def addHistToTGraphPoisson(self, h, g, w=1.):
for i in range(0, g.GetN()):
# shifted by +1, i.e. over/underflow
err = h.GetBinError(i + 1)
y = h.GetBinContent(i + 1)
binWidth = h.GetBinWidth(i + 1)
# From https://twiki.cern.ch/twiki/bin/view/CMS/PoissonErrorBars
alpha = 1. - 0.6827
n = int(
round(y * binWidth /
w)) # Round is necessary due to, well, rounding errors
l = Math.gamma_quantile(alpha / 2., n, 1.) if n != 0. else 0.
u = Math.gamma_quantile_c(alpha, n + 1, 1) if n != 0. else 0.
g.SetPointEYlow(
i,
math.sqrt(((n - l) / binWidth * w)**2 + g.GetErrorYlow(i)**2))
g.SetPointEYhigh(
i,
math.sqrt(((u - n) / binWidth * w)**2 + g.GetErrorYhigh(i)**2))
gx = Double(0.)
gy = Double(0.)
g.GetPoint(i, gx, gy)
g.SetPoint(i, gx, y + gy)
def convertToPoisson(h):
graph = TGraphAsymmErrors()
q = (1-0.6827)/2.
for i in range(1,h.GetNbinsX()+1):
x=h.GetXaxis().GetBinCenter(i)
xLow =h.GetXaxis().GetBinLowEdge(i)
xHigh =h.GetXaxis().GetBinUpEdge(i)
y=h.GetBinContent(i)
yLow=0
yHigh=0
if y !=0.0:
yLow = y-Math.chisquared_quantile_c(1-q,2*y)/2.
yHigh = Math.chisquared_quantile_c(q,2*(y+1))/2.-y
graph.SetPoint(i-1,x,y)
graph.SetPointEYlow(i-1,yLow)
graph.SetPointEYhigh(i-1,yHigh)
graph.SetPointEXlow(i-1,0.0)
graph.SetPointEXhigh(i-1,0.0)
graph.SetMarkerStyle(20)
graph.SetLineWidth(2)
graph.SetMarkerSize(1.)
graph.SetMarkerColor(kBlack)
return graph
def __init__( self, process_list, sf = None, df = None ):
self.__processes = process_list
if sf and df:
self.__sf = sf
self.__df = df
alpha = 1 - 0.6827
self.__sfCRGraph = TGraphAsymmErrors(self.__sf)
self.__dfCRGraph = TGraphAsymmErrors(self.__df)
for g in [self.__sfCRGraph, self.__dfCRGraph]:
for i in range(g.GetN()):
N = g.GetY()[i]
LowErr = 0 if N == 0 else Math.gamma_quantile(alpha/2, N, 1.)
UpErr = Math.gamma_quantile_c(alpha/2, N+1, 1.) # recommended by StatComm (1.8)
# Math.gamma_quantile_c(alpha, N+1, 1.) # gives 1.2, strictly 68% one-sided
g.SetPointEYlow(i, N-LowErr)
g.SetPointEYhigh(i, UpErr-N)
for p in self.__processes:
if p.name() in ['nonpromptSF', 'nonpromptDF']:
nom, low, high = [], [], []
for ib in range(p.nominal().GetXaxis().GetNbins()):
if p.name() in ['nonpromptDF']: hnp = self.__dfCRGraph
else: hnp = self.__sfCRGraph
npcr = hnp.GetY()[ib]
npcrErrLow = hnp.GetEYlow()[ib]
npcrErrHigh = hnp.GetEYhigh()[ib]
np = p.nominal().GetBinContent(ib+1)
npErr = p.nominal().GetBinError(ib+1)
alpha = np/npcr if npcr > 0 else npErr
nom.append(npcr*alpha)
low.append(npcrErrLow*alpha)
high.append(npcrErrHigh*alpha)
hnom = p.nominal().Clone()
for ib in range(hnom.GetXaxis().GetNbins()):
hnom.SetBinContent(ib+1, nom[ib])
npGraph = TGraphAsymmErrors(hnom)
for ib in range(hnom.GetXaxis().GetNbins()):
npGraph.SetPointEYlow(ib, low[ib])
npGraph.SetPointEYhigh(ib, high[ib])
if p.name() in ['nonpromptDF']:
self.__dfGraph = npGraph
else:
self.__sfGraph = npGraph
self.__uncertainties = set()
for p in self.__processes:
self.__uncertainties = self.__uncertainties.union( set( p.uncertaintySources() ) )
def calculatePoissonErrors(n, confidenceInterval=0.6827):
## Calcultes the Poisson error for a given numer
# n number of entries
# confidenceInterval probability covered inside the error band
from ROOT import Math
n = round(n)
invIntegral = (1. - confidenceInterval) / 2.
lo = Math.gamma_quantile(invIntegral, n, 1.) if n != 0 else 0.
