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Python pysam.tabix_compress方法代码示例

本文整理汇总了Python中pysam.tabix_compress方法的典型用法代码示例。如果您正苦于以下问题:Python pysam.tabix_compress方法的具体用法?Python pysam.tabix_compress怎么用?Python pysam.tabix_compress使用的例子?那么恭喜您, 这里精选的方法代码示例或许可以为您提供帮助。您也可以进一步了解该方法所在pysam的用法示例。


在下文中一共展示了pysam.tabix_compress方法的11个代码示例,这些例子默认根据受欢迎程度排序。您可以为喜欢或者感觉有用的代码点赞,您的评价将有助于系统推荐出更棒的Python代码示例。

示例1: _make_vcf_and_read_depths_files

# 需要导入模块: import pysam [as 别名]
# 或者: from pysam import tabix_compress [as 别名]
def _make_vcf_and_read_depths_files(self):
        if not os.path.exists(self.ref_fa + '.fai'):
            pysam.faidx(self.ref_fa)

        tmp_vcf = self.vcf_file + '.tmp'
        with open(tmp_vcf, 'w') as f:
            print(pysam.mpileup(
                '-t', 'INFO/AD,INFO/ADF,INFO/ADR',
                '-L', '99999999',
                '-A',
                '-f', self.ref_fa,
                '-u',
                '-v',
                self.bam,
            ), end='', file=f)

        got = vcfcall_ariba.vcfcall_ariba(tmp_vcf, self.outprefix, self.min_var_read_depth, self.min_second_var_read_depth, self.max_allele_freq)
        if got != 0:
            raise Error('Error parsing vcf file. Cannot contine')

        pysam.tabix_compress(self.outprefix + '.read_depths', self.read_depths_file)
        pysam.tabix_index(self.read_depths_file, seq_col=0, start_col=1, end_col=1)
        os.unlink(self.outprefix + '.read_depths')
        os.unlink(tmp_vcf) 
开发者ID:sanger-pathogens,项目名称:ariba,代码行数:26,代码来源:samtools_variants.py

示例2: ensureIndexed

# 需要导入模块: import pysam [as 别名]
# 或者: from pysam import tabix_compress [as 别名]
def ensureIndexed(bedPath, preset="bed", trySorting=True):
    if not bedPath.endswith(".gz"):
        if not os.path.exists(bedPath+".gz"):
            logging.info("bgzf compressing {}".format(bedPath))
            pysam.tabix_compress(bedPath, bedPath+".gz")
            if not os.path.exists(bedPath+".gz"):
                raise Exception("Failed to create compress {preset} file for {file}; make sure the {preset} file is "
                    "sorted and the directory is writeable".format(preset=preset, file=bedPath))
        bedPath += ".gz"
    if not os.path.exists(bedPath+".tbi"):
        logging.info("creating tabix index for {}".format(bedPath))
        pysam.tabix_index(bedPath, preset=preset)
        if not os.path.exists(bedPath+".tbi"):
            raise Exception("Failed to create tabix index file for {file}; make sure the {preset} file is "
                "sorted and the directory is writeable".format(preset=preset, file=bedPath))

    line = next(pysam.Tabixfile(bedPath).fetch())
    if len(line.strip().split("\t")) < 6 and preset == "bed":
        raise AnnotationError("BED files need to have at least 6 (tab-delimited) fields (including "
            "chrom, start, end, name, score, strand; score is unused)")
    if len(line.strip().split("\t")) < 9 and preset == "gff":
        raise AnnotationError("GFF/GTF files need to have at least 9 tab-delimited fields")

    return bedPath


# def sortFile(uncompressedPath, preset):
#     if preset == "bed":
#         fields = {"chrom":0, "start":1, "end":2}
#     elif preset == "gff":
#         fields = {"chrom":0, "start":3, "end":4}

#     sortCommand = "sort -k{chrom}V -k{start}n -k{end}n".format(**fields)

#     tabixCommand = "{sort} {path} | bgzip > {path}.gz".format(sort=sortCommand, path=uncompressedPath)

#     logging.info("Trying to sort input annotation file with command:")
#     logging.info("  {}".format(tabixCommand))

#     subprocess.check_call(tabixCommand, shell=True) 
开发者ID:svviz,项目名称:svviz,代码行数:42,代码来源:tabix.py

示例3: get_ins

# 需要导入模块: import pysam [as 别名]
# 或者: from pysam import tabix_compress [as 别名]
def get_ins(args, bases = 50000, splitsize = 1000):
    """function to get insertions

