Question: Bioconductor Digest, Vol 138, Issue 27
0
gravatar for Laurent Gatto
5.1 years ago by
Laurent Gatto1.2k
Belgium
Laurent Gatto1.2k wrote:
Dear Anne and Tengfei, The mapping Pbase vignette [1] is an initial description of mapping protein coordinates back to the genome. My plan is to implement what is described in the vignette in the package but haven't had time to do so yet. Please do not hesitate to comment or make suggestions that would be useful to you or inter-operable with your use cases. Best wishes, Laurent [1] http://bioconductor.org/packages/devel/bioc/vignettes/Pbase/inst/d oc/mapping.html On 27 August 2014 11:00, bioconductor-request at r-project.org wrote: > Message: 25 > Date: Tue, 26 Aug 2014 18:37:49 -0400 > From: Tengfei Yin <tengfei.yin at="" sbgenomics.com=""> > To: Anne Deslattes Mays <ad376 at="" georgetown.edu=""> > Cc: Anne Deslattes Mays Cc Routing Num 255071981 > <adeslat at="" sbresearchllc.com="">, Bioconductor mailing list > <bioconductor at="" r-project.org=""> > Subject: Re: [BioC] Positional Details with Features through > UniProt.ws Ultimately to display as tracks in ggbio > Message-ID: > <cagkue7vokqs4guvbcob5c2_23myhjc51lmu1nv7g1_4k2inhoa at="" mail.gmail.com=""> > Content-Type: text/plain; charset="UTF-8" > > Hey Anne, > > So sorry for the late reply. > > Ideally, I should have some kind of mapper function in biovizBase to help > map protein space to genomic space, so you don't have to do it yourself, > but before I have that, a hack would be massage your protein domain data > into a GRanges object, with domain function as coloumn, and use genomic > coordinates, and then create a separate track to plot the object as > rectangle and use color legend to indicate domain function. > > I will try to develop a more general approach for doing this, if you want, > please send me an example RData or example data, so we can work on that > together. > > ps: in case I don't miss your request, feel free to use github page issues > <https: github.com="" tengfei="" ggbio="" issues="">here > > cheers > > Tengfei > > > > > On Sat, Aug 16, 2014 at 6:57 AM, Anne Deslattes Mays <ad376 at="" georgetown.edu=""> > wrote: > >> Dear all, >> >> biocLite(?UniProt.ws?) >> libraryUniProt.ws) >> >> >> selectUniProt.ws,keys=("P02794"),columns=c("DOMAINS","FEATURES"), keytype="UNIPROTKB") >> Getting extra data for P02794 NA NA etc >> UNIPROTKB DOMAINS >> 1 P02794 Ferritin-like diiron domain (1) >> >> >> FEATURES >> 1 Chain (2); Domain (1); Erroneous initiation (1); Helix (6); Initiator >> methionine (1); Metal binding (6); Modified residue (4); Sequence conflict >> (1); Turn (2) >> >> What I want are the positional details for each of these features ? which >> are visible through the uniprot web page. >> FTH1 is 183 amino acids in length. There are 6 metal binding sites, each >> at a specific position. >> This information is there since you can have the web site return the >> positional details. I would like them so I may manipulate them with new >> evidential information. >> >> Ultimately I wish to display them with tracks from ggbio ? >> pb.53A.pos.ga <- readGAlignmentsFromBam(pb.53A.pos.bamfile, >> param = ScanBamParam(which = >> genesymbol["FTH1"],what=c("seq")), >> use.names = TRUE) >> >> FTH1.ga <- geom_alignment(data = txdb,which=genesymbol["FTH1"]) >> >> So here I have sample information which I have aligned to the reference >> genome. I retrieve that information from a bam file. >> # create the GAlignments objects for each isoform >> FTH1.isoform.1 <- pb.53A.pos.ga[c(7)] >> FTH1.isoform.2 <- pb.53A.pos.ga[c(15)] >> FTH1.isoform.3 <- pb.53A.pos.ga[c(13)] >> FTH1.isoform.4 <- pb.53A.pos.ga[c(8)] >> FTH1.isoform.5 <- pb.53A.pos.ga[c(2)] >> FTH1.isoform.6 <- pb.53A.pos.ga[c(1)] >> >> >> p1 <- autoplot(FTH1.isoform.1, fill = "brown", color = "brown") >> p2 <- autoplot(FTH1.isoform.2, fill = "blue", color = "blue") >> p3 <- autoplot(FTH1.isoform.3, fill = "brown", color = "brown") >> p4 <- autoplot(FTH1.isoform.4, fill = "brown", color = "brown") >> p5 <- autoplot(FTH1.isoform.5, fill = "brown", color = "brown") >> p6 <- autoplot(FTH1.isoform.6, fill = "brown", color = "brown") >> >> tracks( FTH1=p1.FTH1, >> "Iso 1"=p1, >> "Iso 2"=p2, >> "Iso 3"=p3, >> "Iso 4"=p4, >> "Iso 5"=p5, >> "Iso 6"=p6) >> >> >> I then can autopilot each of the separate isoforms. What I want to do >> however, is annotate the isoforms so that they each show the coding region >> with the full height of the bar, and a reduced height for the non- coding >> regions. >> >> Additionally, I want to color the graphic with the details for the >> protein, such as the metal binding sites, domains, etc. So that >> computationally I can generate an informative picture which explains what >> is lost or gained in separate isoforms. >> >> Thoughts? >> >> Anne >> R version 3.1.0 (2014-04-10) >> Platform: x86_64-apple-darwin13.1.0 (64-bit) >> >> locale: >> [1] en_US.UTF-8/en_US.UTF-8/en_US.UTF-8/C/en_US.UTF-8/en_US.UTF-8 >> >> attached base packages: >> [1] parallel stats graphics grDevices utils datasets methods >> [8] base >> >> other attached packages: >> [1] UniProt.ws_2.4.2 >> [2] RCurl_1.95-4.3 >> [3] bitops_1.0-6 >> [4] RSQLite_0.11.4 >> [5] DBI_0.2-7 >> [6] biomaRt_2.20.0 >> [7] BiocInstaller_1.14.2 >> [8] GenomicAlignments_1.0.5 >> [9] BSgenome_1.32.0 >> [10] Rsamtools_1.16.1 >> [11] Biostrings_2.32.1 >> [12] XVector_0.4.0 >> [13] ggbio_1.12.8 >> [14] ggplot2_1.0.0 >> [15] TxDb.Hsapiens.UCSC.hg19.knownGene_2.14.0 >> [16] GenomicFeatures_1.16.2 >> [17] AnnotationDbi_1.26.0 >> [18] Biobase_2.24.0 >> [19] GenomicRanges_1.16.4 >> [20] GenomeInfoDb_1.0.2 >> [21] IRanges_1.22.10 >> [22] BiocGenerics_0.10.0 >> >> loaded via a namespace (and not attached): >> [1] BatchJobs_1.3 BBmisc_1.7 BiocParallel_0.6.1 >> [4] biovizBase_1.12.1 brew_1.0-6 checkmate_1.2 >> [7] cluster_1.15.2 codetools_0.2-8 colorspace_1.2-4 >> [10] dichromat_2.0-0 digest_0.6.4 fail_1.2 >> [13] foreach_1.4.2 Formula_1.1-2 grid_3.1.0 >> [16] gridExtra_0.9.1 gtable_0.1.2 Hmisc_3.14-4 >> [19] iterators_1.0.7 labeling_0.2 lattice_0.20-29 >> [22] latticeExtra_0.6-26 MASS_7.3-33 munsell_0.4.2 >> [25] plyr_1.8.1 proto_0.3-10 RColorBrewer_1.0-5 >> [28] Rcpp_0.11.2 reshape2_1.4 rtracklayer_1.24.2 >> [31] scales_0.2.4 sendmailR_1.1-2 splines_3.1.0 >> [34] stats4_3.1.0 stringr_0.6.2 survival_2.37-7 >> [37] tcltk_3.1.0 tools_3.1.0 >> VariantAnnotation_1.10.5 >> [40] XML_3.98-1.1 zlibbioc_1.10.0 >> [[alternative HTML version deleted]] >> >> >> _______________________________________________ >> Bioconductor mailing list >> Bioconductor at r-project.org >> https://stat.ethz.ch/mailman/listinfo/bioconductor >> Search the archives: >> http://news.gmane.org/gmane.science.biology.informatics.conductor -- Laurent Gatto http://cpu.sysbiol.cam.ac.uk/
