コード例 #1
0
ファイル: automaton.py プロジェクト: kvefimov/jcvi_062915
def pairs(args):
    """
    %prog pairs folder reference.fasta

    Estimate insert size distribution. Compatible with a variety of aligners,
    including CLC, BOWTIE and BWA.
    """
    p = OptionParser(pairs.__doc__)
    p.set_firstN()
    p.set_mates()
    p.set_aligner()
    opts, args = p.parse_args(args)

    if len(args) != 2:
        sys.exit(not p.print_help())

    cwd = os.getcwd()
    aligner = opts.aligner
    work = "-".join(("pairs", aligner))
    mkdir(work)

    if aligner == "clc":
        from jcvi.apps.clc import align
        from jcvi.formats.cas import pairs as ps
    else:
        from jcvi.formats.sam import pairs as ps

    if aligner == "bowtie":
        from jcvi.apps.bowtie import align
    elif aligner == "bwa":
        from jcvi.apps.bwa import align

    folder, ref = args
    ref = get_abs_path(ref)
    messages = []
    for p, prefix in iter_project(folder, 2):
        samplefq = op.join(work, prefix + ".first.fastq")
        first([str(opts.firstN)] + p + ["-o", samplefq])

        os.chdir(work)
        align_args = [ref, op.basename(samplefq)]
        outfile, logfile = align(align_args)
        bedfile, stats = ps([outfile, "--rclip={0}".format(opts.rclip)])
        os.chdir(cwd)

        median = stats.median
        tag = "MP" if median > 1000 else "PE"
        median = str(median)
        pf, sf = median[:2], median[2:]
        if sf and int(sf) != 0:
            pf = str(int(pf) + 1)  # Get the first two effective digits
        lib = "{0}-{1}".format(tag, pf + "0" * len(sf))
        for i, xp in enumerate(p):
            suffix = "fastq.gz" if xp.endswith(".gz") else "fastq"
            link = "{0}-{1}.{2}.{3}".format(lib, prefix.replace("-", ""), i + 1, suffix)
            m = "\t".join(str(x) for x in (xp, link))
            messages.append(m)

    messages = "\n".join(messages)
    write_file("f.meta", messages, tee=True)
コード例 #2
0
def pairs(args):
    """
    %prog pairs folder reference.fasta

    Estimate insert size distribution. Compatible with a variety of aligners,
    including BOWTIE and BWA.
    """
    p = OptionParser(pairs.__doc__)
    p.set_firstN()
    p.set_mates()
    p.set_aligner()
    opts, args = p.parse_args(args)

    if len(args) != 2:
        sys.exit(not p.print_help())

    cwd = os.getcwd()
    aligner = opts.aligner
    work = "-".join(("pairs", aligner))
    mkdir(work)

    from jcvi.formats.sam import pairs as ps

    if aligner == "bowtie":
        from jcvi.apps.bowtie import align
    elif aligner == "bwa":
        from jcvi.apps.bwa import align

    folder, ref = args
    ref = get_abs_path(ref)
    messages = []
    for p, prefix in iter_project(folder):
        samplefq = []
        for i in range(2):
            samplefq.append(
                op.join(work, prefix + "_{0}.first.fastq".format(i + 1)))
            first([str(opts.firstN)] + [p[i]] + ["-o", samplefq[i]])

        os.chdir(work)
        align_args = [ref] + [op.basename(fq) for fq in samplefq]
        outfile, logfile = align(align_args)
        bedfile, stats = ps([outfile, "--rclip={0}".format(opts.rclip)])
        os.chdir(cwd)

