コード例 #1
0
if __name__ == "__main__":
	# Load required modules
	import sys, os, json
	sys.path.append('../')
	import comet as C, run_comet_simple as RC, run_exhaustive as RE

	# Hard-coded results of earlier runs
	trueMCMC = [["CDK4(A),CDKN2A(D),TP53 EGFR,PDGFRA(A),PTEN(D)", 36, 30.44954813369114], ["CDK4(A),CDKN2A(D),TP53 EGFR,PTEN,PTEN(D)", 47, 30.31560877273872], ["CDK4(A),CDKN2A(D),TP53 EGFR,PDGFRA(A),RB1(D)", 6, 28.487778643951266], ["CDK4(A),CDKN2A(D),TP53 PDGFRA(A),PTEN,PTEN(D)", 2, 27.986374758844306], ["CDK4(A),CDKN2A(D),TP53 EGFR,PTEN(D),RB1(D)", 1, 27.207736477342962], ["CDK4(A),CDKN2A(D),TP53 EGFR,MDM4(A),RB1(D)", 1, 26.9059191024149], ["CDK4(A),CDKN2A(D),RB1(D) EGFR,PDGFRA(A),PTEN(D)", 3, 26.35048099140887], ["CDK4(A),CDKN2A(D),RB1(D) EGFR,PTEN,PTEN(D)", 1, 26.216541630456447], ["CDK4(A),CDKN2A(D),TP53 MDM4(A),PTEN(D),RB1(D)", 1, 24.99799710738864], ["CDK4(A),CDKN2A(D),TP53 EGFR,MDM4(A),PTEN", 1, 24.910765737533954], ["CDK4(A),CDKN2A(D),TP53 PDGFRA(A),PTEN,RB1(D)", 1, 24.633365961904023]]
	trueExhaustive = [[["CDK4(A)", "CDKN2A(D)", "TP53"], 0.0, 24.61051], [["CDK4(A)", "CDKN2A(D)", "RB1(D)"], 0.0, 20.51144], [["CDKN2A(D)", "RB1(D)", "TP53"], 0.0, 15.30173], [["CDKN2A(D)", "PDGFRA(A)", "TP53"], 0.0, 14.35459], [["CDK4(A)", "CDKN2A(D)", "PTEN(D)"], 1e-05, 11.92406], [["CDKN2A(D)", "PTEN(D)", "TP53"], 1e-05, 11.90466], [["CDK4(A)", "CDKN2A(D)", "EGFR"], 1e-05, 11.49421], [["CDKN2A(D)", "MDM4(A)", "TP53"], 2e-05, 10.68068], [["CDK4(A)", "CDKN2A(D)", "MDM4(A)"], 4e-05, 10.07425], [["CDKN2A(D)", "PTEN", "TP53"], 7e-05, 9.55559], [["CDKN2A(D)", "EGFR", "TP53"], 0.00015, 8.82747], [["CDK4(A)", "CDKN2A(D)", "PTEN"], 0.00035, 7.96747], [["CDK4(A)", "CDKN2A(D)", "PDGFRA(A)"], 0.00048, 7.6389], [["EGFR", "PDGFRA(A)", "PTEN(D)"], 0.00291, 5.83904], [["EGFR", "PTEN", "PTEN(D)"], 0.00333, 5.7051], [["EGFR", "PDGFRA(A)", "RB1(D)"], 0.02071, 3.87727], [["CDK4(A)", "PTEN", "PTEN(D)"], 0.02471, 3.70061], [["CDK4(A)", "EGFR", "RB1(D)"], 0.03291, 3.41404], [["PDGFRA(A)", "PTEN", "PTEN(D)"], 0.03419, 3.37587], [["CDK4(A)", "EGFR", "PTEN(D)"], 0.04911, 3.01377], [["PTEN", "PTEN(D)", "TP53"], 0.0636, 2.75514], [["EGFR", "PTEN(D)", "RB1(D)"], 0.07448, 2.59723], [["EGFR", "PTEN(D)", "TP53"], 0.07453, 2.59651], [["CDKN2A(D)", "EGFR", "RB1(D)"], 0.08983, 2.40983], [["MDM4(A)", "PTEN(D)", "TP53"], 0.09648, 2.33843], [["EGFR", "MDM4(A)", "RB1(D)"], 0.10072, 2.29541], [["CDKN2A(D)", "EGFR", "PTEN"], 0.12616, 2.0702], [["PTEN", "PTEN(D)", "RB1(D)"], 0.13519, 2.00109], [["EGFR", "MDM4(A)", "PDGFRA(A)"], 0.15149, 1.88723], [["CDK4(A)", "EGFR", "PDGFRA(A)"], 0.17147, 1.76336], [["EGFR", "MDM4(A)", "TP53"], 0.18851, 1.66862], [["MDM4(A)", "PTEN", "PTEN(D)"], 0.19338, 1.64308], [["CDKN2A(D)", "MDM4(A)", "RB1(D)"], 