Displaying 20 results from an estimated 1000 matches similar to: "Question about correlation"
2017 Jul 05
0
Question about correlation
Hi Chin Yi,
If you are trying to correlate "Health" with "Disease", i.e.
cydf<-read.table(text="OTU ID Health Disease
Bacterial 1 0.29 0.34
Bacterial 2 0.25 0.07
Bacterial 3 0.06 0.06
Bacterial 4 0.07 0.09
Bacterial 5 0.02 0.05",
header=TRUE)
print(cor(cydf$Health,cydf$Disease))
[1] 0.7103517
If you are getting that error, it probably means that
2017 Jul 05
2
Question about correlation
On 2017-07-05 11:56, Jim Lemon wrote:
> Hi Chin Yi,
> If you are trying to correlate "Health" with "Disease", i.e.
>
> cydf<-read.table(text="OTU ID Health Disease
> Bacterial 1 0.29 0.34
> Bacterial 2 0.25 0.07
> Bacterial 3 0.06 0.06
> Bacterial 4 0.07 0.09
> Bacterial 5 0.02 0.05",
> header=TRUE)
>
2017 Jul 14
3
Conduct Network Analysis
Greeting.
Dear Mr/Mrs/Miss,
I want to create a network by using R but I only have a table that contain
OTU ID and the abundance value of two samples ONLY.
Isn't possible? If can, which package can be used?
Greatly appreciated to any suggestions and helps.
Thank you.
Best regards,
Kang Chin Yi
[[alternative HTML version deleted]]
2017 Jul 06
0
Question about correlation
Please keep the conversation on the list: Others may be able to help you
better than I can.
On 2017-07-06 10:38, SEB140004 Student wrote:
> Ya. I had successfully got the result. Thank you very much. :)
>
> Isn't possible for me to obtain the network from the correlation matrix?
I know nothing about correlation networks, but by googling I found two R
packages, ggraph and corrr,
2017 Jul 05
0
Question about correlation
I think that Goran is right, I didn't take "cor(data)" literally.
Jim
On Thu, Jul 6, 2017 at 3:38 AM, G?ran Brostr?m <goran.brostrom at umu.se> wrote:
> On 2017-07-05 11:56, Jim Lemon wrote:
>>
>> Hi Chin Yi,
>> If you are trying to correlate "Health" with "Disease", i.e.
>>
>> cydf<-read.table(text="OTU ID Health
2009 Mar 29
2
re form data for aov()?
I have data in a file named hands.dat, which is given at the end of this
question. (It's from a stats textbook example on anova). I'd like to do an
aov on this, which I guess would be
d <- read.table("~/hands.dat", header=TRUE)
aov(Bacterial.Counts ~ Water + Soap + Antibacterial.Soap + Alcohol.Spray,
data=d)
but this fails. Do I need to break d$Method up into columns for
2013 Apr 30
1
vegan -varpart is bigger than 100% in total?
I am trying to find the percentage of the parameters explaining the bacterial community composition. I have one data matrix with relative abundance of OTUs and one with environmental parameters. I used varpart in vegan package but the values in the venn diagram is bigger than 100% in total.How is it possible? What might be the reason? Thank you
library(vegan)
gotud <-
2005 Jan 20
5
glm and percentage data with many zero values
Dear all,
I am interested in correctly testing effects of continuous environmental
variables and ordered factors on bacterial abundance. Bacterial
abundance is derived from counts and expressed as percentage. My problem
is that the abundance data contain many zero values:
Bacteria <-
2005 Sep 27
6
Locomotive 0.2.4 for Mac OS X 10.3+
I am pleased to announce the newest release of Locomotive!
http://locomotive.sourceforge.net
Mostly a bug fix release. If you are using Locomotive on 10.4 you
should definitely upgrade.
New in 0.2.4
============
* Rename application entries in status window
* Run/Restart/Stop buttons now immediately update
* Bundle choosing is fixed for Mac OS X 10.4
* Missing gem dependencies in Rails 0.13.1
2010 Aug 05
2
colour of label points on a boxplot
Hi all,
I have 6 datasets(dataframes Assem_ContigsLen7 through all_ContigsLen12)
containing 3 columns (contig_id, contig_length, read_count).
Each dataset is composed of 3 types of contigs (assemblies of genomic
fragments), 1- all Bacterial fragments, 2 - all Viral fragments, 3 -
mixed fragments.
