similar to: No NT domain controller is available problem

Hi all, I have samba server 2.2.8a to act as a PDC on a mixed WinXP/Win2k/WinNT network. I joined all my workstations to the domain with no problem... And users can login into the domain and access their folders/printers, BUT!!! Every now and then they cannot log in getting error message that domain controller cannot be found.... I'm trying to track the problem down :-) When I went thru

> chromosomes id refseq name length 1 0 NC_000001.9 Homo sapiens chromosome 1 247249719 2 1 NC_000002.10 Homo sapiens chromosome 2 242951149 3 2 NC_000003.10 Homo sapiens chromosome 3 199501827 4 3 NC_000004.10 Homo sapiens chromosome 4 191273063 5 4 NC_000005.8 Homo sapiens chromosome 5 180857866 6 5 NC_000006.10 Homo sapiens chromosome 6

Through converting a miRNAs file from FASTA to character format I get a vector which looks like the following: > nml [1] "hsa-let-7a MIMAT0000062 Homo sapiens let-7a" [2] "hsa-let-7b MIMAT0000063 Homo sapiens let-7b" [3] "hsa-let-7c MIMAT0000064 Homo sapiens let-7c" [4] "hsa-let-7d MIMAT0000065 Homo sapiens

I have the following vector of strings (shown only the first 3 elements) > desc[1:3] [1] "hsa-let-7a MIMAT0000062 Homo sapiens let-7a" [2] "hsa-let-7a* MIMAT0004481 Homo sapiens let-7a*" [3] "hsa-let-7a-2* MIMAT0010195 Homo sapiens let-7a-2*" > is.vector(desc) [1] TRUE > A <- unlist(strsplit(desc[1:3], " ")) > A [1]

Hello R-user community! I am running R 2.7.0 on a Power Book (Tiger). (I am still R and statistics beginner) I did the following : pdf("InLnegthMaxHomogeneity.pdf") boxplot(inflorescence_length_Max~Sex, main="Bartletts Homogeneity for inflorescence length",data=FemMal_Sex) Homo<-bartlett.test(FemMal_Sex$inflorescence_length_Max,FemMal_Sex$Sex) text( 2, 500,

Dear All, I need to fetch GO ontologies for Homo sapiens with their mappings to corresponding Uniprot identifiers. I would be using this information to compare result from a clustering algorithm with existing protein complexes. This would be a test to check how the clustering algorithm accurately captures GO terms with respect to the known protein complexes. Can anyone suggest a simple workflow

I was having a problem with my Samba PDC with LDAP backend. Some of my workstations (W2kSP4) couln't log into the domain. I removed the machines from the domain, changed the name, created a new machine-account, but I still can't add the machine to the domain. smbclient -L localhost Enter root's password: Anonymous login successful Domain=[DCHOMO] OS=[Unix]

Hi ALL, I have very simple question regarding pattern matching. Could anyone tell me how to I can use R to retrieve string pattern from text file. for example my file contain following information SpeciesCommon=(Human);SpeciesScientific=(Homo sapiens);ReactiveCentres=(N,C,C,C,+ H,O,C,C,C,C,O,H);BondInvolved=(C-H);EzCatDBID=(S00343);BondFormed=(O-H,O-H);Bond+

I have checked that section already. Sorry, I should have mentioned that. Memory limit increase does not work. Installtion of msvcrt.dll does not work either. Thank you. -----Original Message----- From: ripley at stats.ox.ac.uk [mailto:ripley at stats.ox.ac.uk] Sent: Wednesday, March 05, 2003 2:44 PM To: Igor Oleinik Cc: r-help at stat.math.ethz.ch Subject: Re: [R] problem with cclust[er]