hi = Math.gamma_quantile_c(invIntegral, n + 1, 1.)
return n - lo, hi - n
def GetZVal(p, excess):
'''The function normal_quantile converts a p-value into a significance,
i.e. the number of standard deviations corresponding to the right-tail of
Gaussian
'''
if excess:
zval = Math.normal_quantile(1 - p, 1)
else:
zval = Math.normal_quantile(p, 1)
return zval
def getDataPoissonErrors(hist,
kPoisson=False,
drawZeroBins=False,
drawXbars=False,
centerBin=True):
'''Make data poisson errors for a histogram with two different methods:
- TH1.kPoisson
- chi-squared quantile
'''
# https://github.com/DESY-CMS-SUS/cmgtools-lite/blob/8_0_25/TTHAnalysis/python/plotter/mcPlots.py#L70-L102
# https://github.com/DESY-CMS-SUS/cmgtools-lite/blob/8_0_25/TTHAnalysis/python/plotter/susy-1lep/RcsDevel/plotDataPredictWithSyst.py#L12-L21
if kPoisson: hist.SetBinErrorOption(TH1D.kPoisson)
Nbins = hist.GetNbinsX()
xaxis = hist.GetXaxis()
alpha = (1 - 0.6827) / 2.
graph = TGraphAsymmErrors(Nbins)
graph.SetName(hist.GetName() + "_graph")
graph.SetTitle(hist.GetTitle())
for i in xrange(1, Nbins + 1):
N = hist.GetBinContent(i)
if N <= 0 and not drawZeroBins: continue
dN = hist.GetBinError(i)
yscale = 1
if centerBin:
x = xaxis.GetBinCenter(i)
else:
x = xaxis.GetBinLowEdge(i)
if N > 0 and dN > 0 and abs(dN**2 / N -
1) > 1e-4: # check is error is Poisson
yscale = (dN**2 / N)
N = (N / dN)**2
if kPoisson:
EYlow = hist.GetBinErrorLow(i)
EYup = hist.GetBinErrorUp(i)
else:
EYlow = (N - Math.chisquared_quantile_c(1 - alpha, 2 * N) /
2.) if N > 0 else 0
EYup = Math.chisquared_quantile_c(alpha, 2 * (N + 1)) / 2. - N
y = yscale * N
EXup = xaxis.GetBinUpEdge(i) - x if drawXbars else 0
EXlow = x - xaxis.GetBinLowEdge(i) if drawXbars else 0
graph.SetPoint(i - 1, x, y)
graph.SetPointError(i - 1, EXlow, EXup, EYlow, EYup)
#print ">>> getDataPoissonErrors - bin %2d: (x,y) = ( %3.1f - %4.2f + %4.2f, %4.2f - %4.2f + %4.2f )"%(i,x,EXlow,EXup,y,EYlow,EYup)
graph.SetLineWidth(hist.GetLineWidth())
graph.SetLineColor(hist.GetLineColor())
graph.SetLineStyle(hist.GetLineStyle())
graph.SetMarkerSize(hist.GetMarkerSize())
graph.SetMarkerColor(hist.GetMarkerColor())
graph.SetMarkerStyle(hist.GetMarkerStyle())
return graph
def pass_lepton_RelIso(lid, ltightId):
"""Return True if lepton passes tightID.
Args:
lid (int): Lepton ID.
ltightId (bool): Tight ID.
"""
if abs(lid) == 11:
return ltightId
elif abs(lid) == 13:
if ltightId <
return True if
else:
return False
# We have 2 good (loose) leptons which MAY form a Z candidate.
loose_lep_arr = []
# Do an OSSF check:
if (lid1 + lid2) != 0:
if verbose:
print(f"Event {evt_num} failed OSSF check.")
continue
# Do we want tight Z1 leptons?
if force_z1_leps_tightID:
if (not ltightId1) or (not ltightId2):
continue
lorvec_lep1 = Math.PtEtaPhiMVector(lpt1, leta1, lphi1, lmass1)
lorvec_lep2 = Math.PtEtaPhiMVector(lpt2, leta2, lphi2, lmass2)
z_cand = lorvec_lep1 + lorvec_lep2
if (z_cand.M() < 12) or (z_cand.M() > 120):
print(f"Event {evt_num} failed m(Z1) window.")
continue
# Good Z candidate! Save these lepton indices.
z_cand_lep_ndcs.append((ndx1, ndx2))
# Need to check lepton kinematics (dxy, dz, SIP3D)
# if make_valid_z1_candidate(lep1, lep2):
# All Z1 candidates found!
# my_lep_ls =
# z1_cand_ls = get_all_z1_candidates()
# If the event made it this far, the leptons are good!
evt_info_d["n_evts_ge4_passing_leps"] += 1
def get_LorentzVector(self, include_FSR=True):
"""Return a Lorentz vector version of this lepton."""
