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  • louis7781x
    Member
    • Oct 2010
    • 74

    #1

    Want to use extract_genomic_dna in command line

    Hi everyone ,I want to use command line to run extract_genomic_dna.py from tool of galaxy.

    Here is code of extract_genomic_dna.py.

    In the beginning,need to import some module.

    import sys, string, os, re
    from bx.cookbook import doc_optparse
    import bx.seq.nib
    import bx.seq.twobit

    Does anyone know what is bx.seq.nib and bx.seq.twobit?

    Both it are also python code?

    I know doc_optparse which is python code [link-->https://bitbucket.org/ajish/bx-omelo...ib/bx/cookbook]

    #!/usr/bin/env python
    """
    usage: %prog $input $out_file1
    -1, --cols=N,N,N,N: Columns for start, end, strand in input file
    -o, --output_format=N: the data type of the output file
    -s, --seq_path=N: the directory containing the chromosome fasta files
    -l, --left_flank=N: extra bases on the left
    -r, --right_flank=N: extra bases on the right
    """
    import sys, string, os, re
    from bx.cookbook import doc_optparse
    import bx.seq.nib
    import bx.seq.twobit

    assert sys.version_info[:2] >= ( 2, 4 )

    def stop_err( msg ):
    sys.stderr.write( msg )
    sys.exit()

    # Default chrom, start, end, strand cols for a bed file
    BED_DEFAULT_COLS = 0, 1, 2, 5

    def parse_cols_arg( cols ):
    """Parse a columns command line argument into a four-tuple"""
    if cols:
    # Handle case where no strand column included - in this case, cols
    # looks something like 1,2,3,
    if cols.endswith( ',' ):
    cols += '0'
    col_list = map( lambda x: int( x ) - 1, cols.split(",") )
    return col_list
    else:
    return BED_DEFAULT_COLS

    def reverse_complement( s ):
    complement_dna = {"A":"T", "T":"A", "C":"G", "G":"C", "a":"t", "t":"a", "c":"g", "g":"c", "N":"N", "n":"n" }
    reversed_s = []
    for i in s:
    reversed_s.append( complement_dna[i] )
    reversed_s.reverse()
    return "".join( reversed_s )

    def __main__():

    lflank = 0
    rflank = 0

    options, args = doc_optparse.parse( __doc__ )
    try:
    chrom_col, start_col, end_col, strand_col = parse_cols_arg( options.cols )
    output_format = options.output_format
    seq_path = options.seq_path
    if ( options.left_flank): lflank = int(options.left_flank)
    if ( options.right_flank): rflank = int( options.right_flank)
    input_filename, output_filename = args
    except:
    doc_optparse.exception()
    includes_strand_col = strand_col >= 0
    strand = None
    nibs = {}
    twobits = {}
    if not os.path.exists( seq_path ):
    # If this occurs, we need to fix the metadata validator.
    print "No sequences are available for '%s', request them by reporting this error."

    skipped_lines = 0
    first_invalid_line = 0
    invalid_line = ''
    fout = open( output_filename, "w" )
    warnings = []
    warning = ''
    twobitfile = None
    dbkey=seq_path

    for i, line in enumerate( open( input_filename ) ):
    line = line.rstrip( '\r\n' )
    if line and not line.startswith( "#" ):
    fields = line.split( '\t' )
    try:
    chrom = fields[chrom_col]
    ostart = int( fields[start_col] )
    oend = int( fields[end_col] )
    start = ostart - lflank
    end = oend + rflank
    if includes_strand_col:
    strand = fields[strand_col]
    except:
    warning = "Invalid chrom, start or end column values. "
    warnings.append( warning )
    skipped_lines += 1
    if not invalid_line:
    first_invalid_line = i + 1
    invalid_line = line
    continue
    if start > end:
    warning = "Invalid interval, start '%d' > end '%d'. " % ( start, end )
    warnings.append( warning )
    skipped_lines += 1
    if not invalid_line:
    first_invalid_line = i + 1
    invalid_line = line
    continue