0.20638, 1.57806], [["CDK4(A)", "EGFR", "PTEN"], 0.20825, 1.56901], [["PDGFRA(A)", "PTEN(D)", "RB1(D)"], 0.21409, 1.54137], [["CDK4(A)", "PTEN(D)", "RB1(D)"], 0.23869, 1.43258], [["PDGFRA(A)", "PTEN(D)", "TP53"], 0.24857, 1.39204], [["CDKN2A(D)", "PDGFRA(A)", "PTEN"], 0.27821, 1.27939], [["MDM4(A)", "PDGFRA(A)", "TP53"], 0.29567, 1.21851], [["PTEN(D)", "RB1(D)", "TP53"], 0.3062, 1.18352], [["CDKN2A(D)", "PDGFRA(A)", "RB1(D)"], 0.31956, 1.14081], [["CDK4(A)", "EGFR", "MDM4(A)"], 0.3235, 1.12854], [["CDKN2A(D)", "PTEN", "RB1(D)"], 0.41747, 0.87355], [["CDK4(A)", "EGFR", "TP53"], 0.44446, 0.81089], [["MDM4(A)", "PDGFRA(A)", "RB1(D)"], 0.4468, 0.80566], [["CDK4(A)", "MDM4(A)", "RB1(D)"], 0.47088, 0.75315], [["MDM4(A)", "RB1(D)", "TP53"], 0.47495, 0.74454], [["EGFR", "PDGFRA(A)", "TP53"], 0.53346, 0.62837], [["EGFR", "PDGFRA(A)", "PTEN"], 0.53346, 0.62837], [["MDM4(A)", "PDGFRA(A)", "PTEN(D)"], 0.54257, 0.61144], [["EGFR", "MDM4(A)", "PTEN(D)"], 0.58204, 0.54122], [["CDKN2A(D)", "PTEN(D)", "RB1(D)"], 0.59467, 0.51974], [["CDK4(A)", "PTEN(D)", "TP53"], 0.60326, 0.50541], [["MDM4(A)", "PDGFRA(A)", "PTEN"], 0.62282, 0.47349], [["MDM4(A)", "PTEN", "TP53"], 0.62456, 0.4707], [["CDK4(A)", "MDM4(A)", "TP53"], 0.65547, 0.42241], [["MDM4(A)", "PTEN(D)", "RB1(D)"], 0.67876, 0.38749], [["CDKN2A(D)", "MDM4(A)", "PTEN"], 0.68465, 0.37884], [["CDK4(A)", "PDGFRA(A)", "PTEN(D)"], 0.70878, 0.34421], [["CDKN2A(D)", "EGFR", "PDGFRA(A)"], 0.7178, 0.33157], [["CDK4(A)", "MDM4(A)", "PTEN(D)"], 0.71914, 0.3297], [["EGFR", "RB1(D)", "TP53"], 0.73762, 0.30432], [["EGFR", "MDM4(A)", "PTEN"], 0.74063, 0.30026], [["CDK4(A)", "PDGFRA(A)", "RB1(D)"], 0.75931, 0.27534], [["CDKN2A(D)", "PTEN", "PTEN(D)"], 0.77636, 0.25314], [["PDGFRA(A)", "RB1(D)", "TP53"], 0.80285, 0.21958], [["CDK4(A)", "MDM4(A)", "PTEN"], 0.82971, 0.18668], [["CDKN2A(D)", "EGFR", "PTEN(D)"], 0.83641, 0.17864], [["CDKN2A(D)", "EGFR", "MDM4(A)"], 0.83641, 0.17864], [["CDKN2A(D)", "MDM4(A)", "PTEN(D)"], 0.8707, 0.13846], [["CDKN2A(D)", "PDGFRA(A)", "PTEN(D)"], 0.8759, 0.1325], [["CDKN2A(D)", "MDM4(A)", "PDGFRA(A)"], 0.8759, 0.1325], [["EGFR", "PTEN", "RB1(D)"], 0.88503, 0.12214], [["EGFR", "PTEN", "TP53"], 0.88751, 0.11933], [["CDK4(A)", "PTEN", "TP53"], 0.88937, 0.11725], [["CDK4(A)", "PDGFRA(A)", "PTEN"], 0.91005, 0.09426], [["CDK4(A)", "PTEN", "RB1(D)"], 0.91538, 0.08841], [["PTEN", "RB1(D)", "TP53"], 0.95692, 0.04404], [["CDK4(A)", "MDM4(A)", "PDGFRA(A)"], 0.95942, 0.04142], [["CDK4(A)", "RB1(D)", "TP53"], 0.96379, 0.03688], [["PDGFRA(A)", "PTEN", "RB1(D)"], 0.9774, 0.02286], [["PDGFRA(A)", "PTEN", "TP53"], 0.98084, 0.01935], [["MDM4(A)", "PTEN", "RB1(D)"], 0.98887, 0.01119], [["CDK4(A)", "PDGFRA(A)", "TP53"], 0.9892, 0.01086]]

