ups

fluents/lib/blmfuncs.py

@@ -197,7 +197,7 @@ class PLS(Model):
         Model.__init__(self, id, name)
         self._options = PlsOptions()
         
-    def validation(self, amax, n_sets, cv_val_method):
+    def validation(self):
         """Returns rmsep for pls model.
         """
         m, n = self.model['E0'].shape
@@ -207,7 +207,7 @@ class PLS(Model):
             val_engine = pls_val
         if self._options['calc_cv']==True:
             rmsep, aopt = val_engine(self.model['E0'], self.model['F0'],
-                                     amax, n_sets)
+                                     self._options['amax'], self._options['n_sets'])
             self.model['rmsep'] = rmsep[:,:-1]
             self.model['aopt'] = aopt
         else:
@@ -319,7 +319,7 @@ class PLS(Model):
             self.model['E0'] = self._data['X']
             self.model['F0'] = self._data['Y']
         
-        self.validation(**options.validation_options())
+        self.validation()
         self.make_model(self.model['E0'], self.model['F0'],
                         **options.make_model_options())
         # variance captured

fluents/lib/engines.py

@@ -6,81 +6,189 @@ There is almost no typechecking of any kind here, just focus on speed
 import math
 from scipy.linalg import svd,inv
 from scipy import dot,empty,eye,newaxis,zeros,sqrt,diag,\
-     apply_along_axis,mean,ones,randn,empty_like,outer,c_,\
+     apply_along_axis,mean,ones,randn,empty_like,outer,r_,c_,\
-     rand,sum,cumsum,matrix
+     rand,sum,cumsum,matrix, expand_dims,minimum,where
 has_sym=True
 try:
-    import symmeig
+    from symeig import symeig
 except:
     has_sym = False
+has_sym=False
+
+def pca(a, aopt,scale='scores',mode='normal',center_axis=-1):
+    """ Principal Component Analysis.
+
+    Performs PCA on given matrix and returns results in a dictionary.
+
+    :Parameters:
+        a : array
+    Data measurement matrix, (samples x variables)
+        aopt : int
+    Number of components to use, aopt<=min(samples, variables)
+
+    :Returns:  
+    results : dict
+        keys -- values,  T -- scores, P -- loadings, E -- residuals,
+        lev --leverages, ssq -- sum of squares, expvar -- cumulative
+        explained variance, aopt -- number of components used
+    
+    :OtherParameters:
+    mode : str
+        Amount of info retained, ('fast', 'normal', 'detailed')
+    center_axis : int
+        Center along given axis. If neg.: no centering (-inf,..., matrix modes)
+  
+    :SeeAlso:
+        - pcr : other blm
+        - pls : other blm
+        - lpls : other blm
+ 
+    Notes
+    -----
+
+    Uses kernel speed-up if m>>n or m<<n.
+
+    If residuals turn rank deficient, a lower number of component than given
+    in input will be used. The number of components used is given in results-dict. 
+    
+    Examples
+    --------
+    
+    >>> import scipy,engines
+    >>> a=scipy.asarray([[1,2,3],[2,4,5]])
+    >>> dat=engines.pca(a, 2)
+    >>> dat['expvar']
+    array([0.,99.8561562,  100.])
 
-def pca(a, aopt, scale='scores', mode='normal'):
-    """ Principal Component Analysis model
-    mode:
-         -- fast : returns smallest dim scaled (T for n<=m, P for n>m )
-         -- normal : returns all model params and residuals after aopt comp
-         -- detailed    : returns all model params and all residuals
     """
-    
+    if center_axis>=0:
+        a = a - expand_dims(a.mean(center_axis), center_axis)
     m, n = a.shape
-    #print "rows: %s    cols: %s" %(m,n)
     if m>(n+100) or n>(m+100):
-        u, s, v = esvd(a)
+        u, e, v = esvd(a)
+        s = sqrt(e)
     else:
         u, s, vt = svd(a, 0)
         v = vt.T
-    eigvals = (1./m)*s
+        e = s**2
+    tol = 1e-10
+    eff_rank = sum(s>s[0]*tol)
+    aopt = minimum(aopt, eff_rank)
     T = u*s
+    s = s[:aopt]
+    e = e[:aopt]
     T = T[:,:aopt]
     P = v[:,:aopt]
     
