similar to: Selecting biological data

Displaying 20 results from an estimated 100 matches similar to: "Selecting biological data"

2009 Aug 24
2
create list entry from variable
Hi; assume i<-10 how can i create a list having key=10 and value=11 list(i=11) generates a list with 'i' [1] 11 and not 10 [1] 11 any help? Thanks _________________________________________________________________ Facebook. :ON:WL:en-US:SI_SB_facebook:082009 [[alternative HTML version deleted]]
2007 Jul 16
1
[LLVMdev] not to break 'for' statement into basic blocks
Thank you so much but could you tell me a little bit more in detail about that you suggested? Sorry, I'm just a greenhorn. Thanks, Seung J. Lee ---- Original message ---- >Date: Sat, 14 Jul 2007 21:26:14 -0500 >From: "David A. Greene" <greened at obbligato.org> >Subject: Re: [LLVMdev] not to break 'for' statement into basic blocks >To: llvmdev at
2010 Feb 17
2
Clustering apache
I'm a greenhorn when it comes to clustering in RHEL/CentOS and recently setup an active/standby clustering using Apache & Heartbeat. It seems to be a good entry step into clustering however after testing it I was disappointed in that the resource manager does not start httpd on node2 if httpd on node1 is dead (only starts httpd on node2 if the heartbeat daemon on node1 is dead). Is there
2012 May 11
1
ANOVA question
Hello all, I'm very satisfied to say that my grip on both R and statistics is showing the first hints of firmness, on a very greenhorn level. I'm faced with a problem that I intend to analyze using ANOVA, and to test my understanding of a primitive, one-way ANOVA I've written the self-contained practice script below. It works as expected. But here's my question: How can I not
2023 Jan 12
1
Upgrading system from non-RAID to RAID1
> On 01/11/2023 01:33 PM, H wrote: >> On 01/11/2023 02:09 AM, Simon Matter wrote: >>> What I usually do is this: "cut" the large disk into several pieces of >>> equal size and create individual RAID1 arrays. Then add them as LVM PVs >>> to >>> one large VG. The advantage is that with one error on one disk, you >>> wont >>>
2007 Aug 08
4
[LLVMdev] Destination register needs to be valid after callee saved register restore when tail calling
Hello, Arnold. > Is there a way to indicate that the register the tail call > instruction uses as destination needs to be valid after the callee > saved registers have been restored? (some X86InstrInfo.td foo magic > maybe ?) It's wrong way to do the things. Because in this case you either violate the ABI for callee, or you're restricted to do tail call lowering only for
2010 Feb 05
4
CentOS 5.4 x86_64 authenticating against AD (Server 2008r2)
Hey All, Just wondering if any of you have been able to setup CentOS 5.4 to authenticate against AD on a Server 2008r2 Domain Controller. I am trying to complete this particular setup however I have run into some difficulties such as not being able to lookup domain users via getent passwd. Thanks for your input, Dan
2023 Jan 12
2
Upgrading system from non-RAID to RAID1
On 01/11/2023 01:33 PM, H wrote: > On 01/11/2023 02:09 AM, Simon Matter wrote: >> What I usually do is this: "cut" the large disk into several pieces of >> equal size and create individual RAID1 arrays. Then add them as LVM PVs to >> one large VG. The advantage is that with one error on one disk, you wont >> lose redundancy on the whole RAID mirror but only on
2007 Aug 08
2
[LLVMdev] Destination register needs to be valid after callee saved register restore when tail calling
Hello, Arnold. > with the sentence i tried to express the question whether there is a > way to persuade the code generator to use another register to load (or > move) the function pointer to (right before the callee saved register > restore) but thinking a little further that's nonsense. Why don't define some special op for callee address and custom lower it? I really
2007 Aug 08
0
[LLVMdev] Destination register needs to be valid after callee saved register restore when tail calling
Hi Anton and Dale first thanks for your answers. On 8 Aug 2007, at 16:43, Anton Korobeynikov wrote: > Hello, Arnold. > >> Is there a way to indicate that the register the tail call >> instruction uses as destination needs to be valid after the callee >> saved registers have been restored? (some X86InstrInfo.td foo magic >> maybe ?) > It's wrong way to do the
2006 Jan 11
3
SPSS and R ? do they like each other?