    """
    if not args.out:
        if args.bed is None:
            args.out = '.'.join(os.path.basename(args.bam).split('.')[0:-1])
        else:
            args.out = '.'.join(os.path.basename(args.bed).split('.')[0:-1])
    if args.bed is None:
        chrs = read_chrom_sizes_from_bam(args.bam)
        chunks = ChunkList.convertChromSizes(chrs, splitsize = splitsize)
        sets = chunks.split(items = bases/splitsize)
    else:
        chunks = ChunkList.read(args.bed)
        chunks.merge()
        sets = chunks.split(bases = bases)
    maxQueueSize = max(2,int(2 * bases / np.mean([chunk.length() for chunk in chunks])))
    pool1 = mp.Pool(processes = max(1,args.cores-1))
    out_handle = open(args.out + '.ins.bedgraph','w')
    out_handle.close()
    write_queue = mp.JoinableQueue(maxsize = maxQueueSize)
    write_process = mp.Process(target = _writeIns, args=(write_queue, args.out))
    write_process.start()
    for j in sets:
        if args.smooth:
            tmp = pool1.map(_insHelperSmooth, zip(j,itertools.repeat(args)))
        else:
            tmp = pool1.map(_insHelper, zip(j,itertools.repeat(args)))
        for track in tmp:
            write_queue.put(track)
    pool1.close()
    pool1.join()
    write_queue.put('STOP')
    write_process.join()
    pysam.tabix_compress(args.out + '.ins.bedgraph', args.out + '.ins.bedgraph.gz', force = True)
    shell_command('rm ' + args.out + '.ins.bedgraph')
    pysam.tabix_index(args.out + '.ins.bedgraph.gz', preset = "bed", force = True) 
开发者ID:GreenleafLab,项目名称:NucleoATAC,代码行数:40,代码来源:get_ins.py

示例4: get_cov

# 需要导入模块: import pysam [as 别名]
# 或者: from pysam import tabix_compress [as 别名]
def get_cov(args, bases = 50000, splitsize = 1000):
    """function to get coverages

    """
    if not args.out:
        if args.bed is None:
            args.out = '.'.join(os.path.basename(args.bam).split('.')[0:-1])
        else:
            args.out = '.'.join(os.path.basename(args.bed).split('.')[0:-1])
    if args.bed is None:
        chrs = read_chrom_sizes_from_bam(args.bam)
        chunks = ChunkList.convertChromSizes(chrs, splitsize = splitsize)
        sets = chunks.split(items = bases/splitsize)
    else:
        chunks = ChunkList.read(args.bed)
        chunks.merge()
        sets = chunks.split(bases = bases)
    maxQueueSize = max(2,int(2 * bases / np.mean([chunk.length() for chunk in chunks])))
    pool1 = mp.Pool(processes = max(1,args.cores-1))
    out_handle = open(args.out + '.cov.bedgraph','w')
    out_handle.close()
    write_queue = mp.JoinableQueue(maxsize = maxQueueSize)
    write_process = mp.Process(target = _writeCov, args=(write_queue, args.out))
    write_process.start()
    for j in sets:
        tmp = pool1.map(_covHelper, zip(j,itertools.repeat(args)))
        for track in tmp:
            write_queue.put(track)
    pool1.close()
    pool1.join()
    write_queue.put('STOP')
    write_process.join()
    pysam.tabix_compress(args.out + '.cov.bedgraph', args.out + '.cov.bedgraph.gz', force = True)
    shell_command('rm ' + args.out + '.cov.bedgraph')
    pysam.tabix_index(args.out + '.cov.bedgraph.gz', preset = "bed", force = True) 
开发者ID:GreenleafLab,项目名称:NucleoATAC,代码行数:37,代码来源:get_cov.py

示例5: tabix_bedgraph

# 需要导入模块: import pysam [as 别名]
# 或者: from pysam import tabix_compress [as 别名]
def tabix_bedgraph(bedgraph):
    pysam.tabix_compress(bedgraph,bedgraph+'.gz')
    pysam.tabix_index(bedgraph+'.gz', seq_col=0, start_col=1, end_col=2, zerobased=True) 
开发者ID:GreenleafLab,项目名称:NucleoATAC,代码行数:5,代码来源:bedgraph.py

