about running gsva on mac
2
0
Entering edit mode
Ed ▴ 230
@ed-4683
Last seen 9.6 years ago
Hi there, I used the examples in ?gsva and got the following errors on my mac. However, I run it also on the linux and it worked. Please suggest. Thanks, Weiwei > library(limma) > > p <- 10 ## number of genes > n <- 30 ## number of samples > nGrp1 <- 15 ## number of samples in group 1 > nGrp2 <- n - nGrp1 ## number of samples in group 2 > > ## consider three disjoint gene sets > geneSets <- list(set1=paste("g", 1:3, sep=""), + set2=paste("g", 4:6, sep=""), + set3=paste("g", 7:10, sep="")) > > ## sample data from a normal distribution with mean 0 and st.dev. 1 > y <- matrix(rnorm(n*p), nrow=p, ncol=n, + dimnames=list(paste("g", 1:p, sep="") , paste("s", 1:n, sep=""))) > > ## genes in set1 are expressed at higher levels in the last 10 samples > y[geneSets$set1, (nGrp1+1):n] <- y[geneSets$set1, (nGrp1+1):n] + 2 > > ## build design matrix > design <- cbind(sampleGroup1=1, sampleGroup2vs1=c(rep(0, nGrp1), rep(1, nGrp2))) > > ## fit linear model > fit <- lmFit(y, design) > > ## estimate moderated t-statistics > fit <- eBayes(fit) > > ## genes in set1 are differentially expressed > topTable(fit, coef="sampleGroup2vs1") ID logFC t P.Value adj.P.Val B 2 g2 2.43865785 6.79741169 1.490585e-09 1.490585e-08 11.467181 1 g1 1.81349993 5.04733755 2.590932e-06 1.295466e-05 4.218446 3 g3 1.68971708 4.54930258 1.812937e-05 6.043122e-05 2.348424 5 g5 0.25263973 0.65201092 5.161890e-01 9.308575e-01 -6.688660 10 g10 0.16766254 0.49082930 6.248376e-01 9.308575e-01 -6.780571 9 g9 0.13478444 0.40143265 6.891295e-01 9.308575e-01 -6.820434 8 g8 -0.12067327 -0.32614302 7.451340e-01 9.308575e-01 -6.847833 7 g7 -0.08002351 -0.23401984 8.155437e-01 9.308575e-01 -6.873660 4 g4 0.07875803 0.20538583 8.377717e-01 9.308575e-01 -6.879960 6 g6 -0.03196719 -0.08251146 9.344379e-01 9.344379e-01 -6.897676 > > ## estimate GSVA enrichment scores for the three sets > gsva_es <- gsva(y, geneSets, mx.diff=1)$es.obs | | 0%The process has forked and you cannot use this CoreFoundation functionality safely. You MUST exec(). Break on __THE_PROCESS_HAS_FORKED_AND_YOU_CANNOT_USE_THIS_COREFOUNDATION_FUNCTI ONALITY___YOU_MUST_EXEC__() to debug. The process has forked and you can > version _ platform x86_64-apple-darwin10.8.0 arch x86_64 os darwin10.8.0 system x86_64, darwin10.8.0 status major 3 minor 0.1 year 2013 month 05 day 16 svn rev 62743 language R version.string R version 3.0.1 (2013-05-16) nickname Good Sport > sessionInfo() R version 3.0.1 (2013-05-16) Platform: x86_64-apple-darwin10.8.0 (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 base other attached packages: [1] limma_3.16.7 GSVA_1.8.0 GSEABase_1.22.0 graph_1.38.3 [5] annotate_1.38.0 AnnotationDbi_1.22.6 Biobase_2.20.1 BiocGenerics_0.6.0 [9] BiocInstaller_1.10.3 loaded via a namespace (and not attached): [1] DBI_0.2-7 grid_3.0.1 IRanges_1.18.2 lattice_0.20-15 Matrix_1.0-12 [6] RSQLite_0.11.4 stats4_3.0.1 tools_3.0.1 XML_3.95-0.2 xtable_1.7-1 > [[alternative HTML version deleted]]
PROcess GSVA PROcess GSVA • 1.5k views
ADD COMMENT
0
Entering edit mode
Dan Tenenbaum ★ 8.2k
@dan-tenenbaum-4256
