e pros and cons of graphical
interfaces. Let me just say you're doing an excellent service to the
community, both with your package and your replies to this forum, which
shows you're a really kind person and deserve all our appreciation.
Best wishes
Gabriele Pallotti (Italy)
Il giorno ven
I managed to get Rcmdr working simply by deleting the .Rdata and .Rhistory
file from the work directory. It is rather weird, as I thought they only
contained data and settings, but probably some of these belonged to the
older version of R/Rcmdr and were not compatible with the new version.
I'll kee
Hallo
I've been using R and R commander (Rcmdr) for some years, never had
problems. I'm on Xubuntu 16.04. Yesterday I updated R from 3.4.4 to 3.6.1
and all sorts of problems occurred. Firstly I completely removed R from my
system, including old directories (with some hiccups, I must admit). Then I
They are attributes, not nodes so, if I understood the question:
"//DischargeMedication/Medication/@MedAdmin"
"//DischargeMedication/Medication/@MedID"
should do.
HTH,
Gabriele
From: Andrew Lachance [mailto:alach...@bates.edu]
Sent: Wednesday, January 25, 2017 3:12 PM
To
Hello Andrew,
as you are "clean slate" anyway in handling XML files, you could take a look to
XSLT processing -- also an off-topic area.
There are free tools available around, and many examples of "XML to CSV XSLT"
on StackOverflow.
HTH,
Gabriele
-Original Messag
I found also knitr + html + the ReporteRs package a good combination,
and less intimidating than Latex. Have a look at their FlexTable tool.
HTH,
Gabriele
-Original Message-
From: Tom Wright [mailto:t...@maladmin.com]
Sent: Tuesday, November 25, 2014 9:12 PM
To: r-help@r-project.org
Hello,
R is good at handling XML, but in this case I would rather do the first
step with an XSLT transformation, e.g. with Saxon, possibly to a CSV
file.
HTH,
Gabriele
-Original Message-
From: Anika Masters [mailto:anika.mast...@gmail.com]
Sent: Tuesday, January 29, 2013 3:01 AM
To: r
\n', sep=""))
}
sink(paste('my_file.xml', sep=""))
cat ('\n')
cat ('\n')
# invisible avoids returning a NULL in the file
invisible(apply(my_df, 1, buildEntry))
cat ("" )
sink()
And it took very little time.
HTH,
Gabriele
---
model?
thanks
gabriele
2012/8/28 Ingmar Visser :
> use str(dentistry.lca2) to see all values of the output; among them a value
> np for number of parameters, in this case 5*2 for the 5 binary items of 2
> classes + 1 for the class proportions, total 11.
> hth, Ingmar
>
> On Mon,
Can anybody, please, explain me how many parameter are estimated using
randomLCA?
For examples, model "dentistry.lca2random" estimate 1 scale (or
variance, b_j) parameter and 2 position parameters (a_cj)? Doesn't
it?
Do I need at least 4 diagnostic tests for such a model?
What happens if I
3d
visualization of the results?
Thanks for your support,
Gabriele
--
View this message in context:
http://r.789695.n4.nabble.com/Correspondence-Analysis-of-Textual-Data-and-Visualization-of-Correspondence-Results-in-a-3d-plot-wit-tp3676450p3676450.html
Sent from the R help mailing list
m the minimum pointing upwards?
Thanks!
Gabriele Zoppoli, MD
Ph.D. Fellow, Experimental and Clinical Oncology and Hematology, University of
Genova, Genova, Italy
Guest Researcher, LMP, NCI, NIH, Bethesda MD
Work: 301-451-8575
Mobile: 301-204-5642
Email: zoppo...@mail.ni
Hi,
I want to generate a number of vectors and store them with different names,
like this:
x=1
while (x<100)
{
vector#x# = rnorm(100)
x=x+1
}
where each vector has, at its hand, instead of #x# a number which goes from 1
to 99.
How can I do this?
Thanks
Gabriele Zoppoli, MD
P
self and I misuse some words, hope it's clear anyway) that a
matrix is all numeric? by doing as.numeric(x), it transforms everything in a
long colum of number, but loses the matrix structure...
Thank you all guys! You're really precious!
Now, how can you "explain" (sorry
crazy stuff!!! I tried to reload the txt file, and now it's working...
this is the original (attached)
thanks!
Gabriele Zoppoli, MD
Ph.D. Fellow, Experimental and Clinical Oncology and Hematology, University of
Genova, Genova, Italy
Guest Researcher, LMP, NCI, NIH, Bethesda MD
Work: 30
.miR.204" "hsa.miR.210" "Tissue"
It doesn't make much sense to me...
I would like to have the second column ordered from max to min, or from min to
max (with the argument decreasing=TRUE), but "order" seems to reorder
everything without considering
68" "0.67884" "Lung"
64 "RE:RXF_393" "-3.49615" "2.59144" "Renal"
22 "CO:HCT_15" "-3.45342" "0.16357" "Colon"
12 "BR:T47D""-3.41228" &q
0.03737 CNS
45 ME:MDA_N 0.21077 0.05502 Melanoma
50 ME:UACC_62 0.52503 0.1605 Melanoma
46ME:SK_MEL_2 0.55255 -1.6667 Melanoma
47 ME:SK_MEL_28 1.7425 1.45266 Melanoma
48ME:SK_MEL_5 1.74749 -1.47817 Melanoma
Gabriele Zopp
RAM values (3 Gb recognized
by Windows).
The isse is, when I try to do
memory.limit (size = 3000 )
the error doesn't resolve, and when I type
> memory.size ()
I always get
[1] 26.85
I'm confused here. Can anybody help me?
Thanks!
Gabriele Zoppoli, MD
Ph.D. Fellow, Experimen
Hi Jim,
thanks! With just the rgl package I cannot do that. For the moment, I
merged two values into one and use triax.plot in the package plotrix,
but that's not fully satisfactory. If you find something, let me know,
thank you a lot!
Gabriele
On Mon, May 3, 2010 at 2:29 PM, Jim Lemon
lp me!
Best,
Gabriele Esposito
__
R-help@r-project.org mailing list
https://stat.ethz.ch/mailman/listinfo/r-help
PLEASE do read the posting guide http://www.R-project.org/posting-guide.html
and provide commented, minimal, self-contained, reproducible code.
Hi
I'm looking for a package to perform quality control, normalization and
analysis of high throughput cell-based chemical screens. I know that the
cellHTS2 package provides this for siRNA screens.
Does anybody know if something like what I'm looking for exists?
Thank you!
Gabrie
Hi
how can I find, in a vector of characters, which is the most frequent one?
Thanks
Gabriele Zoppoli, MD
Ph.D. Fellow, Experimental and Clinical Oncology and Hematology, University of
Genova, Genova, Italy
Guest Researcher, LMP, NCI, NIH, Bethesda MD
Work: 301-451-8575
Mobile: 301-204-5642
Hi
I'm looking for a package to perform quality control, normalization and
analysis of high throughput cell-base chemical screens. I know that the
cellHTS2 package provides this for siRNA screens.
Does anybody know if something like what I'm looking for exists?
Thank you!
Gabrie
e",neval=100,phi=30,main="",xtrim=-0.2)
Thanks!
Gabriele Zoppoli, MD
Ph.D. Fellow, Experimental and Clinical Oncology and Hematology, University of
Genova, Genova, Italy
Guest Researcher, LMP, NCI, NIH, Bethesda MD
Work: 301-451-8575
Mobile: 301-204-5642
Email
/04/01","2012/07/01","2010/10/01"),format=Ymd.format))
vgridlab<-
c("Jan","Feb","Mar","Apr","May","Jun","Jul","Aug","Sep","Oct","Nov","Dec&
substitute it with 1/a
I know that for some of you it must be overeasy, but I swear I googled for two
hours with keywords "operations", "calculations", "data matrices", "data
tables", and "CRAN", and I didn't find anything useful.
Thank yo
he redundant rows with:
> A<-unique(A)
Guess I'm doing something really wrong here... Sorry for the inexperience, I'm
trying to improve...
Gabriele Zoppoli, MD
Ph.D. Fellow, Experimental and Clinical Oncology and Hematology, University of
Genova, Genova, Italy
Guest Researcher
Sorry, maybe it's easy but I haven't found anything useful:
how can I obtain a list C that contains all the members in the list B that are
not in list A? This are lists of nanes, not numbers!
Thank you
Gabriele Zoppoli, MD
Ph.D. Fellow, Experimental and Clinical Oncology and
pecified subset and randomly chosen ones from the
"mother" list.
How could I do that? What would be an appropriate statistical test?
Thank you for your help!
Gabriele Zoppoli, MD
Ph.D. Fellow, Experimental and Clinical Oncology and Hematology, University of
Genova, Genova, Italy
Guest Re
r inside each intersection. I think
the issue lyes in the non-numeric nature of the list, but I don't know if a
solution for this exists...
If anybody can help, this would be a great thing.
Thanks!
Gabriele Zoppoli, MD
Ph.D. Fellow, Experimental and Clinical Oncology and Hematology, Uni
Hi all,
if I transpose a matrix with t(data), the newly created colums do not appear to
have the first row as header. How can I do to have all the newly created
columns have their first row as a header?
Thanks
Gabriele Zoppoli, MD
Ph.D. Fellow, Experimental and Clinical Oncology and
3 9.522 12.362
49Renal3 9.487 12.030
50Renal3 8.322 12.798
51Renal3 9.359 12.714
52Renal3 11.611 13.344
53Renal3 9.663 12.004
54Renal3 9.819 13.214
Please help me
Thank you so much
Gabriele Zoppoli, MD
Ph.D. Fellow, Experimental and
ble",header=TRUE,sep="\t")
>histogram(table)
Please help me!!!
Thanks
Gabriele Zoppoli, MD
Ph.D. Fellow, Experimental and Clinical Oncology and Hematology, University of
Genova, Genova, Italy
Guest Researcher, LMP, NCI, NIH, Bethesda MD
Work: 301-451-8575
Mobile:
Hello Chris,
I had the same problem, and I ended up driving R Gui through an Autoit
script, see http://www.autoitscript.com/autoit3/ Regards,
Gabriele Franzini
-Original Message-
From: cr...@binghamton.edu [mailto:cr...@binghamton.edu]
Sent: 22 September 2009 19:37
To: r-help@r
omeuser") # double quotes
required, it will ask for the password
# Return rows from an SQL query
mydata <- sqlQuery (channel, "Select put your query here ...") #
same as before
odbcClose(channel) # When you're done
HTH,
Gabriele Franzini
ICT Applications Manager
Nerv
Hello Harsh,
I found useful the fgui package (
http://www.people.fas.harvard.edu/~tjhoffm/fgui.html ).
Regards,
Gabriele Franzini
ICT Applications Manager
Nerviano Medical Sciences SRL
Nerviano Italy
-Original Message-
From: Barry Rowlingson [mailto:b.rowling...@lancaster.ac.uk
Hi,
I had a similar problem, and I took the direction of squeezing the
output into a minipage, e.g.:
...
@
\begin{minipage}[c]{0.6\textwidth}
<>=
plot(...)
abline(...)
@
\end{minipage}
...
HTH,
Gabriele Franzini
ICT Applications Manager
Nerviano Medical Sciences SRL
Nerviano
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