allpy: allpy/base.py annotate

allpy

annotate allpy/base.py @ 299:21c2358cb5e7

Implemented allpy.base.Alignment row/column model: methods rows(), *_as_lists()

author	Daniil Alexeyevsky <me.dendik@gmail.com>
date	Thu, 16 Dec 2010 18:51:05 +0300
parents	c305a80cdb75
children	5d355141f37d

rev	line source
me@261	1 import sys
me@261	2 import os
me@262	3 import os.path
me@261	4 from tempfile import NamedTemporaryFile
me@262	5 import urllib2
me@261	6
me@261	7 import config
me@284	8 import fasta
me@261	9 from graph import Graph
me@262	10 from Bio.PDB.DSSP import make_dssp_dict
me@260	11 import data.codes
me@260	12
me@260	13 class MonomerType(object):
me@260	14 """Class of monomer types.
me@260	15
me@260	16 Each MonomerType object represents a known monomer type, e.g. Valine,
me@260	17 and is referenced to by each instance of monomer in a given sequence.
me@260	18
me@260	19 - `name`: full name of monomer type
me@260	20 - `code1`: one-letter code
me@260	21 - `code3`: three-letter code
me@260	22 - `is_modified`: either of True or False
me@260	23
me@260	24 class atributes:
me@260	25
me@260	26 - `by_code1`: a mapping from one-letter code to MonomerType object
me@260	27 - `by_code3`: a mapping from three-letter code to MonomerType object
me@260	28 - `by_name`: a mapping from monomer name to MonomerType object
me@260	29 - `instance_type`: class of Monomer objects to use when creating new
me@260	30 objects; this must be redefined in descendent classes
me@260	31
me@260	32 All of the class attributes MUST be redefined when subclassing.
me@260	33 """
me@260	34
me@260	35 by_code1 = {}
me@260	36 by_code3 = {}
me@260	37 by_name = {}
me@260	38 instance_type = None
me@260	39
me@260	40 def __init__(self, name="", code1="", code3="", is_modified=False):
me@260	41 self.name = name.capitalize()
me@260	42 self.code1 = code1.upper()
me@260	43 self.code3 = code3.upper()
me@260	44 self.is_modified = bool(is_modified)
me@260	45 if not is_modified:
me@260	46 self.by_code1[self.code1] = self
me@260	47 self.by_code3[code3] = self
me@260	48 self.by_name[name] = self
me@260	49 # We duplicate distinguished long names into MonomerType itself,
me@260	50 # so that we can use MonomerType.from_code3 to create the relevant
me@260	51 # type of monomer.
me@260	52 MonomerType.by_code3[code3] = self
me@260	53 MonomerType.by_name[name] = self
me@260	54
me@260	55 @classmethod
me@260	56 def _initialize(cls, type_letter, codes=data.codes.codes):
me@260	57 """Create all relevant instances of MonomerType.
me@260	58
me@260	59 `type_letter` is either of:
me@260	60
me@260	61 - 'p' for protein
me@260	62 - 'd' for DNA
me@260	63 - 'r' for RNA
me@260	64
me@260	65 `codes` is a table of monomer codes
me@260	66 """
me@260	67 for type, code1, is_modified, code3, name in codes:
me@260	68 if type == type_letter:
me@260	69 cls(name, code1, code3, is_modified)
me@260	70
me@260	71 @classmethod
me@260	72 def from_code1(cls, code1):
me@260	73 """Return monomer type by one-letter code."""
me@260	74 return cls.by_code1[code1.upper()]
me@260	75
me@260	76 @classmethod
me@260	77 def from_code3(cls, code3):
me@260	78 """Return monomer type by three-letter code."""
me@260	79 return cls.by_code3[code3.upper()]
me@260	80
me@260	81 @classmethod
me@260	82 def from_name(cls, name):
me@260	83 """Return monomer type by name."""
