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 <dstr7...@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@r-project.org mailing list > https://stat.ethz.ch/mailman/listinfo/bioc-devel > [[alternative HTML version deleted]] _______________________________________________ Bioc-devel@r-project.org mailing list https://stat.ethz.ch/mailman/listinfo/bioc-devel