ADD COMMENTlink modified 5.1 years ago by Tengfei Yin490 • written 5.1 years ago by Laurent Gatto1.2k
Answer: Bioconductor Digest, Vol 138, Issue 27
0
gravatar for Anne Deslattes Mays
5.1 years ago by
United States
Anne Deslattes Mays30 wrote:
Hi Laurent, As you consider use cases ? consider a user wanting to add their own data. You may have then, canonical transcript isoforms, sample specific transcript isoforms. So you have canonical proteins, with their annotations. If the sample specific alters that, say causes a loss of a domain, or metal binding sites, etc. These are potentially important functional changes. Anne On Aug 27, 2014, at 6:42 AM, Laurent Gatto <lg390 at="" cam.ac.uk=""> wrote: > > Dear Anne and Tengfei, > > The mapping Pbase vignette [1] is an initial description of mapping protein > coordinates back to the genome. My plan is to implement what is > described in the vignette in the package but haven't had time to do so > yet. > > Please do not hesitate to comment or make suggestions that would be > useful to you or inter-operable with your use cases. > > Best wishes, > > Laurent > > [1] http://bioconductor.org/packages/devel/bioc/vignettes/Pbase/inst /doc/mapping.html > > > On 27 August 2014 11:00, bioconductor-request at r-project.org wrote: > >> Message: 25 >> Date: Tue, 26 Aug 2014 18:37:49 -0400 >> From: Tengfei Yin <tengfei.yin at="" sbgenomics.com=""> >> To: Anne Deslattes Mays <ad376 at="" georgetown.edu=""> >> Cc: Anne Deslattes Mays Cc Routing Num 255071981 >> <adeslat at="" sbresearchllc.com="">, Bioconductor mailing list >> <bioconductor at="" r-project.org=""> >> Subject: Re: [BioC] Positional Details with Features through >> UniProt.ws Ultimately to display as tracks in ggbio >> Message-ID: >> <cagkue7vokqs4guvbcob5c2_23myhjc51lmu1nv7g1_4k2inhoa at="" mail.gmail.com=""> >> Content-Type: text/plain; charset="UTF-8" >> >> Hey Anne, >> >> So sorry for the late reply. >> >> Ideally, I should have some kind of mapper function in biovizBase to help >> map protein space to genomic space, so you don't have to do it yourself, >> but before I have that, a hack would be massage your protein domain data >> into a GRanges object, with domain function as coloumn, and use genomic >> coordinates, and then create a separate track to plot the object as >> rectangle and use color legend to indicate domain function. >> >> I will try to develop a more general approach for doing this, if you want, >> please send me an example RData or example data, so we can work on that >> together. >> >> ps: in case I don't miss your request, feel free to use github page issues >> <https: github.com="" tengfei="" ggbio="" issues="">here >> >> cheers >> >> Tengfei >> >> >> >> >> On