Comments (3)
@dendesfelder Would this also apply for translocations and micronuclei? Or should we only use the empirical error for them?
from biodosetools.
I'm trying this implementation at the moment:
disp <- case_data[["DI"]]
if (disp >= 1) {
# Use empirical error sqrt(var / N) if disp >= 1
if (aberr_module == "dicentrics" | aberr_module == "micronuclei") {
lambda_est_sd <- case_data[["y_err"]]
} else if (aberr_module == "translocations") {
lambda_est_sd <- case_data[["Fg_err"]]
}
} else {
# Use Poisson error if disp < 1
lambda_est_sd <- sqrt(case_data[["X"]]) / case_data[["N"]]
}
Would these results make sense? Using C0=5
, and C1=2
and the fitting curve from IAEA:
Before fix | After fix |
---|---|
![]() |
![]() |
from biodosetools.
Seems to make sense. Which calibration curve coefficients did you use for dose estimation. I would say that the same applies for translocations and Micronuclei, too. For very high doses of low-LET we would expect some degree of underdispersion and we might therefore slightly overestimate the uncertainty with this approach. However, I believe it's better to overestimate than underestimate.
from biodosetools.
Related Issues (20)
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