        median = stats.median
        tag = "MP" if median > 1000 else "PE"
        median = str(median)
        pf, sf = median[:2], median[2:]
        if sf and int(sf) != 0:
            pf = str(int(pf) + 1)  # Get the first two effective digits
        lib = "{0}-{1}".format(tag, pf + "0" * len(sf))
        for i, xp in enumerate(p):
            suffix = "fastq.gz" if xp.endswith(".gz") else "fastq"
            link = "{0}-{1}.{2}.{3}".format(lib, prefix.replace("-", ""),
                                            i + 1, suffix)
            m = "\t".join(str(x) for x in (xp, link))
            messages.append(m)

    messages = "\n".join(messages)
    write_file("f.meta", messages, tee=True)
コード例 #3
0
ファイル: automaton.py プロジェクト: Nicholas-NVS/jcvi
    def make_link(self, firstN=0):
        mkdir(self.genome)
        if firstN > 0:
            first([str(firstN), self.fastq, "--outfile={0}".format(self.link)])
            return

        if op.islink(self.link):
            os.unlink(self.link)
        os.symlink(get_abs_path(self.fastq), self.link)
コード例 #4
0
    def make_link(self, firstN=0):
        mkdir(self.genome)
        if firstN > 0:
            first([str(firstN), self.fastq, "--outfile={0}".format(self.link)])
            return

        if op.islink(self.link):
            os.unlink(self.link)
        os.symlink(get_abs_path(self.fastq), self.link)
コード例 #5
0
ファイル: preprocess.py プロジェクト: Nicholas-NVS/jcvi
def expand(args):
    """
    %prog expand bes.fasta reads.fastq

    Expand sequences using short reads. Useful, for example for getting BAC-end
    sequences. The template to use, in `bes.fasta` may just contain the junction
    sequences, then align the reads to get the 'flanks' for such sequences.
    """
    import math

    from jcvi.formats.fasta import Fasta, SeqIO
    from jcvi.formats.fastq import readlen, first, fasta
    from jcvi.formats.blast import Blast
    from jcvi.formats.base import FileShredder
    from jcvi.apps.bowtie import align, get_samfile
    from jcvi.apps.align import blast

    p = OptionParser(expand.__doc__)
    p.set_depth(depth=200)
    p.set_firstN()
    opts, args = p.parse_args(args)

    if len(args) != 2:
        sys.exit(not p.print_help())

    bes, reads = args
    size = Fasta(bes).totalsize
    rl = readlen([reads])
    expected_size = size + 2 * rl
    nreads = expected_size * opts.depth / rl
    nreads = int(math.ceil(nreads / 1000.)) * 1000

    # Attract reads
    samfile, logfile = align([bes, reads, "--reorder", "--mapped",
           "--firstN={0}".format(opts.firstN)])

    samfile, mapped, _ = get_samfile(reads, bes, bowtie=True, mapped=True)
    logging.debug("Extract first {0} reads from `{1}`.".format(nreads, mapped))

    pf = mapped.split(".")[0]
    pf = pf.split("-")[0]
    bespf = bes.split(".")[0]
    reads = pf + ".expand.fastq"
    first([str(nreads), mapped, "-o", reads])

    # Perform mini-assembly
    fastafile = reads.rsplit(".", 1)[0] + ".fasta"
    qualfile = ""
    if need_update(reads, fastafile):
        fastafile, qualfile = fasta([reads])

    contigs = op.join(pf, "454LargeContigs.fna")
    if need_update(fastafile, contigs):
        cmd = "runAssembly -o {0} -cpu 8 {1}".format(pf, fastafile)
        sh(cmd)
    assert op.exists(contigs)

    # Annotate contigs
    blastfile = blast([bes, contigs])
    mapping = {}
    for query, b in Blast(blastfile).iter_best_hit():
        mapping[query] = b

    f = Fasta(contigs, lazy=True)
    annotatedfasta = ".".join((pf, bespf, "fasta"))
    fw = open(annotatedfasta, "w")
    keys = list(Fasta(bes).iterkeys_ordered())  # keep an ordered list
    recs = []
    for key, v in f.iteritems_ordered():
        vid = v.id
        if vid not in mapping:
            continue
        b = mapping[vid]
        subject = b.subject
        rec = v.reverse_complement() if b.orientation == '-' else v
        rec.id = rid = "_".join((pf, vid, subject))
        rec.description = ""
        recs.append((keys.index(subject), rid, rec))

    recs = [x[-1] for x in sorted(recs)]
    SeqIO.write(recs, fw, "fasta")
    fw.close()

