#!/opt/chipster/tools/Python-2.7.12/bin/python """ 'Tile' the blocks of a maf file over each of a set of intervals. The highest scoring block that covers any part of a region will be used, and pieces not covered by any block filled with "-" or optionally "*". The list of species to tile is specified by `tree` (either a tree or just a comma separated list). The `seq_db` is a lookup table mapping chromosome names to nib file for filling in the reference species. Maf files must be indexed. NOTE: See maf_tile_2.py for a more sophisticated version of this program, I think this one will be eliminated in the future. usage: %prog tree maf_files... -m, --missingData: Inserts wildcards for missing block rows instead of '-' """ import psyco_full from bx.cookbook import doc_optparse import bx.align.maf import bx.align as align from bx import misc import bx.seq.nib import os import string import sys tree_tx = string.maketrans( "(),", " " ) def main(): options, args = doc_optparse.parse( __doc__ ) try: sources = args[0].translate( tree_tx ).split() seq_db = load_seq_db( args[1] ) index = bx.align.maf.MultiIndexed( args[2:] ) out = bx.align.maf.Writer( sys.stdout ) missing_data = bool(options.missingData) except: doc_optparse.exception() for line in sys.stdin: ref_src, start, end = line.split()[0:3] do_interval( sources, index, out, ref_src, int( start ), int( end ), seq_db, missing_data ) out.close() def load_seq_db( fname ): db = {} for line in open( fname ): fields = line.split(',') src = fields[1] + "." + fields[2] seq = fields[4] db[src]=seq.strip() return db def do_interval( sources, index, out, ref_src, start, end, seq_db, missing_data ): assert sources[0].split('.')[0] == ref_src.split('.')[0], "%s != %s" % ( sources[0].split('.')[0], ref_src.split('.')[0] ) base_len = end - start blocks = index.get( ref_src, start, end ) # From low to high score blocks.sort( lambda a, b: cmp( a.score, b.score ) ) mask = [ -1 ] * base_len # print len( blocks ) # print blocks[0] ref_src_size = None for i, block in enumerate( blocks ): ref = block.get_component_by_src_start( ref_src ) ref_src_size = ref.src_size assert ref.strand == "+" slice_start = max( start, ref.start ) slice_end = min( end, ref.end ) for j in range( slice_start, slice_end ): mask[j-start] = i #print >>sys.stderr, mask tiled = [] for i in range( len( sources ) ): tiled.append( [] ) for ss, ee, index in intervals_from_mask( mask ): if index < 0: tiled[0].append( bx.seq.nib.NibFile( open( seq_db[ ref_src ] ) ).get( start+ss, ee-ss ) ) for row in tiled[1:]: if missing_data: row.append( "*" * ( ee - ss ) ) else: row.append( "-" * ( ee - ss ) ) else: slice_start = start + ss slice_end = start + ee block = blocks[index] ref = block.get_component_by_src_start( ref_src ) sliced = block.slice_by_component( ref, slice_start, slice_end ) sliced = sliced.limit_to_species( sources ) sliced.remove_all_gap_columns() for i, src in enumerate( sources ): comp = sliced.get_component_by_src_start( src ) if comp: tiled[i].append( comp.text ) else: if missing_data: tiled[i].append( "*" * sliced.text_size ) else: tiled[i].append( "-" * sliced.text_size ) a = align.Alignment() for i, name in enumerate( sources ): text = "".join( tiled[i] ) size = len( text ) - text.count( "-" ) if i == 0: if ref_src_size is None: ref_src_size = bx.seq.nib.NibFile( open( seq_db[ ref_src ] ) ).length c = align.Component( ref_src, start, end-start, "+", ref_src_size, text ) else: c = align.Component( name + ".fake", 0, size, "?", size, text ) a.add_component( c ) out.write( a ) def intervals_from_mask( mask ): start = 0 last = mask[0] for i in range( 1, len( mask ) ): if mask[i] != last: yield start, i, last start = i last = mask[i] yield start, len(mask), last main()