def compute_snp(collect):
snp = collect[0]
id = collect[1]
# result = []
# Check SNPs for missing values
x = snp[keep].reshape((n,1)) # all the SNPs
v = np.isnan(x).reshape((-1,))
if v.sum():
keeps = True - v
xs = x[keeps,:]
if keeps.sum() <= 1 or xs.var() <= 1e-6:
# PS.append(np.nan)
# TS.append(np.nan)
# result.append(formatResult(id,np.nan,np.nan,np.nan,np.nan))
# continue
return formatResult(id,np.nan,np.nan,np.nan,np.nan)
# Its ok to center the genotype - I used options.normalizeGenotype to
# force the removal of missing genotypes as opposed to replacing them with MAF.
if not options.normalizeGenotype:
xs = (xs - xs.mean()) / np.sqrt(xs.var())
Ys = Y[keeps]
X0s = X0[keeps,:]
Ks = K[keeps,:][:,keeps]
if options.kfile2:
K2s = K2[keeps,:][:,keeps]
Ls = LMM_withK2(Ys,Ks,X0=X0s,verbose=options.verbose,K2=K2s)
else:
Ls = LMM(Ys,Ks,X0=X0s,verbose=options.verbose)
if options.refit:
Ls.fit(X=xs,REML=options.REML)
else:
#try:
Ls.fit(REML=options.REML)
#except: pdb.set_trace()
ts,ps,beta,betaVar = Ls.association(xs,REML=options.REML,returnBeta=True)
else:
if x.var() == 0:
# PS.append(np.nan)
# TS.append(np.nan)
# result.append(formatResult(id,np.nan,np.nan,np.nan,np.nan)) # writes nan values
return formatResult(id,np.nan,np.nan,np.nan,np.nan)
# continue
if options.refit:
L.fit(X=x,REML=options.REML)
# This is where it happens
ts,ps,beta,betaVar = L.association(x,REML=options.REML,returnBeta=True)
return formatResult(id,beta,np.sqrt(betaVar).sum(),ts,ps)
def fitTwo(y, K1, K2, X0=None, wgrids=100):
'''
Simple function to fit a model with two variance components.
It works by running the standard pylmm algorithm in a loop
where at each iteration of the loop a new kinship is generated
as a linear combination of the original two.
'''
# Create a uniform grid
W = np.array(range(wgrids)) / float(wgrids)
Res = []
LLs = []
for w in W:
# heritability will be estimated for linear combo of kinships
K = w * K1 + (1.0 - w) * K2
sys.stderr.write("Fitting weight %0.2f\n" % (w))
L = LMM(y, K, X0=X0)
R = L.fit()
Res.append(R)
LLs.append(R[-1])
del K
L = np.array(LLs)
i = np.where(L == L.max())[0]
if len(i) > 1:
sys.stderr.write("WARNING: Found multiple maxes using first one\n")
i = i[0]
hmax, beta, sigma, LL = Res[i]
w = W[i]
h1 = w * hmax
h2 = (1.0 - w) * hmax
e = (1.0 - hmax)
return h1, h2, e, beta, sigma, LL
def fitTwo(y,K1,K2,X0=None,wgrids=100):
'''
Simple function to fit a model with two variance components.
It works by running the standard pylmm algorithm in a loop
where at each iteration of the loop a new kinship is generated
as a linear combination of the original two.