if include_FSR:
return Math.PtEtaPhiMVector(
self.lpt,
self.leta,
self.lphi,
self.lmass
)
return Math.PtEtaPhiMVector(
self.lpt_NoFSR,
self.leta_NoFSR,
self.lphi_NoFSR,
self.lmass_NoFSR
)
def __call__(self, population, signalYield, signalSample, backgroundYield,
backgroundSample):
# Loop over the chromosomes in the population
for genome in population:
# Get a nn describe by the chromosome (feed foreward)
net = nn.create_ffphenotype(genome)
error = 0.0
# Loop over the events
for event in signalSample:
# Extract variables and weight
variables = event[1:]
weight = event[0] / signalYield
# Not strictly necessary in feedforward nets
net.flush()
# Computing the error
error = error + weight * (
1 - net.sactivate(variables)[0])**self.norm
# Loop over the events
for event in backgroundSample:
# Extract variables and weight
variables = event[1:]
weight = event[0] / backgroundYield
# Not strictly necessary in feedforward nets
net.flush()
# Computing the error
error = error + weight * (
net.sactivate(variables)[0])**self.norm
# Set the fitness value to the chomosome
genome.fitness = 1 - Math.pow(error / 2, 1. / self.norm)
def __call__(self, population, signalYield, signalSample, backgroundYield, backgroundSample):
# Loop over the chromosomes in the population
for genome in population:
# Get a nn describe by the chromosome (feed foreward)
net = nn.create_ffphenotype(genome)
error = 0.0
# Loop over the events
for event in signalSample:
# Extract variables and weight
variables = event[1:]
weight = event[0]/signalYield
# Not strictly necessary in feedforward nets
net.flush()
# Computing the error
error = error + weight*(1 - net.sactivate(variables)[0])**self.norm
# Loop over the events
for event in backgroundSample:
# Extract variables and weight
variables = event[1:]
weight = event[0]/backgroundYield
# Not strictly necessary in feedforward nets
net.flush()
# Computing the error
error = error + weight*(net.sactivate(variables)[0])**self.norm
# Set the fitness value to the chomosome
genome.fitness = 1 - Math.pow(error/2, 1./self.norm)
def cdf_generator(self, histo, binN):
mean = histo.GetBinContent(binN)
sdev = TMath.Sqrt(mean)
maxK = mean + 4 * sdev # mean + 4 * mean
ks = linspace(0, maxK, 101) # xrange(maxK)# [k for k in xrange(maxK)]
cdf = {pos: [ks[pos], Math.inc_gamma_c(ks[pos]+1, mean)] for pos in xrange(len(ks))} # dictionary wich contains the x and y info of the cdf in a list of two elements. e.g. cdf[1] -> [0, 0].
return deepcopy(cdf)
def getprobability(S, dof):
""".. function:: checkchisquared(S,dof) -> p
Knowing that S follows a chi square distribution (with dof degrees of freem),
return the probability that S is fulfill the hypothesis
"""
from ROOT import Math
return Math.chisquared_cdf(S, dof)
def get_pt(vector):
# Get pT from a given Lorentz vector
pT = None
try:
pT = vector.Perp()
except AttributeError:
pT = Math.sqrt(vector.Perp2())
return pT
def createTGraphPoisson(self, h, w=1.):
self.tfile.cd()
g = TGraphAsymmErrors(h)
for i in range(0, g.GetN()):
y = h.GetBinContent(i+1)
binWidth = h.GetBinWidth(i+1)
# From https://twiki.cern.ch/twiki/bin/view/CMS/PoissonErrorBars
alpha = 1. - 0.6827
n = int(round(y*binWidth/w)) # Round is necessary due to, well, rounding errors
l = Math.gamma_quantile(alpha/2., n, 1.) if n != 0. else 0.
u = Math.gamma_quantile_c(alpha, n+1, 1)
# print y*binWidth/w, n, y, u, l
g.SetPointEYlow(i, (n-l)/binWidth*w)
g.SetPointEYhigh(i, (u-n)/binWidth*w)
return g
def getprobability(S,dof): """.. function:: checkchisquared(S,dof) -> p Knowing that S follows a chi square distribution (with dof degrees of freem), return the probability that S is fulfill the hypothesis """ from ROOT import Math return Math.chisquared_cdf(S,dof)
def get_lorentz_vector_new(particle):
# Get the Lorentz Vector of a given particle (Math::LorentzVector class)
vector = Math.PxPyPzMVector()
vector.SetPx(particle.core.p4.px)
vector.SetPy(particle.core.p4.py)
vector.SetPz(particle.core.p4.pz)
vector.SetM(particle.core.p4.mass)
return vector
def LineShapePDF(shapes, mass, histo):
# import ROOT
from ROOT import Math
x = shapes.binxcenters
y = np.array([])
if mass in shapes.shapes.keys():
y = np.array(shapes.shapes[mass])
else:
input_masses = shapes.shapes.keys()
min_mass = min(input_masses)
max_mass = max(input_masses)
ml = mass
yl = np.array([])
mh = mass
yh = np.array([])
if mass < min_mass:
print "** WARNING: ** Attempting to extrapolate below the lowest input mass. The extrapolated shape(s) might not be reliable."
