search for: sohal

...an you please supply a link. As this is a commercial project maybe you could advise me of somebody that maybe able to help on a small contrcat basis. This may help us speed up development. We have a small budget set aside and can pay for any help with this matter. Thanks in advance. Regards Bobby Sohal _________________________________________________________________ Free games, great prizes - get gaming at Gamesbox. http://www.searchgamesbox.com -------------- next part -------------- An HTML attachment was scrubbed... URL: http://lists.xiph.org/pipermail/speex-dev/attachments/20071220/5aae10...

...h 12byte frame to the card. Once I have finished encoding I update the FA table and have the speex frames written to a card. All I need to do now Is attach a header to this data so that it can be played back. I would greatly appreciate any help you can offer with this problem. Regards Bobby Sohal -------------- next part -------------- An HTML attachment was scrubbed... URL: http://lists.xiph.org/pipermail/speex-dev/attachments/20071022/ae32131a/attachment-0001.htm

Hi all, Here's an interesting (for me, at least!) problem I came across: I have a correlation matrix, let's say with 6 variables, A to F, as column headings and the same 6 as row headings. The matrix is filled with correlation coefficients. Therefore, the diagonal is all 1's, and each of the two triangles formed by the diagonal has the same 15 correlation coefficients. I need to

...s recorder from start->programs->accesories->entertainment->sound recorder, in the file->properties choose the speex codec. now you can record and play speex files. i suggest that the 'small budget set aside' be donated to red cross. - farhan On Thu, 20 Dec 2007, jagjit sohal wrote: > > Hi Jean, > This is my last attempt at trying to use speex for a project we are working on. I have contacted you before, but i have had no joy what so ever trying to find a working example in c++ that shows how to add a header to a raw speex file, so that it an be played using w...

Hi, I am new to R...a recent convert from SAS. I have a dataset that looks like this: SEQ A1 A2 A 532.5 554.5 B 25.5 35.5 C 265.2 522.2 D 245.55 521.56 E 546.52 141.52 F 243.25 32.56 G 452.55 635.56 H 15.14 16.54 I 543.4 646.56 J 54.4 654.5 K 646.5 64.54 L 645.4 614.46 M 646.54 634.46 I want to make a histogram

...sories->entertainment->sound recorder, in the > file->properties choose the speex codec. > > now you can record and play speex files. > > i suggest that the 'small budget set aside' be donated to red cross. > > - farhan > > On Thu, 20 Dec 2007, jagjit sohal wrote: > >> >> Hi Jean, >> This is my last attempt at trying to use speex for a project we are >> working on. I have contacted you before, but i have had no joy what so >> ever trying to find a working example in c++ that shows how to add a >> header to a raw...

Hi, I am making a dendrogram with 180 terminal values. Whether I keep it horizontal or vertical, it gives a 'squished' graph that refuses to be stretched beyond the window size and I cannot read the labels. (I'm using hclust and then plot to make the tree.) Is there a way to stretch the graph in R, or by exporting it somehow, so that I can read the 180 values and see what the results

Hi, I'm using R on Windows and upgraded the computer memory to 4GB, as R was telling me that it is out of memory (for making heatmaps). It still says that the maximum memory is 1024Mb, even if I increase it using memory.limit and memory.size. Is there a way to permanently increase R's memory quota to 4GB? Please help. Many thanks, -DS. [[alternative HTML version deleted]]

Hi, I'm new to R; this is my second email to this forum. I have a dataset that looks like this: Gene A B C D A 511 6116 1515 1515 B 164 115 1515 494 C 21646 D

Hi all, I'm using Pelora (supclust) package for supervised clustering of a microarray dataset. The original package does not delete the genes that are present in the earlier clusters for further cluster identification. This leaves us with mostly redundant clusters. I played around with the source code but couldn't get around it. Is there a way to fix it so that the genes already identified

Hello all, I am doing SAM and the median of positive genes in the permutated sets is = false positives, and the "parent set" gives true positives. FDR = FP/TP * 100. My FDR comes to greater than 100. Is that possible? Please help! Thanks, -D. [[alternative HTML version deleted]]