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Python MutableSeq.reverse_complement方法代码示例

本文整理汇总了Python中Bio.Seq.MutableSeq.reverse_complement方法的典型用法代码示例。如果您正苦于以下问题:Python MutableSeq.reverse_complement方法的具体用法?Python MutableSeq.reverse_complement怎么用?Python MutableSeq.reverse_complement使用的例子?那么, 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Bio.Seq.MutableSeq的用法示例。


在下文中一共展示了MutableSeq.reverse_complement方法的6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: create_genome_seq

# 需要导入模块: from Bio.Seq import MutableSeq [as 别名]
# 或者: from Bio.Seq.MutableSeq import reverse_complement [as 别名]
def create_genome_seq(aligned):

    aligned_seq = aligned.seq if type(aligned.seq) == str else aligned.seq.decode('UTF-8')
        
    genome_seq = MutableSeq(aligned_seq)

    # see samtools documentation for MD string
    
    err = re.findall(MD_REGEX, aligned.opt("MD"))
    
    seq_ix = 0
    
    # step through sequence
    for matched_bases, curr_err in err:
        
        seq_ix += int(matched_bases)
        
        assert '^' not in curr_err
        assert curr_err != genome_seq[seq_ix]
        
        genome_seq[seq_ix] = curr_err
        seq_ix += 1
    
    if aligned.is_reverse:
        genome_seq.reverse_complement()

    return genome_seq
开发者ID:StoreyLab,项目名称:sparta,代码行数:29,代码来源:calculate_mismatch_probs.py

示例2: add_to_pileup_dict

# 需要导入模块: from Bio.Seq import MutableSeq [as 别名]
# 或者: from Bio.Seq.MutableSeq import reverse_complement [as 别名]
def add_to_pileup_dict(sams, aligned_read_set, pileup_dict):
    
    # sanity check that all the qnames (RNA read IDs) are the same
    for read in aligned_read_set:
        assert read.qname == aligned_read_set[0].qname

    if not True in [read.is_unmapped for read in aligned_read_set]:
        
        # all alignments mapped
        for read in aligned_read_set:
            
            for op, op_len in read.cigar:
                
                if op > 0 and op < 7:
                    # do not sample reads where there are insertions or deletions   
                    return
                    
            assert len(read.seq) == len(aligned_read_set[0].seq)
          
        # if aligned reads are reversed, we reverse them and hold on to that info.
        
        pos_dicts = [dict(read.aligned_pairs) for read in aligned_read_set]
        genome_seqs = [create_genome_seq(read) for read in aligned_read_set]
        qual = bytearray(aligned_read_set[0].qual, 'utf-8')
        seq = MutableSeq(aligned_read_set[0].seq if type(aligned_read_set[0].seq) == str else aligned_read_set[0].seq.decode('UTF-8'))  
        if aligned_read_set[0].is_reverse:
            seq.reverse_complement()
            qual = qual[::-1]
        
        for genome_seq in genome_seqs:
            assert len(genome_seq) == len(seq)

        for i in range(0, len(seq)):
                        
            # need (chrom, pos, genome_seq[i]) tuples for each aligned_read
            chroms = [sam.getrname(a.tid) for sam, a in izip(sams, aligned_read_set)]
            positions = [d[i] if not a.is_reverse else d[len(seq) - i - 1] for d, a in zip(pos_dicts, aligned_read_set)]
            genome_seq_i = [g[i] for g in genome_seqs]
            
            genomic_locs = tuple(zip(chroms, positions, genome_seq_i))
            
            pileup_dict[genomic_locs][seq[i]][qual[i]] += 1
开发者ID:StoreyLab,项目名称:sparta,代码行数:44,代码来源:calculate_mismatch_probs.py