	# Run CoMEt MCMC using a fixed seed
	seed = 23
	mcmcArgs = [ "-m", "../example_datasets/gbm/GBM.m2",  "-o", "tmp-mcmc",
				 "-g", "../example_datasets/gbm/GBM.glst", "-N", "10000",
				 "--seed", str(seed), "-mf", "30", "-ks", "3", "3", "--noviz"]
	mcmcResults = RC.run(RC.get_parser().parse_args(mcmcArgs))
	if os.path.exists("tmp-mcmc.para.k33.10K.1.json"):
		os.unlink("tmp-mcmc.para.k33.10K.1.json")
	if os.path.exists("tmp-mcmc-sum.k33.10K.1.tsv"):
		os.unlink("tmp-mcmc.sum.k33.10K.1.tsv")
		
	# Run exhaustive
	exhaustArgs = ["-m", "../example_datasets/gbm/GBM.m2", "-o", "tmp",
				   "-g", "../example_datasets/gbm/GBM.glst", "-k", "3",
				   "-mf", "30"]
	exhaustResults = RE.run(RE.get_parser().parse_args(exhaustArgs))
	exhaustResults = [ (genes, round(phi, 5), round(score, 5)) for genes, phi, score in exhaustResults]

	if os.path.exists("tmp-k3-exact-exhaustive.tsv"):
		os.unlink("tmp-k3-exact-exhaustive.tsv")
コード例 #2
0
ファイル: run_comet_full.py プロジェクト: mruffalo/comet
def runComet(cometArgs):
    return RC.run( RC.get_parser().parse_args(cometArgs) )
コード例 #3
0
def run(args):

    # Set up the arguments for a general CoMEt run on real data
    realOutputDir = "{}/comet-results".format(args.output_directory)
    realCometArgs = []
    permuteFlags = ["-np", "--parallel", "--keep_temp_files", "-o"]
    for i, arg in enumerate(sys.argv[1:]):
        if arg not in permuteFlags and sys.argv[i] not in permuteFlags:
            realCometArgs.append(arg)

    realCometArgs += ["-o", realOutputDir, "--noviz"]
    # perform simple run without viz first.
    results = runComet(realCometArgs)

    # Load mutation data using Multi-Dendrix and output as a temporary file
    realMutations = C.load_mutation_data(args.mutation_matrix,
                                         args.patient_file, args.gene_file,
                                         args.min_freq, args.subtype)
    m, n, genes, patients, geneToCases, patientToGenes, subtypes = realMutations

    if args.verbose:
        print(f'* Mutation data: {m} genes x {n} patients')

    # Construct bipartite graph from mutation data
    if args.verbose: print('* Creating bipartite graph...')
    G = C.construct_mutation_graph(geneToCases, patientToGenes)
    if args.verbose:
        print('\t- Graph has', len(G.edges()), 'edges among', len(G.nodes()),
              'nodes.')

