def valid_covalue(data, parts):
count = 0
total = 0
for i in range(0, len(parts) - 1):
for j in range(i + 1, len(parts)):
for partone in range(0, len(parts[i])):
for parttwo in range(0, len(parts[j])):
left_i = parts[i][partone]
right_i = parts[j][parttwo]
left = data[left_i].astype(bool)
right = data[right_i].astype(bool)
k = np.count_nonzero(np.bitwise_and(left, right))
prb = hypergeom.cdf(k, len(left), np.count_nonzero(left),
np.count_nonzero(right))
if 1 - prb < 0.05:
count += 1
total += 1
print 'false positive %d' % ((1.0 * count) / total)
count = 0
total = 0
for i in range(0, len(parts)):
for k in range(0, len(parts[i])):
for j in range(k, len(parts[i])):
left_i = parts[i][k]
right_i = parts[i][j]
left = data[left_i].astype(bool)
right = data[right_i].astype(bool)
k = np.count_nonzero(np.bitwise_and(left, right))
prb = hypergeom.cdf(k, len(left), np.count_nonzero(left),
np.count_nonzero(right))
if 1 - prb > 0.05:
count += 1
total += 1
print 'true positive %d' % (1.0 * count / total)
def get_dic_pvalue(dic_fasta, dic_control, ctrl_all, fasta_all):
"""
Calculate the p-value with an hypergeomtric test of the count
of the hexanucleotide, di-nucleotide, codon, codon position nucleotides,
amino acids, or others in a control set of exons and the exons in the fasta file
:param dic_fasta:(dictionary of int) the count of the hexanucleotide, di-nucleotide,
codon, codon position nucleotides, amino acids, or others in the fasta file given by the user
:param dic_control:(dictionary of int) the count of the hexanucleotide, di-nucleotide,
codon, codon position nucleotides, amino acids, or others in the control exons (exons CCE/ALL/ACE of fasterDB)
:param ctrl_all: (int) the total number of the hexanucleotide, di-nucleotide,
codon, codon position nucleotides, amino acids, or others in the control set of exons
:param fasta_all:(int) the total number of the hexanucleotide, di-nucleotide,
codon, codon position nucleotides, amino acids, or others in the fasta file
:return: (dictionary of float) for each element give it's calculated p-value
"""
p_val = {}
for key in dic_fasta.keys():
p1 = hypergeom.cdf(dic_fasta[key], ctrl_all, dic_control[key], fasta_all)
p2 = 1 - hypergeom.cdf(dic_fasta[key], ctrl_all, dic_control[key], fasta_all)
if p1 < p2:
p_val[key] = p1
else:
p_val[key] = p2
return p_val
def test_hypergeometric():
assert_almost_equal(hypergeometric(4, 10, 5, 6, 'greater'),
1 - hypergeom.cdf(3, 10, 5, 6))
assert_almost_equal(hypergeometric(4, 10, 5, 6, 'less'),
hypergeom.cdf(4, 10, 5, 6))
assert_almost_equal(hypergeometric(4, 10, 5, 6, 'two-sided'),
2 * (1 - hypergeom.cdf(3, 10, 5, 6)))
def test_hypergeometric():
"""Clopper-Pearson."""
np.testing.assert_almost_equal(hypergeometric(4, 10, 5, 6, 'greater'),
1 - hypergeom.cdf(3, 10, 5, 6))
np.testing.assert_almost_equal(hypergeometric(4, 10, 5, 6, 'less'),
hypergeom.cdf(4, 10, 5, 6))
np.testing.assert_almost_equal(hypergeometric(4, 10, 5, 6, 'two-sided'),
2 * (1 - hypergeom.cdf(3, 10, 5, 6)))
def hypergeom_conf_interval(n, x, N, cl=0.975, alternative="two-sided", G=None,
**kwargs):
"""
Confidence interval for a hypergeometric distribution parameter G, the number of good
objects in a population in size N, based on the number x of good objects in a simple
random sample of size n.
Parameters
----------
n : int
The number of draws without replacement.
x : int
The number of "good" objects in the sample.
N : int
The number of objects in the population.
cl : float in (0, 1)
The desired confidence level.
alternative : {"two-sided", "lower", "upper"}
Indicates the alternative hypothesis.
G : int in [0, N]
Starting point in search for confidence bounds for the hypergeometric parameter G.
kwargs : dict
Key word arguments
Returns
-------
tuple
lower and upper confidence level with coverage (at least)
1-alpha.
Notes
-----
xtol : float
Tolerance
rtol : float
Tolerance
maxiter : int
Maximum number of iterations.
"""
assert alternative in ("two-sided", "lower", "upper")
if G is None:
G = (x / n)*N
ci_low = 0
ci_upp = N
if alternative == 'two-sided':
cl = 1 - (1-cl)/2
if alternative != "upper" and x > 0:
f = lambda q: cl - hypergeom.cdf(x-1, N, q, n)
ci_low = math.ceil(brentq(f, 0.0, G, *kwargs))
if alternative != "lower" and x < n:
f = lambda q: hypergeom.cdf(x, N, q, n) - (1-cl)
ci_upp = math.floor(brentq(f, G, N, *kwargs))
return ci_low, ci_upp
def hypergeom_conf_interval(n, x, N, cl=0.975, alternative="two-sided", G=None,
**kwargs):
"""
Confidence interval for a hypergeometric distribution parameter G, the number of good
objects in a population in size N, based on the number x of good objects in a simple
random sample of size n.
Parameters
----------
n : int
The number of draws without replacement.
x : int
The number of "good" objects in the sample.
N : int
The number of objects in the population.
cl : float in (0, 1)
The desired confidence level.
alternative : {"two-sided", "lower", "upper"}
Indicates the alternative hypothesis.
G : int in [0, N]
Starting point in search for confidence bounds for the hypergeometric parameter G.
kwargs : dict
Key word arguments
Returns
-------
tuple
lower and upper confidence level with coverage (at least)
1-alpha.
Notes
-----
xtol : float
Tolerance
rtol : float
Tolerance
maxiter : int
Maximum number of iterations.
"""
assert alternative in ("two-sided", "lower", "upper")
if G is None:
G = (x / n) * N
ci_low = 0
ci_upp = N
if alternative == 'two-sided':
cl = 1 - (1 - cl) / 2
if alternative != "upper" and x > 0:
f = lambda q: cl - hypergeom.cdf(x - 1, N, q, n)
ci_low = math.ceil(brentq(f, 0.0, G, *kwargs))
if alternative != "lower" and x < n:
f = lambda q: hypergeom.cdf(x, N, q, n) - (1 - cl)
ci_upp = math.floor(brentq(f, G, N, *kwargs))
return ci_low, ci_upp
def score(self, x_t: Union[np.ndarray, Any]) -> np.ndarray:
"""
Compute the test-statistic (FET) between the reference window(s) and test window.
If a given test-window is not yet full then a test-statistic of np.nan is returned for that window.
Parameters
----------
x_t
A single instance.
Returns
-------
Estimated FET test statistics (1-p_val) between reference window and test windows.
"""
values = set(np.unique(x_t))
if not set(values).issubset(['0', '1', True, False]):
raise ValueError(
"The `x_t` data must consist of only (0,1)'s or (False,True)'s for the "
"FETDriftOnline detector.")