示例3: seq_batch_query

# 需要导入模块: from Bio.Seq import MutableSeq [as 别名]
# 或者: from Bio.Seq.MutableSeq import reverse_complement [as 别名]
def seq_batch_query():
    con = sqlite3.connect('./data/DB')
    cur = con.cursor()
    list_file = input('list file name:\n')
    with open(list_file, 'r') as In:
        organism_list = In.read().split(sep='\n')
    cur.execute('CREATE TABLE IF NOT EXISTS tasklist (Name TEXT);')
    for organism in organism_list:
        cur.execute('INSERT INTO tasklist (Name) VALUES (?);', (organism,))
    cur.execute(
        'SELECT Taxon, Organism, Name, Type, Strand, Sequence, Head FROM main WHERE Organism IN (SELECT Name FROM tasklist) ORDER BY Head',
        (organism))
    result = cur.fetchall()
    cur.execute('DROP TABLE tasklist;')
    cur.close()
    con.close()
    query_result = []
    for i in result:
        title = '|'.join([str(i[0]), i[1], i[2], i[3]])
        filename = i[2]
        sequence = MutableSeq(i[5])
        if i[4] == '-1':
            sequence.seq = sequence.reverse_complement()
        record = [title, filename, sequence]
        query_result.append(record)
    for i in query_result:
        with open(''.join(['./out/', i[1], '.fasta']), 'a') as Fileout:
            Fileout.write('>%s\n%s\n' % (i[0], i[2]))
            # rps12 may have larger than 50k fragments,  here to filter it
    rps12 = SeqIO.parse('./out/rps12.fasta', 'fasta')
    rps12short = list()
    for item in rps12:
        if len(item.seq) < 4000:
            rps12short.append(item)
    SeqIO.write(rps12short, './out/rps12short.fasta', 'fasta')
    print('Done.\n')
开发者ID:jangwen,项目名称:python,代码行数:38,代码来源:portable.py

示例4: TestMutableSeq

# 需要导入模块: from Bio.Seq import MutableSeq [as 别名]
# 或者: from Bio.Seq.MutableSeq import reverse_complement [as 别名]

#.........这里部分代码省略.........
                         self.mutable_s)

    def test_inserting(self):
        self.mutable_s.insert(4, "G")
        self.assertEqual(MutableSeq("TCAAGAAGGATGCATCATG", IUPAC.ambiguous_dna),
                         self.mutable_s)

    def test_popping_last_item(self):
        self.assertEqual("G", self.mutable_s.pop())

    def test_remove_items(self):
        self.mutable_s.remove("G")
        self.assertEqual(MutableSeq("TCAAAAGATGCATCATG", IUPAC.ambiguous_dna),
                         self.mutable_s, "Remove first G")

        self.assertRaises(ValueError, self.mutable_s.remove, 'Z')

    def test_count(self):
        self.assertEqual(7, self.mutable_s.count("A"))
        self.assertEqual(2, self.mutable_s.count("AA"))

    def test_index(self):
        self.assertEqual(2, self.mutable_s.index("A"))
        self.assertRaises(ValueError, self.mutable_s.index, "8888")

    def test_reverse(self):
        """Test using reverse method"""
        self.mutable_s.reverse()
        self.assertEqual(MutableSeq("GTACTACGTAGGAAAACT", IUPAC.ambiguous_dna),
                         self.mutable_s)

    def test_reverse_with_stride(self):
        """Test reverse using -1 stride"""
        self.assertEqual(MutableSeq("GTACTACGTAGGAAAACT", IUPAC.ambiguous_dna),
                         self.mutable_s[::-1])

    def test_complement(self):
        self.mutable_s.complement()
        self.assertEqual(str("AGTTTTCCTACGTAGTAC"), str(self.mutable_s))

    def test_complement_rna(self):
        seq = Seq.MutableSeq("AUGaaaCUG", IUPAC.unambiguous_rna)
        seq.complement()
        self.assertEqual(str("UACuuuGAC"), str(seq))

    def test_complement_mixed_aphabets(self):
        seq = Seq.MutableSeq("AUGaaaCTG")
        with self.assertRaises(ValueError):
            seq.complement()

    def test_complement_rna_string(self):
        seq = Seq.MutableSeq("AUGaaaCUG")
        seq.complement()
        self.assertEqual('UACuuuGAC', str(seq))