me@260	84 return cls.by_name[name.capitalize()]
me@260	85
me@260	86 def instance(self):
me@260	87 """Create a new monomer of given type."""
me@260	88 return self.instance_type(self)
me@260	89
me@260	90 def __eq__(self, other):
me@260	91 if hasattr(other, "type"):
me@260	92 return self is other.type
me@260	93 return self is other
me@260	94
me@260	95 class Monomer(object):
me@260	96 """Monomer object.
me@260	97
me@260	98 attributes:
me@260	99
me@260	100 - `type`: type of monomer (a MonomerType object)
me@260	101
me@282	102 class attributes:
me@282	103
me@282	104 - `monomer_type`: either MonomerType or one of it's subclasses, it is used
me@282	105 when creating new monomers. It SHOULD be redefined when subclassing
me@282	106 Monomer.
me@260	107 """
me@260	108 monomer_type = MonomerType
me@260	109
me@260	110 def __init__(self, type):
me@260	111 self.type = type
me@260	112
me@260	113 @classmethod
me@260	114 def from_code1(cls, code1):
me@260	115 return cls(cls.monomer_type.by_code1[code1.upper()])
me@260	116
me@260	117 @classmethod
me@260	118 def from_code3(cls, code3):
me@260	119 return cls(cls.monomer_type.by_code3[code3.upper()])
me@260	120
me@260	121 @classmethod
me@260	122 def from_name(cls, name):
me@260	123 return cls(cls.monomer_type.by_name[name.capitalize()])
me@260	124
me@260	125 def __eq__(self, other):
me@260	126 if hasattr(other, "type"):
me@260	127 return self.type is other.type
me@260	128 return self.type is other
bnagaev@239	129
bnagaev@239	130 class Sequence(list):
me@274	131 """Sequence of Monomers.
bnagaev@243	132
me@274	133 This behaves like list of monomer objects. In addition to standard list
me@274	134 behaviour, Sequence has the following attributes:
me@270	135
me@274	136 * name -- str with the name of the sequence
me@274	137 * description -- str with description of the sequence
me@274	138 * source -- str denoting source of the sequence
me@266	139
me@274	140 Any of them may be empty (i.e. hold empty string)
me@275	141
me@275	142 Class attributes:
me@282	143
me@275	144 * monomer_type -- type of monomers in sequence, must be redefined when
me@275	145 subclassing
me@274	146 """
me@270	147
me@275	148 monomer_type = Monomer
me@270	149
me@275	150 name = ''
me@275	151 description = ''
me@275	152 source = ''
me@275	153
me@275	154 def __init__(self, sequence=[], name=None, description=None, source=None):
me@275	155 super(Sequence, self).__init__(sequence)
me@275	156 if hasattr(sequence, 'name'):
me@275	157 vars(self).update(vars(sequence))
me@275	158 if name:
me@275	159 self.name = name
me@275	160 if description:
me@275	161 self.description = description
me@275	162 if source:
me@275	163 self.source = source
me@270	164
me@262	165 def __str__(self):
me@275	166 """Returns sequence in one-letter code."""
me@275	167 return ''.join(monomer.code1 for monomer in self)
me@270	168
me@273	169 @classmethod
me@273	170 def from_string(cls, string, name='', description=''):
me@273	171 """Create sequences from string of one-letter codes."""
me@273	172 monomer = cls.monomer_type.from_code1
me@273	173 monomers = [monomer(letter) for letter in string]
me@273	174 return cls(monomers, name, description)
me@262	175
me@284	176 @classmethod
me@284	177 def from_fasta(cls, file):
me@284	178 """Read sequence from FASTA file.
me@286	179
me@284	180 File must contain exactly one sequence.
me@284	181 """
me@284	182 sequences = fasta.parse_file(file)
me@284	183 assert len(sequences) == 1
me@287	184 name, description = sequences.keys()[0]
me@284	185 return cls(sequences[header], name, description, file.name)
me@284	186
me@295	187 class Alignment(object):
me@295	188 """Alignment. It is a list of Columns."""
