Description Usage Arguments Value Note See Also
Post process Estimation of binding site positions obtained from PING. Refit mixture models with stronger prior in candidate regions contain potential problems, and then convert final result into dataframe.
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 |
ping |
A |
seg |
An object of class |
rho2, sigmaB2, alpha2, beta2 |
Integer values, the parameters in the prior of mixture models to be re-fitted. |
min.dist |
The minimum distance of two adjacent nucleosomes predicted from different candidate regions, smaller than that will be treated as duplicated predictions for the same nucleosomes. |
paraEM |
A |
paraPrior |
A |
score |
A |
dataType |
A |
nCores |
An |
makePlot |
A |
FragmentLength |
An |
mart, seg.boundary, DupBound, datname |
Plotting parameters and options. |
IP |
A |
minK |
An |
maxK |
An |
tol |
A |
B |
An |
mSelect |
A |
mergePeaks |
A |
mapCorrect |
A |
xi |
An |
rho |
An |
alpha |
An |
beta |
An |
lambda |
An |
dMu |
An |
A data.frame
containing the estimated binding site positions
Based on our experiemt on a few real data sets, we suggestion to use following values of parameters. For sonication data we use rho1=1.2; sigmaB2=6400; rho=15; alpha1=10; alpha2=98; beta2=200000. For MNase data we use rho1=3; sigmaB2=4900; rho=8; alpha1=20; alpha2=100; beta2=100000. The value of xi depends on specs of sample, since that affect the length of linker-DNA. For example, we use xi=160 for yeast and xi=200 for mouse.
PING, plotSummary
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