mthapower (version 0.1.1)

mthacases: Sample size calculations - mtDNA haplogroups

Description

Determine the minimum number of cases (Ncmin), required to detect: either a change from p0 (haplogroup frequency in controls) to p1 (haplogroup frequency in cases), or a given OR, with a predefined confidence interval, in a study with Nh haplogroups. Note: I assume that case-control equations are valid for cohorts with a balanced number of cases and controls. This function may not be generalizable for all studies involving mtDNA haplogroups.

Usage

mthacases(p0 = p0, Nh = Nh, OR.cas.ctrl = OR.cas.ctrl,
  power = power, sig.level = sig.level)

Arguments

p0

the frequency of the haplogroup in the control population, (that is, the controls among exposed). It depends on haplogroup baseline frequency.

Nh

number of haplogroup categories. Usually 10 haplogroups plus one category for rare haplogroups: Nh <- 11.

OR.cas.ctrl

(p1 / (1-p1)) / (p0 / (1-p0)) the OR you want to detect with your data. It can be either a single value, or a sequence: OR.cas.ctrl <- 2; OR.cas.ctrl <- seq(1.25,3 by=0.5).

power

the power to detect a given OR in my study (usually 80-90).

sig.level

the alpha error accepted. Can take 3 possible values: 0.05, 0.01 and 0.001 (see [Table 2] of Samuels et al).

Value

Gives the result in a data frame, easy to print in a plot.

References

1. DC Samuels, AD Carothers, R Horton, PF Chinnery. The Power to Detect Disease Associations with Mitochondrial DNA Haplogroups. AJHG, 2006. 78(4):713-720. DOI:10.1086/502682.

2. Source code: github.com/aurora-mareviv/mthapower.

3. Shiny app: aurora.shinyapps.io/mtDNA_power_calc.

Examples

# NOT RUN {
mydata <- mthacases(p0=0.445, Nh=11,
                    OR.cas.ctrl=c(2), power=80,
                    sig.level=0.05) # Baudouin study
mydata <- mthacases(p0=0.445, Nh=11,
                    OR.cas.ctrl=c(1.25,1.5,1.75,2,2.25,2.5,2.75,3),
                    power=80, sig.level=0.05)
mydata <- mydata[c(2,6)]
mydata
plot(mydata)

# }