    FileShredder([samfile, logfile, mapped, reads, fastafile, qualfile, blastfile, pf])
    logging.debug("Annotated seqs (n={0}) written to `{1}`.".\
                    format(len(recs), annotatedfasta))

    return annotatedfasta
コード例 #6
0
def expand(args):
    """
    %prog expand bes.fasta reads.fastq

    Expand sequences using short reads. Useful, for example for getting BAC-end
    sequences. The template to use, in `bes.fasta` may just contain the junction
    sequences, then align the reads to get the 'flanks' for such sequences.
    """
    import math

    from jcvi.formats.fasta import Fasta, SeqIO
    from jcvi.formats.fastq import readlen, first, fasta
    from jcvi.formats.blast import Blast
    from jcvi.formats.base import FileShredder
    from jcvi.apps.bowtie import align, get_samfile
    from jcvi.apps.align import blast

    p = OptionParser(expand.__doc__)
    p.set_depth(depth=200)
    p.set_firstN()
    opts, args = p.parse_args(args)

    if len(args) != 2:
        sys.exit(not p.print_help())

    bes, reads = args
    size = Fasta(bes).totalsize
    rl = readlen([reads])
    expected_size = size + 2 * rl
    nreads = expected_size * opts.depth / rl
    nreads = int(math.ceil(nreads / 1000.)) * 1000

    # Attract reads
    samfile, logfile = align([bes, reads, "--reorder", "--mapped",
           "--firstN={0}".format(opts.firstN)])

    samfile, mapped, _ = get_samfile(reads, bes, bowtie=True, mapped=True)
    logging.debug("Extract first {0} reads from `{1}`.".format(nreads, mapped))

    pf = mapped.split(".")[0]
    pf = pf.split("-")[0]
    bespf = bes.split(".")[0]
    reads = pf + ".expand.fastq"
    first([str(nreads), mapped, "-o", reads])

    # Perform mini-assembly
    fastafile = reads.rsplit(".", 1)[0] + ".fasta"
    qualfile = ""
    if need_update(reads, fastafile):
        fastafile, qualfile = fasta([reads])

    contigs = op.join(pf, "454LargeContigs.fna")
    if need_update(fastafile, contigs):
        cmd = "runAssembly -o {0} -cpu 8 {1}".format(pf, fastafile)
        sh(cmd)
    assert op.exists(contigs)

    # Annotate contigs
    blastfile = blast([bes, contigs])
    mapping = {}
    for query, b in Blast(blastfile).iter_best_hit():
        mapping[query] = b

    f = Fasta(contigs, lazy=True)
    annotatedfasta = ".".join((pf, bespf, "fasta"))
    fw = open(annotatedfasta, "w")
    keys = list(Fasta(bes).iterkeys_ordered())  # keep an ordered list
    recs = []
    for key, v in f.iteritems_ordered():
        vid = v.id
        if vid not in mapping:
            continue
        b = mapping[vid]
        subject = b.subject
        rec = v.reverse_complement() if b.orientation == '-' else v
        rec.id = rid = "_".join((pf, vid, subject))
        rec.description = ""
        recs.append((keys.index(subject), rid, rec))

    recs = [x[-1] for x in sorted(recs)]
    SeqIO.write(recs, fw, "fasta")
    fw.close()

    FileShredder([samfile, logfile, mapped, reads, fastafile, qualfile, blastfile, pf])
    logging.debug("Annotated seqs (n={0}) written to `{1}`.".\
                    format(len(recs), annotatedfasta))

    return annotatedfasta