m_temp = input_masses
m_temp.sort()
ml = m_temp[0]
mh = m_temp[1]
elif mass > max_mass:
print "** WARNING: ** Attempting to extrapolate above the highest input mass. The extrapolated shape(s) might not be reliable."
m_temp = input_masses
m_temp.sort(reverse=True)
ml = m_temp[1]
mh = m_temp[0]
else:
ml = max([ m for m in input_masses if m<mass ])
mh = min([ m for m in input_masses if m>mass ])
yl = np.array(shapes.shapes[ml])
yh = np.array(shapes.shapes[mh])
y = ((yh - yl)/float(mh-ml))*float(mass - ml) + yl
# define interpolator
interpolator = Math.Interpolator(len(x))
interpolator.SetData(len(x), array('d',x), array('d',y.tolist()))
for i in range(0, histo.GetNbinsX()+1):
xcenter = histo.GetBinCenter(i)/float(mass)
if xcenter > shapes.binxcenters[0] and xcenter < shapes.binxcenters[-1]:
xlow = histo.GetXaxis().GetBinLowEdge(i)/float(mass)
if xlow < shapes.binxcenters[0]: xlow = shapes.binxcenters[0]
xhigh = histo.GetXaxis().GetBinUpEdge(i)/float(mass)
if xhigh > shapes.binxcenters[-1]: xhigh = shapes.binxcenters[-1]
integral = interpolator.Integ(xlow, xhigh)
histo.SetBinContent( i, (integral if integral >= 0. else 0.) )
else:
histo.SetBinContent(i, 0.)
# histo.Scale( 1./histo.Integral() )
histo.Scale( sum(y)/histo.Integral() )
def createTGraphPoisson(self, h, w=1.):
self.tfile.cd()
g = TGraphAsymmErrors(h)
for i in range(0, g.GetN()):
y = h.GetBinContent(i + 1)
binWidth = h.GetBinWidth(i + 1)
# From https://twiki.cern.ch/twiki/bin/view/CMS/PoissonErrorBars
alpha = 1. - 0.6827
n = int(
round(y * binWidth /
w)) # Round is necessary due to, well, rounding errors
l = Math.gamma_quantile(alpha / 2., n, 1.) if n != 0. else 0.
u = Math.gamma_quantile_c(alpha, n + 1, 1)
# print y*binWidth/w, n, y, u, l
g.SetPointEYlow(i, (n - l) / binWidth * w)
g.SetPointEYhigh(i, (u - n) / binWidth * w)
return g
def addHistToTGraphPoisson(self, h, g, w=1.):
for i in range(0, g.GetN()):
# shifted by +1, i.e. over/underflow
err = h.GetBinError(i+1)
y = h.GetBinContent(i+1)
binWidth = h.GetBinWidth(i+1)
# From https://twiki.cern.ch/twiki/bin/view/CMS/PoissonErrorBars
alpha = 1. - 0.6827
n = int(round(y*binWidth/w)) # Round is necessary due to, well, rounding errors
l = Math.gamma_quantile(alpha/2., n, 1.) if n != 0. else 0.
u = Math.gamma_quantile_c(alpha, n+1, 1) if n != 0. else 0.
g.SetPointEYlow(i, math.sqrt(((n-l)/binWidth*w)**2 + g.GetErrorYlow(i)**2))
g.SetPointEYhigh(i, math.sqrt(((u-n)/binWidth*w)**2 + g.GetErrorYhigh(i)**2))
gx = Double(0.)
gy = Double(0.)
