calcMLE | R Documentation |
Optimizes the likelihood function of the DNA mixture model
calcMLE(
nC,
samples,
popFreq,
refData = NULL,
condOrder = NULL,
knownRef = NULL,
kit = NULL,
DEG = TRUE,
BWS = TRUE,
FWS = TRUE,
AT = 50,
pC = 0.05,
lambda = 0.01,
fst = 0,
knownRel = NULL,
ibd = NULL,
minF = NULL,
normalize = TRUE,
steptol = 1e-04,
nDone = 3,
delta = 1,
difftol = 0.01,
seed = NULL,
verbose = FALSE,
priorBWS = NULL,
priorFWS = NULL,
maxThreads = 0,
adjQbp = FALSE
)
nC |
Number of contributors in model. |
samples |
A List with samples which for each samples has locus-list elements with list elements adata and hdata. 'adata' is a qualitative (allele) data vector and 'hdata' is a quantitative (peak heights) data vector. |
popFreq |
A list of allele frequencies for a given population. |
refData |
Reference objects has locus-list element [[i]] with a list element 'r' which contains a 2 long vector with alleles for each references. |
condOrder |
Specify conditioning references from refData (must be consistent order). For instance condOrder=(0,2,1,0) means that we restrict the model such that Ref2 and Ref3 are respectively conditioned as 2. contributor and 1. contributor in the model. |
knownRef |
Specify known non-contributing references from refData (index). For instance knownRef=(1,2) means that reference 1 and 2 is known non-contributor in the hypothesis. This affectes coancestry correction. |
kit |
shortname of kit: Obtained from getKit() |
DEG |
Boolean of whether Degradation model should be used |
BWS |
Boolean of whether back-stutter model should be used |
FWS |
Boolean of whether for-stutter model should be used |
AT |
The analytical threshold given. Used when considering probability of allele drop-outs. |
pC |
A numeric for allele drop-in probability. Default is 0. |
lambda |
Parameter in modeled peak height shifted exponential model. Default is 0. |
fst |
is the coancestry coeffecient. Default is 0. |
knownRel |
gives the index of the reference which the 1st unknown is related to. |
ibd |
the identical by decent coefficients of the relationship (specifies the type of relationship) |
minF |
The freq value included for new alleles (new alleles as potential stutters will have 0). Default NULL is using min.observed in popFreq. |
normalize |
Whether normalization should be applied or not. Default is FALSE. |
steptol |
Argument used in the nlm function for faster return from the optimization (tradeoff is lower accuracy). |
nDone |
Number of optimizations required providing equivalent results (same logLik value obtained) |
delta |
Scaling of variation of normal distribution when drawing random startpoints. Default is 1. |
difftol |
Tolerance for being exact in log-likelihood value (relevant when nDone>1) |
seed |
The user can set seed if wanted |
verbose |
Whether printing limits to integrate over. Printing progress if maxEval>0. Default is TRUE. |
priorBWS |
Prior function for BWS-parameter. Flat prior on [0,1] is default. |
priorFWS |
Prior function for FWS-parameter. Flat prior on [0,1] is default. |
maxThreads |
Maximum number of threads to be executed by the parallelization |
adjQbp |
Indicate whether fragmenth length of Q-allele is based on averaged weighted with frequencies |
Fitted maximum likelihood object
Oyvind Bleka
## Not run:
kit = "ESX17"
AT = 50 #analytical threshold
sep0 = .Platform$file.sep
popfn = paste(path.package("euroformix"),"FreqDatabases",paste0(kit,"_Norway.csv"),sep=sep0)
evidfn = paste(path.package("euroformix"),"examples",paste0(kit,"_3p.csv"),sep=sep0)
reffn = paste(path.package("euroformix"),"examples",paste0(kit,"_refs.csv"),sep=sep0)
popFreq = freqImport(popfn)[[1]] #population frequencies
samples = sample_tableToList(tableReader(evidfn)) #evidence samples
refData = sample_tableToList(tableReader(reffn)) #reference sample
plotEPG2(samples,kit,refData,AT)
condOrder = c(1,2,0) #assuming C1=ref1,C2=ref2
mlefit = contLikMLE(3,samples,popFreq,refData,condOrder,kit=kit)
plotTopEPG2(mlefit)
## End(Not run)
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