randomizeBE 0.3-5 [🇷 for BE/BA]

posted by Helmut Homepage – Vienna, Austria, 2019-08-25 18:26 (2126 d 04:40 ago) – Posting: # 20517
Views: 6,138

Hi Yung-jin,

❝ That means I cannot use RL4(...,seqs=seqs) where seqs=squences(...) if I prefer using "R", "T", "T1", "T2" for treatment abbreviated, instead of "A", "B", "C" etc.. Am I correct?


I’m not sure whether I understand you correctly. See ?sequences. Only designs listed there are implemented. Hence, you can’t randomize a parallel design with >2 groups.
However,

sequences("4x4", tmts=c("R1", "R2", "T1", "T2"))
# [1] "R1T2R2T1" "R2T1T2R1" "T1R2R1T2" "T2R1T1R2"

williams(ntmt=4, tmts=c("R1", "R2", "T1", "T2"))
# [1] "R1T2T1R2" "R2T1T2R1" "T1R1R2T2" "T2R2R1T1"

work as designed.

Dif-tor heh smusma 🖖🏼 Довге життя Україна! [image]
Helmut Schütz
[image]

The quality of responses received is directly proportional to the quality of the question asked. 🚮
Science Quotes

Complete thread:

UA Flag
Activity
 Admin contact
23,424 posts in 4,927 threads, 1,674 registered users;
40 visitors (0 registered, 40 guests [including 10 identified bots]).
Forum time: 23:07 CEST (Europe/Vienna)

Complex, statistically improbable things are by their nature
more difficult to explain than
simple, statistically probable things.    Richard Dawkins

The Bioequivalence and Bioavailability Forum is hosted by
BEBAC Ing. Helmut Schütz
HTML5