Sat, Aug 16, 2014 at 6:57 AM, Anne Deslattes Mays <ad376 at="" georgetown.edu=""> >> wrote: >> >>> Dear all, >>> >>> biocLite(?UniProt.ws?) >>> libraryUniProt.ws) >>> >>> >>> selectUniProt.ws,keys=("P02794"),columns=c("DOMAINS","FEATURES"), keytype="UNIPROTKB") >>> Getting extra data for P02794 NA NA etc >>> UNIPROTKB DOMAINS >>> 1 P02794 Ferritin-like diiron domain (1) >>> >>> >>> FEATURES >>> 1 Chain (2); Domain (1); Erroneous initiation (1); Helix (6); Initiator >>> methionine (1); Metal binding (6); Modified residue (4); Sequence conflict >>> (1); Turn (2) >>> >>> What I want are the positional details for each of these features ? which >>> are visible through the uniprot web page. >>> FTH1 is 183 amino acids in length. There are 6 metal binding sites, each >>> at a specific position. >>> This information is there since you can have the web site return the >>> positional details. I would like them so I may manipulate them with new >>> evidential information. >>> >>> Ultimately I wish to display them with tracks from ggbio ? >>> pb.53A.pos.ga <- readGAlignmentsFromBam(pb.53A.pos.bamfile, >>> param = ScanBamParam(which = >>> genesymbol["FTH1"],what=c("seq")), >>> use.names = TRUE) >>> >>> FTH1.ga <- geom_alignment(data = txdb,which=genesymbol["FTH1"]) >>> >>> So here I have sample information which I have aligned to the reference >>> genome. I retrieve that information from a bam file. >>> # create the GAlignments objects for each isoform >>> FTH1.isoform.1 <- pb.53A.pos.ga[c(7)] >>> FTH1.isoform.2 <- pb.53A.pos.ga[c(15)] >>> FTH1.isoform.3 <- pb.53A.pos.ga[c(13)] >>> FTH1.isoform.4 <- pb.53A.pos.ga[c(8)] >>> FTH1.isoform.5 <- pb.53A.pos.ga[c(2)] >>> FTH1.isoform.6 <- pb.53A.pos.ga[c(1)] >>> >>> >>> p1 <- autoplot(FTH1.isoform.1, fill = "brown", color = "brown") >>> p2 <- autoplot(FTH1.isoform.2, fill = "blue", color = "blue") >>> p3 <- autoplot(FTH1.isoform.3, fill = "brown", color = "brown") >>> p4 <- autoplot(FTH1.isoform.4, fill = "brown", color = "brown") >>> p5 <- autoplot(FTH1.isoform.5, fill = "brown", color = "brown") >>> p6 <- autoplot(FTH1.isoform.6, fill = "brown", color = "brown") >>> >>> tracks( FTH1=p1.FTH1, >>> "Iso 1"=p1, >>> "Iso 2"=p2, >>> "Iso 3"=p3, >>> "Iso 4"=p4, >>> "Iso 5"=p5, >>> "Iso 6"=p6) >>> >>> >>> I then can autopilot each of the separate isoforms. What I want to do >>> however, is annotate the isoforms so that they each show the coding region >>> with the full height of the bar, and a reduced height for the non- coding >>> regions. >>> >>> Additionally, I want to color the graphic with the details for the >>> protein, such as the metal binding sites, domains, etc. So that >>> computationally I can generate an informative picture which explains what >>> is lost or gained in separate isoforms. >>> >>> Thoughts? >>> >>> Anne >>> R version 3.1.0 (2014-04-10) >>> Platform: x86_64-apple-darwin13.1.0 (64-bit) >>> >>> locale: >>> [1] en_US.UTF-8/en_US.UTF-8/en_US.UTF-8/C/en_US.UTF-8/en_US.UTF-8 >>> >>> attached base packages: >>> [1] parallel stats graphics grDevices utils datasets methods >>> [8] base >>> >>> other attached packages: >>> [1] UniProt.ws_2.4.2 >>> [2] RCurl_1.95-4.3 >>> [3] bitops_1.0-6 >>> [4] RSQLite_0.11.4 >>> [5] DBI_0.2-7 >>> [6] biomaRt_2.20.0 >>> [7] BiocInstaller_1.14.2 >>> [8] GenomicAlignments_1.0.5 >>> [9] BSgenome_1.32.0 >>> [10] Rsamtools_1.16.1 >>> [11] Biostrings_2.32.1 >>> [12] XVector_0.4.0 >>> [13] ggbio_1.12.8 >>> [14] ggplot2_1.0.0 >>> [15] TxDb.Hsapiens.UCSC.hg19.knownGene_2.14.0 >>> [16] GenomicFeatures_1.16.2 >>> [17] AnnotationDbi_1.26.0 >>> [18] Biobase_2.24.0 >>> [19] GenomicRanges_1.16.4 >>> [20] GenomeInfoDb_1.0.2 >>> [21] IRanges_1.22.10 >>> [22] BiocGenerics_0.10.0 >>> >>> loaded via a namespace (and not attached): >>> [1] BatchJobs_1.3 BBmisc_1.7 BiocParallel_0.6.1 >>> [4] biovizBase_1.12.1 brew_1.0-6 checkmate_1.2 >>> [7] cluster_1.15.2 codetools_0.2-8 colorspace_1.2-4 >>> [10] dichromat_2.0-0 digest_0.6.4 fail_1.2 >>> [13] foreach_1.4.2 Formula_1.1-2 grid_3.1.0 >>> [16] gridExtra_0.9.1 gtable_0.1.2 Hmisc_3.14-4 >>> [19] iterators_1.0.7 labeling_0.2 lattice_0.20-29 >>> [22] latticeExtra_0.6-26 MASS_7.3-33 munsell_0.4.2 >>> [25] plyr_1.8.1 proto_0.3-10 RColorBrewer_1.0-5 >>> [28] Rcpp_0.11.2 reshape2_1.4 rtracklayer_1.24.2 >>> [31] scales_0.2.4 sendmailR_1.1-2 splines_3.1.0 >>> [34] stats4_3.1.0 stringr_0.6.2 survival_2.37-7 >>> [37] tcltk_3.1.0 tools_3.1.0 >>> VariantAnnotation_1.10.5 >>> [40] XML_3.98-1.1 zlibbioc_1.10.0 >>> [[alternative HTML version deleted]] >>> >>> >>> _______________________________________________ >>> Bioconductor mailing list >>> Bioconductor at r-project.org >>> https://stat.ethz.ch/mailman/listinfo/bioconductor >>> Search the archives: >>> http://news.gmane.org/gmane.science.biology.informatics.conductor > > -- > Laurent Gatto > http://cpu.sysbiol.cam.ac.uk/
ADD COMMENTlink written 5.1 years ago by Anne Deslattes Mays30
Answer: Bioconductor Digest, Vol 138, Issue 27
0
gravatar for Tengfei Yin
5.1 years ago by
Tengfei Yin490
Tengfei Yin490 wrote:
Hey Laurent, Thanks a lot, just quickly go through it, this is very useful for me! I will look into it. cheers Tengfei On Wed, Aug 27, 2014 at 6:42 AM, Laurent Gatto <lg390 at="" cam.ac.uk=""> wrote: > > Dear Anne and Tengfei, > > The mapping Pbase vignette [1] is an initial description of mapping protein > coordinates back to the genome. My plan is to implement what is > described in the vignette in the package but haven't had time to do so > yet. > > Please do not hesitate to comment or make suggestions that would be > useful to you or inter-operable with your use cases. > > Best wishes, > > Laurent > > [1] > http://bioconductor.org/packages/devel/bioc/vignettes/Pbase/inst/doc /mapping.html > > > On 27 August 2014 11:00, bioconductor-request at r-project.org wrote: > > > Message: 25 > > Date: Tue, 26 Aug 2014 18:37:49 -0400 > > From: Tengfei Yin <tengfei.yin at="" sbgenomics.com=""> > > To: Anne Deslattes Mays <ad376 at="" georgetown.edu=""> > > Cc: Anne Deslattes Mays Cc Routing Num 255071981 > > <adeslat at="" sbresearchllc.com="">, Bioconductor mailing list > > <bioconductor at="" r-project.org=""> > > Subject: Re: [BioC] Positional Details with Features through > > UniProt.ws Ultimately to display as tracks in ggbio > > Message-ID: > > < > CAGkUe7VoKqS4GuVBcoB5C2_23myhJC51LMu1nV7g1_4k2iNHoA