示例6: make_bias_track

# 需要导入模块: import pysam [as 别名]
# 或者: from pysam import tabix_compress [as 别名]
def make_bias_track(args, bases = 500000, splitsize = 1000):
    """function to compute bias track

    """
    if args.out is None:
        if args.bed is not None:
            args.out = '.'.join(os.path.basename(args.bed).split('.')[0:-1])
        else:
            args.out = '.'.join(os.path.basename(args.fasta).split('.')[0:-1])
    params = _BiasParams(args.fasta, args.pwm)
    if args.bed is None:
        chunks = ChunkList.convertChromSizes(params.chrs, splitsize = splitsize)
        sets = chunks.split(items = bases/splitsize)
    else:
        chunks = ChunkList.read(args.bed)
        chunks.checkChroms(params.chrs.keys())
        chunks.merge()
        sets = chunks.split(bases = bases)
    maxQueueSize = max(2,int(2 * bases / np.mean([chunk.length() for chunk in chunks])))
    pool = mp.Pool(processes = max(1,args.cores-1))
    out_handle = open(args.out + '.Scores.bedgraph','w')
    out_handle.close()
    write_queue = mp.JoinableQueue(maxsize = maxQueueSize)
    write_process = mp.Process(target = _writeBias, args=(write_queue, args.out))
    write_process.start()
    for j in sets:
        tmp = pool.map(_biasHelper, zip(j,itertools.repeat(params)))
        for track in tmp:
            write_queue.put(track)
    pool.close()
    pool.join()
    write_queue.put('STOP')
    write_process.join()
    pysam.tabix_compress(args.out + '.Scores.bedgraph', args.out + '.Scores.bedgraph.gz', force = True)
    shell_command('rm ' + args.out + '.Scores.bedgraph')
    pysam.tabix_index(args.out + '.Scores.bedgraph.gz', preset = "bed", force = True) 
开发者ID:GreenleafLab,项目名称:NucleoATAC,代码行数:38,代码来源:make_bias_track.py

示例7: run_diff

# 需要导入模块: import pysam [as 别名]
# 或者: from pysam import tabix_compress [as 别名]
def run_diff(args, bases = 500000):
    """run differential occupancy calling

    """
    chrs = read_chrom_sizes_from_bam(args.bam)
    pwm = PWM.open(args.pwm)
    chunks = ChunkList.read(args.bed, chromDict = chrs, min_offset = args.flank + args.upper/2 + max(pwm.up,pwm.down))
    chunks.merge()
    maxQueueSize = max(2,int(100 * bases / np.mean([chunk.length() for chunk in chunks])))
    #get fragmentsizes
    fragment_dist1 = FragmentMixDistribution(0, upper = args.upper)
    fragment_dist1.fragmentsizes = FragmentSizes(0, args.upper, vals = FragmentSizes.open(args.sizes1).get(0,args.upper))
    fragment_dist1.modelNFR()
    fragment_dist2 = FragmentMixDistribution(0, upper = args.upper)
    fragment_dist2.fragmentsizes = FragmentSizes(0, args.upper, vals = FragmentSizes.open(args.sizes2).get(0,args.upper))
    fragment_dist2.modelNFR()
    params = OccupancyParameters(fragment_dist, args.upper, args.fasta, args.pwm, sep = args.nuc_sep, min_occ = args.min_occ,
            flank = args.flank, bam = args.bam, ci = args.confidence_interval)
    sets = chunks.split(bases = bases)
    pool1 = mp.Pool(processes = max(1,args.cores-1))
    diff_handle = open(args.out + '.occdiff.bed','w')
    diff_handle.close()
    diff_queue = mp.JoinableQueue()
    diff_process = mp.Process(target = _writeDiff, args=(diff_queue, args.out))
    diff_process.start()
    nuc_dist = np.zeros(args.upper)
    for j in sets:
        tmp = pool1.map(_occHelper, zip(j,itertools.repeat(params)))
        for result in tmp:
            diff_queue.put(result[1])
    pool1.close()
    pool1.join()
    diff_queue.put('STOP')
    diff_process.join()
    pysam.tabix_compress(args.out + '.occdiff.bed', args.out + '.occdiff.bed.gz',force = True)
    shell_command('rm ' + args.out + '.occdiff.bed')
    pysam.tabix_index(args.out + '.occdiff.bed.gz', preset = "bed", force = True) 
开发者ID:GreenleafLab,项目名称:NucleoATAC,代码行数:39,代码来源:diff_occ.py