g.GetPoint(i, gx, gy)
g.SetPoint(i, gx, y + gy)
def __call__(self, population, signalYield, signalSample, backgroundYield,
backgroundSample):
# Histogram holders
signalHistogram = TH1F('signalHistogram', 'signal', self.nbins, 0, 1)
backgroundHistogram = TH1F('backgroundHistogram', 'background',
self.nbins, 0, 1)
# Loop over the chromosomes in the population
for genome in population:
# Reset histograms
signalHistogram.Reset()
backgroundHistogram.Reset()
# Get a nn describe by the chromosome (feed foreward)
net = nn.create_ffphenotype(genome)
# Loop over the events creating signal histogram
for event in signalSample:
# Extract variables and weight
variables = event[1:]
weight = event[0]
# Not strictly necessary in feedforward nets
net.flush()
# Net output
output = net.sactivate(variables)[0]
# Filling histograms
signalHistogram.Fill(output, weight)
# Loop over the events creating background histogram
for event in backgroundSample:
# Extract variables and weight
variables = event[1:]
weight = event[0]
# Not strictly necessary in feedforward nets
net.flush()
# Net output
output = net.sactivate(variables)[0]
# Filling histograms
backgroundHistogram.Fill(output, weight)
fitness = 0
# Computing fitness
for bin in xrange(1, signalHistogram.GetNbinsX() + 1):
signal = signalHistogram.GetBinContent(bin)
background = backgroundHistogram.GetBinContent(bin)
total = signal + background
if total > 0:
fitness = fitness + signal**2 / (signal + background)
# Adding fitness to genome
genome.fitness = Math.sqrt(fitness)
def __call__(self, population, signalYield, signalSample, backgroundYield, backgroundSample):
# Histogram holders
signalHistogram = TH1F('signalHistogram', 'signal', self.nbins, 0, 1)
backgroundHistogram = TH1F('backgroundHistogram', 'background', self.nbins, 0, 1)
# Loop over the chromosomes in the population
for genome in population:
# Reset histograms
signalHistogram.Reset()
backgroundHistogram.Reset()
# Get a nn describe by the chromosome (feed foreward)
net = nn.create_ffphenotype(genome)
# Loop over the events creating signal histogram
for event in signalSample:
# Extract variables and weight
variables = event[1:]
weight = event[0]
# Not strictly necessary in feedforward nets
net.flush()
# Net output
output = net.sactivate(variables)[0]
# Filling histograms
signalHistogram.Fill(output, weight)
# Loop over the events creating background histogram
for event in backgroundSample:
# Extract variables and weight
variables = event[1:]
weight = event[0]
# Not strictly necessary in feedforward nets
net.flush()
# Net output
output = net.sactivate(variables)[0]
# Filling histograms
backgroundHistogram.Fill(output, weight)
fitness = 0
# Computing fitness
for bin in xrange(1,signalHistogram.GetNbinsX()+1):
signal = signalHistogram.GetBinContent(bin)
background = backgroundHistogram.GetBinContent(bin)
total = signal + background
if total > 0:
fitness = fitness + signal**2/(signal+background)
# Adding fitness to genome
genome.fitness = Math.sqrt(fitness)
def mean_poisson_pval(d, b, b_error, conv_width=3, step_size=1):
"""
Mostly transcribed from
https://svnweb.cern.ch/trac/atlasoff/browser/Trigger/TrigFTK/SuPlot/trunk/src/bumphunter/StatisticsAnalysis.C
(including the docstring)
Convolve a Gaussian (non-negative part) with a Poisson. Background is b+-b_error, and
we need the mean Poisson probability to observe at least d (if d >=b, else at most d),
given this PDF for b.
The way is to cut the PDF or b into segments, whose area is exactly calculable, take the
Poisson probability at the center of each gaussian slice, and average the probabilities
using the area of each slice as weight.
But here, currently, we are guaranteed to have d > b so some of this simplifies.
d - data counts
b - background counts
b_error - error in bkg counts
conv_width - range of l in convolution loop (I think this is how many sigmas of to convolve)
step_size - step size for convolution
TODO: I think there might be a better way to do this using ROOT.TMath
"""
if b_error == 0:
