similar to: Code works, but not as function.

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

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

Hi, I have the following data: Path_Number <- 5 ID.Path <- c(1:Path_Number) # Make vector of ID's. No_of_X <- sample(50:550, length(ID.Path), replace=TRUE) # X <- split(sample(1:10000, sum(No_of_X), replace=TRUE), rep(ID.Path, No_of_X)) Y <- lapply(X,function(x) sample(x, round(runif(1, min=10, max=50)))) X and Y are both lists, and I've made the following function to

Hi, I've been modelling some data over the past few days, of my work, repeatedly challenging microbes to a certain concentration of cleaner, until the required concentration to inhibit or kill them increaces, at which point they are challenged to a slightly higher concentration each day. I'm doing ths for two different cleaners and I'm collecting the required concentration to

On 15 Jul 2019, at 23.17, Ralf Hildebrandt via dovecot <dovecot at dovecot.org> wrote: > > * Ralf Hildebrandt via dovecot <dovecot at dovecot.org>: >> We're using dovecot (via LMTP) as a backup for all incoming mail. >> >> I upgraded from 2.3.6 to 2.3.7 on the 12th: >> 2019-07-12 14:35:44 upgrade dovecot-imapd:amd64 2:2.3.6-2~bionic 2:2.3.7-8~bionic

Hello, I need to chenge axes orirentation in triangle plot. (function triangle.plot in ade4 package) I want to plot elasticities of some species in demographic triangle, where axes values commnly increace "clockwise". If some better imangination is needed, see http://www.open.ac.uk/science/biosci/personalpages/j.silvertown/pdfs/Silvertown%20et%20al.%201993.pdf I am sorry if I just

-------- Original Message -------- Subject: Re: [R] Simulation - Natrual Selection Date: Wed, 05 Jan 2011 17:24:05 +0000 From: Ben Ward <benjamin.ward@bathspa.org> To: Bert Gunter <gunter.berton@gene.com> CC: Mike Marchywka <marchywka@hotmail.com> On 05/01/2011 17:08, Bert Gunter wrote: > Couple of brief comments inline below. -- Bert > > On Wed, Jan 5, 2011 at

We're using dovecot (via LMTP) as a backup for all incoming mail. I upgraded from 2.3.6 to 2.3.7 on the 12th: 2019-07-12 14:35:44 upgrade dovecot-imapd:amd64 2:2.3.6-2~bionic 2:2.3.7-8~bionic and it seems that 2.3.7 is slower than 2.3.6 -- mail to the backup IMAP box is suddenly taking quite some time to get delivered and is piling up in the queue. doveconf -n: ============

Hi all, I read in a text book, that you can examine a variable that is colinear with others, and giving different ANOVA output and explanatory power when ordered differently in the model forula, by modelling that explanatory variable, against the others colinear with it. Then, using that information to split the vector (explanatory variable) in question, into two new vectors, one should

I use the step() function occasionally, and I think I understand its objective, proper use, and limitations. Now I see stepwise model selection being used in what seems to be an unusual way, and I wonder if it is right or wrong. May I describe? Genetic mapping tries to find where in an animal's genome are genetic elements that influence a particular physical trait. Say there are 100

Hello All ! why freebd user can't member more than 15 group ? my system is FreeBSD 4.8-RC I need that scripts running from user "master" make some changes if files that owned by other users. Shurely i can set UID of master to "0" but this increace vunerability of system. in /etc/group I add user1:*:1001:master ... user15:*:1015:master --- all work Ok user master member

Hello, I used iproute2 to do iif specific routing on wifi routers with 2 wifi 802.11b interfaces on non overlapping interfaces. I set rule as follows on router-2 (shown below) use table 100 if incomming interface is wlan0 use table 200 if incomming interface is wlan1 all routes in table 100 have wlan1 as oif all routes in table 200 have wlan0 as oif --wlan0--

* Ralf Hildebrandt via dovecot <dovecot at dovecot.org>: > We're using dovecot (via LMTP) as a backup for all incoming mail. > > I upgraded from 2.3.6 to 2.3.7 on the 12th: > 2019-07-12 14:35:44 upgrade dovecot-imapd:amd64 2:2.3.6-2~bionic 2:2.3.7-8~bionic > > and it seems that 2.3.7 is slower than 2.3.6 -- mail to the backup > IMAP box is suddenly taking quite

* Timo Sirainen via dovecot <dovecot at dovecot.org>: > > And alas, I had a look at the monitoring and found that disk IO has > > increase A LOT after the update: https://www.arschkrebs.de/images/dovecot-disk-io-increase.png > > > > I zoomed in and found that the sudden increace in IO coincides with > > the update to 2.3.7 (14:35):

COMPUTATIONAL ANALYSIS OF NEXT GENERATION SEQUENCE DATA (http://bioinformatics.nki.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

On 16 Jul 2019, at 11.15, Ralf Hildebrandt via dovecot <dovecot at dovecot.org> wrote: > > * Timo Sirainen via dovecot <dovecot at dovecot.org>: > >>> And alas, I had a look at the monitoring and found that disk IO has >>> increase A LOT after the update: https://www.arschkrebs.de/images/dovecot-disk-io-increase.png >>> >>> I zoomed in

Hi All, Can anyone suggest how to make rsync work in order to replicate double-byte characters ? Thanks to anyone who can help aslay

Hi, I wonder if anyone could advise me with this: I've been trying to make a standard curve in R with lm() of some standards from a spectrophotometer, so as I can express the curve as a formula, and so obtain values from my treated samples by plugging in readings into the formula, instead of trying to judge things by eye, with a curve drawn by hand. It is a curve and so I used the