     if scale=='loads':
-        tnorm = apply_along_axis(vnorm, 0, T)
+        T = T/s
-        T = T/tnorm
+        P = P*s
-        P = P*tnorm
 
     if mode == 'fast':
-        return {'T':T, 'P':P}
+        return {'T':T, 'P':P, 'aopt':aopt}
     
     if mode=='detailed':
-        """Detailed mode returns residual matrix for all comp.
-        That is E, is a three-mode matrix: (amax, m, n) """
         E = empty((aopt, m, n))
+        ssq = []
+        lev = []
+        expvarx = empty((aopt, aopt+1))
         for ai in range(aopt):
-            e = a - dot(T[:,:ai+1], P[:,:ai+1].T)
+            E[ai,:,:] = a - dot(T[:,:ai+1], P[:,:ai+1].T)
-            E[ai,:,:] = e.copy()
+            ssq.append([(E[ai,:,:]**2).sum(0), (E[ai,:,:]**2).sum(1)])
+            if scale=='loads':
+                lev.append([((s*T)**2).sum(1), (P**2).sum(1)])
             else:
+                lev.append([(T**2).sum(1), ((s*P)**2).sum(1)])
+        
+            expvarx[ai,:] = r_[0, 100*e.cumsum()/e.sum()]
+        
+    else:
+        # residuals
         E = a - dot(T, P.T)
+        SEP = E**2
+        ssq = [SEP.sum(0), SEP.sum(1)]
+        # leverages
+        if scale=='loads':
+            lev = [(1./m)+(T**2).sum(1), (1./n)+((P/s)**2).sum(1)]
+        else:
+            lev = [(1./m)+((T/s)**2).sum(1), (1./n)+(P**2).sum(1)]
+        # variances        
+        expvarx = r_[0, 100*e.cumsum()/e.sum()]
         
-    return {'T':T, 'P':P, 'E':E}
+    return {'T':T, 'P':P, 'E':E, 'expvarx':expvarx, 'levx':lev, 'ssqx':ssq, 'aopt':aopt}
 
-
+def pcr(a, b, aopt, scale='scores',mode='normal',center_axis=0):
-def pcr(a, b, aopt=2, scale='scores', mode='normal'):
     """ Principal Component Regression.
 
-    Returns 
+    Performs PCR on given matrix and returns results in a dictionary.
+
+    :Parameters:
+        a : array
+    Data measurement matrix, (samples x variables)
+        b : array
+    Data response matrix, (samples x responses)
+        aopt : int
+    Number of components to use, aopt<=min(samples, variables)
+
+    :Returns:  
+    results : dict
+        keys -- values,  T -- scores, P -- loadings, E -- residuals,
+        levx -- leverages, ssqx -- sum of squares, expvarx -- cumulative
+        explained variance, aopt -- number of components used
+    
+    :OtherParameters:
+    mode : str
+        Amount of info retained, ('fast', 'normal', 'detailed')
+    center_axis : int
+        Center along given axis. If neg.: no centering (-inf,..., matrix modes)
+  
+    :SeeAlso:
+        - pcr : other blm
+        - pls : other blm
+        - lpls : other blm
+ 
+    Notes
+    -----
+
+    Uses kernel speed-up if m>>n or m<<n.
+
+    If residuals turn rank deficient, a lower number of component than given
+    in input will be used. The number of components used is given in results-dict. 
+    
+
+    Examples
+    --------
+    
+    >>> import scipy,engines
+    >>> a=scipy.asarray([[1,2,3],[2,4,5]])
+    >>> dat=engines.pca(a, 2)
+    >>> dat['expvar']
+    array([0.,99.8561562,  100.])
 
