similar to: Moving HTML out of a model

I''d like to add an event listener for dragging markers, but it looks like YM4R GM (and Mapstraction) doesn''t support this. I need an init like: marker = new GMarker(... GEvent.addListener(marker, "dragend", function() { }) but the current setup makes "anonymous" markers - never creates variable that can be used to access them. Has anyone thought about

Hey there all. I have a mapping app that uses ym4r_gm to build with google maps. The markers i generate use the status of a machine to determine their color. This way our customers can pull up the map and see a color coded drawing where their machine is. So, how would i go about making this to where it could update each marker every 10 minutes or so. I would like to allow our customers to leave

Dear R users,   I am new user for elastic net. I am trying to use elasticnet library. I have marker data with 359 markers and 168 samples, and response is metabolites. I am trying to do regression between a metabolite and markers.  But i am getting the following error:   > en<-enet(marker,as.numeric(vio),lambda=0.5,normalize=FALSE,intercept=TRUE) Error in one %*% x : requires numeric

Hi All, I''m looking for a good example of client-side marker clustering with Mapstraction. It would be especially valuable if it was easily reusable code, similar to MarkerClusterer for Google Maps: http://gmaps-utility-library.googlecode.com/svn/trunk/markerclusterer/1.0/docs/reference.html If no such thing exists for Mapstraction (and I haven''t seen one), what are the

Dear R listers, I have a data file looks like the following: Testing marker: s_1 --------------------------------------------- Allele df(0) -LnLk(0) df(T) -LnLk(T) ChiSq p 3 7995 29320.30 7994 29311.85 16.90 4e-05 (2229/8000 probands) Testing marker: s_2 --------------------------------------------- Allele df(0)

The existing lifetime start/end is not very well defined (by spec, or by code) in what it means, so you could have nested lifetime markers if you wanted. If you made the spec well-defined, they would be meaningful (for loops, etc). There are a number of open bugs/complaints about lifetime markers and the fact that the scope is not well defined (the spec says "This intrinsic indicates that

Hello, I'm writing some genetic simulations in R where I would like to place genes along a chromosome proportional to the density of markers in a given region. For example, a chromosome can be presented as a list of marker locations: Chr1<-c(0, 6.5, 17.5, 26.2, 30.5, 36.4, 44.8, 45.7, 47.8, 48.7, 49.2, 50.9, 52.9, 54.5, 56.5, 58.9, 61.2, 64.1) Where the numbers refer to the locations of

Hi list, I'm using the package XML to create a simple XML document. Unfortunately constructing the XML tree is extremely slow. My code (see below) adds only about 100 nodes per second on an Intel i5 machine. There's clearly something wrong but I don't see what. Here's a sample of the XML document: <?xml version="1.0" encoding="utf-8"?>

Hi guys (and gals), The code formatting is so nice on SO.com, so I thought I''d just share my post in hopes that someone from the group can help. http://stackoverflow.com/questions/9643786/cartographer-shows-correct-info-box-but-over-wrong-marker Feel free to answer back via email if you don''t have an SO account. Thanks! Abram -- You received this message because you are

Dear list   I have 5 markers that can be used to detect an infection in combination. Could you please advise me how to use functions in ROCR/ other package to produce the ROC curve for a combination of markers?   I have used the following to get ROC statistics for each marker. pred <- prediction(y$marker1, y$infectn) perf <-performance(pred,"tpr","fpr")

Dear R-Helpers, I am not very experienced in using lattice and I am still in the learning stage I have a data set which looks like this: (I have deleted a few lines in order to save space) Chromosome marker Marker.Name Distance 1 1 1 PeMm261 0.0000 2 1 2 Xtxp8 10.1013 .. 20 1 20 EbMi148 210.3099 21 1 21 Xtxp25

Hello I have two data frames, SNP4 and SNP1: > head(SNP4) Animal Marker Y 3213 194073197 P1001 0.021088 1295 194073197 P1002 0.021088 915 194073197 P1004 0.021088 2833 194073197 P1005 0.021088 1487 194073197 P1006 0.021088 1885 194073197 P1007 0.021088 > head(SNP1) Animal Marker x 3213 194073197 P1001 2 1295 194073197 P1002 1 915 194073197

I am attempting to sample 10 markers from each chr, with a maximum distance of 14, calculated by the location of the marker in each chromosome as loc[i+1] - loc[i]. I presume the easiest way to do this is with a while loop, so that the function keeps resampling when the max distains is greater than 14. Example code is below. I have gon as far as to select markers and calculate the distances, A

Hi! Your plugin is really great! Thanks. One more little question. Is it possible to add event listeners to the maps via your plugin? greetings /till -------------- next part -------------- An HTML attachment was scrubbed... URL: http://rubyforge.org/pipermail/ym4r-user/attachments/20061106/6b1c6f4f/attachment.html

Hi, I am new to R and I need to perform multiple chi-square tests. I manage to perform one at a time, but is there a specific command to do multiple tests? For example, I have a table that looks like this: Marker Treatment Genotype1 Genotype2 Genotype3 1 A 23 57 32 1 B 43 59 12 ... ... n A ## ## ## n

Hi, after spending hours on getting geokit and ym4r running I don''t know how to do or how to getting a test running. I have try the tutorial from http://www.railslodge.com/plugins/179-ym4r but I don''t get it :(. Has sone one other tutorials he can recommend? Maybe someone knows were I did my mistake (I only want to show a fixed address, no database connection so far, pure

Hi R-ers, I am struggling with my x-axis in a association plot. What I would like is to place the labels of the x-axis between the tick markers and normally the labels are printed at the place where the tick marker is placed. I don???t want to move the tick marker (it gives the switch between one chromosome and the next) but I just want to put the chromosome number in between the

Hi Baolu, On Tue, May 30, 2023 at 01:37:07PM +0800, Lu Baolu wrote: > - The timeout value for the pending page fault messages. Ideally we > should determine the timeout value from the device configuration, but > I failed to find any statement in the PCI specification (version 6.x). > A default 100 milliseconds is selected in the implementation, but it > leave the room for

Hi, Rafael Inlined asm markup inside functions and on the top level is used to split asm prologue/epilogue parts in very fine-grained manner. So, splitting source c won't give the same result. Regards, Sergey Y. 2010/2/22 Rafael Espindola <espindola at google.com> I haven't looked at the code, but why can't you split the .c files > into multiple files instead of splitting

-----BEGIN PGP SIGNED MESSAGE----- Hash: SHA1 Hi Milan! Thanks for your comments ont he requirement list. [Milan Zamazal, Dienstag, 26. Oktober 2004 20:58] > [Since the mailing list apparently hasn't been created yet, I continue > in private not to freeze the discussion for too long.] > I have just asked David Stone when we can start using the list. > BTW, this might be