[Bioc-devel] Is there a way to change the name of R package that is already published on bioconductor?

Hervé Pagès hpages at fredhutch.org
Wed Dec 2 22:52:13 CET 2015


Hi Marcin,

BTW I noticed that RTCGA has no biocViews (only Software). Populating
the biocViews field with appropriate and specific terms will make
your packages show up in the corresponding views here

   http://bioconductor.org/packages/release/BiocViews.html#___Software

and thus will greatly improve the chances that the user in the need
of functionalities like the ones you provide will discover your package.

Cheers,
H.

On 11/22/2015 10:39 AM, Morgan, Martin wrote:
> Marcin -- I join with Herve in strongly discouraging you from this approach. Because you wish only to change upper versus lower case of your package name, and because some operating systems ignore case, your package will go through a release where it is not available under either upper- or lower-case variant. This will confuse and alienate your users, even more than changing the package name to something completely different. There are a number of packages, including some of our own, where the name could have been chosen more carefully, but we have learned to live with our changes of mind. After all, you can still claim to be consistent with the naming convention of the RTCGA.clinical and RTCGA.mutations package ;)
>
> I guess Dario was referring to
>
>    library(AnnotationHub)
>    hub = AnnotationHub()
>    eset = query(hub, "GSE62944")[[1]]
>
> with
>
>> eset
> ExpressionSet (storageMode: lockedEnvironment)
> assayData: 23368 features, 7706 samples
>    element names: exprs
> protocolData: none
> phenoData
>    sampleNames: TCGA-02-0047-01A-01R-1849-01
>      TCGA-02-0055-01A-01R-1849-01 ... TCGA-ZG-A8QZ-01A-11R-A37L-07 (7706
>      total)
>    varLabels: bcr_patient_barcode bcr_patient_uuid ... CancerType (421
>      total)
>    varMetadata: labelDescription
> featureData: none
> experimentData: use 'experimentData(object)'
> Annotation:
>> table(eset$CancerType)
>
> BLCA BRCA COAD  GBM HNSC KICH KIRC KIRP LAML  LGG LIHC LUAD LUSC   OV PRAD READ
>   273 1082  468  170  481   66  540  226  164  528  212  514  490  344  423  164
> SKCM STAD THCA UCEC
>   373  146  506  536
>> print(object.size(eset), units="auto")
> 264.5 Mb
>> ov = eset[, eset$CancerType == "OV"]   ## ovarian samples
>
> The data are Rsubread summarized counts from before the May update. In the near term, we are actively expanding offerings derived from that GSE to include the May update; this is in conjunction with efforts to develop an 'ExperimentHub' analog of AnnotationHub, for more experiment-centric, heavily curated resources.
>
> It is a little unclear whether the AnnotationHub and your data are redundant or complementary, and whether they can be combined into a single offering. One philosophical difference is the use of semantically rich and integrated ExpressionSet versus basic data structures (data.frame, in your case). We also differ in when we separate data into cancer types; we opted for the entire data set because it is not impossibly large. And our data are AnnotationHub-based rather than package-based. Obviously, avoiding redundant access to the same data is beneficial. One possibility is to collaboratively curate the data into AnnotationHub / ExperimentHub resources, and to tailor access via packages that reference the resource (e.g., one can retrieve the GRASP2 data base through AnnotationHub as resource AH21414, or via grasp2db::GRASP2(); the latter comes with documentation for manipulating the resource).
>
> It seems like there are similar opportunities for collaboration and reduced redundancy between the RTCGA, RTCGAToolbox, and TCGAbiolinks packages.
>
> Martin Morgan
> Bioconductor
>
> ________________________________________
> From: Bioc-devel [bioc-devel-bounces at r-project.org] on behalf of Marcin Kosiński [m.p.kosinski at gmail.com]
> Sent: Sunday, November 22, 2015 11:37 AM
> To: Dario Strbenac
> Cc: bioc-devel at r-project.org
> Subject: Re: [Bioc-devel] Is there a way to change the name of R package that is already published on bioconductor?
>
> Hi Herve,
>
> I think I would like to proceed with such technical possibility.
> I'd like to keep consistency with the RTCGA.miRNASeq package that I am
> uploading to bioconductor with issue 1335.
> Can we schedule such operation?
>
> Best,
> Marcin
>
>
>
> Hi Dario,
>
> Do you want to tell me that there is a possibility to load RNASeq datasets
> for all available 38 cancer types/cohorts from the last release date
> (21-08-2015) of datasets from The Cancer Genome Atlas with the use of
> AnnotationHub?
>
> Is it as simple as:
>
> library(AnnotationHub)
> BRCA.RNASeq -> x
>
> ?
>
> Best,
> Marcin
>
> 2015-11-17 0:00 GMT+01:00 Dario Strbenac <dstr7320 at uni.sydney.edu.au>:
>
>> Hello,
>>
>> How does your package differ to importing GSE62944 into R with
>> AnnotationHub
>> http://bioinformatics.oxfordjournals.org/content/31/22/3666.long ? It
>> seems like unnecessary duplication.
>>
>> --------------------------------------
>> Dario Strbenac
>> PhD Student
>> University of Sydney
>> Camperdown NSW 2050
>> Australia
>> _______________________________________________
>> Bioc-devel at r-project.org mailing list
>> https://stat.ethz.ch/mailman/listinfo/bioc-devel
>>
>
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-- 
Hervé Pagès

Program in Computational Biology
Division of Public Health Sciences
Fred Hutchinson Cancer Research Center
1100 Fairview Ave. N, M1-B514
P.O. Box 19024
Seattle, WA 98109-1024

E-mail: hpages at fredhutch.org
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