Bump version: 1.0.9 → 1.1.0

sigven · Jun 10, 2022 · 1cc2cd3 · 1cc2cd3
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Showing 6 changed files with 6 additions and 6 deletions.
diff --git a/.bumpversion.cfg b/.bumpversion.cfg
@@ -1,5 +1,5 @@
 [bumpversion]
-current_version = 1.0.9
+current_version = 1.1.0
 commit = True
 tag = False
 

diff --git a/.github/workflows/pkgdown.yaml b/.github/workflows/pkgdown.yaml
@@ -8,7 +8,7 @@ on:
   workflow_dispatch:
 
 env:
-  VERSION: '1.0.9' #versioned by bump2version
+  VERSION: '1.1.0' #versioned by bump2version
 
 name: pkgdown
 

diff --git a/DESCRIPTION b/DESCRIPTION
@@ -1,7 +1,7 @@
 Package: oncoEnrichR
 Type: Package
 Title: Cancer-dedicated gene set interpretation
-Version: 1.0.9
+Version: 1.1.0
 Date: 2022-06-10
 Authors@R: 
     c(person(given = "Sigve",

diff --git a/README.md b/README.md
@@ -2,7 +2,7 @@
 
 **oncoEnrichR** is an R package for functional interrogation of human genesets in the context of cancer. The package leverages an extensive amount of prior molecular knowledge for geneset interpretation along multiple dimensions.
 
-Web-based access to **oncoEnrichR** is available at [**https://oncotools.elixir.no**](https://oncotools.elixir.no/tool_runner?tool_id=galaxy-ntnu.bioinfo.no%2Ftoolshed_nels%2Frepos%2Fradmilko%2Foncoenrichr%2Foncoenrichr_wrapper%2F1.0.9)
+Web-based access to **oncoEnrichR** is available at [**https://oncotools.elixir.no**](https://oncotools.elixir.no/tool_runner?tool_id=galaxy-ntnu.bioinfo.no%2Ftoolshed_nels%2Frepos%2Fradmilko%2Foncoenrichr%2Foncoenrichr_wrapper%2F1.1.0)
 
 **oncoEnrichR** is primarily intended for exploratory analysis and prioritization of a gene list (referred to here as **query set**) from high-throughput cancer biology experiments, e.g. genetic screens (siRNA/CRISPR), protein proximity labeling, or transcriptomics (differential expression). The tool queries a number of high-quality data resources in order to assemble useful gene annotations and analyses in an interactive report.
 

diff --git a/pkgdown/index.md b/pkgdown/index.md
@@ -8,7 +8,7 @@
 
 **oncoEnrichR** can be used to interrogate results from e.g. genetic screens (siRNA/CRISPR), protein proximity labeling, or transcriptomics (differential expression). The tool queries a variety of high-quality data resources in order to assemble useful gene annotations and analyses in an interactive report (examples from the report shown below).
 
-Web-based access to **oncoEnrichR** is available at <font size="4"> **[https://oncotools.elixir.no](https://oncotools.elixir.no/tool_runner?tool_id=galaxy-ntnu.bioinfo.no%2Ftoolshed_nels%2Frepos%2Fradmilko%2Foncoenrichr%2Foncoenrichr_wrapper%2F1.0.9)**</font>
+Web-based access to **oncoEnrichR** is available at <font size="4"> **[https://oncotools.elixir.no](https://oncotools.elixir.no/tool_runner?tool_id=galaxy-ntnu.bioinfo.no%2Ftoolshed_nels%2Frepos%2Fradmilko%2Foncoenrichr%2Foncoenrichr_wrapper%2F1.1.0)**</font>
 
 <br>
 

diff --git a/vignettes/installation.Rmd b/vignettes/installation.Rmd
@@ -4,5 +4,5 @@ output: rmarkdown::html_document
 ---
 
 1.  `install.packages('devtools')`
-2.  `devtools::install_github('sigven/oncoEnrichR', ref = "v1.0.9")`
+2.  `devtools::install_github('sigven/oncoEnrichR', ref = "v1.1.0")`
 3.  `library(oncoEnrichR)`