ||
# browseVignettes(\'anor\')', msg) packageStartupMessage(msg) | ||
Sys.setenv(R_TESTS = "") | ||
invisible() | ||
} |
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