bnagaev@249	189
me@287	190 sequence_type = Sequence
me@289	191 """Type of sequences in alignment. SHOULD be redefined when subclassing."""
me@288	192
me@289	193 sequences = None
me@289	194 """Ordered list of sequences in alignment. Read, but DO NOT FIDDLE!"""
bnagaev@249	195
me@287	196 def __init__(self):
me@287	197 """Initialize empty alignment."""
me@287	198 super(Alignment, self).__init__()
me@287	199 self.sequences = []
me@295	200 self.columns = []
me@282	201
me@299	202 # Alignment modification methods
me@299	203 # ==============================
me@299	204
me@294	205 def append_sequence(self, sequence):
me@294	206 """Add sequence to alignment.
me@294	207
me@294	208 If sequence is too short, pad it with gaps on the right.
me@294	209 """
me@294	210 self.sequences.append(sequence)
me@294	211 for i, monomer in enumerate(sequence):
me@295	212 self.columns[i][sequence] = monomer
me@294	213
me@294	214 def append_gapped_line(self, line, name='', description='', source=''):
me@287	215 """Add row from a line of one-letter codes and gaps."""
me@287	216 Sequence = cls.sequence_type
me@287	217 not_gap = lambda (i, char): char != "-"
me@287	218 no_gaps = line.replace("-", "")
me@287	219 sequence = Sequence(no_gaps, name, description, source)
me@287	220 for i, (j, char) in enumerate(filter(not_gap, enumerate(line))):
me@295	221 self.columns[j][seq] = sequence[i]
me@287	222 self.sequences.append(sequence)
me@287	223
me@299	224 # Alignment IO methods
me@299	225 # ====================
me@299	226
me@287	227 @classmethod
me@287	228 def from_fasta(cls, file):
me@287	229 """Create new alignment from FASTA file."""
me@287	230 self = cls()
me@287	231 for ((name, description), body) in fasta.parse_file(file):
me@294	232 self.append_gapped_line(body, name, description)
me@287	233 return self
bnagaev@249	234
me@292	235 def to_fasta(self, file):
me@292	236 """Write alignment in FASTA file as sequences with gaps."""
me@292	237 def char(monomer):
me@292	238 if monomer:
me@292	239 return monomer.code1
me@292	240 return "-"
me@292	241 for row in self.rows_as_lists():
me@292	242 seq = row.sequence
me@292	243 line = "".join(map(char, row))
me@292	244 fasta.save_file(file, line, seq.name, seq.description)
me@292	245
me@299	246 # Data access methods for alignment
me@299	247 # =================================
me@299	248
me@299	249 def rows(self):
me@299	250 """Return list of rows (temporary objects) in alignment.
me@299	251
me@299	252 Each row is a dictionary of { column : monomer }.
me@299	253
me@299	254 For gap positions there is no key for the column in row.
me@299	255
me@299	256 Each row has attribute `sequence` pointing to the sequence the row is
me@299	257 describing.
me@299	258
me@299	259 Modifications of row have no effect on the alignment.
me@299	260 """
me@299	261 # For now, the function returns a list rather than iterator.
me@299	262 # It is yet to see, whether memory performance here becomes critical,
me@299	263 # or is random access useful.
me@299	264 rows = []
me@299	265 for sequence in self.sequences:
me@299	266 row = util.UserDict()
me@299	267 row.sequence = sequence
me@299	268 for column in self.columns:
me@299	269 if sequence in column:
me@299	270 row[column] = column[sequence]
me@299	271 rows.append(row)
me@299	272 return rows
me@299	273
me@299	274 def rows_as_lists(self):
me@299	275 """Return list of rows (temporary objects) in alignment.
me@299	276
me@299	277 Each row here is a list of either monomer or None (for gaps).