     """
-    m, n = m_shape(a)
+    k, l = m_shape(b)
-    B = empty((aopt, n, l))
+    if center_axis>=0:
-    dat = pca(a, aopt=aopt, scale=scale, mode='normal', center_axis=0)
+        b = b - expand_dims(b.mean(center_axis), center_axis)
+    dat = pca(a, aopt=aopt, scale=scale, mode=mode, center_axis=center_axis)
     T = dat['T']
-    weigths = apply_along_axis(vnorm, 0, T)
+    weights = apply_along_axis(vnorm, 0, T)
     if scale=='loads':
         # fixme: check weights
-        Q = dot(b.T, T*weights)
+        Q = dot(b.T, T*weights**2)
     else:
         Q = dot(b.T, T/weights**2)
 
     if mode=='fast':
-        return {'T', T:, 'P':P, 'Q':Q}
+        dat.update({'Q':Q})
+        return dat
     if mode=='detailed':
-        for i in range(1, aopt+1, 1):
+        F = empty((aopt, k, l))
-            F[i,:,:] = b - dot(T[:,i],Q[:,:i].T)
+        for i in range(aopt):
+            F[i,:,:] = b - dot(T[:,:i+1], Q[:,:i+1].T)
     else:
         F = b - dot(T, Q.T)
     #fixme: explained variance in Y + Y-var leverages
-    dat.update({'Q',Q, 'F':F})
+    dat.update({'Q':Q, 'F':F})
     return dat
 
 def pls(a, b, aopt=2, scale='scores', mode='normal', ab=None):
@@ -271,7 +379,6 @@ def nipals_lpls(X, Y, Z, a_max, alpha=.7, mean_ctr=[2, 0, 1], mode='normal', sca
         X, mnX = center(X, xctr)
         Y, mnY = center(Y, xctr)
         Z, mnZ = center(Z, zctr)
-        print Z.mean(1)
 
     varX = pow(X, 2).sum()
     varY = pow(Y, 2).sum()
@@ -365,7 +472,7 @@ def nipals_lpls(X, Y, Z, a_max, alpha=.7, mean_ctr=[2, 0, 1], mode='normal', sca
 def m_shape(array):
     return matrix(array).shape
 
-def esvd(data):
+def esvd(data, amax=None):
     """SVD with the option of economy sized calculation
     Calculate subspaces of X'X or XX' depending on the shape
     of the matrix.
@@ -378,15 +485,28 @@ def esvd(data):
     m, n = data.shape
     if m>=n:
         kernel = dot(data.T, data)
+        if has_sym:
+            if not amax:
+                amax = n
+            pcrange = [n-amax, n]
+            s, v = symeig(kernel, range=pcrange, overwrite=True)
+            s = s[::-1]
+            v = v[:,arange(n, -1, -1)]
+        else:
             u, s, vt = svd(kernel)
-        u = dot(data, vt.T)
             v = vt.T
+        u = dot(data, v)
         for i in xrange(n):
             s[i] = vnorm(u[:,i])
             u[:,i] = u[:,i]/s[i]
     else:
         kernel = dot(data, data.T)
-        #data = (data + data.T)/2.0
+        if has_sym:
+            if not amax:
+                amax = m
+            pcrange = [m-amax, m]
+            s, u = symeig(kernel, range=pcrange, overwrite=True)
+        else:
             u, s, vt = svd(kernel)
             v = dot(u.T, data)
         for i in xrange(m):

scripts/lpls/rpy_go.py

@@ -3,32 +3,14 @@ import scipy
 import rpy
 silent_eval = rpy.with_mode(rpy.NO_CONVERSION, rpy.r)
 
-def get_term_sim(termlist, method = "JiangConrath", verbose=False):
-    """Returns the similariy matrix between go-terms.
 
-    Arguments:
+def goterms_from_gene(genelist, ontology='BP', garbage=None):
-        termlist: character vector of GO terms
-        method: one of
-        ("JiangConrath","Resnik","Lin","CoutoEnriched","CoutoJiangConrath","CoutoResnik","CoutoLin")
-        verbose: print out various information or not
-    """
-    _methods = ("JiangConrath","Resnik","Lin","CoutoEnriched","CoutoJiangConrath","CoutoResnik","CoutoLin")
-    assert(method in _methods)
-    assert(termlist[0][:2]=='GO')
-    rpy.r.library("GOSim")
-    return rpy.r.getTermSim(termlist, method = method, verbose = verbose)
-
-def get_gene_sim(genelist, similarity='OA',
-                 distance="Resnick"):
-    rpy.r.library("GOSim")
-    rpy.r.assign("ids", genelist)
-    silent_eval('a<-getGeneSim(ids)', verbose=FALSE)
-
-def goterms_from_gene(genelist, ontology=['BP'], garbage = ['IEA', 'ISS', 'ND']):
     """ Returns the go-terms from a specified genelist (Entrez id).
 
