Dear R-helpers,
Lists in R are stumbling block for me.
I kindly ask you to help me able to write a
data-frame.
I have a list of lists.
sls[1:2]
$Andromeda_maya1
x y
[1,] 369 103
[2,] 382 265
[3,] 317 471
[4,] 169 465
[5,] 577 333
$Andromeda_maya2
x y
[1,] 173 507
[2,]
Dear group,
i have 114 files (all have 5 columns) and variable
number of rows.
I want to read all the files and select the first
column and 4th column and fill the values into a big
matrix. I have a pre-made matrix that would have all
rownames (1st column) and coloumn names (4th column
from
dear group,
i have 100 files starting with 'hsa-*'.
ex. file:
fruit p-value
apple 0.0003
orange 0.004
kiwi 0.0003
peach 0.0004
I want to read all these files and create a single
matrix. here each file may have different fruit names.
in the matrix i want to have a
Dear marc: thank you for your tip.
cat(x.new, \n)
3\',5\'-cyclic-nucleotide phosphodiesterase activity
here cat is printing on screen.
how can I direct the output to an object.
I cannot do:
y - cat(x.new, \n)
is there any other way.
thanks
srini
Try this:
x -
Dear all:
I have a character object x with ' (single-quote)
character.
x - c('hydrolase activity,actin
binding,3',5'-cyclic-nucleotide phosphodiesterase
activity)
I want to write a function that will identify ' and
replaces with \'
myf - function(term){
if (grep(',term))
{ sub(',\',term)}
}
Hello :
I have matrix with dimensions(200 X 20,000). I
have another
file, a tab-delim file where first column
variables are row
names and second column variables are column
names. Tab-delim file has smaller values than the
matrix.
Matrix = tmat
tab-delim file read as data.frame = tb
My aim
1 1 00
O 1 1 0 00
M 0 0 1 00
G 0 0 0 00
S 1 1 1 00
HTH,
Andy
From: Srinivas Iyyer
hi:
I have matrix with dimensions(200 X 20,000). I
have another
file, a tab-delim file where
hi:
I have matrix with dimensions(200 X 20,000). I have
another file, a tab-delim file where first column
variables are row names and second column variables
are column names.
For instance:
tmat
Apple Orange Mango Grape Star
A 0 0 0 00
O 0 0 0 00
M
Dear group,
I have a matrix with (190,2) dimensions.
The values range from : -973.8149 to 807.4688
I want to select the values less than -200 and want to
know what are the names of row and columns.
m1 m2 m3 m4 .. mn
k1
k2
k3
k4
.
.
.
kj
mymat[1:4,1:4]
1-Dec
hello:
I have 3 data.frame objects.
First df object:
Of dim (149,31). Columns 2:31 are marked as T1..T14
and N1..N16.
Name T1T2N1 T3 N2 N3 N4 T4
mu1 1010910 9 9 8 10
mu2 1111911 9 9 9 11
...
muN 1212911 9
dear group,
i have a sample matrix
name v1 v2 v3 v4
cat 1011 12 15
dog 3 12 10 14
cat 9 12 12 15
cat 5 12 10 11
dog 12113 123 31
...
since cat is repeated 3 times, I want a mean value for
it. Like wise for every element of the name
hi group,
I have a list of 100 elements (genes), that are to be
queried in postgres. The out of the file is processed
for fisher test and written back as a file with
pvalues.
For one such operation there are 54 lines of code.
I replicated the same code changing the query element
and file name
Hi group,
I ran the file again and after 10 min. of run, the
process got interrupted.
Here is the output of the file
$bash: R CMD BATCH grand.R grand.log
R CMD BATCH grand.R
/usr/local/lib64/R/bin/BATCH: line 55: 1758 Broken
pipe ( echo invisible(options(echo =
TRUE)); cat
Dear group,
I am a novice programmer in R. I have a list that
has a length of 27 elements. Each element is derived
from table function.
lls - table(drres)
legnth(lls)
27
I want to plot all these elements in 9x3 plot (9 rows
and 3 columns)
par(9,3)
mypltfunc - function(mydata){
+ for (i in
hi sarah,
thanks for your mail.
