similar to: Call for Papers: ManLang 2018 (Sept. 10-14, Linz, Austria)

Displaying 20 results from an estimated 500 matches similar to: "Call for Papers: ManLang 2018 (Sept. 10-14, Linz, Austria)"

2018 Mar 12
0
Call for Papers: ManLang 2018 (Sept. 10-14, Linz, Austria)
Dear Person That Posted This Email, Please be aware that calls for papers are only on-topic for this email list if they are specifically about LLVM. For example, a call for a workshop on LLVM in Scientific Computing would be on topic whereas a general compiler call for papers (like the one below) is not. That said, I hope you receive many strong submissions. Your conference looks
2011 Sep 01
3
betareg question - keeping the mean fixed?
Hello, I have a dataset with proportions that vary around a fixed mean, is it possible to use betareg to look at variance in the dispersion parameter while keeping the mean fixed? I am very new to R but have tried the following: svec<-c(qlogis(mean(data1$scaled)),0,0,0) f<-betareg(scaled~-1 | expt_label + grouped_hpi, data=data1, link.phi="log",
2014 Mar 26
1
Conflicting definitions for function redefined as S4 generics
[cross-posted to R-devel and bioc-devel] Hi, I am trying to implement a 'sort' method in one of the CRAN packages I am maintaining ('apcluster'). I started with using setMethod("sort", ...) in my package, which worked fine. Since many users of my package are from the bioinformatics field, I want to ensure that my package works smoothly with Bioconductor. The problem
2011 Sep 12
1
findFreqTerms vs minDocFreq in Package 'tm'
I am using 'tm' package for text mining and facing an issue with finding the frequently occuring terms. From the definition it appears that findFreqTerms and minDocFreq are equivalent commands and both tries to identify the documents with terms appearing more than a specified threshold. However, I am getting drastically different results with both. I have given the results from both the
2012 Dec 14
1
Strange, most probably unjustified, codoc mismatch for S4 method with one argument plus '...' (re-try)
Hi, I just figured out that I accidentally posted my message in HTML, so I am retrying in plain text only. Sorry. I am currently extending one of our CRAN packages and ran into an unexpected problem when checking the source package. I got some warnings in the step "* checking for code/documentation mismatches". I double checked everything and did not see anything that would
2011 Mar 01
1
Problem on flexmix when trying to apply signature developed in one model to a new sample
Problem on flexmix when trying to apply signature developed in one model to a new sample. Dear R Users, R Core Team, I have a problem when trying to know the classification of the tested cases using two variables with the function of flexmix: After importing the database and creating a matrix: BM<-cbind(Data$var1,Data$var2) I see that the best model has 2 groups and use: ex2
2014 Mar 26
5
Conflicting definitions for function redefined as S4 generics
That might be worth thinking about generally, but it would still be nice to have the base generics pre-defined, so that people are not copy and pasting the definitions everywhere, hoping that they stay consistent. On Wed, Mar 26, 2014 at 6:13 AM, Gabriel Becker <gmbecker@ucdavis.edu>wrote: > Perhaps a patch to R such that generics don't clobber each-other's method > tables
2012 Mar 09
6
unir 2 dataframe con con igual caso pero distinto valor en igual variable
Estimados usarios de R: Tengo una base de datos madre en formato .sav de SPSS y la quiero modificar usando datos de otras base de datos .sav y otra en .csv a las que llamare hijos. No tengo problema en convertirlas en data.frame. Todos los archivos tienen en comĂșn una variable que es Ășnica. En aquellos casos que les falta un valor a una variable en el archivo madre lo relleno con el valor del
2012 Jun 18
2
Need to append vector to all levels of nested list WITHOUT a loop
Hi everyone, I have a list betaMoments with 2 levels, e.g. > beta1 = list( + m = 4, + v = 5 + ) > beta2 = list( + m = 6, + v = 7 + ) > > betaMoments = list() > betaMoments[[1]] = beta1 > betaMoments[[2]] = beta2 and I have a matrix Names which has the same number of lines as the list has first level elements (here 2; beta1 and beta2). Now I need to make
2009 Jul 11
2
[LLVMdev] ANTLR?