x_t = super()._preprocess_xt(x_t)
self._update_state(x_t)
stats = np.zeros((len(self.window_sizes), self.n_features),
dtype=np.float32)
for k, ws in enumerate(self.window_sizes):
if self.t >= ws:
sum_last_ws = np.sum(self.xs[-ws:, :], axis=0)
# Perform FET with hypergeom.cdf (this is vectorised over features)
if self.alternative == 'greater':
p_vals = hypergeom.cdf(self.sum_ref, self.n + ws,
self.sum_ref + sum_last_ws, self.n)
else:
p_vals = hypergeom.cdf(sum_last_ws, self.n + ws,
self.sum_ref + sum_last_ws, ws)
# Compute test stat and apply smoothing
stats_k = 1 - p_vals
for f in range(self.n_features):
if len(self.test_stats) != 0 and not np.isnan(
self.test_stats[-1, k, f]):
stats_k[f] = (1 - self.lam) * self.test_stats[
-1, k, f] + self.lam * stats_k[f]
stats[k, :] = stats_k
else:
stats[k, :] = np.nan
return stats
def enrichment(geneList1, geneList2, allGenes):
tmp = set(geneList1).intersection(geneList2)
x = len(tmp)
M = allGenes
n = len(geneList1)
N = len(geneList2)
return [x,tmp,M,n,N,1-hypergeom.cdf(x, M, n, N)]
def _TEST_(block, exptotal, bkgtotal, pseudo_count):
sigPoi = 0
sigHyp = 0
ind = block.index
for i in block.index:
lamda = block.loc[i, 'BkgHop_withBonus']
obs = block.loc[i, 'ExpHop_withBonus']
BkgHop = block.loc[i, 'BkgHop']
ExpHop = block.loc[i, 'ExpHop']
P_poisson = 1 - poisson.cdf(int(obs) - 1, lamda + pseudo_count)
if int(BkgHop) < 100000000 and int(ExpHop) < 100000000:
P_hyper = 1 - hypergeom.cdf(ExpHop - 1,
(bkgtotal + exptotal), exptotal,
(ExpHop + BkgHop))
else:
P_hyper = '***'
block.loc[i, 'BkgFraction'] = float(BkgHop / bkgtotal)
block.loc[i, 'ExpFraction'] = float(ExpHop / exptotal)
block.loc[i, 'P_Hyper'] = P_hyper
block.loc[i, 'P_Poisson'] = P_poisson
if P_poisson < alpha and lamda * obs != 0:
sigPoi = sigPoi + 1
if P_hyper < alpha:
sigHyp = sigHyp + 1
return block, sigPoi, sigHyp
def hypergeom_test(data, sort_fdr=True):
p_value_list = []
ratio_in_study_list = []
ratio_in_pop_list = []
classes = []
hit_genes = []
hit_links = []
path_names, typeIIs, typeIs = list(), list(), list()
for study_hitnumber, pop_number, pop_hitnumber, study_number, each_class, associated_diff_info, link, path_name, typeII, typeI in data:
p_value = 1 - hypergeom.cdf(study_hitnumber - 1, pop_number, pop_hitnumber, study_number)
ratio_in_study = str(study_hitnumber) + '/' + str(study_number)
ratio_in_pop = str(pop_hitnumber) + '/' + str(pop_number)
p_value_list.append(p_value)
ratio_in_study_list.append(ratio_in_study)
ratio_in_pop_list.append(ratio_in_pop)
classes.append(each_class)
hit_genes.append(associated_diff_info)
hit_links.append(link)
path_names.append(path_name)
typeIIs.append(typeII)
typeIs.append(typeI)
q_value_list = multipletests(p_value_list, method='fdr_bh')[1]
number = len(q_value_list)
# print(number)
databases = ['KEGG PATHWAY'] * number
result = zip(path_names, databases, classes, ratio_in_study_list, ratio_in_pop_list, p_value_list, q_value_list,
hit_genes, hit_links, typeIIs, typeIs)
if sort_fdr:
sorted_result = sorted(result, key=lambda x: (x[6], x[5]))
else:
sorted_result = sorted(result, key=lambda x: (x[5], x[6]))
# num = sum([1 for x in p_value_list if x < 1])
# return sorted_result[0:num]
return sorted_result
def co_test_single(self, i, j):
left = self.data[i].astype(bool)
right = self.data[j].astype(bool)
k = np.count_nonzero(np.bitwise_and(left, right))
prb = hypergeom.cdf(k, len(left), np.count_nonzero(left),
np.count_nonzero(right))
return 1 - prb
def test_hypergeom_cdf_lower(self):
# check hypergeom cdf to return right value
from scipy.stats import hypergeom
h = HyperCI(n_pop=100, n_draw=20, k_s_obs=5)
k_s = 30
res = hypergeom.cdf(h.k_s_obs, h.n_pop, k_s, h.n_draw)
self.assertEqual(res, 0.4009887932548518)
def run_analysis(self,
pvalue_cutoff: float = 0.05,
method: str = "hyperg",
limiter: int = 0) -> pd.DataFrame:
results = []
population = self.pathway_data["population"]
num_cpds = len(self.compound_list)
for pathway in self.pathway_data["pathways"]:
pth_info = self.pathway_data["pathways"][pathway]
pth_name = pth_info["name"]
dbids = list(pth_info["compounds"].keys())
pth_cpds = [pth_info["compounds"][x] for x in dbids]
num_dbids = len(dbids)
if num_dbids >= limiter:
pathway_hits = self._check_if_in_pathway(pth_cpds)
num_hits = len(pathway_hits)
if method == "hyperg":
p_value = 1 - hypergeom.cdf(num_hits - 1, population -
num_dbids, num_cpds, num_dbids)
else:
_, p_value = fisher_exact(
[[num_hits, num_cpds - num_hits],
[
num_dbids - num_hits,
((population - num_dbids) - num_cpds) + num_hits
]])
in_pathway_str = self._generate_string(pathway_hits, dbids)
importance = self._calc_cov(num_hits, num_dbids)
results.append([
pathway, pth_name, num_hits, num_dbids, p_value,
importance, in_pathway_str
])
results = pd.DataFrame(results,
columns=[
"Pathway ID", "Pathway Name", "Hits",
"Pathway Compounds", "p", "Coverage",
"Identifiers"
])
results.set_index("Pathway ID", inplace=True)
_, holm_p, _, _ = multipletests(results["p"].values, method="holm")
results.insert(4, "Holm p", holm_p)
results = results[results["Holm p"] <= pvalue_cutoff]
results.sort_values("p", inplace=True)
self.results = results
def Random_strongInteraction(part1, part2, cluster_pool1, cluster_pool2):
global min_interaction, p_value
''' This is for counputing FDR using random permutation '''
c_interaction = {}
for i in range(len(part1)):
region1 = str(part1[i])
region2 = str(part2[i])
inter = "%d--%d" % (part1[i].cluster, part2[i].cluster)
if c_interaction.has_key(inter):
c_interaction[inter] += 1
else:
c_interaction[inter] = 0
k = 0 # record for strong interactions
n = 0
for interaction in c_interaction:
n = n + 1
count = c_interaction[interaction]
if count < min_interaction: continue
i = int(interaction.split("--")[0])
j = int(interaction.split("--")[1])
try: # we select clusters with size no less than 5, so some interactions cannot be found in clusters
count1 = cluster_pool1[i].cluster
count2 = cluster_pool2[j].cluster
except:
continue
real_p = 1 - hypergeom.cdf(count, len(part1), count1, count2)
if real_p <= p_value:
k = k + 1
return [n, k]
def hyperConfidence(db, antc, consq):
total = db.shape[0]
cxy = raMetricas.abSupp(db, antc, consq)
cx = raMetricas.abSupp(db, antc)
cy = raMetricas.abSupp(db, consq)
result = hypergeom.cdf(k=cxy - 1, M=total, n=cy, N=cx)
return result
def calc_hyp(node_list, cui_to_genes, N, Q):
n = len(node_list)
(assoc_count, assoc_genes) = get_assoc(node_list)
assoc_analy = []
for (a, k) in assoc_count.items():
K = len(cui_to_genes[a])
prb = 1 - hypergeom.cdf(k, N, K, n)
assoc_analy.append([a, k, K, prb])
# Q = 0.001
sort_assoc = sorted(assoc_analy, key=lambda x: (x[3], x[0]))
m = len(sort_assoc)
mhc_assoc = []
for (i, [a, k, K, prb]) in enumerate(sort_assoc):
BH = (float(i + 1) /
m) * Q # calculate Benjamini-Hochberg based on ranked data
mhc_assoc.append([i + 1, a, k, K, prb, BH])
sig_assoc = []
for [rank, phen, assnet, assint, prb, BH] in mhc_assoc:
if prb < BH and assint > 24:
genes = sorted(assoc_genes[phen])
gene_str = ','.join(genes)
phen_term = cui_to_phens[phen][
0] # use the first phenotype as the descriptor
sig_assoc.append(
[rank, phen_term, phen, assnet, assint, prb, BH, gene_str])
elif prb > BH:
break
return sig_assoc
def Random_strongInteraction(part1,part2,cluster_pool1,cluster_pool2):
global min_interaction, p_value
''' This is for counputing FDR using random permutation '''
c_interaction={}
for i in range(len(part1)):
region1=str(part1[i])
region2=str(part2[i])
inter="%d--%d"%(part1[i].cluster,part2[i].cluster)
if c_interaction.has_key(inter):
c_interaction[inter]+=1
else:
c_interaction[inter]=0
k=0 # record for strong interactions
n=0
for interaction in c_interaction:
n=n+1
count=c_interaction[interaction]
if count<min_interaction: continue
i=int(interaction.split("--")[0])
j=int(interaction.split("--")[1])
try: # we select clusters with size no less than 5, so some interactions cannot be found in clusters
count1=cluster_pool1[i].cluster
count2=cluster_pool2[j].cluster
except:
continue
real_p=1-hypergeom.cdf(count,len(part1),count1,count2)
if real_p<=p_value:
k=k+1
return [n,k]
def zeta(L, s, Nmutated, a):
# zeta(L,s,Nmut,a)=P[H(L+Nmut,L-Nmut,s) >= a]
# i.e. the tail of a hypergeometric distribution
# in the manuscript, zeta(L,s,n,a) is F_n(a) for a given L and s
#
# see
# https://docs.scipy.org/doc/scipy/reference/generated/scipy.stats.hypergeom.html#scipy.stats.hypergeom
#
# hypergeom.cdf(k,M,n,N)
# k = number of red balls drawn = a-1 (not a)
# M = total number of balls = L+Nmutated
# n = number of red balls = L-Nmutated
# N = number of draws = s
#if (showZetaCalls):
# callStr = "zeta(%s,%s,%s,%s) = 1-hypergeom.cdf(%s,%s,%s,%s) = %.12f" \
# % (L,s,Nmutated,a,
# a-1,L+Nmutated,L-Nmutated,s,
# 1 - hypergeom.cdf(a-1,L+Nmutated,L-Nmutated,s))
# cacheKey = (L,s,Nmutated,a)
# if (cacheKey in zeta_cache): callStr += " (from cache)"
# print(callStr,file=stderr)
if (useCache):
cacheKey = (L, s, Nmutated, a)
if (cacheKey in zeta_cache):
return zeta_cache[cacheKey]
p = 1 - hypergeom.cdf(a - 1, L + Nmutated, L - Nmutated, s)
if (useCache):
zeta_cache[cacheKey] = p
return p
def pval(R, n_basepairs, q_size):
t = R[:,0]
pvals = np.zeros(len(t))
for i in range(0, len(t)):
pvals[i] = hypergeom.cdf(t[i], n_basepairs, q_size, R[i,2])
return 1 - pvals
def specificities(freqMotifParDep):
"""
Calcule la spécificité du motif dans chaque département
- entrée : dataframe contenant la fréquence du motif recherché par département
- sortie : dictionnaire contenant pour chaque département la spécificité du motif
"""
freqTot = 31868064