示例8: convert_VariantFile_to_IndexedVariantFile

# 需要导入模块: import pysam [as 别名]
# 或者: from pysam import tabix_compress [as 别名]
def convert_VariantFile_to_IndexedVariantFile(vf_path, ivf_path):
    make_basedir(ivf_path)
    tmp_path = get_tmp_path(ivf_path)
    pysam.tabix_compress(vf_path, tmp_path, force=True)
    os.rename(tmp_path, ivf_path)

    pysam.tabix_index(
        filename=ivf_path, force=True,
        seq_col=0, start_col=1, end_col=1, # note: `pysam.tabix_index` calls the first column `0`, but cmdline `tabix` calls it `1`.
        line_skip=1, # skip header
    ) 
开发者ID:statgen,项目名称:pheweb,代码行数:13,代码来源:file_utils.py

示例9: _compress_and_index_file

# 需要导入模块: import pysam [as 别名]
# 或者: from pysam import tabix_compress [as 别名]
def _compress_and_index_file(infile, log_fh=None):
        if log_fh is not None:
            print('Compressing file', infile, file=log_fh, flush=True)
        pysam.tabix_compress(infile, infile + '.gz')
        pysam.tabix_index(infile + '.gz', seq_col=0, start_col=1, end_col=1) 
开发者ID:sanger-pathogens,项目名称:ariba,代码行数:7,代码来源:read_store.py

示例10: run_nuc

# 需要导入模块: import pysam [as 别名]
# 或者: from pysam import tabix_compress [as 别名]
def run_nuc(args):
    """run occupancy calling

    """
    vmat = VMat.open(args.vmat)
    if args.fasta:
        chrs = read_chrom_sizes_from_fasta(args.fasta)
    else:
        chrs = read_chrom_sizes_from_bam(args.bam)
    pwm = PWM.open(args.pwm)
    chunks = ChunkList.read(args.bed, chromDict = chrs, min_offset = vmat.mat.shape[1] + vmat.upper/2 + max(pwm.up,pwm.down) + args.nuc_sep/2, min_length = args.nuc_sep * 2)
    chunks.slop(chrs, up = args.nuc_sep/2, down = args.nuc_sep/2)
    chunks.merge()
    maxQueueSize = args.cores*10
    if args.sizes is not None:
        fragment_dist = FragmentSizes.open(args.sizes)
    else:
        fragment_dist = FragmentSizes(0, upper = vmat.upper)
        fragment_dist.calculateSizes(args.bam, chunks)
    params = NucParameters(vmat = vmat, fragmentsizes = fragment_dist, bam = args.bam, fasta = args.fasta, pwm = args.pwm,
                           occ_track = args.occ_track,
                           sd = args.sd, nonredundant_sep = args.nuc_sep, redundant_sep = args.redundant_sep,
                           min_z = args.min_z, min_lr = args.min_lr , atac = args.atac)
    sets = chunks.split(items = args.cores*5)
    pool1 = mp.Pool(processes = max(1,args.cores-1))
    if args.write_all:
        outputs = ['nucpos','nucpos.redundant','nucleoatac_signal','nucleoatac_signal.smooth',
                       'nucleoatac_background','nucleoatac_raw']
    else:
        outputs = ['nucpos','nucpos.redundant','nucleoatac_signal','nucleoatac_signal.smooth']
    handles = {}
    write_queues = {}
    write_processes = {}
    for i in outputs:
        if i not in ['nucpos','nucpos.redundant','nfrpos']:
            handles[i] = open(args.out + '.'+i+'.bedgraph','w')
        else:
            handles[i] = open(args.out + '.'+i+'.bed','w')
        handles[i].close()
        write_queues[i] = mp.JoinableQueue(maxsize = maxQueueSize)
        write_processes[i] = mp.Process(target = _writeFuncs[i], args=(write_queues[i], args.out))
        write_processes[i].start()
    for j in sets:
        tmp = pool1.map(_nucHelper, zip(j,itertools.repeat(params)))
        for result in tmp:
            for i in outputs:
                write_queues[i].put(result[i])
    pool1.close()
    pool1.join()
    for i in outputs:
        write_queues[i].put('STOP')
    for i in outputs:
        write_processes[i].join()
        if i not in ['nucpos','nucpos.redundant']:
            pysam.tabix_compress(args.out + '.' + i + '.bedgraph', args.out +  '.' + i + '.bedgraph.gz',force = True)
            shell_command('rm ' + args.out +  '.' + i + '.bedgraph')
            pysam.tabix_index(args.out +  '.' + i + '.bedgraph.gz', preset = "bed", force = True)
        else:
            pysam.tabix_compress(args.out + '.' + i + '.bed', args.out +  '.' + i + '.bed.gz',force = True)
            shell_command('rm ' + args.out +  '.' + i + '.bed')
            pysam.tabix_index(args.out +  '.' + i + '.bed.gz', preset = "bed", force = True) 
开发者ID:GreenleafLab,项目名称:NucleoATAC,代码行数:63,代码来源:run_nuc.py

