search for: 0.206

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2010 Sep 27
2
subtraction based on two groups in a dataframe
Hello I have a data set like below: plate.id well.id Group HYB rlt1 1 P1 A1 Control SKOV3hyb 0.190 2 P1 A2 Control SKOV3hyb 0.210 3 P1 A3 Control SKOV3hyb 0.205 4 P1 A4 Control SKOV3hyb 0.206 5 P1 A5 Control SKOV3hyb 0.184 385 P1 A1 ovca SKOV3hyb 0.184 386 P1 A2 ovca SKOV3hyb 0.229 387
2008 Mar 25
1
Subset of matrix
Dear R users I have a big matrix like 6021 1188 790 290 1174 1015 1990 6613 6288 100714 6021 1 0.658 0.688 0.474 0.262 0.163 0.137 0.32 0.252 0.206 1188 0.658 1 0.917 0.245 0.331 0.122 0.148 0.194 0.168 0.171 790 0.688 0.917 1 0.243 0.31 0.122 0.15 0.19 0.171 0.174 290 0.474
2008 Apr 11
4
Format regression result summary
Hello to the whole group. I am a newbie to R, but I got my way through and think it is a lot easier to handle than other software packages (far less clicks necessary). However, I have a problem with respect to the summary of regression results. The summary function gives sth like: Residuals: Min 1Q Median 3Q Max -0.46743 -0.09772 0.01810 0.11175 0.42252
2010 Feb 18
1
aggregate by column names
Hi, I've this dataframe: V1 V5 V6 1 MOD13Q1_2000049 0.1723 A1 2 MOD13Q1_2000049 0.1824 B1 3 MOD13Q1_2000049 0.1824 C1 4 MOD13Q1_2000049 0.1774 A2 5 MOD13Q1_2000049 0.1953 B2 6 MOD13Q1_2000049 0.1824 C2 7 MOD13Q1_2000065 0.1921 A1 8 MOD13Q1_2000065 0.1938 B1 9 MOD13Q1_2000065 0.2009 C1 10 MOD13Q1_2000065 0.2035 A2 11 MOD13Q1_2000065 0.2157 B2 12
2012 Aug 27
0
ping latency using vhost_net, macvtap and virtio
Hi all, I have been testing network throughput and latency and I was wondering if my measurements are as expected. For the test, I used Fedora 17 for both host and guest, using kernel 3.5.2-3.fc17.86_64. Pinging an external server on the LAN from the host, using a gigabit interface, the results are: # ping -c 10 172.16.1.1 PING 172.16.1.1 (172.16.1.1) 56(84) bytes of data. 64 bytes from
2012 Aug 27
0
ping latency using vhost_net, macvtap and virtio
Hi all, I have been testing network throughput and latency and I was wondering if my measurements are as expected. For the test, I used Fedora 17 for both host and guest, using kernel 3.5.2-3.fc17.86_64. Pinging an external server on the LAN from the host, using a gigabit interface, the results are: # ping -c 10 172.16.1.1 PING 172.16.1.1 (172.16.1.1) 56(84) bytes of data. 64 bytes from
2006 Nov 21
1
crossprod(x) vs crossprod(x,x)
I found out the other day that crossprod() will take a single matrix argument; crossprod(x) notionally returns crossprod(x,x). The two forms do not return identical matrices: x <- matrix(rnorm(3000000),ncol=3) M1 <- crossprod(x) M2 <- crossprod(x,x) R> max(abs(M1-M2)) [1] 1.932494e-08 But what really surprised me is that crossprod(x) is slower than crossprod(x,x): R>
2003 May 01
0
factanal
# I have a question about how factanal is calculating the regression factor # scores based on an oblique rotation (promax) of the factors. # # As is explained in the help file, regression factor scores are # obtained as # # hat f = Lambda' Sigma^-1 x # # However, according to Harman's "Modern Factor Analysis" (e.g. second # edition, pp. 351-352) the formula is # # hat f = Phi
2010 Feb 17
2
extract the data that match
Hi r-users,   I would like to extract the data that match.  Attached is my data: I'm interested in matchind the value in column 'intg' with value in column 'rand_no' > cbind(z=z,intg=dd,rand_no = rr)             z  intg rand_no    [1,]  0.00 0.000   0.001    [2,]  0.01 0.000   0.002    [3,]  0.02 0.000   0.002    [4,]  0.03 0.000   0.003    [5,]  0.04 0.000   0.003    [6,] 
2005 Jan 25
1
CODA vs. BOA discrepancy
Dear List: the CODA and BOA packages for the analysis of MCMC output yield different results on two dignostic test of convergence: 1) Geweke's convergence diagnostic; 2) Heidelberger and Welch's convergence diagnostic. Does that imply that the CODA and BOA packages implement different ``flavors'' of the same test? I paste below an example. Geweke's test
2005 Feb 04
5
How to access results of survival analysis