freqTotParDep = pd.read_hdf('./static/freqByDep.hdf', 'freqTokensByDep')
freqTotMotif = freqMotifParDep.sum().sum()
df_freqTotMotif = pd.DataFrame(freqMotifParDep.sum(axis=1), columns=["0"])
# Calcul de la fréquence attendue du motif dans chaque département
expectedCounts = df_freqTotMotif.dot(freqTotParDep) / freqTot
specif = freqMotifParDep.copy()
"""
Pour chaque département, la spécificité du motif est calculée à partir de :
- la fréquence du motif dans le département en question (à partir de freqMotifParDep)
- la fréquence totale de tous les tokens (freqTot)
- la fréquence totale du motif (freqTotMotif)
- la fréquence totale de tous les tokens dans le département (à partir de freqTotParDep)
"""
for dep in freqMotifParDep.columns:
if (freqMotifParDep.loc["freq", dep] < expectedCounts.loc["freq",
dep]):
specif.loc["freq",
dep] = hypergeom.cdf(freqMotifParDep.loc["freq", dep],
freqTot, freqTotMotif,
freqTotParDep.transpose().loc[dep])
else:
specif.loc["freq", dep] = 1 - hypergeom.cdf(
freqMotifParDep.loc["freq", dep] - 1, freqTot, freqTotMotif,
freqTotParDep.transpose().loc[dep])
specif = np.log10(specif)
specif[freqMotifParDep >=
expectedCounts] = -specif[freqMotifParDep >= expectedCounts]
# Les valeurs qui ne sont pas entre -10 et 10 sont tronquées
for dep in specif:
specif.loc[specif[dep] > 10, dep] = 10
specif.loc[specif[dep] < -10, dep] = -10
specif.rename(index={"freq": "specif"}, inplace=True)
specif = pd.DataFrame.to_dict(specif)
return specif
def cHgPvl(x,M,n,N):
"""
x=randVar
M=popSize
n=totalSuccesses
N=samplSize
"""
return 1-hypergeom.cdf(x,M,n,N)+hypergeom.pmf(x,M,n,N)
def _hypergeom_wrapper(self, x):
from scipy.stats import hypergeom
p = hypergeom.cdf(x['lonely triplets at pos'],
x['Num Triplets at Gene'],
x['lonely triplets at gen'],
x['Num Triplets at Pos'])
return p
def compHyperGemP(hits, bg_all, bg_hits, query_size):
'''
Returns P(X>=occ);fold-enrichment
'''
p = 1 - hypergeom.cdf(hits - 1, bg_all, bg_hits,
query_size) # calculates P(X>=occ)
fe = hits / ((bg_hits / bg_all) * query_size)
return p, fe
def GO_enrichment(geneList, ontology, expressedGenes = None, printIt=False, pCut = 1000000, xRef = {}):
lenAllGenes, lenTheseGenes = len(expressedGenes), len(geneList)
pValues = defaultdict()
nCmps = 0
for GOTerm, GOGenes in ontology.items():
inBoth = GOGenes['genes'].intersection(geneList)
expressedGOGenes = GOGenes['genes'].intersection(expressedGenes)
if len(inBoth) <= 3 or len(expressedGOGenes) < 5:
pValues[GOTerm] = 'notest'
continue
pVal = (1.-hypergeom.cdf(len(inBoth), lenAllGenes, len(expressedGOGenes), lenTheseGenes))
if pVal < 0:
pVal = 0
symbols = []
for ensg in inBoth:
if ensg in xRef:
symbols.append(xRef[ensg])
else:
symbols.append(ensg)
pValues[GOTerm] = (pVal, len(inBoth), len(expressedGOGenes), len(GOGenes['genes']), inBoth, symbols)
for k, v in pValues.items():
try:
pValues[k][0] = v * float(nCmps) #bonferroni correction
except:
pass
import operator
y = []
sorted_x = sorted(pValues.iteritems(), key=operator.itemgetter(1))
for k, v in sorted_x:
if v == "notest":
continue
if not type(k) == str:
continue
try:
if v[0] > pCut:
continue
if printIt:
[k, "|".join(ontology[k]['name']), v[0], v[1], v[2], v[3], ",".join(v[4]), ",".join(v[5])]
#print k, "|".join(ontology[k]['name']), "%.3e" %v[0], v[1], v[2], v[3], "|".join(v[3])
y.append([k, "|".join(ontology[k]['name']), v[0], v[1], v[2], v[3], ",".join(v[4]), ",".join(v[5])])
except:
pass
try:
df = pd.DataFrame(y, columns=['GO Term ID', 'GO Term Description', 'Bonferroni-corrected Hypergeometric p-Value', 'N Genes in List and GO Category', 'N Expressed Genes in GO Category', 'N Genes in GO category', 'Ensembl Gene IDs in List', 'Gene symbols in List'])
df.set_index('GO Term ID', inplace=True)
except:
df = pd.DataFrame(None, columns=['GO Term ID', 'GO Term Description', 'Bonferroni-corrected Hypergeometric p-Value', 'N Genes in List and GO Category', 'N Expressed Genes in GO Category', 'N Genes in GO category', 'Ensembl Gene IDs in List', 'Gene symbols in List'])
return df
def get_pa(N, n, c, p):
"""
Get the probability of acceptance
N = lot size
n = sample size
c = tolerable defective rate
p = defective rate
"""
return hypergeom.cdf(c, N, N * p, n)
def summary_to_hypergeometric_pvals(summary):
#sys.stderr.write("C1\n")
hypergeometric_pvals = {}
for dbk in dbs.keys():
#if dbk != 'jaspar':
# continue
for p in paddings:
# reduce padding-specific tuples in summary[k][p] to find TF indices where there are overlaps
tf_overlaps = {}
ordered_tfs = summary[dbk]['ordered_tfs']
mapped_tfs = summary[dbk]['mapped_tfs']
totals = summary[dbk]['totals']
tups = summary[dbk][str(p)]
for tup in tups:
(probe, bitstring) = tup
bits = list(bitstring)
for idx, bit in enumerate(bits):
if bit == '1':
if ordered_tfs[idx] not in tf_overlaps:
tf_overlaps[ordered_tfs[idx]] = 0
tf_overlaps[ordered_tfs[idx]] += 1
#print(tf_overlaps)
# use these indices to count TF-overlap totals over set of probes, and then over all probes via summary[k]['totals']
all_overlaps = {}
for tfk in tf_overlaps.keys():
idx = mapped_tfs[tfk]
all_overlaps[tfk] = totals[idx]
#print(all_overlaps)
# for each TF, calculate a hypergeometric p-value
for tfk in tf_overlaps.keys():
# number of probes ("balls") in probe-subset ("sample") that overlap TF (sample of "red balls")
x = int(tf_overlaps[tfk])
# number of probes ("balls") in set ("urn") ("all balls, black and red")
M = int(total_number_of_probes)
# number of probes in set ("urn") that overlap TF (all "red balls")
n = int(all_overlaps[tfk])
# number of probes in probe-subset ("sample")
N = int(len(probes))
#print('\t'.join([tfk, str(x), str(M), str(n), str(N)]))
pval = 1.0 - hypergeom.cdf(x, M, n, N)
if pval == 0.0:
pval = 2.2250738585072014e-308
ip = str(p)
if dbk not in hypergeometric_pvals:
hypergeometric_pvals[dbk] = {}
if ip not in hypergeometric_pvals[dbk]:
hypergeometric_pvals[dbk][ip] = []
hypergeometric_pvals[dbk][ip].append({
'id': tfk,
'score': pval
})
#sys.stderr.write("C2\n")
return hypergeometric_pvals
def diff_of_tail_area_and_cl(self, k_s_x, lf='left'):
"""
Calculate left/right tail probability minus (confidence level)*0.5 for hypergeometric distribution.
:param k_s_x: number of success in the population
:param lf: left tail or right tail
:return:
when lf='left' it returns sum of density among [0:k_s_t+1] minus (confidence level) *0.5
when lf='right' it returns sum of density [k_s_t:n_pop+1] minus (confidence level) *0.5
"""
if lf == 'left': # left tailを計算
return abs(
hypergeom.cdf(self.k_s_obs, self.n_pop, k_s_x, self.n_draw) -
self.cl * 0.5)
elif lf == 'right': # right tailを計算
return abs(1 - hypergeom.cdf(self.k_s_obs -
1, self.n_pop, k_s_x, self.n_draw) -
self.cl * 0.5)
else:
raise TypeError('lf must be "left" or "right"')
def hypergeom_function(white_balls_drawn, population, white_balls_in_population, total_balls_drawn): """ hypergeometric function for probability value @param white_balls_drawn -- associated gene in input genesubset @param population -- population (here use the offical home sapiens genes in NCBI) @param white_balls_in_population -- assoicated genes in population @param total_balls_drawn -- input genelist size """ prob = 1-hypergeom.cdf(white_balls_drawn-1, population, white_balls_in_population, total_balls_drawn) return prob
def _hypergeom_wrapper(self, x):
from scipy.stats import hypergeom
p = hypergeom.cdf(
x["lonely triplets at pos"],
x["Num Triplets at Gene"],
x["lonely triplets at gen"],
x["Num Triplets at Pos"],
)
return p
def calculate_enrichment(genes_file,
peaks_file,
clusters,
n_genes,
working_dir,
distance=None,
report_entire_feature=False,
bedtools_exe="bedtools"):
"""
Calculate enrichment for a single peak set and distance
genes_file (str): path to BED file with all genes
distance (int): distance to calculate enrichments at
peaks_file (list): BED file containing the ChIP-seq peaks
clusters (list): cluster files
n_genes (int): total number of genes in the genes BED file
report_entire_feature (bool): if True then run intersectBed
with the -wa option (to report the entire feature, not just
the overlap)
bedtools_exe (str): 'bedtools' executable to use
Returns tuple (pvalue,counts) i.e. col1 for p-val, col2 for
number of genes)
"""
# Initialise result arrays
pvalues = np.zeros([len(clusters)])
counts = np.zeros([len(clusters)])
# Get set of genes overlapping this peak set for this distance
overlap_genome = get_overlapping_genes(
genes_file,
peaks_file,
distance,
working_dir=working_dir,
report_entire_feature=report_entire_feature)
# Find subsets of overlapping genes in each RNA-seq cluster
# and calculate enrichments
for i, cluster_file in enumerate(clusters):
# Read cluster file
genes_cls = set(
np.loadtxt(cluster_file,
delimiter='\t',
ndmin=1,
usecols=[0],
dtype=np.str))
# No. of genes in current cluster (sample size)
n = len(genes_cls)
# Total number of overlapping genes (for set of all genes)
K_i = len(overlap_genome)
# Genes from the input regions based set, which are also in this cluster
n_i = len(overlap_genome.intersection(genes_cls))
# Calculate and store enrichment from hypergeometric function
pvalues[i] = max(MIN_PVALUE, 1.0 - hg.cdf(n_i - 1, n_genes, n, K_i))
counts[i] = n_i
return (pvalues, counts)
def _one_fit(self):
print("\nCreating downsampled doublets...")
self._createDoublets()
# Normalize combined augmented set
print("Normalizing...")
aug_counts = self.normalizer(
np.append(self._raw_counts, self._raw_synthetics, axis=0))
self._norm_counts = aug_counts[:self._num_cells]
self._synthetics = aug_counts[self._num_cells:]
print("Running PCA...")
