similar to: Memory Leak

Hi, on a CentOS 6.4-workstation we have the problem, that Xorg fills up /var/log/Xorg.0.log with AUDIT messages faster than one can read. Within four hours the logfile grew to 160 MB and usually within 1-2 days applications and sometimes the OS crash because /var becomes full. Here a small extract of /var/log/Xorg.0.log: [...] [ 24272.458] AUDIT: Wed Oct 2 15:41:44 2013: 2625: client 28

I can't seem to dial out with Voicepulse Open Access service using *. Incoming works fine. Another user posted a few weeks back that they were having problems and there are some threads at dslreports.com about this as well. Maybe someone here can figure out what the issue is from the sip debug info below. I am at a loss. The audible error message from Allison is 0984 (from VP server) Here is

I've recently had an Asterisk 1.4.x install system crash, luckily I was well into configuring a replacement system. Initially, the system was running: Debian 6 64BIT Asteirsk 11.3 USB sound card (to paging amp) Audio file is sent to the console via /dev/dsp1 on a 3 second time delayed call file. Initial testing shows this working well, but the day before I was to deliver and install, I

On 7 June 2016 at 10:54, Shi, Steven <steven.shi at intel.com> wrote: > Hi Rafael, > I finally enable the clang LTO build with small code model and PIE, and my clang LTO Uefi firmware works now. Thank you! But I have one more issue on the clang normal build (without LTO) now. I find the small code model + "-fpie" build option will let clang generate some R_X86_64_GOTPCREL

Hi, hm i don?t think that it has something to do with the trus-relationship if it where so than every user on that pc would get a permision denied. what does the error message exactly says? example: Access denied, the network path was not found... -----Ursprungliche Nachricht----- Von: Bert_De_Ridder@peopleware.be [mailto:Bert_De_Ridder@peopleware.be] Gesendet: Dienstag, 27. Juli 2004

I have a confusing error from R CMD check that I don't get when running the example manually by hand. In the \examples section of an Rd file, I create a GRanges object, then I call a function with the GRanges object, whose first 2 lines are require(GenomicRanges) annoDF <- as.data.frame(anno) # anno is the GRanges object. and that second line gives: Error in

Hi, I am soliciting input from the ZFS engineers and/or ZFS users on an extension to "zfs list". Thanks in advance for your feedback. Quick Background: The pNFS project (http://opensolaris.org/os/project/nfsv41/) is adding a new DMU object set type which is used on the pNFS data server to store pNFS stripe DMU objects. A pNFS dataset gets created with the "zfs

Hello, I am using R 2.11.0. I have a curious problem where I get a warning in R CMD check which is seemingly not relevant to my Rd file. The warning says : * checking Rd \usage sections ... WARNING Bad \usage lines found in documentation object 'enrichmentCalc': <unescaped bksl>S4method{enrichmentCalc}{GenomeDataList, BSgenome}(rs, organism, seqLen=NULL, ...) <unescaped

Hello, I am using R 2.11.0. I have a curious problem where I get a warning in R CMD check which is seemingly not relevant to my Rd file. The warning says : * checking Rd \usage sections ... WARNING Bad \usage lines found in documentation object 'enrichmentCalc': <unescaped bksl>S4method{enrichmentCalc}{GenomeDataList, BSgenome}(rs, organism, seqLen=NULL, ...) <unescaped

Help please- I am running 3.3.1 on Centos using a 10GB network. I get reasonable write speeds, although I think they could be faster. But my read speeds are REALLY slow. Executive summary: On gluster client- Writes average about 700-800MB/s Reads average about 70-80MB/s On server- Writes average about 1-1.5GB/s Reads average about 2-3GB/s Any thoughts? Here are some additional details:

Hi All, I have an CBS segmentation algorithm output for 10 tumor samples each from 2 different tumors. Now, I am in an urgent need to assign gene (followed by all genes present) that belong to a particular segment after I removed all the CNVs from segment data. The format of the data is: Sample Chromosome Start End Num_Probes Segment_Mean Sample1A-TA 1 51598 76187 15

Hi all, I am using the package ChIPpeakAnno, and I have a problem with the function getAllPeakSequence. This is related to object oriented programming I think, I have the following message: > peaksWithSequences <- getAllPeakSequence(peakList, upstream = 100, > downstream = 100, genome = Hsapiens) Error in validObject(.Object) : invalid class "GRanges" object: superclass

I've got two tables.... first one(table1): ID chrom start end Ex1 2 152 180 Ex2 10 2000 2220 Ex3 15 3000 4000 second one ( table2): chrom location name 2 160 Alv 2 190 GNN 2 100

Hello, I'm trying to use coxph() function to fit a very simple Cox proportional hazards regression model (only one covariate) but the parameter space is restricted to an open set (0, 1). Can I still obtain a valid estimate by using coxph function in this scenario? If yes, how? Any suggestion would be greatly appreciated. Thanks!!! [[alternative HTML version deleted]]

Il gio, 2004-07-29 alle 07:55, Bert_De_Ridder@peopleware.be ha scritto: > That is for roaming profiles, right ? > Why would I want to set that ? No, isn't. but you have to try; 'cos, in my opinion, of course, you won't login in bdc; but, the roaming profiles (home directory) must be in pdc; if that works, you will try set (in bdc): logon path = \\PDC\blablabla... (for win

I'm in the process of converting some S3 methods to S4 methods. I have this function : setGeneric("enrichmentCalc", function(rs, organism, seqLen, ...){standardGeneric("enrichmentCalc")}) setMethod("enrichmentCalc", c("GenomeDataList", "BSgenome"), function(rs, organism, seqLen, ...) { ... ... ... })

I do have a bunch of genes ( nearly ~50000) from the whole genome, which read in genomic ranges A range(gene) can be seem as an observation has three columns chromosome, start and end, like that seqnames start end width strand gene1 chr1 1 5 5 + gene2 chr1 10 15 6 + gene3 chr1 12 17 6 + gene4 chr1 20 25 6 + gene5

Hi, I want to merge multiple chromosomal regions based on their common intersecting regions. I tried couple of things using while and if loops but did not work out. I would appreciate if anyone could provide me a small piece of code in R to get the intersection of following example: chr1: 100-150 chr1: 79-250 chr1: 100-175 chr1: 300-350 I want the intersection of all four regions as follow:

Hi everybody, I would like to know whether it is possible to compare to tables for certain parameters. I have these two tables: gene table name chr start end str accession Length gen1 4 646752 646838 + MI0005806 86 gen12 2L 243035 243141 - MI0005821 106 gen3 2L 159838 159928 + MI0005813 90 gen7 2L

Hello, I have start and end coordinates from different experiments (DNase hypersensitivity data) and now I would like to combine overlapping intervals. For instance (see my test data below) (2) 30-52 and (3) 49-101 are combined to 30-101. But 49-101 and 70-103 would not be combined because they are on different chromosomes (chr a and chr b). Does anybody have an idea? Thanks Hermann > df