me@299	278
me@299	279 Each row has attribute `sequence` pointing to the sequence of row.
me@299	280
me@299	281 Modifications of row have no effect on the alignment.
me@299	282 """
me@299	283 rows = []
me@299	284 for sequence in self.sequences:
me@299	285 row = util.UserList()
me@299	286 row.sequence = sequence
me@299	287 for column in self.columns:
me@299	288 row.append(column.get(sequence))
me@299	289 rows.append(row)
me@299	290 return rows
me@299	291
me@299	292 def columns_as_lists(self):
me@299	293 """Return list of columns (temorary objects) in alignment.
me@299	294
me@299	295 Each column here is a list of either monomer or None (for gaps).
me@299	296
me@299	297 Items of column are sorted in the same way as alignment.sequences.
me@299	298
me@299	299 Modifications of column have no effect on the alignment.
me@299	300 """
me@299	301 columns = []
me@299	302 for column in self.columns:
me@299	303 col = []
me@299	304 for sequence in self.sequences:
me@299	305 col.append(column.get(sequence))
me@299	306 columns.append(col)
me@299	307 return columns
me@299	308
me@292	309 ## Unclean code follows
me@292	310
bnagaev@249	311 def length(self):
me@287	312 """Return width, ie length of each sequence with gaps."""
bnagaev@249	313 return max([len(line) for line in self.body.values()])
bnagaev@249	314
bnagaev@249	315 def height(self):
bnagaev@249	316 """ The number of sequences in alignment (it's thickness). """
bnagaev@249	317 return len(self.body)
bnagaev@249	318
bnagaev@249	319 def identity(self):
bnagaev@249	320 """ Calculate the identity of alignment positions for colouring.
bnagaev@249	321
bnagaev@249	322 For every (row, column) in alignment the percentage of the exactly
bnagaev@249	323 same residue in the same column in the alignment is calculated.
me@270	324 The data structure is just like the Alignment.body, but istead of
bnagaev@249	325 monomers it contains float percentages.
bnagaev@249	326 """
bnagaev@249	327 # Oh, God, that's awful! Absolutely not understandable.
bnagaev@249	328 # First, calculate percentages of amino acids in every column
bnagaev@249	329 contribution = 1.0 / len(self.sequences)
bnagaev@249	330 all_columns = []
bnagaev@249	331 for position in range(len(self)):
bnagaev@249	332 column_percentage = {}
bnagaev@249	333 for seq in self.body:
bnagaev@249	334 if self.body[seq][position] is not None:
bnagaev@249	335 aa = self.body[seq][position].code
bnagaev@249	336 else:
bnagaev@249	337 aa = None
bnagaev@249	338 if aa in allpy.data.amino_acids:
bnagaev@249	339 if aa in column_percentage.keys():
bnagaev@249	340 column_percentage[aa] += contribution
bnagaev@249	341 else:
bnagaev@249	342 column_percentage[aa] = contribution
bnagaev@249	343 all_columns.append(column_percentage)
bnagaev@249	344 # Second, map these percentages onto the alignment
bnagaev@249	345 self.identity_percentages = {}
bnagaev@249	346 for seq in self.sequences:
bnagaev@249	347 self.identity_percentages[seq] = []
bnagaev@249	348 for seq in self.identity_percentages:
bnagaev@249	349 line = self.identity_percentages[seq]
bnagaev@249	350 for position in range(len(self)):
bnagaev@249	351 if self.body[seq][position] is not None:
bnagaev@249	352 aa = self.body[seq][position].code
bnagaev@249	353 else:
bnagaev@249	354 aa = None
bnagaev@249	355 line.append(all_columns[position].get(aa))
bnagaev@249	356 return self.identity_percentages
bnagaev@249	357
bnagaev@249	358 class Block(object):
me@261	359 """ Block of alignment