Hi R-users, I have a data frame like this: photographer category picture points Hannu kalat limamikko 1 Teemu kalat verkkovaja 3 Hate kalat munat puoliks padassa 6 Hannu kalat isokala 8 Teemu kasvit, sienet ja muut eliöt harppi 2 Hate kasvit, sienet ja muut eliöt pyynikki 2 Petteri kasvit, sienet ja muut eliöt harmaaleppä 5 Lauri kasvit, sienet ja muut eliöt lumipuu 9 Teemu linnut kainostelua 1

I deal with a huge amount of Biology data stored in different databases. The databases belongig to Bioconductor organization can be accessed through Bioconductor packages. Unluckily some useful data is stored in databases like, for instance, miRDB, miRecords, etc ... which offer just an interactive HTML interface. See for instance http://mirdb.org/cgi-bin/search.cgi,

Hi, Am am plotting aggregated frequency data (extracted from an RDBMS) relating to DNA sequence features for each of the human chromosomes as described in the table chromosomes below (the frequency data is in a table 'hits' that has a value (or not) for each of a set of bins across each chromosome). I would like to mark the extent of the chromosome (according to the length value in

Hi R-users, I have a dataset like this: kuvaaja kuva yhteispisteet Hannu isokala 8 Hannu kaapin alta löytynyt 2 Hannu kaapin alta löytynyt 2 8 Hannu limamikko 1 Hannu maukasta marmeladia 8 Hannu skrinnareita 4 Hate madekoukkujen suojelupyhimys 3 Hate matka aikaan joka ei enää palaa 3 Hate munat puoliks padassa 6 Hate pyynikki 2 Hate vailla armeerausta 2

I have 3 variables relating to the successful introductions of species to 95 different areas: introduction frequency; number of successes pre 1906; number of successes post 1906 The data are not normal, nor homo-skedatic, so I am using non-parametric statistics. I have calculated Kendall's tau between both introduction & successes pre 1906 (tau=0.3903) and introduction & successes

On 13 October 2015 at 16:41, Rafael Espíndola <llvm-dev at lists.llvm.org> wrote: >> - *Be welcoming.* We strive to be a community that welcomes and supports >> people of all backgrounds and identities. This includes, but is not limited >> to members of any race, ethnicity, culture, national origin, colour, >> immigration status, social and economic class, educational

Hi All, I've been using samba 2.2.8a running on RedHat 9 as a PDC for almost a year by now. Everything works great even though it required some time to configure everything properly. Our company decided to move to Active Directory running on Win2003 server.... I want to leave Samba as our file server, so I plan to use Samba 3.0.4 as a domain member server. I got one problem, though

Dear all, I have data.frame object in R. I want to export it in tab-delimited file with several lines of header initiated with comment sign (#). I do not know how to do that in R. Could you please give helps on this problem? Thanks in advance. Best, Jian-Feng, ################################################################## The lines I want to write in the header lines look like, with words

I'm testing a samba4 server join AD (had 1 win2003 dc) as dc. Version: Samba4 DC: samba 4.1.1 with ubuntu (172.16.3.8) Win2003 DC: Win2003 SP2 (172.16.3.3) AD domain name: dotest.com The samba server had joined to AD as DC. When win2003 dc online, it seems works fine. When I test win2003 dc online, simulate the win2003 DC was failue, found the samba4 DC can't work fine along. The AD

I am running Samba 3.5.5 on Solaris 10. This is the latest Sun/Oracle provided build. I have an ldap backend for everything (unix+samba accounts, idmapping for domain trusts.) The Samba server is a PDC for a domain we can call "SAMBA." Each samba account is tied to a unix account. I have a one-way domain trust setup with a Windows 2003 domain which we can call

My AD server is Win2003. And my linux server is ubuntu. Samba version is 2:3.6.3-2ubuntu2.12 and 2:4.1.6+dfsg-1ubuntu2.14.04.7. They are join into the Win2003 AD as normal smb servers (not DC). After Win2003 DC autoupdate last week, I can't use smbclient access all samba server with NTLMv2: ~$ smbclient //172.16.3.13/share -U testuser Enter DOMAIN\testuser's password: session setup