View source: R/MultiGroupTestBMDD.R
| Multi.group.test.bMDD | R Documentation | 
Idea: shift lambda of Poisson distribution until there is a certain proportion of significant results
Multi.group.test.bMDD(
  groups,
  counts,
  control.name = NULL,
  alpha = 0.05,
  shift.step = -0.25,
  bootstrap.runs = 200,
  power = 0.8,
  max.iterations = 1000,
  use.fixed.random.seed = NULL,
  CPCAT.bootstrap.runs = 200,
  Dunnett.GLM.zero.treatment.action = "log(x+1)",
  show.progress = TRUE,
  show.results = TRUE,
  get.effect.and.power = FALSE,
  use.CMP.distribution = FALSE,
  CMP.dispersion.factor = 1,
  test = "CPCAT"
)
groups | 
 Group vector  | 
counts | 
 Vector with count data  | 
control.name | 
 Character string with control group name (optional)  | 
alpha | 
 Significance level  | 
shift.step | 
 Step of shift (negative as a reduction is assumed)  | 
bootstrap.runs | 
 Number of bootstrap runs  | 
power | 
 Proportion of bootstrap.runs that return significant differences  | 
max.iterations | 
 Max. number of iterations to not get stuck in the while loop  | 
use.fixed.random.seed | 
 Use fixed seed, e.g. 123, for reproducible results. If NULL no seed is set.  | 
CPCAT.bootstrap.runs | 
 Bootstrap runs within CPCAT method  | 
Dunnett.GLM.zero.treatment.action | 
 Dunnett.GLM method to be used for treatments only containing zeros  | 
show.progress | 
 Show progress for each shift of lambda  | 
show.results | 
 Show results  | 
get.effect.and.power | 
 Return effect size (percent of control) and power for each step (only for last treatment)  | 
use.CMP.distribution | 
 Use Conway-Maxwell-Poisson distribution for sampling  | 
CMP.dispersion.factor | 
 Dispersion parameter phi has to be sqrt(factor) to scale the variance by this factor  | 
test | 
 Either "CPCAT" or "GLM.Dunnett"  | 
Data frame with results from bMDD analysis
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