[Bioc-devel] Best practices to load data for vignette/tests
Shepherd, Lori
Lor|@Shepherd @end|ng |rom Ro@we||P@rk@org
Tue Jan 22 15:13:23 CET 2019
You could see if there is any existing data already in Bioconductor for use with your package. That would be preferable.
http://bioconductor.org/packages/release/BiocViews.html#___Software
searching for fastq - you could see what data ShortRead, seqTools, and FastqCleaner
similarly you could also search for rna-seq packages to see if any of their data is appropriate.
There are also a number of experiment data packages that may provide the data format you are in need of.
http://bioconductor.org/packages/release/BiocViews.html#___ExperimentData
You could search here as well.
Lastly, Bioconductor has an experimentHub for storing large data files. You can search interactively in R or the web API interface here:
https://experimenthub.bioconductor.org/
If none of those location provide data currently in Bioconductor that is suitable for your package, You can submit your own data to the ExperimentHub.
http://bioconductor.org/packages/devel/bioc/vignettes/ExperimentHub/inst/doc/CreateAnExperimentHubPackage.html
You could download directly but this could be time consuming depending on internet connections and download speeds. The Bioconductor hubs provide a caching mechanism so it is only downloaded once and then it remembers where the file is on the system for later use.
Cheers,
Lori Shepherd
Bioconductor Core Team
Roswell Park Cancer Institute
Department of Biostatistics & Bioinformatics
Elm & Carlton Streets
Buffalo, New York 14263
________________________________
From: Bioc-devel <bioc-devel-bounces using r-project.org> on behalf of Julien Wollbrett <julien.wollbrett using unil.ch>
Sent: Tuesday, January 22, 2019 8:57:23 AM
To: bioc-devel using r-project.org
Subject: [Bioc-devel] Best practices to load data for vignette/tests
Hi everyone,
I am currently working on a R package called BgeeCall allowing to
automatically generate present/absent expression calls from any RNA-Seq
fastq files as long as the species is present in Bgee (https://bgee.org/)
.
The package is almost ready and I am currently writing the vignette and
some tests.
This package can be seen as a workflow taking as input one transcriptome
and at least one fastq file.
My question is how can I import these 2 files to run the vignette/tests?
They are too big to be part of my package.
Can I directly download them from SRA and ensembl (or from my own
server)? Do I need to create a dataset that will be loaded by my package
for this kind of raw and publicly available data?
Do you know if I could reuse some already existing dataset? I am
interested to any best practices infomation.
Thank you for your answers.
Best Regards,
Julien
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