Hello, it seems that the main results of survival analysis with package survival are shown only as side effects of the print method. If I compute e.g. a Kaplan-Meier estimate by > km.survdur<-survfit(s.survdur) then I can simply print the results by > km.survdur Call: survfit(formula = s.survdur) n events median 0.95LCL 0.95UCL 100.0 58.0 46.8 41.0 79.3 Is
2005 Sep 07
1
encoder settings
Hi! Some background: I am trying to create an application that would encode video taken by USB camera using Theora and then send it to the client. I have almost succeeded, but I have one problem. When I grab video frames from the camera and encode them they form 4KB OGG pages, then I send them over TCP/IP to the client application. Since I want to achieve as small latency as possible I
2012 Jun 30
2
Adjusting length of series
Hi I have a follow up question, relating to subsetting to list items. After using the list and min(sapply()) method to adjust the length of the variables, I specify a dynamic regression equation using the variables in the list. My list looks like this: Dcr<- list(Dcre1=DCred1,Dcre2=DCred2,Dcre3=DCred3,Dbobc1=DBoBC1,Dbobc2=DBoBC2,Dbobc3=DBoBC3,...) By specifying the list items with names, I
2012 Feb 07
7
GPLPV, RDP and network latency
Hello! Has anybody experienced network latency problems with combination of Windows 7, GPLPV drivers and RDP connection? Any Windows pop-up message(such as "command not found" error message in "Run command:" dialog, or dividing by zero in windows calc) causes a short freeze of RDP session and looks like that from dom0: PING 192.168.44.65 (192.168.44.65) 56(84) bytes of data.
2006 Mar 11
1
Quicker quantiles?
Motivated by Deepayan's recent inquiries about the efficiency of the R 'quantile' function: http://tolstoy.newcastle.edu.au/R/devel/05/11/3305.html http://tolstoy.newcastle.edu.au/R/devel/06/03/4358.html I decided to try to revive an old project to implement a version of the Floyd and Rivest (1975) algorithm for finding quantiles with O(n) comparisons. I used
2005 Nov 28
1
GLMM: measure for significance of random variable?
Hi, I have three questions concerning GLMMs. First, I ' m looking for a measure for the significance of the random variable in a glmm. I'm fitting a glmm (lmer) to telemetry-locations of 12 wildcat-individuals against random locations (binomial response). The individual is the random variable. Now I want to know, if the individual ("TIER") has a significant effect on the model
2012 Jun 02
2
mgcv (bam) very large standard error difference between versions 1.7-11 and 1.7-17, bug?
Dear useRs, I reran an analysis with bam (mgcv, version 1.7-17) originally conducted using an older version of bam (mgcv, version 1.7-11) and this resulted in the same estimates, but much lower standard errors (in some cases 20 times as low) and lower p-values. This obviously results in a larger set of significant predictors. Is this result expected given the improvements in the new version? Or
2008 Aug 08
2
aggregate
Dear All- I have a dataset that is comprised of the following: doy yr mon day hr hgt1 hgt2 hgt3 co21 co22 co23 sig1 sig2 sig3 dif flag 244.02083 2005 09 01 00 2.6 9.5 17.8 375.665 373.737 373.227 3.698 1.107 0.963 -0.509 PRE 244.0625 2005 09 01 01 2.6 9.5 17.8 393.66 384.773 379.466 15.336 11.033 5.76 -5.307 PRE 244.10417 2005 09 01 02 2.6 9.5 17.8 411.162 397.866 387.755 6.835 5.61 6.728
2008 Jan 18
0
forming a linear discriminant function from the output of lda()
Hello all- I am a relatively new user of R and am working through a graduate course in Statistics that uses Minitab, SAS and some Matlab. I like using R but am having some trouble lining up the output from lda() to that of the other programs' results. The dataset below is a modified set of wine data from the Pinot Noir data set as an illustration of the 2 group LDA scenario. Mo Ba
2013 Jul 10
0
permanova for multivariate repeat measures toxicology data set
Hello, I would like to use a permanova to analyze my repeated measures, multivariate data set using the package vegan (adonis function). I have several explanatory variables and many clinical biochemistry/hematological response variables (all continuous, non-normally distributed). My explanatory variables are: ID - 29 levels - individual subjects Treatment - 2 levels Sex - 2 levels Time -