    def test_complement_dna_string(self):
        seq = Seq.MutableSeq("ATGaaaCTG")
        seq.complement()
        self.assertEqual('TACtttGAC', str(seq))

    def test_reverse_complement(self):
        self.mutable_s.reverse_complement()
        self.assertEqual("CATGATGCATCCTTTTGA", str(self.mutable_s))

    def test_reverse_complement_of_protein(self):
        seq = Seq.MutableSeq("ACTGTCGTCT", Alphabet.generic_protein)
        with self.assertRaises(ValueError):
            seq.reverse_complement()

    def test_to_string_method(self):
        """This method is currently deprecated, probably will need to remove this test soon"""
        with warnings.catch_warnings(record=True):
            self.mutable_s.tostring()

    def test_extend_method(self):
        self.mutable_s.extend("GAT")
        self.assertEqual(MutableSeq("TCAAAAGGATGCATCATGGAT", IUPAC.ambiguous_dna),
                         self.mutable_s)

    def test_extend_with_mutable_seq(self):
        self.mutable_s.extend(MutableSeq("TTT", IUPAC.ambiguous_dna))
        self.assertEqual(MutableSeq("TCAAAAGGATGCATCATGTTT", IUPAC.ambiguous_dna),
                         self.mutable_s)

    def test_delete_stride_slice(self):
        del self.mutable_s[4:6 - 1]
        self.assertEqual(MutableSeq("TCAAAGGATGCATCATG", IUPAC.ambiguous_dna),
                         self.mutable_s)

    def test_extract_third_nucleotide(self):
        """Test extracting every third nucleotide (slicing with stride 3)"""
        self.assertEqual(MutableSeq("TAGTAA", IUPAC.ambiguous_dna), self.mutable_s[0::3])
        self.assertEqual(MutableSeq("CAGGTT", IUPAC.ambiguous_dna), self.mutable_s[1::3])
        self.assertEqual(MutableSeq("AAACCG", IUPAC.ambiguous_dna), self.mutable_s[2::3])

    def test_set_wobble_codon_to_n(self):
        """Test setting wobble codon to N (set slice with stride 3)"""
        self.mutable_s[2::3] = "N" * len(self.mutable_s[2::3])
        self.assertEqual(MutableSeq("TCNAANGGNTGNATNATN", IUPAC.ambiguous_dna),
                         self.mutable_s)
开发者ID:BrianLinSu,项目名称:rop,代码行数:104,代码来源:test_seq.py

示例5: append

# 需要导入模块: from Bio.Seq import MutableSeq [as 别名]
# 或者: from Bio.Seq.MutableSeq import reverse_complement [as 别名]
st=str(seq)		#toString
print st

#tipo de dato secuencia editable
from Bio.Seq import MutableSeq
mut_seq=seq.tomutable()	#convertirlo a tipo seq mutable
print mut_seq
mut_seq[0]='C'
print mut_seq
mut_seq=MutableSeq('ATGCCG',IUPAC.IUPACUnambiguousDNA())
#has methods as a list: append(), insert(), pop(), remove()
mut_seq[1:3]='TTT'
mut_seq.reverse()
mut_seq.complement()
print mut_seq
mut_seq.reverse_complement()
print mut_seq

#tipo de dato metadatos de secuencia
from Bio.SeqRecord import SeqRecord
seqrec=SeqRecord(seq,id='001', name='My Secuencia')
#2 main attributes:
#	id: string identifier, optional, recommended
#	seq: Seq object, required
#additional attributes
#	name, description: name and more info of sequence
#	dbxrefs: list of strings, each string an id of a DB
#	features: list of SeqFeature objects, those found in Genbank records
#	annotations: dictionary with further info, can't be set on initialization
seqrec=SeqRecord(Seq('mdstnvrsgmksrkkkpkttvidddddcmtcsacqsklvkisditkvsldyintmrgntlacaacgsslkllndfas',Bio.Alphabet.generic_protein), id='P20994.1', name='P20994', description='Protein A19', dbxrefs=['Pfam:PF05077', 'InterPro:IPR007769', 'DIP:2186N'])
seqrec.annotations['note']='A simple note'
开发者ID:ajonjoli,项目名称:Mytest,代码行数:33,代码来源:biopython1.py

