Mercurial > repos > nick > sequence_content_trimmer
diff trimmer.py @ 0:7f170cb06e2e draft
planemo upload commit d76a1cf04f3e4bc735d320ccccbf7aecbc193395
author | nick |
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date | Tue, 01 Dec 2015 21:33:27 -0500 |
parents | |
children | 464aee13e2df |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/trimmer.py Tue Dec 01 21:33:27 2015 -0500 @@ -0,0 +1,220 @@ +#!/usr/bin/env python +from __future__ import division +import sys +import argparse +import getreads + +OPT_DEFAULTS = {'win_len':1, 'thres':1.0, 'filt_bases':'N'} +USAGE = "%(prog)s [options] [input_1.fq [input_2.fq output_1.fq output_2.fq]]" +DESCRIPTION = """Trim the 5' ends of reads by sequence content, e.g. by GC content or presence of +N's.""" + + +def main(argv): + + parser = argparse.ArgumentParser(description=DESCRIPTION, usage=USAGE) + parser.set_defaults(**OPT_DEFAULTS) + + parser.add_argument('infile1', metavar='reads_1.fq', nargs='?', type=argparse.FileType('r'), + default=sys.stdin, + help='Input reads (mate 1). Omit to read from stdin.') + parser.add_argument('infile2', metavar='reads_2.fq', nargs='?', type=argparse.FileType('r'), + help='Input reads (mate 2). If given, it will preserve pairs (if one read is filtered out ' + 'entirely, the other will also be lost).') + parser.add_argument('outfile1', metavar='reads.filt_1.fq', nargs='?', type=argparse.FileType('w'), + default=sys.stdout, + help='Output file for mate 1. WARNING: Will overwrite.') + parser.add_argument('outfile2', metavar='reads.filt_2.fq', nargs='?', type=argparse.FileType('w'), + help='Output file for mate 2. WARNING: Will overwrite.') + parser.add_argument('-f', '--format', dest='filetype', choices=('fasta', 'fastq'), + help='Input read format.') + parser.add_argument('-F', '--out-format', dest='out_filetype', choices=('fasta', 'fastq'), + help='Output read format. Default: whatever the input format is.') + parser.add_argument('-b', '--filt-bases', + help='The bases to filter on. Case-insensitive. Default: %(default)s.') + parser.add_argument('-t', '--thres', type=float, + help='The threshold. The read will be trimmed once the proportion of filter bases in the ' + 'window exceed this fraction (not a percentage). Default: %(default)s.') + parser.add_argument('-w', '--window', dest='win_len', type=int, + help='Window size for trimming. Default: %(default)s.') + parser.add_argument('-i', '--invert', action='store_true', + help='Invert the filter bases: filter on bases NOT present in the --filt-bases.') + parser.add_argument('-m', '--min-length', type=int, + help='Set a minimum read length. Reads which are trimmed below this length will be filtered ' + 'out (omitted entirely from the output). Read pairs will be preserved: both reads in a ' + 'pair must exceed this length to be kept. Set to 0 to only omit empty reads.') + parser.add_argument('--error', + help='Fail with this error message (useful for Galaxy tool).') + parser.add_argument('-A', '--acgt', action='store_true', + help='Filter on any non-ACGT base (shortcut for "--invert --filt-bases ACGT").') + parser.add_argument('-I', '--iupac', action='store_true', + help='Filter on any non-IUPAC base (shortcut for "--invert --filt-bases ACGTUWSMKRYBDHVN-").') + + args = parser.parse_args(argv[1:]) + + if args.error: + fail('Error: '+args.error) + + # Catch invalid argument combinations. + if args.infile1 and args.infile2 and not (args.outfile1 and args.outfile2): + fail('Error: If giving two input files (paired end), must specify both output files.') + # Determine filetypes, open input file parsers. + filetype1 = get_filetype(args.infile1, args.filetype) + file1_parser = iter(getreads.getparser(args.infile1, filetype=filetype1)) + if args.infile2: + paired = True + filetype2 = get_filetype(args.infile2, args.filetype) + file2_parser = iter(getreads.getparser(args.infile2, filetype=filetype2)) + else: + filetype2 = None + file2_parser = None + paired = False + # Override output filetypes if it was specified on the command line. + if args.out_filetype: + filetype1 = args.out_filetype + filetype2 = args.out_filetype + + # Determine the filter bases and whether to invert the selection. + filt_bases = args.filt_bases + invert = args.invert + if args.acgt: + filt_bases = 'ACGT' + invert = True + elif args.iupac: + filt_bases = 'ACGTUWSMKRYBDHVN-' + invert = True + + # Do the actual trimming. + try: + trim_reads(file1_parser, file2_parser, args.outfile1, args.outfile2, filetype1, filetype2, + paired, args.win_len, args.thres, filt_bases, invert, args.min_length) + finally: + for filehandle in (args.infile1, args.infile2, args.outfile1, args.outfile2): + if filehandle and filehandle is not sys.stdin and filehandle is not sys.stdout: + filehandle.close() + + +def