at mail.gmail.com> > > Content-Type: text/plain; charset="UTF-8" > > > > Hey Anne, > > > > So sorry for the late reply. > > > > Ideally, I should have some kind of mapper function in biovizBase to help > > map protein space to genomic space, so you don't have to do it yourself, > > but before I have that, a hack would be massage your protein domain data > > into a GRanges object, with domain function as coloumn, and use genomic > > coordinates, and then create a separate track to plot the object as > > rectangle and use color legend to indicate domain function. > > > > I will try to develop a more general approach for doing this, if you > want, > > please send me an example RData or example data, so we can work on that > > together. > > > > ps: in case I don't miss your request, feel free to use github page > issues > > <https: github.com="" tengfei="" ggbio="" issues="">here > > > > cheers > > > > Tengfei > > > > > > > > > > On Sat, Aug 16, 2014 at 6:57 AM, Anne Deslattes Mays < > ad376 at georgetown.edu> > > wrote: > > > >> Dear all, > >> > >> biocLite(?UniProt.ws?) > >> libraryUniProt.ws) > >> > >> > >> > selectUniProt.ws,keys=("P02794"),columns=c("DOMAINS","FEATURES"),ke ytype="UNIPROTKB") > >> Getting extra data for P02794 NA NA etc > >> UNIPROTKB DOMAINS > >> 1 P02794 Ferritin-like diiron domain (1) > >> > >> > >> FEATURES > >> 1 Chain (2); Domain (1); Erroneous initiation (1); Helix (6); Initiator > >> methionine (1); Metal binding (6); Modified residue (4); Sequence > conflict > >> (1); Turn (2) > >> > >> What I want are the positional details for each of these features ? > which > >> are visible through the uniprot web page. > >> FTH1 is 183 amino acids in length. There are 6 metal binding sites, > each > >> at a specific position. > >> This information is there since you can have the web site return the > >> positional details. I would like them so I may manipulate them with new > >> evidential information. > >> > >> Ultimately I wish to display them with tracks from ggbio ? > >> pb.53A.pos.ga <- readGAlignmentsFromBam(pb.53A.pos.bamfile, > >> param = ScanBamParam(which = > >> genesymbol["FTH1"],what=c("seq")), > >> use.names = TRUE) > >> > >> FTH1.ga <- geom_alignment(data = txdb,which=genesymbol["FTH1"]) > >> > >> So here I have sample information which I have aligned to the reference > >> genome. I retrieve that information from a bam file. > >> # create the GAlignments objects for each isoform > >> FTH1.isoform.1 <- pb.53A.pos.ga[c(7)] > >> FTH1.isoform.2 <- pb.53A.pos.ga[c(15)] > >> FTH1.isoform.3 <- pb.53A.pos.ga[c(13)] > >> FTH1.isoform.4 <- pb.53A.pos.ga[c(8)] > >> FTH1.isoform.5 <- pb.53A.pos.ga[c(2)] > >> FTH1.isoform.6 <- pb.53A.pos.ga[c(1)] > >> > >> > >> p1 <- autoplot(FTH1.isoform.1, fill = "brown", color = "brown") > >> p2 <- autoplot(FTH1.isoform.2, fill = "blue", color = "blue") > >> p3 <- autoplot(FTH1.isoform.3, fill = "brown", color = "brown") > >> p4 <- autoplot(FTH1.isoform.4, fill = "brown", color = "brown") > >> p5 <- autoplot(FTH1.isoform.5, fill = "brown", color = "brown") > >> p6 <- autoplot(FTH1.isoform.6, fill = "brown", color = "brown") > >> > >> tracks( FTH1=p1.FTH1, > >> "Iso 