'''
# Create a uniform grid
W = np.array(range(wgrids)) / float(wgrids)
Res = []
LLs = []
for w in W:
# heritability will be estimated for linear combo of kinships
K = w*K1 + (1.0 - w)*K2
sys.stderr.write("Fitting weight %0.2f\n" % (w))
L = LMM(y,K,X0=X0)
R = L.fit()
Res.append(R)
LLs.append(R[-1])
del K
L = np.array(LLs)
i = np.where(L == L.max())[0]
if len(i) > 1:
sys.stderr.write("WARNING: Found multiple maxes using first one\n")
i = i[0]
hmax,beta,sigma,LL = Res[i]
w = W[i]
h1 = w * hmax
h2 = (1.0 - w) * hmax
e = (1.0 - hmax)
return h1,h2,e,beta,sigma,LL
def compute_snp(j, snp_ids, q=None):
# print(j,len(snp_ids),"\n")
result = []
for snp_id in snp_ids:
# j,snp_id = collect
snp, id = snp_id
# id = collect[1]
# result = []
# Check SNPs for missing values
x = snp[keep].reshape((n, 1)) # all the SNPs
v = np.isnan(x).reshape((-1, ))
if v.sum():
# NOTE: this code appears to be unreachable!
if options.verbose:
sys.stderr.write("Found missing values in " + str(x))
keeps = True - v
xs = x[keeps, :]
if keeps.sum() <= 1 or xs.var() <= 1e-6:
# PS.append(np.nan)
# TS.append(np.nan)
# result.append(formatResult(id,np.nan,np.nan,np.nan,np.nan))
# continue
result.append(formatResult(id, np.nan, np.nan, np.nan, np.nan))
continue
# Its ok to center the genotype - I used options.normalizeGenotype to
# force the removal of missing genotypes as opposed to replacing them with MAF.
if not options.normalizeGenotype:
xs = (xs - xs.mean()) / np.sqrt(xs.var())
Ys = Y[keeps]
X0s = X0[keeps, :]
Ks = K[keeps, :][:, keeps]
if options.kfile2:
K2s = K2[keeps, :][:, keeps]
Ls = LMM_withK2(Ys,
Ks,
X0=X0s,
verbose=options.verbose,
K2=K2s)
else:
Ls = LMM(Ys, Ks, X0=X0s, verbose=options.verbose)
if options.refit:
Ls.fit(X=xs, REML=options.REML)
else:
#try:
Ls.fit(REML=options.REML)
#except: pdb.set_trace()
ts, ps, beta, betaVar = Ls.association(xs,
REML=options.REML,
returnBeta=True)
else:
if x.var() == 0:
# Note: this code appears to be unreachable!
# PS.append(np.nan)
# TS.append(np.nan)
# result.append(formatResult(id,np.nan,np.nan,np.nan,np.nan)) # writes nan values
result.append(formatResult(id, np.nan, np.nan, np.nan, np.nan))
continue
if options.refit:
L.fit(X=x, REML=options.REML)
# This is where it happens
ts, ps, beta, betaVar = L.association(x,
REML=options.REML,
returnBeta=True)
result.append(formatResult(id, beta, np.sqrt(betaVar).sum(), ts, ps))
# compute_snp.q.put([j,formatResult(id,beta,np.sqrt(betaVar).sum(),ts,ps)])
# print [j,result[0]]," in result queue\n"
if not q:
q = compute_snp.q
q.put([j, result])
return j
sys.stderr.write("Loading pre-computed eigendecomposition...\n")
Kva = np.load(options.eigenfile + ".Kva")
Kve = np.load(options.eigenfile + ".Kve")
else:
Kva = []
Kve = []
# CREATE LMM object for association
n = K.shape[0]
if not options.kfile2: L = LMM(Y, K, Kva, Kve, X0, verbose=options.verbose)
else: L = LMM_withK2(Y, K, Kva, Kve, X0, verbose=options.verbose, K2=K2)