return TMath.Gamma(d, b) # Guaranteed to have d > b, so this is equivalent to commonFunctions.h:503
# TODO: Pythonify the following
mean, total_weight = 0.0, 0.0
l = -conv_width
while l <= conv_width:
bcenter = max(0, b + l*b_error)
this_slice_weight = Math.normal_cdf(l + 0.5*step_size) - Math.normal_cdf(l - 0.5*step_size)
this_pval = poisson_pval(d, bcenter)
mean += this_pval*this_slice_weight
total_weight += this_slice_weight
l += step_size
return mean / total_weight
def scat(x, par):
"""
A = par[0]
sigma = par[1]
tau = par[2]
b = par[3]
"""
t0 = par[0]
A = par[1]
sigma = par[2]
tau = par[3]
b = par[4]
dt = (x[0] - t0)
t1 = tau * dt
t3 = sigma * sigma
t5 = tau * tau
t9 = math.exp(-(0.4e1 * t1 - t3) / t5 / 0.4e1)
t10 = 1.77245385090552
t19 = Math.erf((0.2e1 * t1 - t3) / sigma / tau / 0.2e1)
return (A * t9 * t10 * sigma * (t19 + 0.1e1) / 0.2e1 + b)
def CalFtest(fit1, fit2):
print fit1.fitname, fit2.fitname
print 1. - Math.fdistribution_cdf(fit1.chindof / fit2.chindof, fit1.ndof,
fit2.ndof)
continue
if in_ev == 1:
# Check the status of this particle
try:
if line.split()[1] is "1":
# We have a final state particle on this line
s.n_particles += 1
PID_v.push_back(int(line.split()[0]))
P_X_v.push_back(float(line.split()[6]))
P_Y_v.push_back(float(line.split()[7]))
P_Z_v.push_back(float(line.split()[8]))
E_v.push_back(float(line.split()[9]))
M_v.push_back(float(line.split()[10]))
VecLep = Math.LorentzVector('ROOT::Math::PxPyPzE4D<float>')(
float(line.split()[6]), float(line.split()[7]),
float(line.split()[8]), float(line.split()[9]))
P4_v.push_back(VecLep)
pass
pass
except:
pass
if in_wgt == 1:
# <wgt id='rwgt_11'> +2.2580107e-03 </wgt>
# Check the weight
try:
wgt = line.rsplit('>')[1].split()[0]
Wgt_v.push_back(float(wgt))
pass
except:
if tmpJetPTTwo > jetPTCut:
#Counter
if not ifTwoBool:
ifTwoCount += 1
ifTwoBool = True
#Getting the eta dif between the two jets
tmpEtaDif = abs(ev.Jet_eta[i] - ev.Jet_eta[j])
#Checking if the eta dif passes the eta dif cut
if tmpEtaDif > jetEtaDifCut:
#Counter
if not ifThreeBool:
ifThreeCount += 1
ifThreeBool = True
#Getting four vectors for the two jets, using pt, eta, phi, and mass
tmpVecOne = Math.PtEtaPhiMVector(
ev.Jet_pt[i], ev.Jet_eta[i], ev.Jet_phi[i],
ev.Jet_mass[i])
tmpVecTwo = Math.PtEtaPhiMVector(
ev.Jet_pt[j], ev.Jet_eta[j], ev.Jet_phi[j],
ev.Jet_mass[j])
#Adding four vectors together and getting their invariant mass
tmpDiJetVec = tmpVecOne + tmpVecTwo
tmpInvMass = tmpDiJetVec.M()
#Checking if their InvMass passes the InvMass cut
if tmpInvMass > jetInvMassCut:
#Counter
if not ifFourBool:
ifFourCount += 1
ifFourBool = True
#Selecting by summed jet pt
def __call__(self, event):
#corrected electrons to put into the event
corre1s = []
corre2s = []
corrgs = []
Zs = []
Zgs = []
corrPtName1 = self._lep1CorrPt
corrPtName2 = self._lep2CorrPt
corrPtNameG = self._gamCorrPt
corrEtaName1 = self._lep1CorrEta
corrEtaName2 = self._lep2CorrEta
corrEtaNameG = self._gamCorrEta
corrPhiName1 = self._lep1CorrPhi
corrPhiName2 = self._lep2CorrPhi
corrPt_1 = getattr(event, corrPtName1)
corrPt_2 = getattr(event, corrPtName2)
corrPt_G = getattr(event, corrPtNameG)
corrEta_1 = getattr(event, corrEtaName1)
corrEta_2 = getattr(event, corrEtaName2)
corrEta_G = getattr(event, corrEtaNameG)
corrPhi_1 = getattr(event, corrPhiName1)
corrPhi_2 = getattr(event, corrPhiName2)
for i in range(event.N_PATFinalState):
#recalculate the photon vector from the PV
corrgs.append(TLorentzVector())
pv = Math.XYZPoint(event.pvX[i], event.pvY[i], event.pvZ[i])
phoSC = Math.XYZPoint(event.gPositionX[i], event.gPositionY[i],
event.gPositionZ[i])
phoTemp = Math.XYZVector(phoSC.X() - pv.X(),
phoSC.Y() - pv.Y(),
phoSC.Z() - pv.Z())
corrE_G = corrPt_G[i] * math.cosh(corrEta_G[i])
phoP3 = phoTemp.unit() * corrE_G
phoP4 = Math.XYZTVector(phoP3.x(), phoP3.y(), phoP3.z(), corrE_G)
corrgs[-1].SetPtEtaPhiM(phoP4.pt(), phoP4.eta(), phoP4.phi(), 0.0)
#create e1 corrected LorentzVector and error
corre1s.append(TLorentzVector())
pt1 = corrPt_1[i]
eta1 = corrEta_1[i]