... and is there also such a nice tool (like spss.get) for exporting data frames to SPSS? write.table does not keep the data frame labels - neither did the other exporting tools that I found. Thanks! Michael [[alternative HTML version deleted]]
2009 Sep 02
1
outbound calls not ringing still
i have posted this before but was unable to resolve it. i have some new info so i figured i would try again. the trace from bandwidth.com are below. they are telling me that the ip that is bold should be our ip not bandwidth.com. i have changed every setting that i can see and nothing fixes this. Where would i change this at? they cannot tell me. INVITE sip:+185993133333 at 216.82.224.202
2008 Aug 12
0
i am is Ruby greenhorn
hello , i am is Ruby greenhorn --~--~---------~--~----~------------~-------~--~----~ You received this message because you are subscribed to the Google Groups "Ruby on Rails: Spinoffs" group. To post to this group, send email to rubyonrails-spinoffs-/JYPxA39Uh5TLH3MbocFFw@public.gmane.org To unsubscribe from this group, send email to
2009 Apr 03
1
Curve fitting,FDA for biological data
Dear all, Another newbie just got attracted to this mailing list. I am a biologist currently working my way through R, had sort play around with python earlier this year. I have some data exhibiting periodicity ** my data consists of peaks and valleys, with peaks arising due to the presence of a repetitive structural unit,** with x being a reference grid (position along a chromosome) and y
2010 Oct 15
0
tessellation from biological data in spatstat
Hi, I'm new to this mailing list so apologies if this is too basic. I have confocal images 512x512 from which I have extracted x,y positions of the coordiates of labelled cells exported from ImageJ as a.csv file. I also have images that define an underlying pattern in the tissue defined as areas of different pixel values 0 or 255 (also 512x512) I've exported these images as .txt
2017 Jun 09
2
Dendogram from RNAseq read count to show correlation between biological replicate using R
Dear all, I need to make dendogram from read count in a csv file across 34 samples including biological replicate. Please share R code or package to do this. Do I also need to normalized read count before using read data? Thanks [[alternative HTML version deleted]]
2013 Oct 24
0
Faculty Position in Biometry / Biological Statistics at Illinois
Assistant/Associate Professor of Biometry Department of Crop Sciences College of Agricultural, Consumer and Environmental Sciences University of Illinois at Urbana ? Champaign The Department of Crop Sciences is seeking candidates for an Assistant/Associate Professor of Statistics. The successful candidate will develop a vigorous, externally funded, and nationally recognized research program with
2009 Sep 24
1
Maximum likelihood estimation of parameters make no biological sense
R-help, I'm trying to estimate some parameters using the Maximum Likehood method. The model describes fish growth using a sigmoidal-type of curve: fn_w <- function(params) { Winf <- params[1] k <- params[2] t0 <- params[3] b <- params[4] sigma <- params[5] what <- Winf * (1-exp(- k *(tt - t0)))^b
2008 Oct 30
1
Is possible, on biological grounds, suggest to fitdistr (MASS library) that the estimated parameters must be between two values?
Sorry if it is a silly question, I haven't found documentation on this and I don't know if it is possible. library(MASS) ## for fitdistr library(msm) ## for dtnorm #prepare truncated normal distribution dtnorm0 <- function(x, mean, sd , log = FALSE) { dtnorm(x, mean, sd, 105, 135, log) } set.seed(1) #Generate normal distribution with the TRUE population mean (day 106 of the
2009 Aug 19
0
ASA John M. Chambers Statistical Software Award - 2010
John M. Chambers Statistical Software Award - 2010 Statistical Computing Section American Statistical Association The Statistical Computing Section of the American Statistical Association announces the competition for the John M. Chambers Statistical Software Award. In 1998 the Association for Computing Machinery presented its Software System Award to John Chambers for the design and development