Last seen 3.2 years ago
United States
On Thu, Aug 1, 2013 at 3:10 PM, Ed <edforum at="" gmail.com=""> wrote: > Hi there, > > I used the examples in ?gsva and got the following errors on my mac. > However, I run it also on the linux and it worked. > > Please suggest. > > Thanks, > > Weiwei > >> library(limma) >> >> p <- 10 ## number of genes >> n <- 30 ## number of samples >> nGrp1 <- 15 ## number of samples in group 1 >> nGrp2 <- n - nGrp1 ## number of samples in group 2 >> >> ## consider three disjoint gene sets >> geneSets <- list(set1=paste("g", 1:3, sep=""), > + set2=paste("g", 4:6, sep=""), > + set3=paste("g", 7:10, sep="")) >> >> ## sample data from a normal distribution with mean 0 and st.dev. 1 >> y <- matrix(rnorm(n*p), nrow=p, ncol=n, > + dimnames=list(paste("g", 1:p, sep="") , paste("s", 1:n, > sep=""))) >> >> ## genes in set1 are expressed at higher levels in the last 10 samples >> y[geneSets$set1, (nGrp1+1):n] <- y[geneSets$set1, (nGrp1+1):n] + 2 >> >> ## build design matrix >> design <- cbind(sampleGroup1=1, sampleGroup2vs1=c(rep(0, nGrp1), rep(1, > nGrp2))) >> >> ## fit linear model >> fit <- lmFit(y, design) >> >> ## estimate moderated t-statistics >> fit <- eBayes(fit) >> >> ## genes in set1 are differentially expressed >> topTable(fit, coef="sampleGroup2vs1") > ID logFC t P.Value adj.P.Val B > 2 g2 2.43865785 6.79741169 1.490585e-09 1.490585e-08 11.467181 > 1 g1 1.81349993 5.04733755 2.590932e-06 1.295466e-05 4.218446 > 3 g3 1.68971708 4.54930258 1.812937e-05 6.043122e-05 2.348424 > 5 g5 0.25263973 0.65201092 5.161890e-01 9.308575e-01 -6.688660 > 10 g10 0.16766254 0.49082930 6.248376e-01 9.308575e-01 -6.780571 > 9 g9 0.13478444 0.40143265 6.891295e-01 9.308575e-01 -6.820434 > 8 g8 -0.12067327 -0.32614302 7.451340e-01 9.308575e-01 -6.847833 > 7 g7 -0.08002351 -0.23401984 8.155437e-01 9.308575e-01 -6.873660 > 4 g4 0.07875803 0.20538583 8.377717e-01 9.308575e-01 -6.879960 > 6 g6 -0.03196719 -0.08251146 9.344379e-01 9.344379e-01 -6.897676 >> >> ## estimate GSVA enrichment scores for the three sets >> gsva_es <- gsva(y, geneSets, mx.diff=1)$es.obs > | > | 0%The process has forked and you cannot use this > CoreFoundation functionality safely. You MUST exec(). > Break on > __THE_PROCESS_HAS_FORKED_AND_YOU_CANNOT_USE_THIS_COREFOUNDATION_FUNC TIONALITY___YOU_MUST_EXEC__() > to debug. > The process has forked and you can > > > >> version > _ > platform x86_64-apple-darwin10.8.0 > arch x86_64 > os darwin10.8.0 > system x86_64, darwin10.8.0 > status > major 3 > minor 0.1 > year 2013 > month 05 > day 16 > svn rev 62743 > language R > version.string R version 3.0.1 (2013-05-16) > nickname Good Sport >> sessionInfo() > R version 3.0.1 (2013-05-16) > Platform: x86_64-apple-darwin10.8.0 (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 > base > > other attached packages: > [1] limma_3.16.7 GSVA_1.8.0 GSEABase_1.22.0 > graph_1.38.3 > [5] annotate_1.38.0 AnnotationDbi_1.22.6 Biobase_2.20.1 > BiocGenerics_0.6.0 > [9] BiocInstaller_1.10.3 > > loaded via a namespace (and not attached): > [1] DBI_0.2-7 grid_3.0.1 IRanges_1.18.2 lattice_0.20-15 > Matrix_1.0-12 > [6] RSQLite_0.11.4 stats4_3.0.1 tools_3.0.1 