# Get phenograph results
pca = PCA(n_components=self.n_components)
print("Clustering augmented data set with Phenograph...\n")
reduced_counts = pca.fit_transform(aug_counts)
fullcommunities, _, _ = phenograph.cluster(
reduced_counts, **self.phenograph_parameters)
min_ID = min(fullcommunities)
self.communities_ = fullcommunities[:self._num_cells]
self.synth_communities_ = fullcommunities[self._num_cells:]
community_sizes = [
np.count_nonzero(fullcommunities == i)
for i in np.unique(fullcommunities)
]
print("Found communities [{0}, ... {2}], with sizes: {1}\n".format(
min(fullcommunities), community_sizes, max(fullcommunities)))
# Count number of fake doublets in each community and assign score
# Number of synth/orig cells in each cluster.
synth_cells_per_comm = collections.Counter(self.synth_communities_)
orig_cells_per_comm = collections.Counter(self.communities_)
community_IDs = orig_cells_per_comm.keys()
community_scores = {
i: float(synth_cells_per_comm[i]) /
(synth_cells_per_comm[i] + orig_cells_per_comm[i])
for i in community_IDs
}
scores = np.array([community_scores[i] for i in self.communities_])
community_p_values = {
i: hypergeom.cdf(synth_cells_per_comm[i], aug_counts.shape[0],
self._synthetics.shape[0],
synth_cells_per_comm[i] + orig_cells_per_comm[i])
for i in community_IDs
}
p_values = np.array([community_p_values[i] for i in self.communities_])
if min_ID < 0:
scores[self.communities_ == -1] = np.nan
p_values[self.communities_ == -1] = np.nan
return scores, p_values
def hypergeom(self, white_balls_drawn, population,
white_balls_in_population, total_balls_drawn):
"""
hypergeometric function for probability value
@param white_balls_drawn -- associated gene in input genesubset
@param population -- population (here use the offical home sapiens genes in NCBI)
@param white_balls_in_population -- assoicated genes in population
@param total_balls_drawn -- input genelist size
"""
prob = 1 - hypergeom.cdf(white_balls_drawn - 1, population,
white_balls_in_population, total_balls_drawn)
return prob
def specificities(lexicalTable,annotationType):
from scipy.stats import hypergeom
M=lexicalTable.sum().sum()
lengths=pd.DataFrame(lexicalTable.sum())
freq=pd.DataFrame(lexicalTable.sum(axis=1))
expectedCounts=(freq.dot(lengths.transpose()))/M
specif=lexicalTable.copy()
for part in lexicalTable.columns:
sys.stdout.write("\r5/6 - "+annotationType+" - Calcul des spécificités pour le département "+str(part))
for word in lexicalTable.index:
if lexicalTable.loc[word,part]<expectedCounts.loc[word,part] :
specif.loc[word,part]=hypergeom.cdf(lexicalTable.loc[word,part],M, freq.loc[word], lengths.loc[part])
else:
specif.loc[word,part]=1-hypergeom.cdf(lexicalTable.loc[word,part]-1,M, freq.loc[word], lengths.loc[part])
specif=np.log10(specif)
specif[lexicalTable>=expectedCounts]=-specif[lexicalTable>=expectedCounts]
sys.stdout.write("\n")
# si on veut des valeurs tronquées
for dep in specif :
specif.loc[specif[dep] > 10,dep] = 10
specif.loc[specif[dep] < -10,dep] = -10
return specif
def accumulative_hypergeometric(k, n, K, N):
'''
[k]: SUCCESS IN THE CLUSTER
[n]: SIZE OF THE CLUSTER
[K]: SUCCESS IN POPULATION
[N]: SIZE OF THE POPULATION
'''
k, n, K, N = int(k), int(n), int(K), int(N)
sf = hyp.sf(k, N, K, n)
if sf < 1:
return sf + hyp.pmf(k, N, K, n)
else:
return 1 - hyp.cdf(k, N, K, n) + hyp.pmf(k, N, K, n)
def hypergeometric(objects_in_bin, total_size, objects_total, bin_size):
p_over = np.log10(
hypergeom.sf(objects_in_bin - 1, total_size, objects_total, bin_size))
p_under = np.log10(
hypergeom.cdf(objects_in_bin, total_size, objects_total, bin_size))
if p_over < p_under:
p = -p_over
else:
p = p_under
if abs(p) > 3:
return p / (abs(p)) * 3
else:
return p
def plotheatmap_hypertest(ann_heatmap,
genes,
groupby,
filename,
vmin=0,
vmax=1.5,
figsize=(23, 2)):
from scipy.stats import hypergeom
ann_heatmap = ann_heatmap.copy()
ann_heatmap.X = ann_heatmap.raw.X
ann_heatmap = ann_heatmap[:, ann_heatmap.var_names.isin(genes)].copy()
ann_heatmap.var['ncells'] = (ann_heatmap.X > 0).sum(axis=0).tolist()[0]
records = {}
htmap_df = pd.DataFrame(columns=ann_heatmap.var_names)
#nn_heatmap.
M = len(ann_heatmap.obs)
for grp in ann_heatmap.obs[groupby].unique():
test_group = ann_heatmap[ann_heatmap.obs[groupby] == grp].copy()
test_group.var['ncells'] = (test_group.X > 0).sum(axis=0).tolist()[0]
N = len(test_group.obs)
records[grp] = []
for g in genes:
n = ann_heatmap.var.loc[g]['ncells']
x = test_group.var.loc[g]['ncells']
# add a small value to avoid 0 as a pvalue
hyper_test_pval = 1 - hypergeom.cdf(x, M, n, N) + 10e-30
records[grp].append(hyper_test_pval)
htmap_df = pd.DataFrame.from_dict(records, orient='index', columns=genes)
htmap_df = htmap_df.sort_index()
f, ax = plt.subplots(1, 1, figsize=figsize)
sns.heatmap(
htmap_df.applymap(lambda x: -np.log10(x)),
square=False,
cmap=sns.light_palette('red', as_cmap=True),
vmin=vmin,
vmax=vmax,
linewidths=.5,
cbar_kws=dict(use_gridspec=False,
aspect=8,
label='$-log(p_{val})$',
anchor=(-0.3, 0.0)),
ax=ax,
)
fn = filename
f.savefig(fn + '.pdf', bbox_inches='tight', dpi=300)
plt.close(f)
return htmap_df
def compare_cols(fg_col, fg_cons, fg_size, fg_weights,
bg_col, bg_cons, bg_size, bg_weights,
aa_freqs, pseudo_size):
"Compare alignments using the hypergeometric model"
# Number of consensus-type residues in the foreground column
fg_cons_count = count_col(fg_col, fg_weights)[fg_cons]
# Consensus residue frequency in the combined alignment column
p_j = count_col(bg_col, bg_weights)[fg_cons] + fg_cons_count
# Round fg counts & size to nearest integer for hypergeometric test
fg_cons_count_i = max(1, int(ceil(fg_cons_count)))
fg_size_i = int(ceil(fg_size))
bg_size_i = int(ceil(bg_size))
# Probability of fg col conservation vs. the combined/main set
pvalue = 1.0 - hypergeom.cdf(fg_cons_count_i - 1, fg_size_i + bg_size_i,
p_j, fg_size_i)
return pvalue
def doHyperG(genelist, allgenes, allterms, assocname):
geneswithterms = allgenes.keys()
termswithgenes = allterms.keys()
M=len(geneswithterms)
N=len(list(set(geneswithterms).intersection(set(genelist))))
pvalues=[]
termsingenelist=[]
termsinbackground=[]
termname=[]
for t in termswithgenes:
n = len(allterms[t])
x = len(list(set(allterms[t]).intersection(set(genelist))))
if x == 0:
continue
pvalue = 1.0 - hypergeom.cdf(x,M,n,N)
pvalues.append(pvalue)
termsingenelist.append(x)
termsinbackground.append(n)
termname.append(t)
adjpvalue = list(fdrcorrection0(pvalues)[1])
print("\t".join(["Term annotation", "pvalue", "fdr adj pvalue","Background","Expected","GeneList","Observed","Genes"]))
for u in range(0,len(adjpvalue)):
gotermname = termname[u]
if termname[u] in assocname.keys():
gotermname = assocname[termname[u]]
print("\t".join([gotermname,
str(pvalues[u]),
str(adjpvalue[u]),
str(M),
str(termsinbackground[u]),
str(N),
str(termsingenelist[u]),
",".join(list(set(allterms[termname[u]]).intersection(set(genelist))))]
)
)
def hypergeometric_test(x, M, n, N):
"""
The hypergeometric distribution models drawing objects from a bin.
- M is total number of objects
- n is total number of Type I objects.