    if strand not in ['+', '-']:
    strand = '+'
    sequence = ''

    if seq_path and os.path.exists( "%s/%s.nib" % ( seq_path, chrom ) ):
    if chrom in nibs:
    nib = nibs[chrom]
    else:
    nibs[chrom] = nib = bx.seq.nib.NibFile( file( "%s/%s.nib" % ( seq_path, chrom ) ) )
    try:
    sequence = nib.get( start, end-start )
    except:
    warning = "Unable to fetch the sequence from '%d' to '%d' for build '%s'. " %( start, end-start, dbkey )
    warnings.append( warning )
    skipped_lines += 1
    if not invalid_line:
    first_invalid_line = i + 1
    invalid_line = line
    continue
    elif seq_path and os.path.isfile( seq_path ):
    if not(twobitfile):
    twobitfile = bx.seq.twobit.TwoBitFile( file( seq_path ) )
    try:
    sequence = twobitfile[chrom][start:end]
    except:
    warning = "Unable to fetch the sequence from '%d' to '%d' for build '%s'. " %( start, end-start, dbkey )
    warnings.append( warning )
    skipped_lines += 1
    if not invalid_line:
    first_invalid_line = i + 1
    invalid_line = line
    continue
    else:
    warning = "Chromosome by name '%s' was not found for build '%s'. " % ( chrom, dbkey )
    warnings.append( warning )
    skipped_lines += 1
    if not invalid_line:
    first_invalid_line = i + 1
    invalid_line = line
    continue
    if sequence == '':
    warning = "Chrom: '%s', start: '%s', end: '%s' is either invalid or not present in build '%s'. " %( chrom, start, end, dbkey )
    warnings.append( warning )
    skipped_lines += 1
    if not invalid_line:
    first_invalid_line = i + 1
    invalid_line = line
    continue
    if includes_strand_col and strand == "-":
    sequence = reverse_complement( sequence )
    sequence = sequence[0:lflank].lower() + sequence[lflank:len(sequence)-rflank+1].upper() + sequence[len(sequence)-rflank+1:len(sequence)].lower()

    if output_format == "fasta" :
    l = len( sequence )
    c = 0
    fields = [dbkey, str( chrom ), str( ostart ), str( oend ), strand]
    meta_data = "_".join( fields )
    fout.write( ">%s\n" % meta_data )
    while c < l:
    b = min( c + 50, l )
    fout.write( "%s\n" % str( sequence[c:b] ) )
    c = b
    else: # output_format == "interval"
    meta_data = "\t".join( fields )
    fout.write( "%s\t%s\n" % ( meta_data, str( sequence ) ) )

    fout.close()

    if warnings:
    warn_msg = "%d warnings, 1st is: " % len( warnings )
    warn_msg += warnings[0]
    print warn_msg
    if skipped_lines:
    print 'Skipped %d invalid lines, 1st is #%d, "%s"' % ( skipped_lines, first_invalid_line, invalid_line )

    if __name__ == "__main__": __main__()
  • Blahah404
    Member
    • Dec 2011
    • 48

    #2
    bx-python is a library for manipulating biological data.

    bx.seq.nib handles DNA sequences, packing the file as 4 bits per character.

    twobit is a patch which uses the 2 bit datatype instead, as mentioned on the galaxy dev discussions.

    If you want to run the script, you have to install the bx-python library, using these instructions.
    Last edited by Blahah404; 12-04-2011, 06:43 AM. Reason: added link to install instructions

    Comment

    • louis7781x
      Member
      • Oct 2010
      • 74

      #3
      Originally posted by Blahah404 View Post
      bx-python is a library for manipulating biological data.

      bx.seq.nib handles DNA sequences, packing the file as 4 bits per character.

      twobit is a patch which uses the 2 bit datatype instead, as mentioned on the galaxy dev discussions.

      If you want to run the script, you have to install the bx-python library, using these instructions.
      Thanks a lot!

      I will install bx-python and try the script again.

      Comment

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