    # reset the arguments for a general CoMEt run on permuted matrices
    cometArgs = []
    permuteFlags = ["-np", "--parallel", "--keep_temp_files", "-m", "-o"]
    for i, arg in enumerate(sys.argv[1:]):
        if arg not in permuteFlags and sys.argv[i] not in permuteFlags:
            cometArgs.append(arg)

    cometArgs.append('--noviz')
    # Create a permuted matrix, and then run it through CoMEt
    import tempfile
    arguments = []
    if args.keep_temp_files:
        directory = args.output_directory
    else:
        directory = tempfile.mkdtemp(dir=".", prefix=".tmp")

    # Generate random seeds for each permutation
    random.seed(args.seed)
    seeds = [
        random.randint(0, 2**31 - 1) for _ in range(args.num_permutations)
    ]

    for i, seed in enumerate(seeds):
        # Print simple progress bar
        sys.stdout.write(
            "* Running CoMEt on permuted matrices... {}/{}\r".format(
                i + 1, args.num_permutations))
        sys.stdout.flush()

        # Create a permuted dataset and save it a temporary file
        mutations = C.permute_mutation_data(G, genes, patients, seed, args.Q)
        _, _, _, _, geneToCases, patientToGenes = mutations
        adj_list = [
            p + "\t" + "\t".join(sorted(patientToGenes[p])) for p in patients
        ]

        permutation_file = "{}/permuted-matrix-{}.m2".format(directory, i + 1)
        with open(permutation_file, 'w') as outfile:
            outfile.write('\n'.join(adj_list))

        # Add the new arguments
        permuteArgs = list(map(str, cometArgs))
        permuteArgs += ["-m", permutation_file]
        permuteArgs += [
            "-o",
            "{}/comet-results-on-permutation-{}".format(directory, i + 1)
        ]
        arguments.append(permuteArgs)

    if args.parallel:
        pool = mp.Pool(25)
        results = pool.map(runComet, arguments)
        pool.close()
        pool.join()
    else:
        results = [runComet(permuteArgs) for permuteArgs in arguments]

    # Find the maximum test statistic on the permuted datasets
    from itertools import islice
    maxStat = 0

    for rf in [
            rf for rf in os.listdir(directory)
            if rf.startswith("comet-results-on-permutation")
    ]:
        for df in [
                df for df in os.listdir("{}/{}/results".format(directory, rf))
                if df.endswith(".tsv")
        ]:
            with open("{}/{}/results/{}".format(directory, rf, df)) as infile:
                for line in islice(infile, 1, 2):
                    score = float(line.split("\t")[1])
                    if score > maxStat:
                        maxStat = score

    print("*" * 80)
    print("Number of permutations:", args.num_permutations)
    print("Max statistic:", maxStat)

    # Prepare comet results on real, mutation data, and output directory for viz
    for rf in [
            rf for rf in os.listdir("{}/results/".format(realOutputDir))
            if (not rf.startswith('.') and rf.endswith(".tsv"))
    ]:
        resultsTable = [
            l.rstrip() for l in open("{}/results/{}".format(realOutputDir, rf))
        ]

    realMutations = (m, n, genes, patients, geneToCases, patientToGenes)
    outputDirViz = realOutputDir + "/viz/"
    C.ensure_dir(outputDirViz)

    # Perform visualization
    C.output_comet_viz(RC.get_parser().parse_args(realCometArgs), realMutations, \
        resultsTable, maxStat, args.num_permutations)

    # Destroy the temporary directory if necessary
    if not args.keep_temp_files:
        import shutil
        shutil.rmtree(directory)
コード例 #4
0
ファイル: run_comet_full.py プロジェクト: mruffalo/comet
def run( args ):

    # Set up the arguments for a general CoMEt run on real data
    realOutputDir = "{}/comet-results".format(args.output_directory)
    realCometArgs = []
    permuteFlags = ["-np", "--parallel", "--keep_temp_files", "-o"]
    for i, arg in enumerate(sys.argv[1:]):
        if arg not in permuteFlags and sys.argv[i] not in permuteFlags:
            realCometArgs.append( arg )

    realCometArgs += [ "-o", realOutputDir, "--noviz"]
    # perform simple run without viz first.
    results = runComet(realCometArgs)