- x (random variate) represents the number of Type I objects in N drawn without replacement from the total population
- http://en.wikipedia.org/wiki/Hypergeometric_distribution
- https://www.biostars.org/p/66729/
- http://docs.scipy.org/doc/scipy-0.14.0/reference/generated/scipy.stats.hypergeom.html
- http://docs.scipy.org/doc/numpy/reference/generated/numpy.random.hypergeometric.html
- http://stackoverflow.com/questions/6594840/what-are-equivalents-to-rs-phyper-function-in-python
"""
assert n <= M
assert x <= n
assert N <= M
pv_le = hypergeom.cdf(x+1, M, n, N)
pv_gt = hypergeom.sf(x-1, M, n, N)# 1-cdf sometimes more accurate
return pv_le, pv_gt
def _TEST_ (block,exptotal,bkgtotal,pseudo_count):
sigPoi=0
sigHyp=0
ind=block.index
for i in block.index:
lamda=block.loc[i,'BkgHop_withBonus']
obs=block.loc[i,'ExpHop_withBonus']
BkgHop=block.loc[i,'BkgHop']
ExpHop=block.loc[i,'ExpHop']
P_poisson=1-poisson.cdf(int(obs)-1,lamda+pseudo_count)
if int(BkgHop) < 100000000 and int(ExpHop) < 100000000:
P_hyper=1-hypergeom.cdf(ExpHop-1,(bkgtotal+exptotal),exptotal, (ExpHop+BkgHop))
else:
P_hyper='***'
block.loc[i,'BkgFraction']=float(BkgHop/bkgtotal)
block.loc[i,'ExpFraction']=float(ExpHop/exptotal)
block.loc[i,'P_Hyper']= P_hyper
block.loc[i,'P_Poisson']=P_poisson
if P_poisson < alpha and lamda*obs != 0:
sigPoi=sigPoi+1
if P_hyper < alpha:
sigHyp=sigHyp+1
return block, sigPoi, sigHyp
def mutual_exclusivity(array_a, array_b, verbose=1):
""" Performs a hypergeometric test assessing the probability of array_a and array_b are mutual exclusive.
Arguements:
array_a, array_b: boolean array - discretised values
Returns:
p-value: float
"""
a, b = np.array(array_a), np.array(array_b)
x = np.sum(np.bitwise_and(a == False, b == True)) - 1
M = len(a)
n = np.sum(a == False)
N = np.sum(b == True)
if verbose > 0:
print '[INFO] x, M, n, N: ', x, M, n, N
return 1.0 - hypergeom.cdf(x, M, n, N)
control.append(get_control(path))
sys.stderr.write("%d blocks were read from\t%s\n" % (len(control[-1]), path))
counts, total = count_conservation(signal, iid2seed, matches);
r_control = []
for maf_control in control:
cc,tc = count_control(maf_control, seeds, matches)
r_control.append((cc,tc))
for k,v in Counter(total).most_common(10):
name = mir_lib.shortname(seed2mirs[k])
a = [name, counts[k], v, counts[k]/float(v)]
for cc,tc in r_control:
rawp = (1 - hypergeom.cdf(counts[k], tc[k] ,cc[k] , v))
p_value = "%.2e" % rawp;
a += [cc[k], tc[k], cc[k]/(tc[k] + 0.1), p_value]
print "\t".join([str(x) for x in a])
#micros = parsing.getDictFromFa(args.micro);
#micros = parsing.to_upper_case(micros);
#for key, value in micros.iteritems():
#seed_dict[reverse_complement(value[1:7])].append(key);
#counts_true, total_true = count_conservation(maf_dict, micros)
#seeds = set([reverse_complement(x[1:7]) for x in micros.values()])
#counts_control, total_control = count_control(maf_control, seeds)
def enrichment_test(the_present_set, the_absent_set, the_grouping_dict, **kwargs):
""" Hypergeometric testing for enrichment.
Arguments:
the_present_set: a list or set of items that were tested and were positive
the_absent_set: a list or set of items that were tested for but
were not present / significant
the_grouping_dict: a dict of items to check for enrichment.
key: grouping name, e.g. GO enrichment category, complex name, etc...
value: a list or set of items in the list to test, e.g. gene or protein id's
kwargs:
filter_items: [True (default) / False]
Whether to filter the items in the_grouping_dict and
the_present_set / the_absent_set so only items
in common are tested.
verbose: [False(default) / True]
method: type of mt testing to apply, default is "none", see
mtcorrect() for more information
direction: ["enrichment" (default), "depletion"]
essentially, whether to look at the right or left tail
returns:
test_result_dict: a dict with:
{the_grouping: {'p': the corrected p-value,
'n_present': number in the grouping that were present,
'n_group': the total size of the group}
"""
from copy import deepcopy
from scipy.stats import hypergeom
method = test_kwarg('method', kwargs, mtcorrect_methods)
filter_items = test_kwarg('filter_items', kwargs, [True, False])
verbose = test_kwarg('verbose', kwargs, [False, True])
method = test_kwarg('method', kwargs, mtcorrect_methods)
direction = test_kwarg('direction', kwargs, ["enrichment", "depletion"])
the_present_set = set(the_present_set)
the_absent_set = set(the_absent_set)
all_test_items_set = the_present_set | the_absent_set
the_grouping_dict = deepcopy(the_grouping_dict)
all_grouping_items_set = set([])
the_groupings_to_test = deepcopy(the_grouping_dict.keys())
for the_grouping in the_groupings_to_test:
the_grouping_dict[the_grouping] = set(the_grouping_dict[the_grouping])
if filter_items:
the_grouping_dict[the_grouping] = the_grouping_dict[the_grouping] & all_test_items_set
all_grouping_items_set.update(the_grouping_dict[the_grouping])
if len(the_grouping_dict[the_grouping]) == 0:
the_grouping_dict.pop(the_grouping)
if filter_items:
the_present_set = the_present_set & all_grouping_items_set
the_absent_set = the_absent_set & all_grouping_items_set
all_test_items_set = all_test_items_set & all_grouping_items_set
test_result_dict = {}
n_present_dict = {}
group_size_dict = {}
for the_grouping in the_grouping_dict.keys():
# x: number of present items in the grouping
# M: total number of items
# n: total number of present items
# N: total number of items in the grouping
the_grouping_set = the_grouping_dict[the_grouping]
x = len(the_present_set & the_grouping_set)
M = len(all_test_items_set)
n = len(the_present_set)
N = len(the_grouping_set)
if direction == "enrichment":
# We want the probability that x or more than x can be chosen randomly,
# so we must subtract 1
if x >= 1:
the_p = hypergeom.sf(x-1,M,n,N,loc=0)
else:
the_p = 1.
else:
the_p = hypergeom.cdf(x,M,n,N,loc=0)
test_result_dict[the_grouping] = the_p
n_present_dict[the_grouping] = x
group_size_dict[the_grouping] = N
corrected_p_dict = mtcorrect(test_result_dict, method = method)
final_result_dict = {}
for the_grouping in the_grouping_dict.keys():
final_result_dict[the_grouping] = {}
final_result_dict[the_grouping]['n_present'] = n_present_dict[the_grouping]
final_result_dict[the_grouping]['n_group'] = group_size_dict[the_grouping]
final_result_dict[the_grouping]['p'] = corrected_p_dict[the_grouping]
return final_result_dict
def Main():
t1=time()
args=ParseArg()
inp = open(args.input, 'r')
min_clusterS=args.min_clusterS
min_interaction=args.min_interaction
p_value=args.p_value
output=open(args.output,'w')
outputIntra = open(args.output_intra, 'w')
hasAnnotation = False
if args.annotation:
dbi = DBI.init(args.annotation, "bed")
hasAnnotation = True
else:
dbi = False
if args.annotation_repeat:
dbirepeat = DBI.init(args.annotation_repeat, "bed")
hasAnnotationRepeat = True
else:
dbirepeat = False
#store count of RNA for part1 and part2
part={}
k=0
sgcount = 0 #single fragment count
print >> sys.stderr,"# Inputing data..."