1"=p1, > >> "Iso 2"=p2, > >> "Iso 3"=p3, > >> "Iso 4"=p4, > >> "Iso 5"=p5, > >> "Iso 6"=p6) > >> > >> > >> I then can autopilot each of the separate isoforms. What I want to do > >> however, is annotate the isoforms so that they each show the coding > region > >> with the full height of the bar, and a reduced height for the non-coding > >> regions. > >> > >> Additionally, I want to color the graphic with the details for the > >> protein, such as the metal binding sites, domains, etc. So that > >> computationally I can generate an informative picture which explains > what > >> is lost or gained in separate isoforms. > >> > >> Thoughts? > >> > >> Anne > >> R version 3.1.0 (2014-04-10) > >> Platform: x86_64-apple-darwin13.1.0 (64-bit) > >> > >> locale: > >> [1] en_US.UTF-8/en_US.UTF-8/en_US.UTF-8/C/en_US.UTF-8/en_US.UTF-8 > >> > >> attached base packages: > >> [1] parallel stats graphics grDevices utils datasets methods > >> [8] base > >> > >> other attached packages: > >> [1] UniProt.ws_2.4.2 > >> [2] RCurl_1.95-4.3 > >> [3] bitops_1.0-6 > >> [4] RSQLite_0.11.4 > >> [5] DBI_0.2-7 > >> [6] biomaRt_2.20.0 > >> [7] BiocInstaller_1.14.2 > >> [8] GenomicAlignments_1.0.5 > >> [9] BSgenome_1.32.0 > >> [10] Rsamtools_1.16.1 > >> [11] Biostrings_2.32.1 > >> [12] XVector_0.4.0 > >> [13] ggbio_1.12.8 > >> [14] ggplot2_1.0.0 > >> [15] TxDb.Hsapiens.UCSC.hg19.knownGene_2.14.0 > >> [16] GenomicFeatures_1.16.2 > >> [17] AnnotationDbi_1.26.0 > >> [18] Biobase_2.24.0 > >> [19] GenomicRanges_1.16.4 > >> [20] GenomeInfoDb_1.0.2 > >> [21] IRanges_1.22.10 > >> [22] BiocGenerics_0.10.0 > >> > >> loaded via a namespace (and not attached): > >> [1] BatchJobs_1.3 BBmisc_1.7 > BiocParallel_0.6.1 > >> [4] biovizBase_1.12.1 brew_1.0-6 checkmate_1.2 > >> [7] cluster_1.15.2 codetools_0.2-8 colorspace_1.2-4 > >> [10] dichromat_2.0-0 digest_0.6.4 fail_1.2 > >> [13] foreach_1.4.2 Formula_1.1-2 grid_3.1.0 > >> [16] gridExtra_0.9.1 gtable_0.1.2 Hmisc_3.14-4 > >> [19] iterators_1.0.7 labeling_0.2 lattice_0.20-29 > >> [22] latticeExtra_0.6-26 MASS_7.3-33 munsell_0.4.2 > >> [25] plyr_1.8.1 proto_0.3-10 > RColorBrewer_1.0-5 > >> [28] Rcpp_0.11.2 reshape2_1.4 > rtracklayer_1.24.2 > >> [31] scales_0.2.4 sendmailR_1.1-2 splines_3.1.0 > >> [34] stats4_3.1.0 stringr_0.6.2 survival_2.37-7 > >> [37] tcltk_3.1.0 tools_3.1.0 > >> VariantAnnotation_1.10.5 > >> [40] XML_3.98-1.1 zlibbioc_1.10.0 > >> [[alternative HTML version deleted]] > >> > >> > >> _______________________________________________ > >> Bioconductor mailing list > >> Bioconductor at r-project.org > >> https://stat.ethz.ch/mailman/listinfo/bioconductor > >> Search the archives: > >> http://news.gmane.org/gmane.science.biology.informatics.conductor > > -- > Laurent Gatto > http://cpu.sysbiol.cam.ac.uk/ > -- Tengfei Yin, PhD Product Manager Seven Bridges Genomics sbgenomics.com One Broadway FL 7 Cambridge, MA 02142 (617) 866-0446 [[alternative HTML version deleted]]
ADD COMMENTlink written 5.1 years ago by Tengfei Yin490
Please log in to add an answer.

Help
Access

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.
Powered by Biostar version 16.09
Traffic: 282 users visited in the last hour