XML_3.95-0.2 > xtable_1.7-1 >> > I can't reproduce this on a Mac with similar sessionInfo. The differences in sessionInfo() suggest things to try: update the XML package: library(BiocInstaller) biocLite("XML") Locale is also different so that would be another thing to explore if these don't work. Also, you have packages loaded that I do not have loaded. So try starting R as follows: R --vanilla Here is my sessionInfo(): > sessionInfo() R version 3.0.1 (2013-05-16) Platform: x86_64-apple-darwin10.8.0 (64-bit) locale: [1] C attached base packages: [1] parallel stats graphics grDevices utils datasets methods [8] base other attached packages: [1] limma_3.16.7 GSVA_1.8.0 GSEABase_1.22.0 [4] graph_1.38.3 annotate_1.38.0 AnnotationDbi_1.22.6 [7] Biobase_2.20.1 BiocGenerics_0.6.0 loaded via a namespace (and not attached): [1] DBI_0.2-7 IRanges_1.18.2 RSQLite_0.11.4 XML_3.98-1.1 stats4_3.0.1 [6] tools_3.0.1 xtable_1.7-1 Dan > [[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
ADD COMMENT
0
Entering edit mode
Devon Ryan ▴ 200
@devon-ryan-6054
Last seen 8.3 years ago
Germany
Are you running this in R.app or R from the terminal? If the former, try running things from the terminal and see if the problem persists. Some parallel computing related packages (e.g. doMC) will give this error in a GUI. Devon ____________________________________________ Devon Ryan, Ph.D. Email: dpryan at dpryan.com Molecular and Cellular Cognition Lab German Centre for Neurodegenerative Diseases (DZNE) Ludwig-Erhard-Allee 2 53175 Bonn, Germany On Aug 2, 2013, at 12:10 AM, Ed wrote: > Hi there, > > I used the examples in ?gsva and got the following errors on my mac. > However, I run it also on the linux and it worked. > > Please suggest. > > Thanks, > > Weiwei > >> library(limma) >> >> p <- 10 ## number of genes >> n <- 30 ## number of samples >> nGrp1 <- 15 ## number of samples in group 1 >> nGrp2 <- n - nGrp1 ## number of samples in group 2 >> >> ## consider three disjoint gene sets >> geneSets <- list(set1=paste("g", 1:3, sep=""), > + set2=paste("g", 4:6, sep=""), > + set3=paste("g", 7:10, sep="")) >> >> ## sample data from a normal distribution with mean 0 and st.dev. 1 >> y <- matrix(rnorm(n*p), nrow=p, ncol=n, > + dimnames=list(paste("g", 1:p, sep="") , paste("s", 1:n, > sep=""))) >> >> ## genes in set1 are expressed at higher levels in the last 10 samples >> y[geneSets$set1, (nGrp1+1):n] <- y[geneSets$set1, (nGrp1+1):n] + 2 >> >> ## build design matrix >> design <- cbind(sampleGroup1=1, sampleGroup2vs1=c(rep(0, nGrp1), rep(1, > nGrp2))) >> >> ## fit linear model >> fit <- lmFit(y, design) >> >> ## estimate moderated t-statistics >> fit <- eBayes(fit) >> >> ## genes in set1 are differentially expressed >> topTable(fit, coef="sampleGroup2vs1") > ID logFC t P.Value adj.P.Val B > 2 g2 2.43865785 6.79741169 1.490585e-09 1.490585e-08 11.467181 > 1 g1 1.81349993 5.04733755 2.590932e-06 1.295466e-05 4.218446 > 3 g3 1.68971708 4.54930258 1.812937e-05 6.043122e-05 2.348424 > 5 g5 0.25263973 0.65201092 5.161890e-01 9.308575e-01 -6.688660 > 10 g10 0.16766254 0.49082930 6.248376e-01 9.308575e-01 -6.780571 > 9 g9 0.13478444 0.40143265 