similar to: Grouping models - table name conflicts

In my usb drive with EXT3 filesystem in /dev/sda1 partition, syslinux uses the first sector on /dev/sda1 but EXT3 filesystem doesn't? On Mon, Oct 21, 2013 at 4:49 PM, Ferenc Wagner <wferi at niif.hu> wrote: > Kun Huang <gareth at unitedstack.com> writes: > > > For a bootable usb drive, syslinux seems use MBR and VBR > > (and some files on the partition) >

Hi, I'm doing anova on a matrix of multivariate data where I want to assess the effect of each column (element). My matrix is 86 rows x 31 columns. I've created a grouping factor of length 86 containing group assignments of 6 types. Then I run: x<- aov(matrix~grouping.factor) summary(aov.fit.raw, test="Wilks") This is working fine enough, but I'm getting different

I thought I had this fixed, but apparently not. It works okay from the console, but not from the view. I have the following: # partial schema create_table "users", :force => true do |t| t.string "login", :null => false t.string "first_name" t.string "last_name" t.string "email", :null => false

When I run a summary(anova) I get output for all of the elements (columns) as these are multiple - single anova results. Can I store the F values? I can't find the attribute of the fitted model attributes(fit) that stores these F values, and for that matter, P values. Thanks -- Gareth Campbell PhD Candidate The University of Auckland P +649 815 3670 M +6421 256 3511 E

I have a firewall with 3 interfaces DMZ, INTERNET, LAN. Does anyone have an example script to do QOS on multiple intefaces using htb? Gareth Segree mailto:Gareth.Segree@gleanerjm.com <mailto:Gareth.Segree@gleanerjm.com> Technical Support Analyst The Gleaner Company Ltd. 7 North Street Kingston Tel: 922-3400

Okay, I posted about this a few days ago but couldn''t replicate it in my test case. I have this page, which everything works fine on... except some of the prototype methods. They do not appear to exist on an extended Element. ie: Element._extended = true Element.up = undefined Element.addClassName = function Element.getElementsBySelector = undefined I''ve been trying to figure

Hi there, I'm plotting some glass RI values just by plotting plot(x) then I put on my lowess smoother lines(lowess(x)) now I want to put on some 95% Confidence Interval bands of the lowess smoother, but don't know how?? Thanks -- Gareth Campbell PhD Candidate The University of Auckland P +649 815 3670 M +6421 256 3511 E gareth.campbell@esr.cri.nz gcam032@gmail.com [[alternative

Hi there, I know this is probably a really simple question, but without the correct keywords, or knowledge of the correct function it is hard to search for on the net or within R. How do I increment a dataframe (or similar) name within a loop and assign data? A simple example would be: for(i in 1:10){ test<-i } BUT I want it to be test[i] --- in other words I want my stored data to

I have 2 connections to the internet. 1 is an ADSL the other is a 3MB link over satellite. This is a portion of my firewall script ip route flush table 3 2> /dev/null ip rule delete table 3 2> /dev/null ip route add table 3 127.0.0.0/8 dev lo scope link ip route add table 3 89.0.0.0/8 dev eth0 scope link ip rule add fwmark 3 table 3 ip route add table 3 default via $isp2_ip dev eth3 ip

Hello, I have a time-series of standards measured for Refractive index. They are daily standards, however, I didn't run one everyday so some days have no data. I can plot the values, but the x-axis does not represent the correct time series (i.e. it's just an evenly spaced 1,2,3 type axis). I want to plot the points with some form of representitive date line on the x-axis. I don't

Hello all, I'm dealing with geochemical analyses of some rocks. If I use the full composition (31 elements or variables), I can get reasonable separation of my 6 sources. Then when I go onto do LDA with the 6 groups, I get excellent separation. I feel like I should be reducing the variables to thos that are providing the most discrimination between the groups as this is important

When using windows NT and Netware there are ways of limiting the logins of users such as only allowing them on between 9am - 5pm and limiting maximum concurrent connection to one. Is there a way of enforcing these restrictions through samba or similar? Many thanks Gareth Norman

Started using dovecot and I am very impressed by its speed. I am confused by what it is expecting the format of the Maildir directory to be in. I currently have ~/Maildir which contains new, cur, and tmp all containing email that should be in my inbox and it pops up correctly as such when I connect to dovecot using Mutt. After the connection a new .INBOX is created under ~/Maildir with sym

Hello, What I am trying to do is: Generate a density plot of a population of data. This data has a bimodal distribution so I've isolated a couple of possible sub-populations and I want to overlay these two density plots over the first to see whether they are contributing to the bimodal population. I can do this fine with plot(density(...)) and lines(density(...)) . But the resulting plots

Hey team, If I have a matrix: 1, 2, 3, 4, 4, 0, 1, 3, 0, 3 2 columns. I want to write an if command that looks at (in this case) row 3 and looks to see if either [3,1] or [3,2] has a zero in it. IF it does have a zero I want the zero to be placed in another matrix in the same position. I know how to do the latter part, I just can't get the if command to look at both cells and deal with

I have some data (REE plots - geochemistry) where I have values 1:14 for the x axis, but have no data for some x values. Here for example, let's say that I don't have data for x=2,5,8. So x<-1:14 y<-c(4, NA, 5, 9, NA, 3.4, 8, NA, 19, 22, 12, 14, 15.3, 15) if I plot the data plot(x,y) and then I want to join with lines lines(x,y) How do I get it so the points join across the

I have a vector: alleles.present<-c("D3", "D16", ... ) The alleles present changes given the case I'm dealing with - i.e. either all of the alleles I use for my calculations are present, or some of them. Depending on what alleles are present, I need to make matrices and do calculations on those alleles present and completely disregard any formula or other use of the

I've made an LDA model on some data from one source. I have some new data that I want to see if I can "place" to the sources in the LDA model. I used the predict function as follows: predict(wak.insitu.ld, wak.alr.alluvial) where wak.insitu.ld is an LDA model generated from some data and wak.alr.alluvial is new data of similar origin. When I look at the results, there is 86

Hi everyone, I have a PCA plot that I'm writing about in the text. There were so many symbols in different colours on it that I didn't include a legend in the plot as it would be useless. So what I was hoping to do was to talk about each set of replicates in the text and when I do that, use their coloured symbol in the text. So what I want to do is to get R to create some high quality

Hi Charles, Thank you so much for getting back to me. I should have given you a bit of background in my last message but I'm actually doing this for my grandmother's benefit! She has Dementia and lives on her own so we want to be notified if she has a power cut... I'd hate to think she might be stumbling around in the dark (which has happened before)! In terms of stopping the older