+    Recalculates the information content if needed based on selected evidence codes.
+    
     """
-    rpy.r.library("GO")
+    rpy.r.library("GOSim")
     _CODES = {"IMP" : "inferred from mutant phenotype",
               "IGI" : "inferred from genetic interaction",
               "IPI" :"inferred from physical interaction",
@@ -42,25 +24,46 @@ def goterms_from_gene(genelist, ontology=['BP'], garbage = ['IEA', 'ISS', 'ND'])
               "IC" : "inferred by curator"
               }
     _ONTOLOGIES = ['BP', 'CC', 'MF']
-    assert(scipy.all([(code in _CODES) for code in garbage]))
+    #assert(scipy.all([(code in _CODES) for code in garbage]) or garbage==None)
-    assert(scipy.all([(ont in _ONTOLOGIES) for ont in ontology]))
+    assert(ontology in _ONTOLOGIES)
-    have_these = rpy.r('as.list(GOTERM)').keys()
+    dummy = rpy.r.setOntology(ontology)
-    goterms = {}
+    ddef = False
+    if ontology=='BP' and garbage!=None:
+        # This is for ont=BP and garbage =['IEA', 'ISS', 'ND']
+        rpy.r.load("ICsBPIMP_IGI_IPI_ISS_IDA_IEP_TAS_NAS_IC.rda")
+        ic = rpy.r.assign("IC",rpy.r.IC, envir=rpy.r.GOSimEnv)
+        print len(ic)
+    else:
+        ic = rpy.r('get("IC", envir=GOSimEnv)')
+    print "loading GO definitions environment"
+    
+    gene2terms = {}
     for gene in genelist:
-        goterms[gene] = []
         info = rpy.r('GOENTREZID2GO[["' + str(gene) + '"]]')
         #print info
         if info:
+            skip=False
             for term, desc in info.items():
-                if term not in have_these:
+                if ic.get(term)==scipy.isinf:
-                    print "GO miss:"
+                    print "\nIC is Inf on this GO term %s for this gene: %s" %(term,gene)
-                    print term
+                    skip=True
-                if desc['Ontology'] in ontology and desc['Evidence'] not in garbage:
+                if ic.get(term)==None:
-                        goterms[gene].append(term)
+                    #print "\nHave no IC on this GO term %s for this gene: %s" %(term,gene)
+                    skip=True
+                if desc['Ontology']!=ontology:
+                    #print "\nThis GO term %s belongs to: %s:" %(term,desc['Ontology'])
+                    skip = True
+                if not skip:
+                    if gene2terms.has_key(gene):
+                        gene2terms[gene].append(term)
+                    else:
+                        gene2terms[gene] = [term]
+        else:
+           print "\nHave no Annotation on this gene: %s" %gene 
 
-    return goterms
+    return gene2terms
 
-def genego_matrix(goterms, tmat, gene_ids, term_ids, func=min):
+def genego_matrix(goterms, tmat, gene_ids, term_ids, func=max):
     ngenes = len(gene_ids)
     nterms = len(term_ids)
     gene2indx = {}
@@ -71,23 +74,46 @@ def genego_matrix(goterms, tmat, gene_ids, term_ids, func=min):
         term2indx[id]=i
     #G = scipy.empty((nterms, ngenes),'d')
     G = []
-    newindex = []
+    new_gene_index = []
     for gene, terms in goterms.items():
         g_ind = gene2indx[gene]
         if len(terms)>0:
             t_ind = []
-            newindex.append(g_ind)
+            new_gene_index.append(g_ind)
             for term in terms:
                 if term2indx.has_key(term): t_ind.append(term2indx[term])
-            print t_ind
             subsim = tmat[t_ind, :]
             gene_vec = scipy.apply_along_axis(func, 0, subsim)
             G.append(gene_vec)
 
