Python FileParser.read方法代码示例

# 需要导入模块: from Bio.PopGen.GenePop import FileParser [as 别名]
# 或者: from Bio.PopGen.GenePop.FileParser import read [as 别名]
def updateAll():
    global rec2, selRec2, popNames, remPops, remLoci, locusFst #,rec
    global summPanel, empiricalPanel, frame
    global myFst, maxRun, minRun # This is really a private var to be reused on report
    empiricalPanel.ignoreChanges = True
    myFst  = -1
    maxRun = -1
    minRun = -1
    selRec2 = FileParser.read(rec2.fname)
    #print rec2.fname, countPops(rec2)
    #for locus in remLoci:
    selRec2.remove_loci_by_name(remLoci, lpath + os.sep + "sr.tmp")
    shutil.copyfile(lpath + os.sep + "sr.tmp",
                    lpath + os.sep + "sr")
    selRec2 = FileParser.read(lpath + os.sep + "sr")

    #print len(popNames), remPops
    for i in range(len(popNames)-1, -1, -1):
        #print i, popNames[i]
        if popNames[i] in remPops:
            selRec2.remove_population(i, lpath + os.sep + "sr.tmp")
            shutil.copyfile(lpath + os.sep + "sr.tmp",
                            lpath + os.sep + "sr")
            selRec2 = FileParser.read(lpath + os.sep + "sr")
            #print i, os.path.getsize(lpath + os.sep + "sr"), countPops(selRec2)
    summPanel.update(rec2, popNames, remPops, remLoci)
    enableAllMenus()
    empiricalPanel.setTotalPops(len(popNames))
    def after():
        chartPanel.setMarkers(locusFst)
        chartPanel.updateChartDataset()
        empiricalPanel.knownPops = countPops(selRec2)
        empiricalPanel.ignoreChanges = False
    runDatacal(after)

# 需要导入模块: from Bio.PopGen.GenePop import FileParser [as 别名]
# 或者: from Bio.PopGen.GenePop.FileParser import read [as 别名]
    def test_remove_features(self):
        """Testing the ability to remove population/loci via class methods."""
        for index in range(len(self.files)):
            fname = self.files[index]
            ftemp = tempfile.NamedTemporaryFile(mode="w+", delete=False)
            ftemp.close()
            rec = FileParser.read(fname)
            rec.remove_loci_by_position([0], ftemp.name)
            with open(ftemp.name, 'r') as ft:
                ft.seek(0)
                rec2 = GenePop.read(iter(ft))
            self.assertEqual(rec.loci_list[1:], rec2.loci_list)

            rec.remove_locus_by_position(0, ftemp.name)
            with open(ftemp.name, 'r') as ft:
                ft.seek(0)
                rec3 = GenePop.read(iter(ft))
            self.assertEqual(rec.loci_list[1:], rec3.loci_list)

            rec.remove_locus_by_name(rec.loci_list[0], ftemp.name)
            with open(ftemp.name, 'r') as ft:
                ft.seek(0)
                rec4 = GenePop.read(iter(ft))
            self.assertEqual(rec.loci_list[1:], rec4.loci_list)

            rec.remove_loci_by_name([rec.loci_list[0]], ftemp.name)
            with open(ftemp.name, 'r') as ft:
                ft.seek(0)
                rec5 = GenePop.read(iter(ft))
            self.assertEqual(rec.loci_list[1:], rec5.loci_list)

            os.remove(ftemp.name)
            rec._handle.close()

# 需要导入模块: from Bio.PopGen.GenePop import FileParser [as 别名]
# 或者: from Bio.PopGen.GenePop.FileParser import read [as 别名]
def _convert_genepop_to_fdist_big(gp_rec, report_pops = None):
    """Converts a big GenePop record to a FDist one.

       Parameters:
       gp_rec - Genepop Record (Big)

       Returns:
       FDist record.
    """
    fd_rec = Bio.PopGen.FDist.Record()

    fd_rec.data_org = 1
    fd_rec.num_loci = len(gp_rec.loci_list)
    num_loci = len(gp_rec.loci_list)
    loci = []
    for i in range(num_loci):
        loci.append(set())
    pops = []
    work_rec = FileParser.read(gp_rec.fname)
    lParser = work_rec.get_individual()

    def init_pop():
        my_pop = []
        for i in range(num_loci):
            my_pop.append({})
        return my_pop

    curr_pop = init_pop()
    num_pops = 1
    if report_pops:
        report_pops(num_pops)
    while lParser:
        if lParser is not True:
            for loci_pos in range(num_loci):
                for al in lParser[1][loci_pos]:
                    if al is not None:
                        loci[loci_pos].add(al)
                        curr_pop[loci_pos][al]= curr_pop[loci_pos].get(al,0)+1
        else:
            pops.append(curr_pop)
            num_pops += 1
            if report_pops:
                report_pops(num_pops)
            curr_pop = init_pop()
        lParser = work_rec.get_individual()
    work_rec._handle.close()  # TODO - Needs a proper fix
    pops.append(curr_pop)
    fd_rec.num_pops = num_pops
    for loci_pos in range(num_loci):
        alleles = list(loci[loci_pos])
        alleles.sort()
        loci_rec = [len(alleles), []]
        for pop in pops:
            pop_rec = []
            for allele in alleles:
                pop_rec.append(pop[loci_pos].get(allele, 0))
            loci_rec[1].append(pop_rec)
        fd_rec.loci_data.append(tuple(loci_rec))
    return fd_rec

# 需要导入模块: from Bio.PopGen.GenePop import FileParser [as 别名]
# 或者: from Bio.PopGen.GenePop.FileParser import read [as 别名]
 def test_convert_big(self):
     """Big interface conversion test.
     """
     for i in range(len(self.names)):
         gp_rec = FileParser.read(self.names[i])
         fd_rec = convert_genepop_to_fdist(gp_rec)
         assert(fd_rec.num_loci == 3)
         assert(fd_rec.num_pops == 3)

# 需要导入模块: from Bio.PopGen.GenePop import FileParser [as 别名]
# 或者: from Bio.PopGen.GenePop.FileParser import read [as 别名]
def loadGenePop(file):
    global rec2, popNames, remPops, remLoci #,rec
    #rec = GenePop.read(open(str(file)))
    try:
        rec2 = FileParser.read(file)
        if isDominant:
            checkAlleles(file)
        remPops = []
        remLoci = []
        #popNames = ['pop' + str(i+1) for i in range(len(rec.populations))]
        popNames = ['pop' + str(i+1) for i in range(countPops(rec2))]
    except:
        error(frame, "Not a genepop file!")

# 需要导入模块: from Bio.PopGen.GenePop import FileParser [as 别名]
# 或者: from Bio.PopGen.GenePop.FileParser import read [as 别名]
 def test_file_record_parser(self):
     """Basic operation of the File Record Parser.
     """
     for index in range(len(self.files)):
         fname = self.files[index]
         rec = FileParser.read(fname)
         assert isinstance(rec, FileParser.FileRecord)
         assert len(rec.loci_list) == self.num_loci[index]
         for skip in range(self.pops_indivs[index][0]):
             if rec.skip_population() == False:
                 raise Error("Not enough populations")
         if rec.skip_population() == True:
                 raise Error("Too much populations")
         for i in range(self.pops_indivs[index][0]):
             continue
             assert len(rec.populations[i]) == \
                        self.pops_indivs[index][1][i]

# 需要导入模块: from Bio.PopGen.GenePop import FileParser [as 别名]
# 或者: from Bio.PopGen.GenePop.FileParser import read [as 别名]
 def test_file_record_parser(self):
     """Basic operation of the File Record Parser."""
     for index in range(len(self.files)):
         fname = self.files[index]
         rec = FileParser.read(fname)
         self.assertIsInstance(rec, FileParser.FileRecord)
         self.assertTrue(str(rec).startswith(
                 "Generated by createGenePop.py - (C) Tiago Antao\n"
                 "136255903\n"
                 "136257048\n"
                 "136257636\n"
                 "Pop\n"), "Did not expect this:\n%s" % rec)
         self.assertEqual(len(rec.loci_list), self.num_loci[index])
         for skip in range(self.pops_indivs[index][0]):
             if rec.skip_population() is False:
                 raise Exception("Not enough populations")
         if rec.skip_population() is True:
             raise Exception("Too much populations")
         for i in range(self.pops_indivs[index][0]):
             continue
         rec._handle.close()  # TODO - Needs a proper fix

# 需要导入模块: from Bio.PopGen.GenePop import FileParser [as 别名]
# 或者: from Bio.PopGen.GenePop.FileParser import read [as 别名]
def checkAlleles(file):
    df = FileParser.read(file)
    countAlleles = []
    for locus in df.loci_list:
        countAlleles.append(set())
    indiv = df.get_individual()
    while indiv:
        if type(indiv) == tuple:
            name, loci = indiv
            for l in range(len(loci)):
                for a in loci[l]:
                    if a: countAlleles[l].add(a)
        indiv = df.get_individual()
    probLoci = []
    for l in range(len(countAlleles)):
        if len(countAlleles[l])>2:
            probLoci.append(df.loci_list[l])
    if probLoci != []:
        if len(probLoci)>5:
            error(frame, "Many (%d) loci have more than 2 alleles" % (len(probLoci)))
        else:
            error(frame, "Some loci have more than 2 alleles: %s" % (str(probLoci)))

# 需要导入模块: from Bio.PopGen.GenePop import FileParser [as 别名]
# 或者: from Bio.PopGen.GenePop.FileParser import read [as 别名]
 def countPops(rec):
     f2 = FileParser.read(rec.fname)
     popCnt = 1
     while f2.skip_population():
         popCnt += 1
     return popCnt

# 需要导入模块: from Bio.PopGen.GenePop import FileParser [as 别名]
# 或者: from Bio.PopGen.GenePop.FileParser import read [as 别名]
def _convert_genepop_to_fdist_big_old(gp_rec, report_loci=None):
    """Converts a big GenePop record to a FDist one.

       Parameters:
       gp_rec - Genepop Record (Big)

       Returns:
       FDist record.
    """
    fd_rec = Bio.PopGen.FDist.Record()

    def countPops(rec):
        f2 = FileParser.read(rec.fname)
        popCnt = 1
        while f2.skip_population():
            popCnt += 1
        return popCnt

    fd_rec.data_org = 0
    fd_rec.num_loci = len(gp_rec.loci_list)
    work_rec0 = FileParser.read(gp_rec.fname)
    fd_rec.num_pops = countPops(work_rec0)

    num_loci = len(gp_rec.loci_list)
    for lc_i in range(num_loci):
        if report_loci:
            report_loci(lc_i, num_loci)
        work_rec = FileParser.read(gp_rec.fname)
        work_rec2 = FileParser.read(gp_rec.fname)

        alleles = []
        pop_data = []
        lParser = work_rec.get_individual()
        while lParser:
            if lParser is not True:
                for al in lParser[1][lc_i]:
                    if al is not None and al not in alleles:
                        alleles.append(al)
            lParser = work_rec.get_individual()
        # here we go again (necessary...)
        alleles.sort()

        def process_pop(pop_data, alleles, allele_counts):
            allele_array = []  # We need the same order as in alleles
            for allele in alleles:
                allele_array.append(allele_counts.get(allele, 0))
            pop_data.append(allele_array)

        lParser = work_rec2.get_individual()
        allele_counts = {}
        for allele in alleles:
            allele_counts[allele] = 0
        allele_counts[None] = 0
        while lParser:
            if lParser is True:
                process_pop(pop_data, alleles, allele_counts)
                allele_counts = {}
                for allele in alleles:
                    allele_counts[allele] = 0
                allele_counts[None] = 0
            else:
                for al in lParser[1][lc_i]:
                    allele_counts[al] += 1
            lParser = work_rec2.get_individual()
        process_pop(pop_data, alleles, allele_counts)
        fd_rec.loci_data.append((len(alleles), pop_data))
    return fd_rec

# 需要导入模块: from Bio.PopGen.GenePop import FileParser [as 别名]
# 或者: from Bio.PopGen.GenePop.FileParser import read [as 别名]
def report(fst):
    global numAttempts
    global fda, fdc, fdRequest, runState, selRec2, splitSize
    global chartPanel, simsDonePanel, systemPanel, empiricalPanel
    global empiricalPanel, menuHandles, statusPanel, frame
    global myFst, maxRun, minRun # This is really a private var to be reused
    global isTemporal, tempSamples, fdt
    if isTemporal:
        fdt.acquire()
    else:
        fda.acquire()
        if myFst < 0:
            myFst = empiricalPanel.getFst()
        if maxRun < 0:
            maxRun = 1.0
            minRun = 0.0
    ext = FDistExtra.getExt()
    fdc = FDistController('.', ext)
    ci = systemPanel.getCI()
    chartPanel.drawCI = True
    confLines = changeChartCI(False)
    simsDonePanel.increment(splitSize / 1000.0)
    if isTemporal:
        desiredNe = empiricalPanel.getNe()
    else:
        desiredFst = empiricalPanel.getFst()
    if simsDonePanel.getRange() == simsDonePanel.getValue():
        #print runState
        if isTemporal:
            fdt.release()  # We are the last one, this is safe
        else:
            fda.release()  # We are the last one, this is safe
        if runState == 'ForceBeforeNeutral' or runState == 'Force':
            os.remove(lpath + os.sep + 'out.dat') #careful, not for 5000 case
            #print "max", maxRun, "min", minRun
            nextFst, maxRun, minRun = approximate_fst(desiredFst, fst, myFst,
                maxRun, minRun)
            #print "obtained", fst, "desired", desiredFst, "next", nextFst, "max", maxRun, "min", minRun
            numAttempts += 1
            if nextFst == myFst or numAttempts == 20:
                numSims = systemPanel.getNumSims()
                if runState == 'Force':
                    statusPanel.setStatus('Running final simulation', Color.YELLOW)
                    runState = 'Final'
                else:
                    runState = 'Neutral'
                    statusPanel.setStatus('Simulation pass to determine initial neutral set', Color.CYAN)
            else:
                statusPanel.setStatus('Forcing correct mean Fst, current error is ' +
                                str(round(abs(fst - desiredFst), 3)), Color.RED)
                numSims = 50000
                myFst = nextFst
            npops = empiricalPanel.getTotalPops()
            nsamples = countPops(selRec2)
            numCores = systemPanel.getNumCores()
            sampSize = empiricalPanel.getSampleSize()
            if isDominant:
                theta = empiricalPanel.getTheta()
                beta = empiricalPanel.getBeta()
                crit = empiricalPanel.getCrit()
                mut = None
            else:
                theta = beta = crit = None
                mutStr = empiricalPanel.mut.getSelectedItem()
                mut = getMut(mutStr)
            if isTemporal:
                pass #XXX
            else:
                runFDistPart(False, selRec2, mut, numSims, npops, nsamples,
                    myFst, sampSize, theta, beta, crit, numCores)
        elif runState == 'Neutral':
            maxRun = -1
            minRun = -1
            myFst  = -1
            if isDominant:
                pv = fdc.run_pv(data_dir =  lpath, version=2)
            else:
                pv = fdc.run_pv(data_dir =  lpath, version=1)
            #pv = get_pv(data_dir = lpath)
            selLoci = getSelLoci(pv)
            if fdRequest == 'Neutral':
                runState = 'Final'
                numSims  = systemPanel.getNumSims()
                statusPanel.setStatus('Running final simulation', Color.YELLOW)
            else:
                runState = 'Force'
                numAttempts = 0
                statusPanel.setStatus('Forcing correct mean Fst for final pass', Color.RED)
                numSims  = 50000
            neutralRec = FileParser.read(selRec2.fname)
            #for locus in selLoci:
            neutralRec.remove_loci_by_name(selLoci, lpath+os.sep+"nr.tmp")
            shutil.copyfile(lpath + os.sep + "nr.tmp",
                    lpath + os.sep + "nr")
            neutralRec = FileParser.read(lpath + os.sep + "nr")
            createInfile(convert_genepop_to_fdist(neutralRec))
            if isTemporal:
                dc = Datacal()
                dc.compute(lpath + os.sep + "infile", lpath + os.sep + "data_fst_outfile")
                dc.computeNe(tempSamples[-1] - tempSamples[0])
#.........这里部分代码省略.........

# 需要导入模块: from Bio.PopGen.GenePop import FileParser [as 别名]
# 或者: from Bio.PopGen.GenePop.FileParser import read [as 别名]
def countPops(rec2):
    f2 = FileParser.read(rec2.fname)
    pop = 1
    while f2.skip_population():
        pop += 1
    return pop