trim_reads(file1_parser, file2_parser, outfile1, outfile2, filetype1, filetype2, paired, + win_len, thres, filt_bases, invert, min_length): + """Trim all the reads in the input file(s), writing to the output file(s).""" + read1 = None + read2 = None + while True: + # Read in the reads. + try: + read1 = next(file1_parser) + if paired: + read2 = next(file2_parser) + except StopIteration: + break + # Do trimming. + read1.seq = trim_read(read1.seq, win_len, thres, filt_bases, invert) + if filetype1 == 'fastq': + # If the output filetype is FASTQ, trim the quality scores too. + # If there are no input quality scores (i.e. the input is FASTA), use dummy scores instead. + # "z" is the highest alphanumeric score (PHRED 89), higher than any expected real score. + qual1 = read1.qual or 'z' * len(read1.seq) + read1.qual = qual1[:len(read1.seq)] + if paired: + read2.seq = trim_read(read2.seq, win_len, thres, filt_bases, invert) + if filetype2 == 'fastq': + qual2 = read2.qual or 'z' * len(read2.seq) + read2.qual = qual2[:len(read2.seq)] + # Output reads if they both pass the minimum length threshold (if any was given). + if min_length is None or (len(read1.seq) >= min_length and len(read2.seq) >= min_length): + write_read(outfile1, read1, filetype1) + write_read(outfile2, read2, filetype2) + else: + # Output read if it passes the minimum length threshold (if any was given). + if min_length is None or len(read1.seq) >= min_length: + write_read(outfile1, read1, filetype1) + + +def get_filetype(infile, filetype_arg): + if infile is sys.stdin: + if filetype_arg: + filetype = filetype_arg + else: + fail('Error: You must specify the --format if reading from stdin.') + elif infile: + if filetype_arg: + filetype = filetype_arg + else: + if infile.name.endswith('.fa') or infile.name.endswith('.fasta'): + filetype = 'fasta' + elif infile.name.endswith('.fq') or infile.name.endswith('.fastq'): + filetype = 'fastq' + else: + fail('Error: Unrecognized file ending on "{}". Please specify the --format.'.format(infile)) + else: + fail('Error: infile is {}'.format(infile)) + return filetype + + +def write_read(filehandle, read, filetype): + if filetype == 'fasta': + filehandle.write('>{name}\n{seq}\n'.format(**vars(read))) + elif filetype == 'fastq': + filehandle.write('@{name}\n{seq}\n+\n{qual}\n'.format(**vars(read))) + + +def trim_read(seq, win_len, thres, filt_bases, invert): + """Trim an individual read and return its trimmed sequence. + This will track the frequency of bad bases in a window of length win_len, and trim once the + frequency goes below thres. The trim point will be just before the first (leftmost) bad base in + the window (the first window with a frequency below thres). The "bad" bases are the ones in + filt_bases if invert is False, or any base NOT in filt_bases if invert is True.""" + # Algorithm: + # The window is a list which acts as a FIFO. As we scan from the left (3') end to the right (5') + # end, we append new bases to the right end of the window and pop them from the left end. + # Each base is only examined twice: when it enters the window and when it leaves it. + # We keep a running total of the number of bad bases in bad_bases_count, incrementing it when bad + # bases enter the window and decrementing it when they leave. + # We also track the location of bad bases in the window with bad_bases_coords so we can figure out + # where to cut if we have to trim. + max_bad_bases = win_len * thres + window = [] + bad_bases_count = 0 + bad_bases_coords = [] + for coord, base in enumerate(seq.upper()): + # Shift window, adjust bad_bases_count and bad_bases_coords list. + window.append(base) + # Is the new base we're adding to the window a bad base? + if invert: + bad_base = base not in filt_bases + else: + bad_base = base in filt_bases + # If so, increment the total and add its coordinate to the window. + if bad_base: + bad_bases_count += 1 + bad_bases_coords.append(coord) + if len(window) > win_len: + first_base = window.pop(0) + # Is the base we're removing (the first base in the window) a bad base? + if invert: + bad_base = first_base not in filt_bases + else: + bad_base = first_base in filt_bases + # If so, decrement the total and remove its coordinate from the window. + if bad_base: + bad_bases_count -= 1 + bad_bases_coords.pop(0) + # print bad_bases_coords + # Are we over the threshold? + if bad_bases_count > max_bad_bases: + break + # If we exceeded the threshold, trim the sequence at the first (leftmost) bad base in the window. + if bad_bases_count > max_bad_bases: + first_bad_base = bad_bases_coords[0] + return seq[0:first_bad_base] + else: + return seq + + +def fail(message): + sys.stderr.write(message+"\n") + sys.exit(1) + + +if __name__ == '__main__': + sys.exit(main(sys.argv))