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Jeremy, Bit of bad news - we had a another runaway SMBD. This time profiles were NOT involved - I was simply copying up an installation of Office2000 and then deleting it. It almost reached the end of the deletion when the processor utilisation went up to 90%. The client connection then dropped with a 'connection is no longer available' and there is now 99% processor utilisation on the

Hello, I am running Samba 2.2.2 with acl-0.7.16 on RedHat 6.2 (2.2.19). The PDC is a Windows 2000 Server and the Samba server is a domain member using Winbind. All the workstations are Windoze 2000 Pro with SP2. Everything seemingly works fine but every day or two I get a runaway SMBD process which hogs the CPU and becomes unkillable. The only resolution is to reboot the server completely.

I think I might have miss understood where it is failing, has this file been added to the DB on the web site or does it fail when you try to onfigure this? Carle Simmonds Infrastructure Consultant Technology Services Experian UK Ltd __________________________________________________ Tel: +44 (0)115 941 0888 (main switchboard) Mobile: +44 (0)7813 854834 E-Mail: carle.simmonds at uk.experian.com

Hi everyone; I have a problem on my 10 nodes cluster with ocfs2 1.2.9 and the OS is RHEL 4.7 AS. 9 nodes can start o2cb service and mount san disks on startup however one node can not do that. My cluster configuration is : node: ip_port = 7777 ip_address = 192.168.5.1 number = 0 name = fa01 cluster = ocfs2 node: ip_port =

Hello list, I'm trying to figure out how exactly the specification of nested random effects works in the lmer function of lme4. To give a concrete example, consider the rat-liver dataset from the R book (rats.txt from: http://www.bio.ic.ac.uk/research/mjcraw/therbook/data/ ). Crawley suggests to analyze this data in the following way: library(lme4) attach(rats) Treatment <-

Ronaldo, Further to my previous posting on your Glycogen nested aov model. Having read Douglas Bates' response and Reflected on his lmer analysis output of your aov nested model example as given.The Glycogen treatment has to be a Fixed Effect.If a 'treatment' isn't a Fixed Effect what is ? If Douglas Bates' lmer model is modified to treat Glycogen Treatment as a purely

Hi, I''m trying to understand the lme output and procedure. I''m using the Crawley''s book. I''m try to analyse the rats example take from Sokal and Rohlf (1995). I make a nested analysis using aov following the book. > summary(rats) Glycogen Treatment Rat Liver Min. :125.0 Min. :1 Min. :1.0 Min. :1 1st Qu.:135.8

Dear all, During my pre-R era I tried (yes, tried) to understand mixed models by working through the 'rat example' in Sokal and Rohlfs Biometry (2000) 3ed p 288-292. The same example was later used by Crawley (2002) in his Statistical Computing p 363-373 and I have seen the same data being used elsewhere in the litterature. Because this example is so thoroughly described, I thought

Hi All, I would like to ask a question on fixed and random effecti in lme. I am fiddlying around Mick Crawley dataset "rats" : http://www.bio.ic.ac.uk/research/mjcraw/statcomp/data/ The advantage is that most work is already done in Crawley's book (page 361 onwards) so I can check what I am doing. I am tryg to reproduce the nested analysis on page 368:

This is third time today that my Asterisk hangs up. It seams that I have problems with h323. I'm using ooh323 from Asterisk add-ons. I have the following configuration Asterisk 1.2.1 Asterisk-addons 1.2.1 Fedora Core 4 I'm using SIP phones and h323 trunk to my VoIP provider Like I said this is third time today that he hang's up. First time, I came at work and Asterisk was down.

Hi everybody: I?m trying to rewrite some routines originally written for SAS?s PROC NLMIXED into LME4's glmer. These examples came from a paper by Nelson et al. (Use of the Probability Integral Transformation to Fit Nonlinear Mixed-Models with Nonnormal Random Effects - 2006). Firstly the authors fit a Poisson model with canonical link and a single normal random effect bi ~ N(0;Sigma^2).The

Hi, I've been doing an experiment, measuring the dead-zone-diameters of bacteria, when they've been grown with paper diffusion disks of antimicrobial. There are two groups, or treatments - one is bacteria that have been cultured in said antimicrobial for the past year, the other group is of the same species, but lab stock and has not gone had any prior contact with the antimicrobial.

====================================================== "To attract men, I wear a perfume called 'New Car Interior'." Rita Rudner ====================================================== Release Announcements --------------------- This is the latest stable release of Samba 4.4. Major enhancements in Samba 4.4.7 include: o Let winbindd discard expired

====================================================== "To attract men, I wear a perfume called 'New Car Interior'." Rita Rudner ====================================================== Release Announcements --------------------- This is the latest stable release of Samba 4.4. Major enhancements in Samba 4.4.7 include: o Let winbindd discard expired

Hi, I make this model using lme m.lme <- lme(Glycogen~Treatment,random=~1|rTrt/Liver) How to make this using lmer? I try > m.lmer <- lmer(Glycogen~Treatment+(1|rTrt/Liver)) Erro em lmer(Glycogen ~ Treatment + (1 | rTrt/Liver)) : entry 0 in matrix[0,0] has row 2147483647 and column 2147483647 Al??m disso: Mensagem de aviso: / not meaningful for factors in: Ops.factor(rTrt, Liver)

Hello, unfortunately I have I big problem I can't solve. I have to analyse if a gene is tissue specific. For example for the gene xyz I have following expression values: Heart Liver Brain 8.998497 10.013561 12.277407 9.743556 10.137574 11.033957 For every tissue I have two values from two different experiments. Now I want to test if Heart is significant higher

Hi - I have a problem that is driving me round the bend. I have installed Suse 9.3 (64-bit) and compiled Samba 3.0.14a from source. The server is going to be part of an ADS network so I have Kerberos working fine and I have joined the domain ('net ads testjoin' works fine). I have compiled and loaded the idmap_rid module and that seems to be working fine too. wbinfo -u gives me all the

Hi, This is a message I already posted on the chan_sccp mailing list, but since this list has a lot of active members, I'm hoping someone might be able to help (And my problem is * related, so I guess it's ok if I post it here also ;) ). I'm trying to get SCCP ATA188s to run with Asterisk. The Asterisk box uses the latest Asterisk@Home image (Version 2.6). I have compiled and

If I fire up asterisk it connects to my MSSQL server via ODBC just fine. However, if I issue a reload it unloads the ODBC.. then loads it again and I get an error... and keep getting it until I On a fresh start: Aug 26 15:43:14 WARNING[13818] cdr_odbc.c: cdr_odbc: table not specified. Assuming cdr Aug 26 15:43:14 VERBOSE[13818] logger.c: -- cdr_odbc: dsn is MSSQL-asterisk Aug 26 15:43:14

Hello list! I?m having an issue when reloading Asterisk, I?ve had this problem in Asterisk 1.6.1.6 so I upgrade to 1.6.2.1 version, but I still have the same error. For example, I send a "reload" in Asterisk CLI and this is the output: isb152*CLI> reload == Parsing '/etc/asterisk/extconfig.conf': == Found == Parsing '/etc/asterisk/manager.conf': == Found