me@270	360
me@261	361 Mandatory data:
me@266	362
me@261	363 * self.alignment -- alignment object, which the block belongs to
me@261	364 * self.sequences - set of sequence objects that contain monomers
me@261	365 and/or gaps, that constitute the block
me@261	366 * self.positions -- list of positions of the alignment.body that
me@261	367 are included in the block; position[i+1] is always to the right from position[i]
me@270	368
me@261	369 Don't change self.sequences -- it may be a link to other block.sequences
me@270	370
me@261	371 How to create a new block:
me@282	372
me@261	373 >>> import alignment
me@261	374 >>> import block
me@261	375 >>> proj = alignment.Alignment(open("test.fasta"))
me@261	376 >>> block1 = block.Block(proj)
me@261	377 """
me@270	378
me@261	379 def __init__(self, alignment, sequences=None, positions=None):
me@261	380 """ Builds new block from alignment
me@270	381
me@261	382 if sequences==None, all sequences are used
me@261	383 if positions==None, all positions are used
me@261	384 """
me@261	385 if sequences == None:
me@261	386 sequences = set(alignment.sequences) # copy
me@261	387 if positions == None:
me@261	388 positions = range(len(alignment))
me@261	389 self.alignment = alignment
me@261	390 self.sequences = sequences
me@261	391 self.positions = positions
me@270	392
me@261	393 def save_fasta(self, out_file, long_line=70, gap='-'):
me@270	394 """ Saves alignment to given file in fasta-format
me@270	395
me@261	396 No changes in the names, descriptions or order of the sequences
me@261	397 are made.
me@261	398 """
me@261	399 for sequence in self.sequences:
me@261	400 alignment_monomers = self.alignment.body[sequence]
me@261	401 block_monomers = [alignment_monomers[i] for i in self.positions]
me@261	402 string = ''.join([m.type.code1 if m else '-' for m in block_monomers])
me@261	403 save_fasta(out_file, string, sequence.name, sequence.description, long_line)
me@270	404
me@270	405 def geometrical_cores(self, max_delta=config.delta,
me@270	406 timeout=config.timeout, minsize=config.minsize,
me@261	407 ac_new_atoms=config.ac_new_atoms,
me@261	408 ac_count=config.ac_count):
me@261	409 """ Returns length-sorted list of blocks, representing GCs
me@270	410
me@282	411 * max_delta -- threshold of distance spreading
me@282	412 * timeout -- Bron-Kerbosh timeout (then fast O(n ln n) algorithm)
me@282	413 * minsize -- min size of each core
me@282	414 * ac_new_atoms -- min part or new atoms in new alternative core
me@282	415 current GC is compared with each of already selected GCs if
me@282	416 difference is less then ac_new_atoms, current GC is skipped
me@261	417 difference = part of new atoms in current core
me@282	418 * ac_count -- max number of cores (including main core)
me@261	419 -1 means infinity
me@282	420
me@261	421 If more than one pdb chain for some sequence provided, consider all of them
me@270	422 cost is calculated as 1 / (delta + 1)
me@282	423
me@261	424 delta in [0, +inf) => cost in (0, 1]
me@261	425 """
me@261	426 nodes = self.positions
me@261	427 lines = {}
me@261	428 for i in self.positions:
me@261	429 for j in self.positions:
me@261	430 if i < j:
me@261	431 distances = []
me@261	432 for sequence in self.sequences:
me@261	433 for chain in sequence.pdb_chains:
me@261	434 m1 = self.alignment.body[sequence][i]
me@261	435 m2 = self.alignment.body[sequence][j]
me@261	436 if m1 and m2:
me@261	437 r1 = sequence.pdb_residues[chain][m1]
me@261	438 r2 = sequence.pdb_residues[chain][m2]
