class Simulation(object):
def __init__(self):
self.markerSetBuilder = MarkerSetBuilder()
self.img = IMG()
self.simContigLen = 10000
def __selectMarkerSet(self, tree, internalNode, metadata, ubiquityThreshold, singleCopyThreshold, queueOut):
"""Select marker set for parent edge of specified internal node."""
# get genomes descendant from each child of the specified internal node
leaves = []
for child in internalNode.child_nodes():
genomeIds = set()
for leaf in child.leaf_nodes():
genomeId = leaf.taxon.label.replace('IMG_', '')
genomeIds.add(genomeId)
duplicateGenomes = self.markerSetBuilder.duplicateSeqs.get(leaf.taxon.label, [])
for dup in duplicateGenomes:
dupId = dup.replace('IMG_', '')
genomeIds.add(dupId)
leaves.append(genomeIds)
# make sure each set of leaves contains at least a minimum number of genomes
orderedLeaves = sorted(leaves, key=len)
if len(orderedLeaves[0]) < 5:
queueOut.put(('NA', -1, -1, -1, -1, -1))
return
# calculate marker genes with all genomes in lineage with the fewest genomes removed
binMarkerGenes, _ = self.markerSetBuilder.buildBinMarkerSet(tree, internalNode, ubiquityThreshold, singleCopyThreshold, bMarkerSet = False, genomeIdsToRemove = orderedLeaves[0])
# evaluate accuracy of completeness and contamination estimations on different partial genomes from lineage with fewest genomes
testGenomeIds = random.sample(orderedLeaves[0], min(len(orderedLeaves[0]), 100))
deltaComp = defaultdict(list)
deltaCont = defaultdict(list)
for testGenomeId in testGenomeIds:
geneDistTable = self.img.geneDistTable([testGenomeId], binMarkerGenes.getMarkerGenes(), spacingBetweenContigs=0)
genomeSize = readFastaBases(os.path.join(self.img.genomeDir, testGenomeId, testGenomeId + '.fna'))
repsPerGenome = 100
for _ in xrange(0, repsPerGenome):
testComp = random.uniform(0.5, 1.0)
testCont = random.uniform(0, 0.2)
trueComp, trueCont, startPartialGenomeContigs = self.markerSetBuilder.sampleGenome(genomeSize, testComp, testCont, self.simContigLen)
for ms in binMarkerGenes.markerSetIter():
containedMarkerGenes = self.markerSetBuilder.containedMarkerGenes(ms.getMarkerGenes(), geneDistTable[testGenomeId], startPartialGenomeContigs, self.simContigLen)
completeness, contamination = ms.genomeCheck(containedMarkerGenes, bIndividualMarkers=True)
if completeness == 0.0:
print ms.getMarkerGenes()
print geneDistTable[testGenomeId]
print startPartialGenomeContigs
print genomeSize
print '*****************' + testGenomeId
sys.exit()
deltaComp[ms.lineageStr].append(completeness - trueComp)
deltaCont[ms.lineageStr].append(contamination - trueCont)
# determine lineage-specific marker set with best average performance
curBest = 1000
bestUID = None
dCompBest = 0
dContBest = 0
for lineageStr in deltaComp:
dComp, dCont = mean(abs(array(deltaComp[lineageStr]))), mean(abs(array(deltaCont[lineageStr])))
if (dComp + dCont) < curBest:
dCompBest = dComp
dContBest = dCont
dCompStdBest = std(abs(array(deltaComp[lineageStr])))
dContStdBest = std(abs(array(deltaCont[lineageStr])))
bestUID = lineageStr.split('|')[0]
curBest = dComp + dCont
queueOut.put((internalNode, bestUID, dCompBest, dCompStdBest, dContBest, dContStdBest))
def __workerThread(self, tree, metadata, ubiquityThreshold, singleCopyThreshold, queueIn, queueOut):
"""Process each data item in parallel."""
while True:
internalNode = queueIn.get(block=True, timeout=None)
if internalNode == None:
break
self.__selectMarkerSet(tree, internalNode, metadata, ubiquityThreshold, singleCopyThreshold, queueOut)
def __writerThread(self, numInternalNodes, writerQueue):
"""Store or write results of worker threads in a single thread."""
fout = open('/tmp/simInferBestMarkerSet.tsv', 'w')
fout.write('Internal node ID\tMarker set ID\tmean % delta comp\tstd % delta comp\tmean % delta cont\tstd % delta cont\n')
itemsProcessed = 0
while True:
internalNode, bestUID, dCompBest, dCompStdBest, dContBest, dContStdBest = writerQueue.get(block=True, timeout=None)
if internalNode == None:
break
itemsProcessed += 1
statusStr = ' Finished processing %d of %d (%.2f%%) internal branches.' % (itemsProcessed, numInternalNodes, float(itemsProcessed)*100/(numInternalNodes))
sys.stdout.write('%s\r' % statusStr)
sys.stdout.flush()
if internalNode != 'NA':
fout.write(internalNode.label + '\t%s\t%.2f\t%.2f\t%.2f\t%.2f\n' % (bestUID, dCompBest, dCompStdBest, dContBest, dContStdBest))
fout.close()
sys.stdout.write('\n')
def run(self, ubiquityThreshold, singleCopyThreshold, numThreads):
random.seed(0)
print '\n Calculating global gene count table.'
metadata = self.img.genomeMetadata()
self.markerSetBuilder.globalGeneCountTable = self.img.geneCountTable(metadata.keys())
print '\n Reading reference genome tree.'
treeFile = os.path.join(os.path.dirname(sys.argv[0]), '..', 'data', 'genome_tree', 'genome_tree_prok.refpkg', 'genome_tree.final.tre')
tree = dendropy.Tree.get_from_path(treeFile, schema='newick', as_rooted=True, preserve_underscores=True)
print ' Evaluating %d internal nodes.' % len(tree.internal_nodes())
workerQueue = mp.Queue()
writerQueue = mp.Queue()
for internalNode in tree.internal_nodes():
if internalNode.parent_node != None:
workerQueue.put(internalNode)
for _ in range(numThreads):
workerQueue.put(None)
metadata = self.img.genomeMetadata()
workerProc = [mp.Process(target = self.__workerThread, args = (tree, metadata, ubiquityThreshold, singleCopyThreshold, workerQueue, writerQueue)) for _ in range(numThreads)]
writeProc = mp.Process(target = self.__writerThread, args = (len(tree.internal_nodes())-1, writerQueue))
writeProc.start()
for p in workerProc:
p.start()
for p in workerProc:
p.join()
writerQueue.put((None, None, None, None, None, None))
writeProc.join()