I identified the type of contig through a merge with another table with
just contig_id and
2012 Jul 10
1
R code help to change table format
I am trying to input an OTU table into EstimateS, however, the format of the
OTU table has to be changed to fit the format EstimateS will accept. In R, I
would like to change the format of the OTU table (from excel). Here is what
I need to do, take Example 1 and create Example 2. The problem is that I
have hundreds of OTUs, so I can't do this by hand (and I'd love to have a
code that I
2005 Dec 30
2
Locomotive 1.0.0 for Mac OS 10.3+
Hi All,
I''m very happy to announce the release of Locomotive 1.0.0.
Locomotive is a one-click development solution for Rails on Mac OS X.
See more details at http://locomotive.sourceforge.net
Get it at:
http://prdownloads.sourceforge.net/locomotive/Locomotive_1.0.0.dmg?download
What''s New?
===========
* Server bundle updated to lighttpd 1.4.8
* Server bundle updated to
2013 Apr 03
2
Ask help
Hello!
I am eager to learn if I only have a data about the relationship between otu and sample, could I use the function capscale, and final make a point plot that x-axis is CAP1 and y-axis is CAP2? Besides, what function could I use to make the different rarefaction curve with different color in the a plot in R? Appreciate very much.
2024 Jan 30
2
Use of geometric mean for geochemical concentrations
Dear Rich,
It depends how the data is generated.
Although I am not an expert in ecology, I can explain it based on a biomedical example.
Certain variables are generated geometrically (exponentially), e.g. MIC or Titer.
MIC = Minimum Inhibitory Concentration for bacterial resistance
Titer = dilution which still has an effect, e.g. serially diluting blood samples;
Obviously, diluting the
2014 Sep 04
1
gplot heatmaps: clustering according to rowsidecolors + key.xtickfun
Hi there,
I have two questions about heatmap.2 in gplot.
My input is a simple square matrix with numeric values between 75 and
100 (it is a similarity matrix based on bacterial DNA sequences).
1. I can sort my input matrix into categories with rowsidecolors (in
this case, very conveniently by bacterial taxa). I do a clustering and
reordering of my matrix by Rowv=TRUE (and
2007 Apr 25
1
heatmap and phylogram / dendogram ploting problem, ape package
I am having trouble displaying a dendrogram of evolutionary
relationships (a phylogram imported from the ape package) as the
vertical component of a heatmap, but keeping the hierarchical
clustering of the horizontal component. The relationships of the
vertical component in the generated heatmap are not that of the
dendrogram, although the ordering is.
In more detail, I am attempting to generate
2009 Sep 21
1
How to use nls when [selfStart] function returns NA or Inf??
Hi Everyone,
I posted this a couple of weeks ago with no responses. My interface (via
gmane) seemed a bit flakey at the time, so I'm venturing to repost with some
additional information.
I'm trying to write selfStart non-linear models for use with nls. In these
models some combinations of parameter values are illegal; the function value
is undefined.
That's OK when calling the
2004 Sep 07
4
Caller id and the number of rings
Hi all,
I have the following setup
PSTN -> ASTERISK -> IVR (using dialogic card)
1) Caller id information is presented to asterisk during the first and
second ring.
2) Hence, Asterisk waits for 2 rings before pickup the call and forwarding
to the appropriate FXS port.
3) The IVR application also waits for 2 rings before picking up the call to
get the caller id.
4) Hence any caller
2007 Sep 17
2
problems with nested loop
Hi, everyone:
R is new to me. I am writing a nested loop to simulate data for t-test. The following code is wrong. The subscript is out of bounds. Could anyone tell me how to revise it? Thanks, Riddle Chin.
result<-matrix(ncol=5, nrow=1000)
colnames(result)<-c('N=20','N=40','N=60','N=80','N=100')
for (i in 1:1000){
for (j in
2013 Aug 30
0
Bioinformatics position at FDA-CFSAN (College Park, MD)
The Biostatistics Analytics Team at the FDA Center for Food Safety and Applied Nutrition seeks an MS/PhD in computer science (or related field) with experience in bioinformatics. The Analytics Team is responsible for computational support for projects involving large chemical and microbial hazard data sets, including bioinformatic and statistical analysis of bacterial genomic data for foodborne