6.891295e-01 9.308575e-01 -6.820434 > 8 g8 -0.12067327 -0.32614302 7.451340e-01 9.308575e-01 -6.847833 > 7 g7 -0.08002351 -0.23401984 8.155437e-01 9.308575e-01 -6.873660 > 4 g4 0.07875803 0.20538583 8.377717e-01 9.308575e-01 -6.879960 > 6 g6 -0.03196719 -0.08251146 9.344379e-01 9.344379e-01 -6.897676 >> >> ## estimate GSVA enrichment scores for the three sets >> gsva_es <- gsva(y, geneSets, mx.diff=1)$es.obs > | > | 0%The process has forked and you cannot use this > CoreFoundation functionality safely. You MUST exec(). > Break on > __THE_PROCESS_HAS_FORKED_AND_YOU_CANNOT_USE_THIS_COREFOUNDATION_FUNC TIONALITY___YOU_MUST_EXEC__() > to debug. > The process has forked and you can > > > >> version > _ > platform x86_64-apple-darwin10.8.0 > arch x86_64 > os darwin10.8.0 > system x86_64, darwin10.8.0 > status > major 3 > minor 0.1 > year 2013 > month 05 > day 16 > svn rev 62743 > language R > version.string R version 3.0.1 (2013-05-16) > nickname Good Sport >> sessionInfo() > R version 3.0.1 (2013-05-16) > Platform: x86_64-apple-darwin10.8.0 (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 > base > > other attached packages: > [1] limma_3.16.7 GSVA_1.8.0 GSEABase_1.22.0 > graph_1.38.3 > [5] annotate_1.38.0 AnnotationDbi_1.22.6 Biobase_2.20.1 > BiocGenerics_0.6.0 > [9] BiocInstaller_1.10.3 > > loaded via a namespace (and not attached): > [1] DBI_0.2-7 grid_3.0.1 IRanges_1.18.2 lattice_0.20-15 > Matrix_1.0-12 > [6] RSQLite_0.11.4 stats4_3.0.1 tools_3.0.1 XML_3.95-0.2 > xtable_1.7-1 >> > > [[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
ADD COMMENT
0
Entering edit mode
It is probably the GUI, the error seems to come from CoreFoundation which is a Mac GUI framework On Thu, Aug 1, 2013 at 6:33 PM, Devon Ryan <dpryan@dpryan.com> wrote: > Are you running this in R.app or R from the terminal? If the former, try > running things from the terminal and see if the problem persists. Some > parallel computing related packages (e.g. doMC) will give this error in a > GUI. > > Devon > > ____________________________________________ > Devon Ryan, Ph.D. > Email: dpryan@dpryan.com > Molecular and Cellular Cognition Lab > German Centre for Neurodegenerative Diseases (DZNE) > Ludwig-Erhard-Allee 2 > 53175 Bonn, Germany > > On Aug 2, 2013, at 12:10 AM, Ed wrote: > > > Hi there, > > > > I used the examples in ?gsva and got the following errors on my mac. > > However, I run it also on the linux and it worked. > > > > Please suggest. > > > > Thanks, > > > > Weiwei > > > >> library(limma) > >> > >> p <- 10 ## number of genes > >> n <- 30 ## number of samples > >> nGrp1 <- 15 ## number of samples in group 1 > >> nGrp2 <- n - nGrp1 ## number of samples in group 2 > >> > >> ## consider three disjoint gene sets > >> geneSets <- list(set1=paste("g", 1:3, sep=""), > > + set2=paste("g", 4:6, sep=""), > > + set3=paste("g", 7:10, sep="")) > >> > >> ## sample data from a normal distribution with mean 0 and st.dev. 1 > >> y <- matrix(rnorm(n*p), nrow=p, ncol=n, > > + dimnames=list(paste("g", 1:p, sep="") , paste("s", 1:n, > > sep=""))) > >> > >> ## genes in set1 are expressed at higher levels in the last 10 samples > >> y[geneSets$set1, (nGrp1+1):n] <- y[geneSets$set1, (nGrp1+1):n] + 2 > >> > >> ## build design matrix > >> design <- cbind(sampleGroup1=1, sampleGroup2vs1=c(rep(0, nGrp1), rep(1, > > nGrp2))) > >> > >> ## fit linear model > >> fit <- lmFit(y, design) > >> > >> ## estimate moderated t-statistics > >> fit <- eBayes(fit) > >> > >> ## genes in set1 are differentially expressed > >> topTable(fit, coef="sampleGroup2vs1") > > ID logFC t P.Value adj.P.Val B > > 2 g2 2.43865785 6.79741169 1.490585e-09 1.490585e-08 11.467181 > > 1 g1 1.81349993 5.04733755 2.590932e-06 1.295466e-05 4.218446 > > 3 g3 1.68971708 4.54930258 1.812937e-05 6.043122e-05 2.348424 > > 5 g5 0.25263973 0.65201092 5.161890e-01 9.308575e-01 -6.688660 > > 10 g10 0.16766254 0.49082930 6.248376e-01 9.308575e-01 -6.780571 > > 9 g9 0.13478444 0.40143265 6.891295e-01 9.308575e-01 -6.820434 > > 8 g8 -0.12067327 -0.32614302 7.451340e-01 9.308575e-01 -6.847833 > > 7 g7 -0.08002351 -0.23401984 8.155437e-01 9.308575e-01 -6.873660 > > 4 g4 0.07875803 0.20538583 8.377717e-01 9.308575e-01 -6.879960 > > 6 g6 -0.03196719 -0.08251146 9.344379e-01 9.344379e-01 -6.897676 > >> > >> ## estimate GSVA enrichment scores for the three sets > >> gsva_es <- gsva(y, geneSets, mx.diff=1)$es.obs > > | > > | 0%The process has forked and you cannot use this > > CoreFoundation functionality safely. You MUST exec(). > > Break on > > > __THE_PROCESS_HAS_FORKED_AND_YOU_CANNOT_USE_THIS_COREFOUNDATION_FUNC TIONALITY___YOU_MUST_EXEC__() > > to debug. > > The process has forked and you can > > > > > > > >> version > > _ > > platform x86_64-apple-darwin10.8.0 > > arch x86_64 > > os darwin10.8.0 > > system x86_64, darwin10.8.0 > > status > > major 3 > > minor 0.1 > > year 2013 > > month 05 > > day 16 > > svn rev 62743 > > language R > > version.string R version 3.0.1 (2013-05-16) > > nickname Good Sport > >> sessionInfo() > > R version 3.0.1 (2013-05-16) > > Platform: x86_64-apple-darwin10.8.0 (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 > > base > > > > other attached packages: > > [1] limma_3.16.7 GSVA_1.8.0 GSEABase_1.22.0 > > graph_1.38.3 > > [5] annotate_1.38.0 AnnotationDbi_1.22.6 Biobase_2.20.1 > > BiocGenerics_0.6.0 > > [9] BiocInstaller_1.10.3 > > > > loaded via a namespace (and not attached): > > [1] DBI_0.2-7 grid_3.0.1 IRanges_1.18.2 lattice_0.20-15 > > Matrix_1.0-12 > > [6] RSQLite_0.11.4 stats4_3.0.1 tools_3.0.1 XML_3.95-0.2 > > xtable_1.7-1 > >> > > > > [[alternative HTML version deleted]] > > > > _______________________________________________ > > Bioconductor mailing list > > Bioconductor@r-project.org > > https://stat.ethz.ch/mailman/listinfo/bioconductor > > Search the archives: > http://news.gmane.org/gmane.science.biology.informatics.conductor > > _______________________________________________ > Bioconductor mailing list > Bioconductor@r-project.org > https://stat.ethz.ch/mailman/listinfo/bioconductor > Search the archives: > http://news.gmane.org/gmane.science.biology.informatics.conductor > [[alternative HTML version deleted]]
ADD REPLY

Login before adding your answer.

Traffic: 764 users visited in the last hour
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6