    # Load mutation data using Multi-Dendrix and output as a temporary file
    realMutations = C.load_mutation_data(args.mutation_matrix, args.patient_file,
                                     args.gene_file, args.min_freq, args.subtype)
    m, n, genes, patients, geneToCases, patientToGenes, subtypes = realMutations

    if args.verbose:
        print('* Mutation data: %s genes x %s patients' % (m, n))

    # Construct bipartite graph from mutation data
    if args.verbose: print("* Creating bipartite graph...")
    G = C.construct_mutation_graph(geneToCases, patientToGenes)
    if args.verbose:
        print('\t- Graph has', len( G.edges() ), 'edges among', len( G.nodes() ), 'nodes.')

    # reset the arguments for a general CoMEt run on permuted matrices
    cometArgs = []
    permuteFlags = ["-np", "--parallel", "--keep_temp_files", "-m", "-o"]
    for i, arg in enumerate(sys.argv[1:]):
        if arg not in permuteFlags and sys.argv[i] not in permuteFlags:
            cometArgs.append( arg )

    cometArgs.append('--noviz')
    # Create a permuted matrix, and then run it through CoMEt
    import tempfile
    arguments = []
    if args.keep_temp_files:
        directory = args.output_directory
    else:
        directory = tempfile.mkdtemp(dir=".", prefix=".tmp")

    # Generate random seeds for each permutation
    random.seed(args.seed)
    seeds = [ random.randint(0, 2**31-1) for _ in range(args.num_permutations) ]

    for i, seed in enumerate(seeds):
        # Print simple progress bar
        sys.stdout.write("* Running CoMEt on permuted matrices... {}/{}\r".format(i+1, args.num_permutations))
        sys.stdout.flush()

        # Create a permuted dataset and save it a temporary file
        mutations = C.permute_mutation_data(G, genes, patients, seed, args.Q)
        _, _, _, _, geneToCases, patientToGenes = mutations
        adj_list = [ p + "\t" + "\t".join( sorted(patientToGenes[p]) ) for p in patients ]

        permutation_file = "{}/permuted-matrix-{}.m2".format(directory, i+1)
        with open(permutation_file, 'w') as outfile: outfile.write('\n'.join(adj_list))

        # Add the new arguments
        permuteArgs = list(map(str, cometArgs))
        permuteArgs += [ "-m", permutation_file ]
        permuteArgs += [ "-o", "{}/comet-results-on-permutation-{}".format(directory, i+1)]
        arguments.append( permuteArgs )

    if args.parallel:
        pool = mp.Pool(25)
        results = pool.map(runComet, arguments)
        pool.close()
        pool.join()
    else:
        results = [ runComet(permuteArgs) for permuteArgs in arguments ]

    # Find the maximum test statistic on the permuted datasets
    from itertools import islice
    maxStat = 0

    for rf in [ rf for rf in os.listdir(directory) if rf.startswith("comet-results-on-permutation") ]:
        for df in [df for df in os.listdir("{}/{}/results".format(directory, rf)  ) if df.endswith(".tsv")]:
            with open("{}/{}/results/{}".format(directory, rf, df)) as infile:
                for line in islice(infile, 1, 2):
                    score = float(line.split("\t")[1])
                    if score > maxStat:
                        maxStat = score

    print("*" * 80)
    print("Number of permutations:", args.num_permutations)
    print("Max statistic:", maxStat)

    # Prepare comet results on real, mutation data, and output directory for viz
    for rf in [rf for rf in os.listdir( "{}/results/".format(realOutputDir) ) if rf.endswith(".tsv")]:
        resultsTable = [l.rstrip() for l in open( "{}/results/{}".format(realOutputDir, rf))]

    realMutations = (m, n, genes, patients, geneToCases, patientToGenes )
    outputDirViz = realOutputDir + "/viz/"
    C.ensure_dir(outputDirViz)

    # Perform visualization
    C.output_comet_viz(RC.get_parser().parse_args(realCometArgs), realMutations,
        resultsTable, maxStat, args.num_permutations)

    # Destroy the temporary directory if necessary
    if not args.keep_temp_files:
        import shutil
        shutil.rmtree(directory)
コード例 #5
0
def runComet(cometArgs):
    return RC.run(RC.get_parser().parse_args(cometArgs))