similar to: Package for Molecular Properties

library(sos) (mp <- findFn('{molecular properties}')) ????? ** found 7 matches in 4 packages and opened two web pages in my default browser with (a) the 7 matches and (b) the 4 packages. The first function was something for amino acids, like you suggested.? Two others returned compound and substance information from PubChem. ????? Does this help? ????? Spencer On

... In addition, you may wish to also post on the Bioconductor list for this sort of thing. -- Bert Bert Gunter "The trouble with having an open mind is that people keep coming along and sticking things into it." -- Opus (aka Berkeley Breathed in his "Bloom County" comic strip ) On Thu, May 3, 2018 at 12:58 AM, Spencer Graves <spencer.graves at effectivedefense.org>

Dear R-helpers: thank your for your attention. i am a newer to R and i am doing some protein category classification based on the amino acid sequence.while i have some questions urgently. 1. any packages for analysis amino acid sequence 2. given two sequences "AAA" and "BBB",how can i combine them into "AAABBB" 3. based on "AAABBB",how can i get some

Hi Sarah Thank you very much for your pointers. Is there a way to specify the date string as POSIXct when reading in? I have tried the following (very inelegant way) and still have no luck. --- Begin Code --- # 1st read in the spreadsheet with stringsAsFactors set to FALSE > abc <- read.csv("gntr1.csv", header=TRUE, stringsAsFactors=FALSE) > abc code tasks.labels

Hi I am trying to generate a complex Gantt chart using the gantt.chart function in the plotrix package. Ideally I would like to use a spreadsheet to populate the activities (tasks) and start and end dates that this function expects and then export the spreadsheet file as a .CSV text file so I can read in this file to generate the gantt chart. Reading through the help file I have not been able to

Dear all, I am a R beginner, and I am looking for a way to do the same thing for all levels of a column in a table. Basically, I have a bunch of protein sequences composed of different amino acid residues, and each residue is represented by an uppercase letter. I want to calculate the ratio of different amino acid residues at each position of the proteins. Here is an example table: Proteins

I have following codes for ggplots. The legends are given in the plot do not match with the values specified in the codes given below. Your helps highly appreciated. Greg library(ggplot2) p <- ggplot(a,aes(x=NO_BMI_FI_beta ,y=FI_beta ,color= Super.Pathway))+ theme_bw() +theme(panel.border=element_blank()) + geom_point(size=3) p2<-p+scale_color_manual(name="Super.Pathway",

>From the help file for plotrix: " ... x - a list of task labels, start/end times and task priorities as returned by get.gantt.info ..." So I try to create an object that will contain this information. abc <- read.csv("gntr1a.csv") # The above csv file was generated from MS .xlsx file containing the tasks and corresponding dates > abc code tasks.labels

Hi, Your attempt didn't work because you didn't do what I suggested, which was make sure that your data frame matched the example given in the help for gantt.chart. Here's what you have: > str(cdfg) 'data.frame': 3 obs. of 3 variables: $ c1d1: Factor w/ 3 levels "task 1","task 3",..: 1 3 2 $ c2d1: POSIXct, format: "2018-04-01"

Hi, The help file for gantt.chart states that dates must be in POSIXct format, and the example shows how to do that. There's no reason that I can see that you can't use a data frame as input to gantt.chart, but you need to be very careful that your data frame matches the correct format. I bet also that your character fields were imported as factors, because you didn't specify not to.

hello every one, How to function more than one loop in R? I have the following problem to be solved with the a method of three loops, can you help me please? The data is attached with this message. The data is composed of two parts, cleaved (denoted by ?cleaved?) and non cleaved (denoted by ?noncleaved?). ? to access to the ith peptide, you can use X$Peptide[i] ? to access to the ith label,

may some one please help me to sort this out, i am trying to writ a R code for calculating the frequencies of the amino acids in 9 different sequences, i want the code to read the sequence from external text file, i used the following code to do so: x<-read.table("sequence.txt",header=FALSE) then i defined an array for 20 amino acids as following:

> On Apr 22, 2018, at 11:50 AM, bbb_aaa at verizon.net wrote: > > Hi > > I am trying to generate a complex Gantt chart using the gantt.chart function in the plotrix package. > > Ideally I would like to use a spreadsheet to populate the activities (tasks) and start and end dates that this function expects and then export the spreadsheet file as a .CSV text file so I can read

Dear mailing list, I'm stuck with a tricky problem here - at least it seems tricky to me, being not really talented in pattern matching and regex matters. I'm analysing amino acid mutations by position and type of mutation. E.g. (fictitious example) in position 92, I can find L92V, L92MV, L92I... L is in this example the wild-type amino-acid, and everything behind the position number is

Hello all: I have a protein sequence alignment in a data frame (align1, 72 x 236), where each row is a protein and each column a site in the alignment. AA is vector of amino acid symbols plus "-" (gap). I can calculate amino acid frequencies at each site by: >align1.F <- matrix(0,nrow=22,ncol=236,dimnames=list(AA,seq(1:236))) >for(i in 1:236) >

Just thought I would mention that there is a new O'Reilly book out, "Developing Bioinformatics Computer Skills", which is ok, pretty superficial about some things but at least it lets you know what is happening and where. R gets a few pages in there, 394-396, mostly nice press and accurate except that Bill Venables (hi Bill) may be surprised to find out that he is a member of the

Hi ! I would like to understand where do affinity.spline.coefs used in function compute.affinities come from ? library(gcrma) data(affinity.spline.coefs) affinity.spline.coefs X1 X2 X3 X4 X5 X1 -0.55004171 -0.58579091 -0.08870557 -0.47774242 0.23205570 0.58002746 X2 X3 X4 X5 X1 X2

Hi, I am trying to use a CGI service (Pubchem PUG) via RCurl and am running into a problem where the data must be supplied via POST - but I don't know the keyword for the argument. The data to be sent is an XML fragment. I can do this via the command line using curl: I save the XML string to a file called query.xml and then do curl -d @query.xml

Hello: I am attempting to use R to analyze amino acid frequencies in aligned protein sequences and need some help. So far, I have imported my sequence alignment into a data frame (lets call it "alignment") with each site in one column, so that I have a data frame consisting of columns of letters (the 21 amino acid symbols plus "-") with row names being the corresponding

Dear users, In my psychometric test i have applied logistic regression on my data. My data consists of 50 predictors (22 continuous and 28 categorical) plus a binary response. Using glm(), stepAIC() i didn't get satisfactory result as misclassification rate is too high. I think categorical variables are responsible for this debacle. Some of them have more than 6 level (one has 10 level).