示例11: run_nfr

# 需要导入模块: import pysam [as 别名]
# 或者: from pysam import tabix_compress [as 别名]
def run_nfr(args):
    """run nfr calling

    """
    if args.bam is None and args.ins_track is None:
        raise Exception("Must supply either bam file or insertion track")
    if not args.out:
        args.out = '.'.join(os.path.basename(args.calls).split('.')[0:-3])
    if args.fasta is not None:
        chrs_fasta = read_chrom_sizes_from_fasta(args.fasta)
        pwm = PWM.open(args.pwm)
        chunks = ChunkList.read(args.bed, chromDict = chrs_fasta, min_offset = max(pwm.up, pwm.down))
    else:
        chunks = ChunkList.read(args.bed)
    if args.bam is not None:
        chrs_bam = read_chrom_sizes_from_bam(args.bam)
        chunks.checkChroms(chrs_bam, chrom_source = "BAM file") 
    chunks.merge()
    maxQueueSize = args.cores * 10 
    params = NFRParameters(args.occ_track, args.calls, args.ins_track, args.bam, max_occ = args.max_occ, max_occ_upper = args.max_occ_upper,
                            fasta = args.fasta, pwm = args.pwm)
    sets = chunks.split(items = args.cores * 5)
    pool1 = mp.Pool(processes = max(1,args.cores-1))
    nfr_handle = open(args.out + '.nfrpos.bed','w')
    nfr_handle.close()
    nfr_queue = mp.JoinableQueue()
    nfr_process = mp.Process(target = _writeNFR, args=(nfr_queue, args.out))
    nfr_process.start()
    if params.ins_track is None:
        ins_handle = open(args.out + '.ins.bedgraph','w')
        ins_handle.close()
        ins_queue = mp.JoinableQueue()
        ins_process = mp.Process(target = _writeIns, args=(ins_queue, args.out))
        ins_process.start()
    for j in sets:
        tmp = pool1.map(_nfrHelper, zip(j,itertools.repeat(params)))
        for result in tmp:
            if params.ins_track is None:
                nfr_queue.put(result[0])
                ins_queue.put(result[1])
            else:
                nfr_queue.put(result)
    pool1.close()
    pool1.join()
    nfr_queue.put('STOP')
    nfr_process.join()
    if params.ins_track is None:
        ins_queue.put('STOP')
        ins_process.join()
    pysam.tabix_compress(args.out + '.nfrpos.bed', args.out + '.nfrpos.bed.gz',force = True)
    shell_command('rm ' + args.out + '.nfrpos.bed')
    pysam.tabix_index(args.out + '.nfrpos.bed.gz', preset = "bed", force = True)
    if params.ins_track is None:
        pysam.tabix_compress(args.out + '.ins.bedgraph', args.out + '.ins.bedgraph.gz', force = True)
        shell_command('rm ' + args.out + '.ins.bedgraph')
        pysam.tabix_index(args.out + '.ins.bedgraph.gz', preset = "bed", force = True) 
开发者ID:GreenleafLab,项目名称:NucleoATAC,代码行数:58,代码来源:run_nfr.py


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