# Fit the null model -- if refit is true we will refit for each SNP, so no reason to run here
if not options.refit:
if options.verbose: sys.stderr.write("Computing fit for null model\n")
L.fit()
if options.verbose and not options.kfile2:
sys.stderr.write("\t heritability=%0.3f, sigma=%0.3f\n" %
(L.optH, L.optSigma))
if options.verbose and options.kfile2:
sys.stderr.write("\t heritability=%0.3f, sigma=%0.3f, w=%0.3f\n" %
(L.optH, L.optSigma, L.optW))
def compute_snp(j, snp_ids, q=None):
# print(j,len(snp_ids),"\n")
result = []
for snp_id in snp_ids:
# j,snp_id = collect
snp, id = snp_id
# id = collect[1]
if options.verbose: sys.stderr.write("Loading pre-computed eigendecomposition...\n")
Kva = np.load(options.eigenfile + ".Kva")
Kve = np.load(options.eigenfile + ".Kve")
else:
Kva = []
Kve = []
# CREATE LMM object for association
n = K.shape[0]
if not options.kfile2: L = LMM(Y,K,Kva,Kve,X0,verbose=options.verbose)
else: L = LMM_withK2(Y,K,Kva,Kve,X0,verbose=options.verbose,K2=K2)
# Fit the null model -- if refit is true we will refit for each SNP, so no reason to run here
if not options.refit:
if options.verbose: sys.stderr.write("Computing fit for null model\n")
L.fit()
if options.verbose and not options.kfile2: sys.stderr.write("\t heritability=%0.3f, sigma=%0.3f\n" % (L.optH,L.optSigma))
if options.verbose and options.kfile2: sys.stderr.write("\t heritability=%0.3f, sigma=%0.3f, w=%0.3f\n" % (L.optH,L.optSigma,L.optW))
# Buffers for pvalues and t-stats
PS = []
TS = []
count = 0
out = open(outFile,'w')
printOutHead()
for snp,id in IN:
count += 1
if options.verbose and count % 1000 == 0:
sys.stderr.write("At SNP %d\n" % count)
def compute_snp(j,snp_ids,q = None):
# print(j,len(snp_ids),"\n")
result = []
for snp_id in snp_ids:
# j,snp_id = collect
snp,id = snp_id
# id = collect[1]
# result = []
# Check SNPs for missing values
x = snp[keep].reshape((n,1)) # all the SNPs
v = np.isnan(x).reshape((-1,))
if v.sum():
# NOTE: this code appears to be unreachable!
if options.verbose:
sys.stderr.write("Found missing values in "+str(x))
keeps = True - v
xs = x[keeps,:]
if keeps.sum() <= 1 or xs.var() <= 1e-6:
# PS.append(np.nan)
# TS.append(np.nan)
# result.append(formatResult(id,np.nan,np.nan,np.nan,np.nan))
# continue
result.append(formatResult(id,np.nan,np.nan,np.nan,np.nan))
continue
# Its ok to center the genotype - I used options.normalizeGenotype to
# force the removal of missing genotypes as opposed to replacing them with MAF.
if not options.normalizeGenotype:
xs = (xs - xs.mean()) / np.sqrt(xs.var())
Ys = Y[keeps]
X0s = X0[keeps,:]
Ks = K[keeps,:][:,keeps]
if options.kfile2:
K2s = K2[keeps,:][:,keeps]
Ls = LMM_withK2(Ys,Ks,X0=X0s,verbose=options.verbose,K2=K2s)
else:
Ls = LMM(Ys,Ks,X0=X0s,verbose=options.verbose)
if options.refit:
Ls.fit(X=xs,REML=options.REML)
else:
#try:
Ls.fit(REML=options.REML)
#except: pdb.set_trace()
ts,ps,beta,betaVar = Ls.association(xs,REML=options.REML,returnBeta=True)
else:
if x.var() == 0:
# Note: this code appears to be unreachable!
# PS.append(np.nan)
# TS.append(np.nan)
# result.append(formatResult(id,np.nan,np.nan,np.nan,np.nan)) # writes nan values
result.append(formatResult(id,np.nan,np.nan,np.nan,np.nan))
continue
if options.refit:
L.fit(X=x,REML=options.REML)
# This is where it happens
ts,ps,beta,betaVar = L.association(x,REML=options.REML,returnBeta=True)
result.append(formatResult(id,beta,np.sqrt(betaVar).sum(),ts,ps))
# compute_snp.q.put([j,formatResult(id,beta,np.sqrt(betaVar).sum(),ts,ps)])
# print [j,result[0]]," in result queue\n"
if not q:
q = compute_snp.q
q.put([j,result])
return j
if options.verbose: sys.stderr.write("Loading pre-computed eigendecomposition...\n")
Kva = np.load(options.eigenfile + ".Kva")
Kve = np.load(options.eigenfile + ".Kve")
else:
Kva = []
Kve = []
# CREATE LMM object for association
n = K.shape[0]
if not options.kfile2: L = LMM(Y,K,Kva,Kve,X0,verbose=options.verbose)
else: L = LMM_withK2(Y,K,Kva,Kve,X0,verbose=options.verbose,K2=K2)
# Fit the null model -- if refit is true we will refit for each SNP, so no reason to run here
if not options.refit:
if options.verbose: sys.stderr.write("Computing fit for null model\n")
L.fit()
if options.verbose and not options.kfile2: sys.stderr.write("\t heritability=%0.3f, sigma=%0.3f\n" % (L.optH,L.optSigma))
if options.verbose and options.kfile2: sys.stderr.write("\t heritability=%0.3f, sigma=%0.3f, w=%0.3f\n" % (L.optH,L.optSigma,L.optW))
def compute_snp(j,snp_ids,q = None):
# print(j,len(snp_ids),"\n")
result = []
for snp_id in snp_ids:
# j,snp_id = collect
snp,id = snp_id
# id = collect[1]
# result = []
# Check SNPs for missing values
x = snp[keep].reshape((n,1)) # all the SNPs
v = np.isnan(x).reshape((-1,))
if v.sum():
if options.verbose: sys.stderr.write("Loading pre-computed eigendecomposition...\n")
Kva = np.load(options.eigenfile + ".Kva")
Kve = np.load(options.eigenfile + ".Kve")
else:
Kva = []
Kve = []
# CREATE LMM object for association
n = K.shape[0]
if not options.kfile2: L = LMM(Y,K,Kva,Kve,X0,verbose=options.verbose)
else: L = LMM_withK2(Y,K,Kva,Kve,X0,verbose=options.verbose,K2=K2)
# Fit the null model -- if refit is true we will refit for each SNP, so no reason to run here
#out = open(outFile,'w') ### Joo Change start
if not options.refit:
if options.verbose: sys.stderr.write("Computing fit for null model\n")
L.fit()
if options.verbose and not options.kfile2:
sys.stderr.write("\t heritability=%0.3f, sigma=%0.3f\n" % (L.optH,L.optSigma))
#out.write("%0.5f\t%0.5f\t%0.5f\n" % (L.optH, L.optH, (1-L.optH)))
out.write("%0.5f\t%0.5f\t%0.5f\n" % (L.optH, L.optH*L.optSigma, L.optSigma*(1-L.optH)))
#out.write("heritability=%0.5f, sigma=%0.5f\n" % (L.optH,L.optSigma))
#out.write("varG=%0.5f, varE=%0.5f\n" %(L.optH*L.optSigma, L.optSigma*(1-L.optH)))
if options.verbose and options.kfile2:
sys.stderr.write("\t heritability=%0.3f, sigma=%0.3f, w=%0.3f\n" % (L.optH,L.optSigma,L.optW))
#out.write("%0.5f\t%0.5f\t%0.5f\n" % (L.optH, L.optH, (1-L.optH)))
out.write("%0.5f\t%0.5f\t%0.5f\n" % (L.optH, L.optH*L.optSigma, L.optSigma*(1-L.optH)))
#out.write("heritability=%0.5f, sigma=%0.5f\n" % (L.optH,L.optSigma))
#out.write("varG=%0.5f, varE=%0.5f\n" %(L.optH*L.optSigma, L.optSigma*(1-L.optH)))
# Buffers for pvalues and t-stats
PS = []