-    return scipy.asarray(G), newindex
+    return scipy.asarray(G), new_gene_index
+
+def genego_sim(gene2go, gene_ids, all_go_terms, STerm, go_term_sim="OA", term_sim="Lin", verbose=False):
+    """Returns go-terms x genes similarity matrix.
+
+    :input:
+           - gene2go: dict: keys: gene_id, values: go_terms
+           - gene_ids: list of gene ids (entrez ids)
+           - STerm: (go_terms x go_terms) similarity matrix
+           - go_terms_sim: similarity measure between a gene and multiple go terms (max, mean, OA)
+           - term_sim: similarity measure between two go-terms
+           - verbose
+    """
+    rpy.r.library("GOSim")
+
+    #gene_ids = gene2go.keys()
+    GG = scipy.empty((len(all_go_terms), len(gene_ids)), 'd')
+    for j,gene in enumerate(gene_ids):
+        for i,go_term in enumerate(all_go_terms):
+            if verbose:
+                print "\nAssigning similarity from %s to terms(gene): %s" %(go_term,gene)
+            GG_ij = rpy.r.getGSim(go_term, gene2go[gene], similarity=go_term_sim,
+                                  similarityTerm=term_sim, STerm=STerm, verbose=verbose)
+            GG[i,j] = GG_ij
+    return GG
 
 def goterm2desc(gotermlist):
-    """Returns the go-terms description keyed by go-term
+    """Returns the go-terms description keyed by go-term.
     """
     rpy.r.library("GO")
     term2desc = {}

scripts/lpls/run_smoker.py

@@ -23,7 +23,7 @@ data = DX.asarray().T
 rpy.r.assign("data", data)
 cl = dot(DY.asarray(), diag([1,2,3])).sum(1)
 rpy.r.assign("cl", cl)
-rpy.r.assign("B", 100)
+rpy.r.assign("B", 20)
 # Perform a SAM analysis.
 print "Starting SAM"
 sam = rpy.r('sam.out<-sam(data=data,cl=cl,B=B,rand=123)')
@@ -32,63 +32,74 @@ print "SAM done"
 qq = rpy.r('qobj<-qvalue(sam.out@p.value)')
 qvals = asarray(qq['qvalues'])
 # cut off
-co = 0.001
+cutoff = 2
-index = where(qvals<0.01)[0]
+index = where(qvals<cutoff)[0]
 
 # Subset data
 X = DX.asarray()
 Xr = X[:,index]
 gene_ids = DX.get_identifiers('gene_ids', index)
-print "\nWorkiing on subset with %s genes " %len(gene_ids)
+print "\nWorking on subset with %s genes " %len(gene_ids)
-### Build GO data ####
+#gene2ind = {}
+#for i, gene in enumerate(gene_ids):
+#    gene2ind[gene] = i
 
