diff --git a/man/exampleRAD.Rd b/man/exampleRAD.Rd index d41916b..dd63e07 100644 --- a/man/exampleRAD.Rd +++ b/man/exampleRAD.Rd @@ -34,7 +34,7 @@ polyRAD/extdata/simulate_rad_data.R. \emph{M. sinensis} sequencing data available at \url{https://www.ncbi.nlm.nih.gov//bioproject/PRJNA207721}, with full genotype -calls at \url{https://doi.org/10.13012/B2IDB-1402948_V1}. +calls at \doi{10.13012/B2IDB-1402948_V1}. } \examples{ diff --git a/man/readTASSELGBSv2.Rd b/man/readTASSELGBSv2.Rd index dc57f9a..f681730 100644 --- a/man/readTASSELGBSv2.Rd +++ b/man/readTASSELGBSv2.Rd @@ -64,9 +64,9 @@ the two input files. \references{ TASSEL GBSv2 pipeline: \url{https://bitbucket.org/tasseladmin/tassel-5-source/wiki/Tassel5GBSv2Pipeline} -Bowtie2: \url{http://bowtie-bio.sourceforge.net/bowtie2/index.shtml} +Bowtie2: \url{https://bowtie-bio.sourceforge.net/bowtie2/index.shtml} -BWA: \url{http://bio-bwa.sourceforge.net/} +BWA: \url{https://bio-bwa.sourceforge.net/} } \author{ Lindsay V. Clark diff --git a/vignettes/isolocus_sorting.Rmd b/vignettes/isolocus_sorting.Rmd index 3898b77..497b0ea 100644 --- a/vignettes/isolocus_sorting.Rmd +++ b/vignettes/isolocus_sorting.Rmd @@ -137,9 +137,9 @@ Depending on the complexity of your dataset, it can be quite a large file. Next, align the FASTQ file generated in step 2 of the previous section to your reference genome. If you have never used -[Bowtie2](http://bowtie-bio.sourceforge.net/bowtie2/index.shtml) +[Bowtie2](https://bowtie-bio.sourceforge.net/bowtie2/index.shtml) on your reference genome before, you will first need to -[make an index](http://bowtie-bio.sourceforge.net/bowtie2/manual.shtml#the-bowtie2-build-indexer). +[make an index](https://bowtie-bio.sourceforge.net/bowtie2/manual.shtml#the-bowtie2-build-indexer). ``` bowtie2-build Msinensis_497_v7.0.hardmasked.fa Msi_DH1_7 diff --git a/vignettes/isolocus_sorting.html b/vignettes/isolocus_sorting.html index 396f3d9..b97351f 100644 --- a/vignettes/isolocus_sorting.html +++ b/vignettes/isolocus_sorting.html @@ -12,10 +12,23 @@ - + Variant and Genotype Calling in Highly Duplicated Genomes + +