similar to: for loop and if problem

Hello, i am heaving issue with some program in wine. When i start it Wine System tray window is shown in screen corner and stay there without icon [Image: http://img15.imageshack.us/img15/6674/screenshotas.png ] (http://img15.imageshack.us/i/screenshotas.png/) Software is working fine i am just heaving issue with tray icon. Is there a way to disable Wine System Tray ? Best regards n24

Hi, I have a question about bundle: RoR + oracle + bind variables. Heaving read forums/blogs/etc I found out RoR does not use bind vars for oracle particularly (and for all adapters in general). Then I found Michael''s patch (http://dev.rubyonrails.org/attachment/ticket/5199/oracle_bind.patch) but it was not added to the following RoR versions (since the end of May). As I suppose it was

On Fri, 16 Jan 2009, r-help-request at r-project.org wrote: > Date: Thu, 15 Jan 2009 13:29:03 +0100 > From: Pablo G Goicoechea <pgoikoetxea at neiker.net> > Subject: Re: [R] How to create a chromosome location map by locus ID > To: Sake <tlep.nav.ekas at hccnet.nl> > Cc: r-help at r-project.org > Message-ID: <496F2C0F.3040304 at neiker.net> > Content-Type:

Hi, everyone When I ran this cript, There is Error in substring(tmp.subject, tmp.end[ex] + 1, tmp.start[ex + 1] - 1) : invalid substring argument(s) Could someone figure out what the problem is? for(i in 1:length(genebody[,1])){ tmp.id<-as.vector(genebody[i,1]) # get gene id tmp.subject<-as.vector(genebody[i,2]) # get gene sequence

Hi, i have two files (file1.txt and file2.txt) which i would like to merge, based on certain criteria, i.e. it combines data based on matching geneID and exons. i have used the merge option, but it does not give me the desired outcome. merged.txt shows the result i would like. *File1. txt* ** AffyProbe ProbeType Flag GeneSymbol GeneID Exons Chrom Strand Affytart AffyEnd 1

Hi, I am given the following table: > head(hsa_refseq) chr genome region start stop nu strand nu.1 nu.2 gene_id 1 chr1 hg19_refGene CDS 67000042 67000051 0 + 0 gene_id NM_032291 2 chr1 hg19_refGene exon 66999825 67000051 0 + . gene_id NM_032291 3 chr1 hg19_refGene CDS 67091530 67091593 0 + 2 gene_id NM_032291 4 chr1 hg19_refGene exon

HI, this is my problem I want to subset this file df, using only unique df$exon printing the line once even if df$exon appear several times: unique(df$exon) will show me the unique exons If I try to print only the unique exon lines with df[unique(df$exon),] -this doesn't print only the unique ones :( could you help? thanks Nat exon size chr start

I'm new to asterisk and fror a cupple of days I heave been googleing the net for digium "clones", because it's very hard for me to get a digium card (X100P). Does anyone Know another substitute for X100P (I know that intel based modem with chip 537/MD3200 is working but I did not find any of those) ? I made it work with an Intel 536 (with a costumised driver that I found on

It's that time again. I'm stuck with a bunch of older Powermac G4's that I either need to repurpose or give the heave ho. I've not tried CentOS on Mac hardware before. Would the following config be suitable for a (somewhat slow) workstation? PowerMac G4 400mhz 256mb RAM 40gig ATA disk Some sort of dual-head ATI video setup with 64mb VRAM (I've forgotten which cards they

Hi, I'm in the process of trying to convince my organization to move from an exchange server, to a samba solution, while retaining their original windows environments, including Outlook clients. I thought I had all my issues covered, and suddenly I'm facing a show stopper. it turns out that a lot of my users "documentation" has been stored on "public folders" on the

I built R 2.2.0 from source on my debian machine yesterday and updated all packages. My problem is that "dates" function from its, that my code heavely uses is now masked by "dates" from chron. How can I specify tehat I want to use dates from its or how can I prevent it from being masked? > library(its) Loading required package: Hmisc Hmisc library by Frank E Harrell Jr

Dear Peter, I am running your g.test() with the william's correction but I have a question about the input numbers. These are my data: "Our data are consistent with those obtained using microarray comparative genome hybridization in that we found significantly fewer variants per Mb on the X compared to the autosomal chromosomes (152 versus 336 respectively, G = 93.4, P < 2e-16, df =

Hello, I am new to R and still feeling my way thru it. I am trying to plot the values from this file below on the X-axis of a plot. I have attached the graph to the email...the one i am trying to recreate. Exon start end 5'UTR 22540060 22540121 1 22540122 22540140 2 22540303 22540493 3 22541552 22541565 4 22542373 22542519 5 22544265 22544432 3'UTR 22544433 22544856 I would like to

I'd like to resurrect this orphaned thread: http://lists.xiph.org/pipermail/icecast/2003-December/006139.html We're using the embedded flash player for listeners of pulverradio.com and can't use 2.2 for relaying from our encoders. Apparently we can use Icecast v1.3 Although this is clearly a problem caused by ActiveX and Microsoft boneheads that is a mountain that may prove

Hello: I was hoping to get some advice about how to return a tree (basically a linked list -- with each node containing a parent, left, and right node pointers) from a C routine back into R. Each node itself contains several attributes (a double, a char *, an int, and a void * ) Initially I was thinking I could just return to R a SEXP containing a pointer to the Root Node, but then realized

Hi, I was wondering I'm going about this in the correct way. I need to test if there are coding sequences or exons in hg19 which match a string of 100bp "D" i.e. [A,G or T]. However I'm getting a strange result. I get a hit on chr7, using the 100bp search however when I search with 60bp sequence of "D" I don't get any hits. library("BSgenome")

As mentioned last night, we''ve been reviewing a proposal for hot spare support in ZFS. Below you can find a current draft of the proposed interfaces. This has not yet been submitted for ARC review, but comments are welcome. Note that this does not include any enhanced FMA diagnosis to determine when a device is "faulted". This will come in a follow-on project, of which some

Alternatively you can just script the window media player control, and bind it to your stream, that should work just fine, assuming you have my directshow filters installed. Zen. ----- Original Message ----- From: "Michael Smith" <msmith@xiph.org> To: "Ian Andrew Bell" <hello@ianbell.com>; "icecast" <icecast@xiph.org> Sent: Monday, October 18,

Rusty, is there a reason why we dont export the virtio headers for 9p, balloon, console, pci, and virtio_ring? kvm uses make sync, but I think it is still useful to heave these headers exported as they might be useful for other userspace tools. I dont export virtio.h, because it does not seem to have useful information for userspace and it requires scatterlist.h which is also not exported.

Hi all, OPC is a standard that specifies a collection of DCOM interfaces heavely used in the industrial automation domain. (http://www.opcfoundation.org) I would like to access these OPC objects that run in Windows from Linux computers, using the DCOM framework. Instead of implementing DCOM from scratch for Linux, I was considering 'stealing' some code off the SAMBA project relating