-print "Go terms ..."
+### Build GO data ####
-goterms = rpy_go.goterms_from_gene(gene_ids)
+print "\n\nFiltering genes by Go terms "
-terms = set()
+gene2goterms = rpy_go.goterms_from_gene(gene_ids)
-for t in goterms.values():
+all_terms = set()
-    terms.update(t)
+for t in gene2goterms.values():
-terms = list(terms)
+    all_terms.update(t)
-print "Number of go-terms: %s" %len(terms)
+terms = list(all_terms)
+print "\nNumber of go-terms: %s" %len(terms)
+# update genelist
+gene_ids = gene2goterms.keys()
+print "\nNumber of genes: %s" %len(gene_ids)
 rpy.r.library("GOSim")
 # Go-term similarity matrix
 methods = ("JiangConrath","Resnik","Lin","CoutoEnriched","CoutoJiangConrath","CoutoResnik","CoutoLin")
-meth = methods[0]
+meth = methods[3]
 print "Term-term similarity matrix (method = %s)" %meth
 if meth=="CoutoEnriched":
     rpy.r('setEnrichmentFactors(alpha=0.1,beta=0.5)')
-print "Calculating term-term similarity matrix"
+print "\nCalculating term-term similarity matrix"
-tmat = rpy.r.getTermSim(terms, verbose=False, method=meth)
+
+rpytmat1 = rpy.with_mode(rpy.NO_CONVERSION, rpy.r.getTermSim)(terms, method=meth,verbose=False)
+tmat1 = rpy.r.assign("haha", rpytmat1)
+
+# check if all terms where found
+nanindex = where(isnan(tmat1[:,0]))[0]
+if len(nanindex)>0:
+    raise valueError("NANs in tmat")
+
+# Z-matrix
+#Z, newind = rpy_go.genego_matrix(terms, tmat, gene_ids, terms,func=mean)
+#Z = Z.T
+Z1 = rpy_go.genego_sim(gene2goterms,gene_ids,terms,rpytmat1,go_term_sim="OA",term_sim=meth)
+
+
+#### do another
+meth = methods[4]
+rpytmat = rpy.with_mode(rpy.NO_CONVERSION, rpy.r.getTermSim)(terms, method=meth,verbose=False)
+tmat = rpy.r.assign("haha", rpytmat)
+
 # check if all terms where found
 nanindex = where(isnan(tmat[:,0]))[0]
-keep=[]
-has_miss = False
 if len(nanindex)>0:
-    has_miss = True
+    raise valueError("NANs in tmat")
-    print "Some terms missing in similarity matrix"
+
-    keep = where(isnan(tmat[:,0])!=True)[0]
-    print "Number of nans: %d" %len(nanindex)
-    tmat_new = tmat[:,keep][keep,:]
-    new_terms = [i for ind,i in enumerate(terms) if ind in keep]
-    bad_terms = [i for ind,i in enumerate(terms) if ind not in keep]
-    # update go-term dict
-    for gene,trm in goterms.items():
-        for t in trm:
-            if t in bad_terms:
-                trm.remove(t)
-                if len(trm)==0:
-                    print "Removing gene: %s" %gene
-                goterms[gene]=trm
-    terms = new_terms
-    tmat = tmat_new
 # Z-matrix
-# func (min, max, median, mean, etc),
+#Z, newind = rpy_go.genego_matrix(terms, tmat, gene_ids, terms,func=mean)
-# func decides on the representation of gene-> goterm when multiple
+#Z = Z.T
-# goterms exist for one gene
+Z = rpy_go.genego_sim(gene2goterms,gene_ids,terms,rpytmat,go_term_sim="OA",term_sim=meth)
-Z, newind = rpy_go.genego_matrix(goterms, tmat, gene_ids, terms,func=mean)
+
-Z = Z.T
+
-# update X matrix (no go-terms available)
+
-Xr = Xr[:,newind]
+# update data (X) matrix
-new_gene_ids = asarray(gene_ids)[newind]
+#newind = [gene2ind[gene] for gene in gene_ids]
+newind = DX.get_indices('gene_ids', gene_ids)
+Xr = X[:,newind]
+#new_gene_ids = asarray(gene_ids)[newind]
 
 
 ######## LPLSR ########
@@ -112,11 +123,14 @@ if alpha_check:
         rmsep , yhat, ce = cv_lpls(Xr, Y, Z, a_max, alpha=alpha)
         Rmsep.append(rmsep)
         Yhat.append(yhat)
-        CE.append(yhat)
+        CE.append(ce)
     Rmsep = asarray(Rmsep)
     Yhat = asarray(Yhat)
     CE = asarray(CE)
 
+    figure(200)
+    
+
 
 # Significance Hotellings T
 Wx, Wz, Wy, = jk_lpls(Xr, Y, Z, aopt)
@@ -135,7 +149,13 @@ for a in range(m):
 ylim([rmsep.min()-.05, rmsep.max()+.05]) 
 title('RMSEP')
 
-figure(2) # Hypoid correlations
+figure(2)
+for a in range(m):
+    bar(arange(a_max)+a*bar_w+.1, class_error[:,a], width=bar_w, color=bar_col[a])
+ylim([class_error.min()-.05, class_error.max()+.05])
+title('Classification accuracy')
+
+figure(3) # Hypoid correlations
 plot_corrloads(Rz, pc1=0, pc2=1, s=tsqz/10.0, c='b', zorder=5, expvar=evz, ax=None)
 ax = gca()
 ylabels = DY.get_identifiers('_cat', sorted=True)