randomizeBE 0.3-5 [R for BE/BA]

posted by Helmut Homepage – Vienna, Austria, 2019-08-25 16:26  – Posting: # 20517
Views: 260

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.

Cheers,
Helmut Schütz
[image]

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

Complete thread:

Activity
 Mix view
Bioequivalence and Bioavailability Forum |  Admin contact
19,781 posts in 4,196 threads, 1,358 registered users;
online 6 (0 registered, 6 guests [including 5 identified bots]).
Forum time (Europe/Vienna): 14:38 CEST

Multivariate analysis: A means of finding the answer
when you don’t know the question.    Stephen Senn

The BIOEQUIVALENCE / BIOAVAILABILITY FORUM is hosted by
BEBAC Ing. Helmut Schütz
HTML5