interaction = {} # store number of interactions for different RNA
selfinteraction = {}
#Types = ["snoRNA","protein_coding","snRNA","lincRNA","tRNA","misc_RNA","pseudogene","miRNA","antisense","sense_intronic","non_coding","processed_transcript","sense_overlapping","rRNA_repeat","rRNA"]
for line in inp.read().split('\n'):
if line=='': continue
line=line.strip().split('\t')
p1=annotated_bed_proper(line[0:10],id=k,cluster=1)
p2=annotated_bed_proper(line[11:],id=k,cluster=1)
if isinstance(p1.start, list):
p1.start=int(p1.start[0])
p1.end=int(p1.end[-1])
if isinstance(p2.start, list):
p2.start=int(p2.start[0])
p2.end=int(p2.end[-1])
if SingleFragment(p1,p2):
sgcount += 1
continue
k+=1
#if p1.subtype=="intron" or p2.subtype=="intron": continue
#if p1.type in Types:
try:
p1_name = GetAnnotationName(p1, hasAnnotation, dbi, hasAnnotationRepeat, dbirepeat)
if p1_name not in part:
part[p1_name]=1
else:
part[p1_name]+=1
#if p2.type in Types:
p2_name = GetAnnotationName(p2, hasAnnotation, dbi, hasAnnotationRepeat, dbirepeat)
if not p1_name == p2_name: # count once for self-interaction
if p2_name not in part:
part[p2_name]=1
else:
part[p2_name]+=1
#if p1.type in Types and p2.type in Types:
if p1_name == p2_name:
if p1_name not in selfinteraction:
selfinteraction[p1_name]=copy.deepcopy(p1)
else:
selfinteraction[p1_name].Update(p1.start, p1.end)
selfinteraction[p1_name].Update(p2.start, p2.end)
selfinteraction[p1_name].cluster += 1
else:
if p1_name>p2_name:
temp = p1
p1 = p2
p2 = temp
tempName = p1_name
p1_name = p2_name
p2_name = tempName
inter_name = p1_name + "--" + p2_name
if inter_name not in interaction:
interaction[inter_name]=[copy.deepcopy(p1),copy.deepcopy(p2)]
else:
interaction[inter_name][0].Update(p1.start,p1.end)
interaction[inter_name][1].Update(p2.start,p2.end)
interaction[inter_name][0].cluster+=1
except Exception as e:
print >> sys.stderr, e
if k%20000==0:
print >> sys.stderr," Reading %d pairs of segments\r"%(k),
print >> sys.stdout,"Get total %d pairs."%(k)
print >> sys.stdout,"Single fragment count: %d."%(sgcount)
print >>sys.stdout," number of different RNAs is %d "%(len(part))
total = k # total pairs used
n=0
k=0 # record number of strong interactions
for i in interaction:
n+=1
count = interaction[i][0].cluster
if count < min_interaction: continue
p1_name = i.split("--")[0]
p2_name = i.split("--")[1]
P1 = interaction[i][0]
P2 = interaction[i][1]
P1.cluster = part[p1_name]
P2.cluster = part[p2_name]
if part[p1_name]<min_clusterS or part[p2_name]<min_clusterS: continue
real_p=1-hypergeom.cdf(count,total,part[p1_name],part[p2_name])
if real_p<=p_value:
k=k+1
try:
log_p = math.log(real_p)
except:
log_p = -float("Inf")
print >> output, str(P1)+'\t'+str(P2)+'\t%d\t%.4f'%(count,log_p)
if n%500==0: print >> sys.stderr, " Progress ( %d / %d )\r"%(n,len(interaction)),
k1=0
for i in selfinteraction:
n+=1
count = selfinteraction[i].cluster
if count < min_interaction: continue
p1_name = i
P1 = selfinteraction[i]
P1.cluster = part[p1_name]
if part[p1_name]<min_clusterS: continue
k1=k1+1
print >> outputIntra, str(P1)+'\t%d'%(count)
if n%500==0: print >> sys.stderr, " Progress ( %d / %d )\r"%(n,len(interaction)),
print >> sys.stdout,"# Find %d strong and %d self interactions. Cost time: %.2f s"%(k,k1,time()-t1)
def Main():
t1=time()
global min_interaction, p_value
args=ParseArg()
inp = open(args.input, 'r')
min_clusterS=args.min_clusterS
min_interaction=args.min_interaction
p_value=args.p_value
output=open(args.output,'w')
ncpus=args.parallel
#store genomic location of part1 and part2
part1=[]
part2=[]
k=0
print >> sys.stderr,"# Inputing data..."
chr_list=[]
for line in inp.read().split('\n'):
if line=='': continue
line=line.strip().split('\t')
p1=annotated_bed(line[0:10],id=k)
p2=annotated_bed(line[11:],id=k)
if isinstance(p1.start, list):
p1.start=int(p1.start[0])
p1.end=int(p1.end[-1])
if isinstance(p2.start, list):
p2.start=int(p2.start[0])
p2.end=int(p2.end[-1])
if SingleFragment(p1,p2): continue
k+=1
part1.append(p1)
part2.append(p2)
if p1.chr not in chr_list: chr_list.append(p1.chr)
if p2.chr not in chr_list: chr_list.append(p2.chr)
if k%20000==0:
print >> sys.stderr," Reading %d pairs of segments\r"%(k),
print >> sys.stderr,"Get total %d pairs."%(k)
if len(part1)!=len(part2):
print >> sys.stderr, "## ERROR: number of regions in two part not match!!"
sys.exit(0)
# sort in genomic order, easy for clustering
part1=sorted(part1, key=attrgetter('start'))
part1=sorted(part1, key=attrgetter('chr'))
part2=sorted(part2, key=attrgetter('start'))
part2=sorted(part2, key=attrgetter('chr'))
# for parallel computing
print >>sys.stderr,"# Generating clusters for two parts..."
# tuple of all parallel python servers to connect with
ppservers = ()
job_server = pp.Server(ncpus, ppservers=ppservers)
jobs1=[]
jobs2=[]
for chro in chr_list:
part1_temp=filter(lambda p: p.chr==chro, part1)
if len(part1_temp)>0:
jobs1.append(job_server.submit(cluster_regions,(part1_temp,min_clusterS),(annotated_bed,),("UnionFind","copy",)))
part2_temp=filter(lambda p: p.chr==chro, part2)
if len(part2_temp)>0:
jobs2.append(job_server.submit(cluster_regions,(part2_temp,min_clusterS),(annotated_bed,),("UnionFind","copy",)))
cluster_pool1={}
part1=[]
for job in jobs1:
try:
part1=part1+job()[1]
cluster_pool1.update(job()[0])
except:
print >> sys.stderr, "Wrong in %s, part1"%(job()[2])
continue
cluster_pool2={}
part2=[]
for job in jobs2:
try:
part2=part2+job()[1]
cluster_pool2.update(job()[0])
except:
continue
print >>sys.stderr," cluster number for part1 is %d "%(len(cluster_pool1))
print >>sys.stderr," cluster number for part2 is %d "%(len(cluster_pool2))
# sort back to pair two parts
part1=sorted(part1, key=attrgetter('id'))
part2=sorted(part2, key=attrgetter('id'))
print >> sys.stderr,"size of part1&2:",len(part1),len(part2)
c_interaction={}
for i in range(len(part1)):
region1=str(part1[i])
region2=str(part2[i])
try:
inter=part1[i].cluster+"--"+part2[i].cluster
except:
print >> sys.stderr,i,part1[i].cluster,part2[i].cluster
sys.exit()
if c_interaction.has_key(inter):
c_interaction[inter]+=1
else:
c_interaction[inter]=1
# annotation file
print >> sys.stderr,"# Indexing annotation files"
dbi_all=DBI.init(args.annotation,"bed")
dbi_detail=DBI.init(args.db_detail,"bed")
dbi_repeat=DBI.init("/home/yu68/bharat-interaction/new_lincRNA_data/mouse.repeat.txt","bed")
print >> sys.stderr,"# finding strong interactions from clusters..."
k=0 # record for strong interactions
n=0
# annotation file
for interaction in c_interaction:
n=n+1
count=c_interaction[interaction]
if count<min_interaction: continue
i=interaction.split("--")[0]
j=interaction.split("--")[1]
try: # we select clusters with size no less than 5, so some interactions cannot be found in clusters
count1=cluster_pool1[i].cluster
count2=cluster_pool2[j].cluster
except:
continue
real_p=1-hypergeom.cdf(count,len(part1),count1,count2)
if real_p<=p_value:
k=k+1
cluster_pool1[i].Annotate(dbi_all,dbi_detail,dbi_repeat)
cluster_pool2[j].Annotate(dbi_all,dbi_detail,dbi_repeat)
try:
log_p = math.log(real_p)
except:
log_p = -float("Inf")
print >> output,str(cluster_pool1[i])+'\t'+str(cluster_pool2[j])+'\t%d\t%.4f'%(count,log_p)
if n%1000==0: print >> sys.stderr, " Progress ( %d / %d )\r"%(n,len(c_interaction)),
print >> sys.stderr,"# Find %d strong interactions. Cost time: %.2f s"%(k,time()-t1)
if args.FDR:
print >> sys.stderr, "# Permutated results:"
for i in range(10):
shuffle(part2)
[n_r_I,n_r_SI]=Random_strongInteraction(part1,part2,cluster_pool1,cluster_pool2)
print >> sys.stderr, " ",i, n_r_I, n_r_SI, n_r_SI*1.0/n_r_I
def enrichment_hypergeo(
termList, entityList, species, useIea=True, asGenes=True, aspect="biological_process", verbose=True
):
"""
termList -- are the terms to be tested
species -- an ncbi taxa id
entityList -- gene or uniprot ids
What is the probability of finding a given number of terms if we randomly select N out of M objects?
M -- genes with at least one annotation
N -- number of draws or size of gene list
k -- the number of genes annotated by a given term (total type I objects)
x -- number of times we observe a term in the gene list (draws)
in R the cdf can be obtained with
phyper(x,k,M-k,N)
hypergeom.pmf(x, M, k, N)
Returns a dict where term id is the key and hypergeo pvalue is the value
"""
## connect to db and get annotations for the species
session, engine = db_connect()
geneAnnots, uniprotAnnots = fetch_taxa_annotations([species], engine, useIea=useIea, verbose=verbose, aspect=aspect)
if asGenes == True:
entity2go = geneAnnots
else:
entity2go = uniprotAnnots
go2entity = {}
for entity, go in entity2go.iteritems():
for term in go:
if not go2entity.has_key(term):
go2entity[term] = set([])
go2entity[term].update([entity])
for go, entity in go2entity.iteritems():
go2entity[go] = list(entity)
print ("total go terms - %s" % (len(go2entity.keys())))
print ("total entities - %s" % (len(entity2go.keys())))
## set variables
M = len(entity2go.keys())
N = len(entityList)
results = {}
for testTerm in termList:
## find
k = len(go2entity[testTerm])
x = 0
for entity in entityList:
if entity in entity2go and testTerm in entity2go[entity]:
x += 1
## get a p-value
if 0 in [x, M, N, k]:
pvalue = np.nan
else:
cdf = hypergeom.cdf(x, M, k, N, loc=0)
if cdf > 0:
pvalue = 2 * (1 - hypergeom.cdf(x, M, k, N))
else:
pvalue = 2 * hypergeom.cdf(x, M, k, N)
results[testTerm] = pvalue
return results
def Main():
t1=time()
global min_interaction, p_value
args=ParseArg()
inp = open(args.input, 'r')
min_clusterS=args.min_clusterS
min_interaction=args.min_interaction
p_value=args.p_value
output=open(args.output,'w')
#store genomic location of part1 and part2
part1=[]
part2=[]
k=0
print >> sys.stderr,"# Inputing data..."
for line in inp.read().split('\n'):
if line=='': continue
line=line.strip().split('\t')
k=k+1
part1.append(annotated_bed(line[0:7],id=k))
part2.append(annotated_bed(line[8:],id=k))
if k%20000==0:
print >> sys.stderr," Reading %d pairs of segments\r"%(k),
print >> sys.stderr,"Get total %d pairs."%(k)
if len(part1)!=len(part2):
print >> sys.stderr, "## ERROR: number of regions in two part not match!!"
sys.exit(0)
# sort in genomic order, easy for clustering
part1=sorted(part1, key=attrgetter('start'))
part1=sorted(part1, key=attrgetter('chr'))
part2=sorted(part2, key=attrgetter('start'))
part2=sorted(part2, key=attrgetter('chr'))
print >>sys.stderr,"# Generating clusters for two parts..."
print >>sys.stderr," Part1:"
cluster_pool1=cluster_regions(part1,min_clusterS)
print >>sys.stderr," cluster number for part1 is %d "%(len(cluster_pool1))
print >>sys.stderr," Part2:"
cluster_pool2=cluster_regions(part2,min_clusterS)
print >>sys.stderr," cluster number for part2 is %d "%(len(cluster_pool2))
# sort back to pair two parts
part1=sorted(part1, key=attrgetter('id'))
part2=sorted(part2, key=attrgetter('id'))
c_interaction={}
for i in range(len(part1)):
region1=str(part1[i])
region2=str(part2[i])
inter="%d--%d"%(part1[i].cluster,part2[i].cluster)
if c_interaction.has_key(inter):
c_interaction[inter]+=1
else:
c_interaction[inter]=0
print >> sys.stderr,"# finding strong interactions from clusters..."
k=0 # record for strong interactions
n=0
for interaction in c_interaction:
n=n+1
count=c_interaction[interaction]
if count<min_interaction: continue
i=int(interaction.split("--")[0])
j=int(interaction.split("--")[1])
try: # we select clusters with size no less than 5, so some interactions cannot be found in clusters
count1=cluster_pool1[i].cluster
count2=cluster_pool2[j].cluster
except:
continue
real_p=1-hypergeom.cdf(count,len(part1),count1,count2)
if real_p<=p_value:
k=k+1
print >> output,str(cluster_pool1[i])+'\t'+str(cluster_pool2[j])+'\t%d\t%.5f'%(count,real_p)
if n%1000==0: print >> sys.stderr, " Progress ( %d / %d )\r"%(n,len(c_interaction)),
print >> sys.stderr,"# Find %d strong interactions. Cost time: %.2f s"%(k,time()-t1)
if args.FDR:
print >> sys.stderr, "# Permutated results:"
for i in range(10):
shuffle(part2)
[n_r_I,n_r_SI]=Random_strongInteraction(part1,part2,cluster_pool1,cluster_pool2)
print >> sys.stderr, " ",i, n_r_I, n_r_SI, n_r_SI*1.0/n_r_I
rxnpvals = np.array(rxnpvals)
recon2subs = np.array(recon2subs)
rxnrangediffs = np.array(rxnrangediffs)
uniqSubs = np.unique(recon2subs)
numrxnspos = []
numsigrxnspos = []
hypergeomparrpos = []
for sub in uniqSubs:
N = len(recon2rxns)
M = sum(recon2subs==sub)
K = sum(np.logical_and(rxnpvals<.05,rxnrangediffs>0))
x = sum(np.logical_and(np.logical_and(rxnpvals<.05,rxnrangediffs>0),recon2subs==sub))
numrxnspos.append(M)
numsigrxnspos.append(x)
hypergeomparrpos.append(1-hypergeom.cdf(x-1,N,M,K))
numrxnsneg = []
numsigrxnsneg = []
hypergeomparrneg = []
for sub in uniqSubs:
N = len(recon2rxns)
M = sum(recon2subs==sub)
K = sum(np.logical_and(rxnpvals<.05,rxnrangediffs<0))
x = sum(np.logical_and(np.logical_and(rxnpvals<.05,rxnrangediffs<0),recon2subs==sub))
numrxnsneg.append(M)
numsigrxnsneg.append(x)
hypergeomparrneg.append(1-hypergeom.cdf(x-1,N,M,K))
labelarr = []
valuesarr = []
youngvals = totalvar['young'].values()
for i in range(len(youngvals)):
def _motif_sig(fore_hits, fore_size, back_hits, back_size):
return (
1 -
hypergeom.cdf(fore_hits, back_size, back_hits, fore_size) +
hypergeom.pmf(fore_hits, back_size, back_hits, fore_size)
)
def cphyper(k, K, n, N):
return 1.0 - hypergeom.cdf(k - 1, N, n, K)
import matplotlib.pyplot as plt from scipy.stats import hypergeom, rv_discrete import numpy as np numargs = hypergeom.numargs #[ M, n, N ] = [100, 10, -1] #Display frozen pmf: rv = hypergeom( 10, 20, 3 ) print rv.dist.b x = np.arange( 0, np.min( rv.dist.b, 3 ) + 1 ) h = plt.plot( x, rv.pmf( x ) ) exit() #Check accuracy of cdf and ppf: prb = hypergeom.cdf( x, M, n, N ) h = plt.semilogy( np.abs( x - hypergeom.ppf( prb, M, n, N ) ) + 1e-20 ) #Random number generation: R = hypergeom.rvs( M, n, N, size=100 ) #Custom made discrete distribution: vals = [np.arange( 7 ), ( 0.1, 0.2, 0.3, 0.1, 0.1, 0.1, 0.1 )] custm = rv_discrete( name='custm', values=vals ) h = plt.plot( vals[0], custm.pmf( vals[0] ) )
def fisher_exact(c) :
"""Performs a Fisher exact test on a 2x2 contingency table.
Parameters
----------
c : array_like of ints
A 2x2 contingency table.
Returns
-------
oddsratio : float
This is prior odds ratio and not a posterior estimate.
p-value : float
P-value for 2-sided hypothesis of independence.
Examples
--------
>>> fisher_exact([[100, 2], [1000, 5]])
(0.25, 0.13007593634330314)
"""
c = np.asarray(c, dtype=np.int64) # int32 is not enough for the algorithm
odssratio = c[0,0] * c[1,1] / float(c[1,0] * c[0,1]) \
if (c[1,0] > 0 and c[0,1] > 0) else np.inf
n1 = c[0,0] + c[0,1]
n2 = c[1,0] + c[1,1]
n = c[0,0] + c[1,0]
mode = int(float((n + 1) * (n1 + 1)) / (n1 + n2 + 2))
pexact = hypergeom.pmf(c[0,0], n1 + n2, n1, n)
pmode = hypergeom.pmf(mode, n1 + n2, n1, n)
epsilon = 1 - 1e-4
if float(np.abs(pexact - pmode)) / np.abs(np.max(pexact, pmode)) <= 1 - epsilon:
return odssratio, 1
elif c[0,0] < mode:
plower = hypergeom.cdf(c[0,0], n1 + n2, n1, n)
if hypergeom.pmf(n, n1 + n2, n1, n) > pexact / epsilon:
return odssratio, plower
# Binary search for where to begin upper half.
min = mode
max = n
guess = -1
while max - min > 1:
guess = max if max == min + 1 and guess == min else (max + min) / 2
pguess = hypergeom.pmf(guess, n1 + n2, n1, n)
if pguess <= pexact and hypergeom.pmf(guess - 1, n1 + n2, n1, n) > pexact:
break
elif pguess < pexact:
max = guess
else:
min = guess
if guess == -1:
guess = min
while guess > 0 and hypergeom.pmf(guess, n1 + n2, n1, n) < pexact * epsilon:
guess -= 1
while hypergeom.pmf(guess, n1 + n2, n1, n) > pexact / epsilon:
guess += 1
p = plower + hypergeom.sf(guess - 1, n1 + n2, n1, n)
if p > 1.0:
p = 1.0
return odssratio, p
else:
pupper = hypergeom.sf(c[0,0] - 1, n1 + n2, n1, n)
if hypergeom.pmf(0, n1 + n2, n1, n) > pexact / epsilon:
return odssratio, pupper
# Binary search for where to begin lower half.
min = 0
max = mode
guess = -1
while max - min > 1:
guess = max if max == min + 1 and guess == min else (max + min) / 2
pguess = hypergeom.pmf(guess, n1 + n2, n1, n)
if pguess <= pexact and hypergeom.pmf(guess + 1, n1 + n2, n1, n) > pexact:
break
elif pguess <= pexact:
min = guess
else:
max = guess
if guess == -1:
guess = min
while hypergeom.pmf(guess, n1 + n2, n1, n) < pexact * epsilon:
guess += 1
while guess > 0 and hypergeom.pmf(guess, n1 + n2, n1, n) > pexact / epsilon:
guess -= 1
p = pupper + hypergeom.cdf(guess, n1 + n2, n1, n)
if p > 1.0:
p = 1.0
return odssratio, p
lc = l.strip("\n").split("\t")
tf[lc[1]] = 1
if lc[1] in expr:
tf_num = tf_num + 1
if lc[1] in degs:
tf_degs = tf_degs + 1
#print expr_num
#print degs_num
#print tf_num
#print tf_degs
## [M, n, N]
[express_genes, degs, tf_binding_genes] = [expr_num, degs_num, tf_num]
#rv = hypergeom(express_genes, degs, tf_binding_genes)
#x = np.arange(0, 10)
#pmf_tfBindDegs = rv.pmf(1)
#print np.sum(pmf_tfBindDegs)
#print 1-np.sum(pmf_tfBindDegs)
# the probability less than tf_degs
prb = hypergeom.cdf(tf_degs, express_genes, degs, tf_binding_genes)
#pvalue = 1 - hypergeom.cdf(tf_degs, express_genes, degs, tf_binding_genes)
#if pvalue > 1:
# print >>sys.stderr, prefix
prefix = sys.argv[4]
print "%s\t%.12f\t%d\t%d\t%d\t%d" % (prefix, prb, express_genes, degs, tf_binding_genes, tf_degs)
def Main():
t1=time()
global min_interaction, p_value
args=ParseArg()
inp = open(args.input, 'r')
min_clusterS=args.min_clusterS
min_interaction=args.min_interaction
p_value=args.p_value
output=open(args.output,'w')
ncpus=args.parallel
#store genomic location of part1 and part2
part=[]
k=0
print >> sys.stderr,"# Inputing data..."
chr_list=[]
for line in inp.read().split('\n'):
if line=='': continue
line=line.strip().split('\t')
p1=annotated_bed(line[0:8],id=k,part=1)
p2=annotated_bed(line[9:],id=k,part=2)
if SingleFragment(p1,p2): continue
k+=1
part.append(p1)
part.append(p2)
if p1.chr not in chr_list: chr_list.append(p1.chr)
if p2.chr not in chr_list: chr_list.append(p2.chr)
if k%20000==0:
print >> sys.stderr," Reading %d pairs of segments\r"%(k),
print >> sys.stderr,"Get total %d pairs."%(k)
# sort in genomic order, easy for clustering
part=sorted(part, key=attrgetter('start'))
part=sorted(part, key=attrgetter('chr'))
# for parallel computing
print >>sys.stderr,"# Generating clusters for two parts..."
# tuple of all parallel python servers to connect with
ppservers = ()
job_server = pp.Server(ncpus, ppservers=ppservers)
jobs=[]
for chro in chr_list:
part_temp=filter(lambda p: p.chr==chro, part)
if len(part_temp)>0:
jobs.append(job_server.submit(cluster_regions,(part_temp,min_clusterS),(annotated_bed,),("UnionFind","copy",)))
cluster_pool={}
part=[]
for job in jobs:
try:
part=part+job()[1]
cluster_pool.update(job()[0])
except:
print >> sys.stderr, "Wrong in %s, part1"%(job()[2])
continue
print >>sys.stderr," cluster number is %d "%(len(cluster_pool))
# sort back to pair two parts
part=sorted(part, key=attrgetter('part'))
part=sorted(part, key=attrgetter('id'))
print >> sys.stderr,"size of part",len(part)
c_interaction={}
i=0
while i<len(part):
P1=part[i]
P2=part[i+1]
assert P1.id==P2.id
i+=2
print >> sys.stderr,"%d\r"%(i),
if P1.cluster==P2.cluster: continue
if P1.cluster<P2.cluster:
inter=P1.cluster+"--"+P2.cluster
else:
inter=P2.cluster+"--"+P1.cluster
if c_interaction.has_key(inter):
c_interaction[inter]+=1
else:
c_interaction[inter]=1
# annotation file
print >> sys.stderr,"# Indexing annotation files"
dbi_all=DBI.init(args.annotation,"bed")
dbi_detail=DBI.init(args.db_detail,"bed")
dbi_repeat=DBI.init("/home/yu68/bharat-interaction/new_lincRNA_data/mouse.repeat.txt","bed")
print >> sys.stderr,"# finding strong interactions from clusters..."
k=0 # record for strong interactions
n=0
# annotation file
for interaction in c_interaction:
n=n+1
count=c_interaction[interaction]
if count<min_interaction: continue
i=interaction.split("--")[0]
j=interaction.split("--")[1]
try: # we select clusters with size no less than 5, so some interactions cannot be found in clusters
count1=cluster_pool[i].cluster
count2=cluster_pool[j].cluster
except:
continue
real_p=1-hypergeom.cdf(count,len(part)/2,count1,count2)
if real_p<=p_value:
k=k+1
cluster_pool[i].Annotate(dbi_all,dbi_detail,dbi_repeat)
cluster_pool[j].Annotate(dbi_all,dbi_detail,dbi_repeat)
try:
log_p = math.log(real_p)
except:
log_p = -float("Inf")
print >> output,str(cluster_pool[i])+'\t'+str(cluster_pool[j])+'\t%d\t%.4f'%(count,log_p)
if n%1000==0: print >> sys.stderr, " Progress ( %d / %d )\r"%(n,len(c_interaction)),
print >> sys.stderr,"# Find %d strong interactions. Cost time: %.2f s"%(k,time()-t1)
def p_hypergeom(self,N_pop,n_chosen,K_pop,k_success): return hypergeom.cdf(k_success,N_pop,K_pop,n_chosen)
def plot_cell_enrichments(
ds,
f=None,
enrichments=None,
ax=None,
title=None,
):
LOGGER.info("Plotting cell type enrichments")
if enrichments is None:
enrichments = brs.enrichments.get_enrichments(
list(ds.species)[0],
)
if f is None:
f = {'p': .05, 'asym_fold': 1.25}
if isinstance(f, dict):
f = [f]
if ax is None:
_, ax = plt.subplots(figsize=(4, 3))
cell_prots = {
cell: [key for key, val in enrichments.items() if val == cell]
for cell in brs.CELL_TYPES
}
display_name = {
'Myelinating Oligodendrocytes': 'Oligodendrocytes',
} if sum([
'Oligo' in cell and len(cell_prots.get(cell, [])) > 0
for cell in brs.CELL_TYPES
]) else {}
vals = []
ds = ds.filter(
protein=set(j for i in cell_prots.values() for j in i),
fn=lambda x: len(x['Proteins']) < 2,
)
hatches = [
"",
"//",
"o",
"x",
".",
]
for cell in brs.CELL_TYPES:
for ind, fil in enumerate(f):
dc = ds.filter(protein=set(cell_prots[cell]))
fore_hits = dc.filter(fil).shape[0]
fore_size = dc.shape[0]
back_hits = ds.filter(fil).shape[0]
back_size = ds.shape[0]
if fore_size < 1 or back_size < 1:
continue
val = (
1 -
hypergeom.cdf(fore_hits, back_size, back_hits, fore_size) +
hypergeom.pmf(fore_hits, back_size, back_hits, fore_size)
)
vals.append(
pd.Series(
OrderedDict([
('cell', display_name.get(cell, cell)),
('fore hits', fore_hits),
('fore size', fore_size),
('back hits', back_hits),
('back size', back_size),
('p-value', val),
('-log10 p-value', -np.log10(val)),
('color', brs.CELL_COLORS[cell]),
('hatch', hatches[ind % len(hatches)]),
('hue', format_title(f=fil)),
])
)
)
df = pd.DataFrame(vals)
ax = sns.barplot(
data=df,
y='cell',
x='-log10 p-value',
hue='hue',
ax=ax,
)
ax.axvline(-np.log10(.01), color='k', linestyle=':')
ax.legend(
handles=[
mpatches.Patch(
facecolor='w',
edgecolor='k',
hatch=i,
label=df['hue'].iloc[ind],
)
for ind, i in enumerate(hatches[:len(f)])
]
)
for hatch, color, p in zip(
df['hatch'],
df['color'],
sorted(ax.patches, key=lambda x: x.xy[1]),
):
p.set_hatch(hatch)
p.set_facecolor(color)
p.set_edgecolor('k')
if title:
ax.set_title(title)
ax.set_ylabel('')
ax.set_xlabel('p-value')
ax.set_xticklabels(['{:.3}'.format(10 ** -i) for i in ax.get_xticks()])
return ax.get_figure(), ax
def Main():
t1=time()
args=ParseArg()
inp = open(args.input, 'r')
min_clusterS=args.min_clusterS
min_interaction=args.min_interaction
p_value=args.p_value
output=open(args.output,'w')
#store count of RNA for part1 and part2
part1={}
part2={}
k=0
print >> sys.stderr,"# Inputing data..."
interaction = {} # store number of interactions for different RNA
Types = ["snoRNA","protein_coding","snRNA","lincRNA","tRNA","misc_RNA","pseudogene","miRNA","antisense","sense_intronic","non_coding","processed_transcript"]
for line in inp.read().split('\n'):
if line=='': continue
line=line.strip().split('\t')
p1=annotated_bed(line[0:8],id=k,cluster=1)
p2=annotated_bed(line[9:],id=k,cluster=1)
if SingleFragment(p1,p2): continue
k+=1
if p1.type in Types:
p1_name = p1.chr+":"+p1.name
if p1_name not in part1:
part1[p1_name]=1
else:
part1[p1_name]+=1
if p2.type in Types:
p2_name = p2.chr+":"+p2.name
if p2_name not in part2:
part2[p2_name]=1
else:
part2[p2_name]+=1
if p1.type in Types and p2.type in Types:
inter_name = p1_name+"--"+p2_name
if inter_name not in interaction:
interaction[inter_name]=[copy.deepcopy(p1),copy.deepcopy(p2)]
else:
interaction[inter_name][0].Update(p1.start,p1.end)
interaction[inter_name][1].Update(p2.start,p2.end)
interaction[inter_name][0].cluster+=1
if k%20000==0:
print >> sys.stderr," Reading %d pairs of segments\r"%(k),
print >> sys.stderr,"Get total %d pairs."%(k)
print >>sys.stderr," number of different RNAs for part1 is %d "%(len(part1))
print >>sys.stderr," number of different RNAs for part2 is %d "%(len(part2))
total = k # total pairs used
n=0
k=0 # record number of strong interactions
for i in interaction:
n+=1
count = interaction[i][0].cluster
if count < min_interaction: continue
p1_name = i.split("--")[0]
p2_name = i.split("--")[1]
P1 = interaction[i][0]
P2 = interaction[i][1]
P1.cluster = part1[p1_name]
P2.cluster = part2[p2_name]
if part1[p1_name]<min_clusterS or part2[p2_name]<min_clusterS: continue
real_p=1-hypergeom.cdf(count,total,part1[p1_name],part2[p2_name])
if real_p<=p_value:
k=k+1
try:
log_p = math.log(real_p)
except:
log_p = -float("Inf")
print >> output, str(P1)+'\t'+str(P2)+'\t%d\t%.4f'%(count,log_p)
if n%100==0: print >> sys.stderr, " Progress ( %d / %d )\r"%(n,len(interaction)),
print >> sys.stderr,"# Find %d strong interactions. Cost time: %.2f s"%(k,time()-t1)