phi1 = corrPhi_1[i]
corre1s[-1].SetPtEtaPhiM(pt1, eta1, phi1, self._leptonMass)
#create e2 corrected LorentzVector and error
corre2s.append(TLorentzVector())
pt2 = corrPt_2[i]
eta2 = corrEta_2[i]
phi2 = corrPhi_2[i]
corre2s[-1].SetPtEtaPhiM(pt2, eta2, phi2, self._leptonMass)
#make composite particles
Zs.append(corre1s[-1] + corre2s[-1])
Zgs.append(corre1s[-1] + corre2s[-1] + corrgs[-1])
#add the newly calculated particles back to the event
#using a common naming
setattr(event, 'ell1', corre1s)
setattr(event, 'ell2', corre2s)
setattr(event, 'gam', corrgs)
setattr(event, 'Z', Zs)
setattr(event, 'Zg', Zgs)
def __call__(self, population, signalYield, signalSample, backgroundYield, backgroundSample):
# Histogram holders
signalHistogram = TH1F('signalHistogram', 'signal', self.nbins, 0, 1)
backgroundHistogram = TH1F('backgroundHistogram', 'background', self.nbins, 0, 1)
# Loop over the chromosomes in the population
for genome in population:
# Reset histograms
signalHistogram.Reset()
backgroundHistogram.Reset()
# Get a nn describe by the chromosome (feed foreward)
net = nn.create_ffphenotype(genome)
# Loop over the events creating signal histogram
for event in signalSample:
# Extract variables and weight
variables = event[1:]
weight = event[0]
# Not strictly necessary in feedforward nets
net.flush()
# Net output
output = net.sactivate(variables)[0]
# Filling histograms
signalHistogram.Fill(output, weight)
# Signal overall normalization scale
signalScale = signalYield/len(signalSample)
# Loop over the events creating background histogram
for event in backgroundSample:
# Extract variables and weight
variables = event[1:]
weight = event[0]
# Not strictly necessary in feedforward nets
net.flush()
# Net output
output = net.sactivate(variables)[0]
# Filling histograms
backgroundHistogram.Fill(output, weight)
# Background overall normalization scale
backgroundScale = backgroundYield/len(backgroundSample)
# Random generators
rcount = TRandom3(int(random.uniform(0,65535)))
rsignal = TRandom3(int(random.uniform(0,65535)))
rbackground = TRandom3(int(random.uniform(0,65535)))
zscore = 0.; sqweight = 0.
# Computing weighted z-score
for bin in xrange(1,signalHistogram.GetNbinsX()+1):
newz = 0.; oldz = 0.
# Computing the zvalue per bin
for point in xrange(1,self.mpoints+1):
# Sample background
background = Math.gamma_quantile(rbackground.Uniform(),
(backgroundHistogram.GetBinContent(bin)/backgroundScale)+1., backgroundScale
)
# Background larger that zero
if background > 0.:
# Sampling signal
signal = Math.gamma_quantile(rsignal.Uniform(),
(signalHistogram.GetBinContent(bin)/signalScale)+1., signalScale
)
# Sampling count
count = rcount.Poisson(signal+background)
# Computing pvalue
pvalue = Math.poisson_cdf_c(count,background) + Math.poisson_pdf(count,background)
# Computing zvalue
zvalue = self.minz
if pvalue < 1.0: zvalue = Math.normal_quantile_c(pvalue,1)
# zvalue iterative average
newz = (zvalue + (point - 1)*oldz)/point
# Computing relative difference
error = math.fabs((newz - oldz)/newz)
# Convergency criteria
if error < self.error: break
# Updating oldz
oldz = newz
if point == self.mpoints:
self.message('Warning reach maximum number of integration %s points.' % point)
weight = self.weight(signalHistogram.GetBinCenter(bin))
zscore = zscore + weight * newz
sqweight = sqweight + weight**2
# Fitness function is zscore transform back to 1 - pvalue
# Set the fitness value to the chomosome
genome.fitness = 1. - Math.normal_cdf_c(zscore/Math.sqrt(sqweight))
import copy
from CMGTools.RootTools.physicsobjects.Particle import Particle
#COLIN should make a module for lorentz vectors (and conversions)
#instanciating template
from ROOT import Math
PtEtaPhiE4DLV = Math.PtEtaPhiE4D(float)
PtEtaPhiM4DLV = Math.PtEtaPhiM4D(float)
class PhysicsObject(Particle):
'''Extends the cmg::PhysicsObject functionalities.'''
def __init__(self, physObj):
self.physObj = physObj
super(PhysicsObject, self).__init__()
def __copy__(self):
'''Very dirty trick, the physObj is deepcopied...'''
