Displaying 7 results from an estimated 7 matches for "effector".
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effectors
2012 Nov 16
1
Code works, but not as function.
Hi,
I have some values in a list format generated by the following:
Path_Number <- 0010
ID.Path <- formatC(0001:Path_Number, width=4, flag=0) # Make vector of ID's.
No_of_Effectors <- sample(1:550, length(ID.Path), replace=TRUE) # Define Number of Effectors each individual gets.
Effectors <- split(sample(1:10000, sum(No_of_Effectors), replace=TRUE), rep(ID.Path, No_of_Effectors)) # Generate effectors and dish them out.
Effectors
And I've written a chunk which is d...
2012 Nov 08
1
Extract cell of many values from dataframe cells and sample from them.
Hi,
First my apologies for a non-working piece of code in a previous submission, I have corrected this error.
I'm doing is individual based modelling of a pathogen and it's host. The way I've thought of doing this is with two dataframes, one of the pathogen and it's genes and effector genes, and one of the host and it's resistance genes. During the simulation, these things can be pulled out of the dataframes and operated on, before being stored again in the dataframes.
Below is how I've created my dataframe and stored my effector genes. In this model, effector genes are...
2012 Oct 28
6
Having some Trouble Data Structures
Hi All,
I'm trying to run a simulation of host-pathogen evolution based around individuals.
What I need to have is a dataframe or table of some description - describing all the individuals of a pathogen population (so far I've implemented this as a matrix):
ID No_of_Effectors Effectors (Sequences)
[1,] 0001 3 ## 3 Random Numbers ##
There will be many such rows for many individuals. They have something called effectors, the number of which is randomly generated, so say you get 3 in the No_of_Effectors column. Then I...
2012 Nov 27
2
Stuck trying to modify a function
...ulation I'm building:
Mutate<-function(x){
l<-0
for(i in x){
l2<-0
l<-l+1
for(i in x[[l]]){
l2<-l2+1
if(runif(1) < 0.9) ifelse(runif(1) <0.5, x[[l]][l2] <- x[[l]][l2]+1, x[[l]][l2] <- x[[l]][l2]-1)
}
}
return(x)
}
I call this with Effectors<-Mutate(X)
The function is designed to alter the values of each element in X by either + or - 1 (50:50 chance wether + or -). However Y, elements of which are a subset of the corresponding elements of X, need to be consistent i.e. if a value in X is changed, and that value is part of the Y subs...
1999 Jun 18
1
Stepwise model selection question
...sts to then treat the results of the stepwise model selection as
yet a fourth analytical tool by which to rank all the mapping markers,
i.e., as further evidence that a marker must be near a genetic element
affecting the trait. "If it's included in the model, it must be close to a
genetic effector of the trait". How does this sound to you? If a stepwise
algorithm ranks possible cofactors--perhaps even assigns them an F
value--can you use that ranking to make any comparisons among possible
cofactors? What do the F values mean?
**********************************************************...
2005 May 20
2
RSYNC with Double-byte
Hi All,
Can anyone suggest how to make rsync work in order to replicate
double-byte characters ?
Thanks to anyone who can help
aslay
2012 Jan 03
0
Job opportunity in AMSTERDAM: ANALYSIS OF NGS CANCER DATA
...nl/vacancies.php)
THREE BIOINFORMATICS POSITIONS
PROJECT OUTLINE
Genomic alterations are major determinant of responses to (targeted) therapies in cancer. In fact, the best positive and negative predictors of responses to targeted therapies are alterations in kinases or their direct downstream effectors. To gain insight into resistance mechanisms to therapy and thus better tailor treatment, we are approaching this problem from two different angles. First, we have acquired large panels of human tumors, on which we are currently performing kinase exon sequencing. More specifically, we are performin...