#
par(mfrow=c(9,3))
mypltfunc(lls)
Error in plot.new() : figure margins too large
par(mfcol=c(9, 3))
mypltfunc(lls)
Error in plot.new() : figure margins too large
Dear Group,
I have been trying to connect postgres with R. I
followed the instructions from :
http://grass.itc.it/statsgrass/r_and_dbms.html.
However, RdbiPgSQL fails to install and throws up
error.
Could any one please help me where the things are
going wrong.
I have attached the log, and
Dear group,
could some one help me how i can split a string into
pieces and access them.
For example:
test = this is a test
typeof(test)
[1] character
strsplit(test,split='is')
[[1]]
[1] th a test
Now I want to get test into : a vector and another
object as list
Also,
Dear Group,
I have a machine which has a 64bit Intel® Xeon
Processor 3.00GHz, 2MB L2 Cache 6T302N - [ 221-7984 ]
processor.
(Dell Precision Workstation 670n Intel® Xeon
Processor)
The OS is RedHat Enterprise Linux version 4 (for
64bit).
I went to /bin/linux/redhat/el4/i386 on CRAN FTP
Dear Group,
I am new to R and Emacs both. Until now I have been
working through R's interactive space. Today I
configured R+XEmacs by following John Fox help file -
how to configure Xemacs + R.
I am very happy to do this. Now the question I have is
can I make XEmacs to be the editor for
Dear Group,
I am a novice R programmer with little statistical
background. I am a molecular biologist by training.
I generated a correlation matrix (157 X 157) for 157
variables.
I want to selection only the unique values (values
that are either side of the diagnol). I want these
unique
Dear Group,
I have a matrix (157 X 157 ) with correlation values.
I want to convert the unique elements into a long list
so that I can add an extra variable and plot them.
Example:
A B C D
alfa 1 0.3 0.8 -0.3
beta 0.2 1 -0.3 0.4
echo 0.9 -0.3 1 0.5
tang -0.5 0.5
Dear group,
I have a matrix with readings for ~180 variables
observed in 240 conditions.
I am doing a hierarchical clustering method (hclust)
by calculating eucledian distances among them.
When I plot the dendrogram from hclust, all my
variables at the end of the branches are cluttered. I
Dear group,
apologies if this is a stupid question. I searched
CRAN sites. I am afraid I missed it.
Can any one help me if I can update my windows version
of 1.9.1 to 2 or higer.
thanks
srini
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Hello Group,
What is the meaning of the error. is there any place
to look for this. I guess 'atomic' seems to be OOP
related concept.
thank you
srini
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PLEASE do
Hi all:
I am trying to do PCA on the following matrix.
N1 N2A1 A2 B1 B2
gene_a 90110190210290310
gene_b 190210390410590610
gene_c 90110110 90120 80
gene_d 200100400 90
Dear Group, I am calculating correlation coeff.
between two populations. After calculating the
cor.coefs I want to represent them as a matrix file.
a b c d
A 1 0 1 1
B 1 1 1 1
C 1 0 1 0
D 0 1 1 1
could any one please help me how can i acheive this:
Dear group,
I have a tab delimitted text file with 21 column and
1988 rows. When I read the file:
D1 -
read.table(file=gist_data1.txt,sep=\t,header=T)
dim(D1)
[1] 1811 20
It reads only 1811 rows from that file.
I saved this file as CSV file and I read it again
using:
D1 -
Dear group,
I am using justRMA in bioconductor to get expression
values. Now I computed fold changes. the fold
changes i get are log2 values.
How can I convert these to log10 values to see them as
actual fold change values.
thank you.
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