# print 'call copy', self
physObj = copy.deepcopy( self.physObj )
newone = type(self)(physObj)
newone.__dict__.update(self.__dict__)
newone.physObj = physObj
return newone
def scaleEnergy( self, scale ):
p4 = self.physObj.p4()
p4 *= scale
self.physObj.setP4( p4 )
## p4 = self.physObj.polarP4()
Nzj = zmumuj_data.Get('TotEvts').GetVal()*ztautauj.Get('NormEvts').GetVal()/zmumuj.Get('NormEvts').GetVal()
#Nwt = (Nevts - (Nqcd + Nzj))*(wtOttbar/(1+wtOttbar))
Nwt = powheg_predictions.Get("Wt_dr_xsec").GetVal() * L * totaleff_wt
Nsig = Nevts - Nqcd - Nzj - Nwt
Nbkg = Nqcd + Nzj + Nwt
acc = TFile("/user2/sfarry/workspaces/top/tuples/ttbar_acc.root")
A = acc.Get('acc').GetVal()
A_err = acc.Get('acc_err').GetVal()
xsec = Nsig * A / (totaleff * L )
from math import floor
#poisson uncertainties
alpha = 1 - 0.68268942
Nwt_err_lo = Nwt - Math.gamma_quantile(alpha/2.0, floor(Nwt),1)
Nzj_err_lo = Nzj - Math.gamma_quantile(alpha/2.0, floor(Nzj),1)
Nqcd_err_lo = Nqcd - Math.gamma_quantile(alpha/2.0, floor(Nqcd),1)
Nbkg_err_lo = Nbkg - Math.gamma_quantile(alpha/2.0, floor(Nbkg),1)
Nwt_err_hi = Math.gamma_quantile_c(alpha/2.0, floor(Nwt)+1,1) - Nwt
Nzj_err_hi = Math.gamma_quantile_c(alpha/2.0, floor(Nzj)+1,1) - Nzj
Nqcd_err_hi = Math.gamma_quantile_c(alpha/2.0, floor(Nqcd)+1,1) - Nqcd
Nbkg_err_hi = Math.gamma_quantile_c(alpha/2.0, floor(Nbkg)+1,1) - Nbkg
stat_err = xsec / sqrt(Nevts)
syst_err = xsec * sqrt(pow(totaleff_err / totaleff, 2) + pow(A_err / A, 2) + pow(Nbkg_err_hi/(Nevts - Nbkg),2))
lumi_err = xsec * 0.039
print "Number of selected events: %f +/- %f" %(Nevts, sqrt(Nevts))
print "Same sign background : %f + %f - %f" %(Nqcd, Nqcd_err_hi, Nqcd_err_lo)
def __call__(self, population, signalYield, signalSample, backgroundYield,
backgroundSample):
# Histogram holders
signalHistogram = TH1F('signalHistogram', 'signal', self.nbins, 0, 1)
backgroundHistogram = TH1F('backgroundHistogram', 'background',
self.nbins, 0, 1)
# Loop over the chromosomes in the population
for genome in population:
# Reset histograms
signalHistogram.Reset()
backgroundHistogram.Reset()
# Get a nn describe by the chromosome (feed foreward)
net = nn.create_ffphenotype(genome)
# Loop over the events creating signal histogram
for event in signalSample:
# Extract variables and weight
variables = event[1:]
weight = event[0]
# Not strictly necessary in feedforward nets
net.flush()
# Net output
output = net.sactivate(variables)[0]
# Filling histograms
signalHistogram.Fill(output, weight)
# Signal overall normalization scale
signalScale = signalYield / len(signalSample)
# Loop over the events creating background histogram
for event in backgroundSample:
# Extract variables and weight
variables = event[1:]
weight = event[0]
# Not strictly necessary in feedforward nets
net.flush()
# Net output
output = net.sactivate(variables)[0]
# Filling histograms
backgroundHistogram.Fill(output, weight)
# Background overall normalization scale
backgroundScale = backgroundYield / len(backgroundSample)
# Random generators
rcount = TRandom3(int(random.uniform(0, 65535)))
rsignal = TRandom3(int(random.uniform(0, 65535)))
rbackground = TRandom3(int(random.uniform(0, 65535)))
zscore = 0.
sqweight = 0.
# Computing weighted z-score
for bin in xrange(1, signalHistogram.GetNbinsX() + 1):
newz = 0.
oldz = 0.
# Computing the zvalue per bin
for point in xrange(1, self.mpoints + 1):
# Sample background
background = Math.gamma_quantile(
rbackground.Uniform(),
(backgroundHistogram.GetBinContent(bin) /
backgroundScale) + 1., backgroundScale)
# Background larger that zero
if background > 0.:
# Sampling signal
signal = Math.gamma_quantile(
rsignal.Uniform(),
(signalHistogram.GetBinContent(bin) / signalScale)
+ 1., signalScale)
# Sampling count
count = rcount.Poisson(signal + background)
# Computing pvalue
pvalue = Math.poisson_cdf_c(
count, background) + Math.poisson_pdf(
count, background)
# Computing zvalue
zvalue = self.minz
if pvalue < 1.0:
zvalue = Math.normal_quantile_c(pvalue, 1)
# zvalue iterative average
newz = (zvalue + (point - 1) * oldz) / point
# Computing relative difference
error = math.fabs((newz - oldz) / newz)
# Convergency criteria
if error < self.error: break
# Updating oldz
oldz = newz
if point == self.mpoints:
self.message(
'Warning reach maximum number of integration %s points.'
% point)
weight = self.weight(signalHistogram.GetBinCenter(bin))
zscore = zscore + weight * newz
sqweight = sqweight + weight**2
# Fitness function is zscore transform back to 1 - pvalue
# Set the fitness value to the chomosome
genome.fitness = 1. - Math.normal_cdf_c(
zscore / Math.sqrt(sqweight))