me@261	439 ca1 = r1['CA']
me@261	440 ca2 = r2['CA']
me@261	441 d = ca1 - ca2 # Bio.PDB feature
me@261	442 distances.append(d)
me@261	443 if len(distances) >= 2:
me@261	444 delta = max(distances) - min(distances)
me@261	445 if delta <= max_delta:
me@261	446 lines[Graph.line(i, j)] = 1.0 / (1.0 + max_delta)
me@261	447 graph = Graph(nodes, lines)
me@261	448 cliques = graph.cliques(timeout=timeout, minsize=minsize)
me@261	449 GCs = []
me@261	450 for clique in cliques:
me@261	451 for GC in GCs:
me@261	452 if len(clique - set(GC.positions)) < ac_new_atoms * len(clique):
me@261	453 break
me@261	454 else:
me@261	455 GCs.append(Block(self.alignment, self.sequences, clique))
me@261	456 if ac_count != -1 and len(GCs) >= ac_count:
me@261	457 break
me@261	458 return GCs
me@270	459
me@261	460 def xstring(self, x='X', gap='-'):
me@261	461 """ Returns string consisting of gap chars and chars x at self.positions
me@270	462
me@261	463 Length of returning string = length of alignment
me@261	464 """
me@261	465 monomers = [False] * len(self.alignment)
me@261	466 for i in self.positions:
me@261	467 monomers[i] = True
me@261	468 return ''.join([x if m else gap for m in monomers])
me@270	469
me@261	470 def save_xstring(self, out_file, name, description='', x='X', gap='-', long_line=70):
me@261	471 """ Save xstring and name in fasta format """
me@261	472 save_fasta(out_file, self.xstring(x=x, gap=gap), name, description, long_line)
me@270	473
me@261	474 def monomers(self, sequence):
me@261	475 """ Iterates monomers of this sequence from this block """
me@261	476 alignment_sequence = self.alignment.body[sequence]
me@261	477 return (alignment_sequence[i] for i in self.positions)
me@270	478
me@261	479 def ca_atoms(self, sequence, pdb_chain):
me@261	480 """ Iterates Ca-atom of monomers of this sequence from this block """
me@261	481 return (sequence.pdb_residues[pdb_chain][monomer] for monomer in self.monomers())
me@270	482
me@261	483 def sequences_chains(self):
me@261	484 """ Iterates pairs (sequence, chain) """
me@261	485 for sequence in self.alignment.sequences:
me@261	486 if sequence in self.sequences:
me@261	487 for chain in sequence.pdb_chains:
me@261	488 yield (sequence, chain)
me@270	489
me@261	490 def superimpose(self):
me@261	491 """ Superimpose all pdb_chains in this block """
me@261	492 sequences_chains = list(self.sequences_chains())
me@261	493 if len(sequences_chains) >= 1:
me@261	494 sup = Superimposer()
me@261	495 fixed_sequence, fixed_chain = sequences_chains.pop()
me@261	496 fixed_atoms = self.ca_atoms(fixed_sequence, fixed_chain)
me@261	497 for sequence, chain in sequences_chains:
me@261	498 moving_atoms = self.ca_atoms(sequence, chain)
me@261	499 sup.set_atoms(fixed_atoms, moving_atoms)
me@261	500 # Apply rotation/translation to the moving atoms
me@261	501 sup.apply(moving_atoms)
me@270	502
me@261	503 def pdb_save(self, out_file):
me@270	504 """ Save all sequences
me@270	505
me@261	506 Returns {(sequence, chain): CHAIN}
me@261	507 CHAIN is chain letter in new file
me@261	508 """
me@261	509 tmp_file = NamedTemporaryFile(delete=False)
me@261	510 tmp_file.close()
me@270	511
me@261	512 for sequence, chain in self.sequences_chains():
me@261	513 sequence.pdb_save(tmp_file.name, chain)
me@261	514 # TODO: read from tmp_file.name
me@261	515 # change CHAIN
me@261	516 # add to out_file
me@270	517
me@261	518 os.unlink(NamedTemporaryFile)
bnagaev@239	519
me@260	520 # vim: set ts=4 sts=4 sw=4 et: