similar to: CLI color using -r

Am I doing something wrong? I can't get this dial command to timeout.... Dial(Zap/g1/xxxxxxx,20) -- Gary White admin@netpathway.com Network Administrator Internet Pathway 105 D East Church Street Voice: 601-776-3355 P. O. Box 777 Fax: 601-776-2314 Quitman, MS 39355

Guys, I have a problem that I can seem to run down. I'm running CVS-HEAD-09/10/04-18:14:15 on a Celeron 500 with an Intel chipset motherboard. The audio from my GS phone to * is sometimes decoded at about twice the normal speed on some outgoing calls. Also.when recordind a message to * from the GS it also does the same. This happens about 1 out of every 5 records or calls. This only

Hello, I am just curious how many people are hooked up with BroadVoice and have recently been experiencing a lot of dificulty. Joel

I am after using a web crm system which has a button to then get asterisk to dial the contact. For this I was looking at call files, which appear good for the job, I have one small problem with them though. 1/ file is created 2/ external number is called 3/ the external party answers 4/ the external party now hears ringing as you extension is now being called - bad! What I would like to

Hello all, I would like to introduce our group's new bioinformatics package to you: pathfindR <https://cran.r-project.org/package=pathfindR> This tool is designed to improve pathway enrichment analysis by firstly identifying active subnetworksin differential expression/methylation data using a protein-protein interaction network. It then performs pathway enrichment analysis

Hello all, I would like to introduce our group's new bioinformatics package to you: pathfindR <https://cran.r-project.org/package=pathfindR> This tool is designed to improve pathway enrichment analysis by firstly identifying active subnetworksin differential expression/methylation data using a protein-protein interaction network. It then performs pathway enrichment analysis

Hi, i'm playing a bit around with vcpus. My guest is Windows 10 1903. This is the excerpt from the config: ... <vcpu placement='static' current='2'>4</vcpu> <vcpus> <vcpu id='0' enabled='yes' hotpluggable='no'/> <vcpu id='1' enabled='yes' hotpluggable='yes'/> <vcpu id='2'

On Fri, Feb 14, 2020 at 16:05:00 +0100, Lentes, Bernd wrote: > Hi, > > i'm playing a bit around with vcpus. > My guest is Windows 10 1903. > This is the excerpt from the config: > ... > <vcpu placement='static' current='2'>4</vcpu> > <vcpus> > <vcpu id='0' enabled='yes' hotpluggable='no'/> >

G'day, My problem is I'm not sure how to extract effect sizes from a nonlinear regression model with a significant interaction term. My data sets are multiple measurements of force response to an agonist with two superimposed treatments each having two levels. This is very similar to the Ludbrook example in Venables and Ripley. The experiment is that a muscle is exposed to an agonist

Esteemed UseRs, This must be embarrassingly trivial to achieve with e.g., melt() and cast(): deduplicating records ("pw.X" in example) for a given set of responses ("cond.Y" in example). Hopefully the runnable example shows clearly what i have and what i'm trying to convert it to. But i'm just not getting it, ?cast that is! So i'd really appreciate some ones

----- On Feb 15, 2020, at 12:47 AM, Marc Roos M.Roos@f1-outsourcing.eu wrote: > Would you mind sharing your xml? I have strange high host load on idle > windows guest/domain <domain type='kvm'> <name>pathway</name> <uuid>8235e5ae-0756-4286-5407-9fa02d372046</uuid> <description>Pathway Studio Dietrich</description> <memory

Hi Dumb question time again, for which I apologise. I have a variable that contains the following numerical text "04010". This is the name to access a list: > as.list(KEGGPATHID2NAME)$"04010" [1] "MAPK signaling pathway" Marvellous! Except I want to do that when "04010" is assigned to a variable called path and I can't figure out how to do it!

I have following codes for ggplots. The legends are given in the plot do not match with the values specified in the codes given below. Your helps highly appreciated. Greg library(ggplot2) p <- ggplot(a,aes(x=NO_BMI_FI_beta ,y=FI_beta ,color= Super.Pathway))+ theme_bw() +theme(panel.border=element_blank()) + geom_point(size=3) p2<-p+scale_color_manual(name="Super.Pathway",

Hi, I'm using GAGE/pathview to analyze my RNA-seq and phospho-protein data. The following error occurs after this command line below: >pv.out.list <- sapply(path.ids2[1:3], function(pid) pathview( gene.data = cnts.d, pathway.id = pid, gene.idtype="SYMBOL",kegg.native = F, same.layer = T, species = "hsa", kegg.dir = "test", out.suffix = "up"))

Gday, This is a repost since I only had one direct reply and I remain mystified- This may be stupidity on my part but it may not be so simple. In brief, my problem is I'm not sure how to extract parameter values/effect sizes from a nonlinear regression model with a significant interaction term. My data sets are dose response curves (force and dose) for muscle that also have two

Greetings all, I have two sets of data that I would like to investigate. The first is gene/genome related data given different 'cell-states'. The second set of data is relates the genes to a biological pathway. /(I think in pictures so here goes.)/ *dataframe1* gene, cell-state1, cell-state2 gene1, x1, y1 gene2, x2, y2 gene.x, ..., ... *dataframe2* pathway1, gene-x1, gene-x2, ...

On Mon, Apr 11, 2016 at 10:37 AM, Karsten Wade <kwade at redhat.com> wrote: > -----BEGIN PGP SIGNED MESSAGE----- > Hash: SHA1 > > On 04/11/2016 09:18 AM, Jim Perrin wrote: >> What are the thoughts or concerns about this sort of workflow >> change? > > Any chance Moin Moin can store wiki source in git and sync > automatically with a central git repository?

On 11/04/16 21:11, Akemi Yagi wrote: > On Mon, Apr 11, 2016 at 10:37 AM, Karsten Wade <kwade at redhat.com> wrote: >> -----BEGIN PGP SIGNED MESSAGE----- >> Hash: SHA1 >> >> On 04/11/2016 09:18 AM, Jim Perrin wrote: >>> What are the thoughts or concerns about this sort of workflow >>> change? >> >> Any chance Moin Moin can store wiki

Hi, * I am using read.table command as follow kegg<-read.table("c:/IDs.tab",header =TRUE,quote= "'", sep="\t") * Fragment of file is as follow: ID Pathway 04916 Melanogenesis 04920 Adipocytokine signaling pathway 04930 Type II diabetes mellitus 04940 Type I diabetes mellitus 04950 Maturity onset diabetes of the young 05010

I have two specific questions regarding the output of lda function in MASS. #Question1: #========= n: sample size, p: number of variables Some articles in the literature say that LDA is singular for p > n-1. However, my experimentation with lda (default arguments) for two class problems shows collinearity for p > n-2. Does anyone know why this is the case? Does lda (MASS) use a different