示例6: seq_query

# 需要导入模块: from Bio.Seq import MutableSeq [as 别名]
# 或者: from Bio.Seq.MutableSeq import reverse_complement [as 别名]
def seq_query():
    """Sequence query function,  to be continued.
    """
    query_type = input(
        '1.Specific fragment\n'
        '2.Specific Organism\n'
        '3.Specific gene\n'
        '4.All\n'
        '5.All cds\n'
    )
    organize = input('Organize output?(y/n)\n')
    if query_type not in ['1', '2', '3', '4', '5']:
        raise ValueError('wrong input!\n')
    con = sqlite3.connect('./data/DB')
    cur = con.cursor()
    if query_type == '1':
        organism = input('Organism:\n')
        gene = input('Gene:\n')
        frag_type = input('Fragment type(gene, cds, rRNA, tRNA, exon, intron, spacer):\n')
        cur.execute(
            'SELECT Taxon, Organism, Name, Type, Strand, Sequence FROM main WHERE Name LIKE ? AND Type = ? AND Organism=?',
            ('%' + gene + '%', frag_type, organism))
        result = cur.fetchall()
    elif query_type == '2':
        organism = input('Organism:\n')
        frag_type = input('Fragment type(gene, cds, rRNA, tRNA, exon, intron, spacer, whole, fragments):\n')
        if frag_type == 'fragments':
            cur.execute(
                'SELECT Taxon, Organism, Name, Type, Strand, Sequence, Head FROM main WHERE Organism = ?  ORDER BY Head',
                (organism,))
        else:
            cur.execute(
                'SELECT Taxon, Organism, Name, Type, Strand, Sequence, Head FROM main WHERE Organism LIKE ? AND Type = ? ORDER BY Head',
                ('%' + organism + '%', frag_type))
        result = cur.fetchall()
    elif query_type == '3':
        gene = input('Gene:\n')
        frag_type = input('Fragment type(gene, cds, rRNA, tRNA, exon, intron, spacer):\n')
        cur.execute(
            'SELECT Taxon, Organism, Name, Type, Strand, Sequence FROM main WHERE Name LIKE ? AND Type = ? ORDER BY Taxon',
            ('%' + gene + '%', frag_type))
        result = cur.fetchall()
    elif query_type == '4':
        cur.execute('SELECT Taxon, Organism, Name, Type, Strand, Sequence, Head FROM main ORDER BY Taxon')
        result = cur.fetchall()
    elif query_type == '5':
        cur.execute(
            'SELECT Taxon, Organism, Name, Type, Strand, Sequence, Head FROM main WHERE type = "cds" ORDER BY Taxon')
        result = cur.fetchall()

    query_result = []
    for i in result:
        title = '|'.join([str(i[0]), i[1], i[2], i[3]])
        sequence = MutableSeq(i[5])
        gene = i[2]
        if i[4] == '-1':
            sequence.seq = sequence.reverse_complement()
        record = [title, gene, sequence]
        query_result.append(record)

    if organize == 'y':
        if not exists('output'):
            makedirs('output')
        for i in query_result:
            file_name = ''.join([
                'output',
                '/',
                i[1].replace('/', ''),
                '.fasta'
            ])
            with open(file_name, 'a') as output_file:
                output_file.write('>%s\n%s\n' % (i[0], i[2]))
    else:
        output = input('Enter output filename:\n')
        with open('.'.join([output, 'fasta']), 'w') as output_file:
            for i in query_result:
                output_file.write('>%s\n%s\n' % (i[0], i[2]))

    cur.close()
    con.close()
    print('Done.\n')
开发者ID:jangwen,项目名称:python,代码行数:83,代码来源:portable.py


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