That sounds like a problem. Just so I understand, do you mean there isn't the run-time support etc. to write back ends for the C++ language, or that the compiler IR is also somehow insufficient to write a code generator? --Vikram Associate Professor, Computer Science University of Illinois at Urbana-Champaign http://llvm.org/~vadve On Jul 11, 2009, at 3:00 PM, Granville Barnett
2016 Feb 04
2
Profiling with LLVM.
Dear Duncan, Thank you a lot for your feedback. I have a problem though. The branch weights counters overflow in some files and thus I get incorrect numbers. Is there any way to find a workaround for that? Is is supposed to be a known bug or is it something that needs configuration on my part? Again, thank you a lot for your reply. Best Regards, Georgios Zacharopoulos 2016-02-03 18:23
2007 Jun 26
3
surprising difference in log()
Hello everybody My collegue and I noticed a strange behaviour of R on different platforms. It's a simple computation, but results are rather different. On Windows XP: > floor(log(8,2)) [1] 3 which is what one should expect. Here's instead the result with Mac OS X (same version, 2.5.0 (2007-04-23)) > floor(log(8,2)) [1] 2 Is it a "bug" in R or in the operating
2016 Feb 05
2
Profiling with LLVM.
Dear Duncan, I am generating branch-weights annotated IR files as described in the documentation of LLVM, using profiling with instrumentation. http://clang.llvm.org/docs/UsersManual.html#profiling-with-instrumentation e.g. llvm-profdata merge -output=$(BENCH).profdata default.profraw > clang -S -emit-llvm -O3 -fprofile-instr-use=$(BENCH).profdata -o > bench.prof.ll bench.c The issue is
2010 Jun 07
1
what`s best memory - speed - pc for R?
Hi all, I need to do massive simulations in the next two years. I estimated that I will need about 64GB memory, if I do not want to split up the calculations. Additionally I would like to have it as fast as possible. Can R handle multi-core processors and can all standard operating systems handle the same amount of memory and speed? Perhaps someone could point me to a webshop that sales
2009 Jul 11
0
[LLVMdev] ANTLR?
When you create a parser via ANTLR you specify the output language of the resulting recursive descent parser, at the moment there exists no C++ output template to my knowledge, thus you would have to generate the parser as C code for which a template exists. The runtime support should be there, at least partially but it won't use things like exceptions, nor will it have a very modular design
2010 May 23
2
Subsetting with a list of vectors
Hi, I have a dataset that looks like the one below. data plot plantno. species H 31 ABC D 2 DEF Y 54 GFE E 12 ERF Y 98 FVD H 4 JKU J 7 JFG A 55 EGD . . . . . . .
2018 Jan 22
2
How to address the following: CRAN packages not using Suggests conditionally
Re-sending, since I forgot to include the list, sorry. I'm including r-package-devel too this time, as it seems more appropriate for this list. El 22 ene. 2018 10:11, "I?aki ?car" <i.ucar86 at gmail.com> escribi?: > > > El 22 ene. 2018 8:12, "Ulrich Bodenhofer" <bodenhofer at bioinf.jku.at> > escribi?: > > Dear colleagues, dear members of
2008 Oct 28
1
Marginal effects in negative binomial
Dear All, I carry out negative binomial estimations using the glm.nb command from the MASS package. Is there a command or a simple procedure for computing marginal effects from a glm.nb fitted object? If these are the same as for a Poisson fitted object (glm), my question remains how to compute them. Thanks in advance for your help. Roberto Patuelli ******************** Roberto Patuelli, Ph.D.
2009 Jan 30
1
Fitted values and residuals from glmmPQL (MASS package)
Dear All, I would like to analyse the residuals from a generalized linear mixed model (GLMM) that I estimated, with random effects, by means of the command glmmPQL, from the MASS package. It is not very clear to me what the actual residuals to analyse are (Y - Yhat): I obtain two columns of residuals, of which the first are population residuals, and the second refer to the grouping used in the
2008 Oct 03
1
Problem with glm.nb estimation
Dear All, I've been using already for a year glm.nb() from the MASS package. But today, R gave me an error message when estimating one of my usual models: > depEsf.nb <- glm.nb(depE ~ manuf00E + corps00E + lngdp00E + lngdp00sqE + > lnpop00E + indshE + scishE + mechshE + elecshE + chemshE + drugshE + > urban_dummyE + aggl_dummyE + + eE1 + eE2 + eE3 + eE4 + eE5 + eE6 + eE7 +