# HG changeset patch
# User greg
# Date 1308663892 14400
# Node ID 81a79b4a3f6fc7b02ba183a96ae712378913e7f0
# Parent 2f3ae18f13edfbac83594399f049ea8560335fcb
Deleted selected fasta files
diff -r 2f3ae18f13ed -r 81a79b4a3f6f bam_to_bigwig/tools/fasta_tools/fasta_filter_by_id.py
--- a/bam_to_bigwig/tools/fasta_tools/fasta_filter_by_id.py Tue Jun 21 09:44:13 2011 -0400
+++ /dev/null Thu Jan 01 00:00:00 1970 +0000
@@ -1,92 +0,0 @@
-#!/usr/bin/env python
-"""Filter a FASTA file with IDs from a tabular file, e.g. from BLAST.
-
-Takes five command line options, tabular filename, ID column numbers
-(comma separated list using one based counting), input FASTA filename, and
-two output FASTA filenames (for records with and without the given IDs).
-
-If either output filename is just a minus sign, that file is not created.
-This is intended to allow output for just the matched (or just the non-matched)
-records.
-
-Note in the default NCBI BLAST+ tabular output, the query sequence ID is
-in column one, and the ID of the match from the database is in column two.
-Here sensible values for the column numbers would therefore be "1" or "2".
-
-This script is copyright 2010 by Peter Cock, SCRI, UK. All rights reserved.
-See accompanying text file for licence details (MIT/BSD style).
-
-This is version 0.0.3 of the script.
-"""
-import sys
-from galaxy_utils.sequence.fasta import fastaReader, fastaWriter
-
-def stop_err( msg ):
- sys.stderr.write( msg )
- sys.exit()
-
-#Parse Command Line
-try:
- tabular_file, cols_arg, in_file, out_positive_file, out_negative_file = sys.argv[1:]
-except ValueError:
- stop_err("Expected five arguments, got %i:\n%s" % (len(sys.argv)-1, " ".join(sys.argv)))
-try:
- columns = [int(arg)-1 for arg in cols_arg.split(",")]
-except ValueError:
- stop_err("Expected list of columns (comma separated integers), got %s" % cols_arg)
-
-#Read tabular file and record all specified identifiers
-ids = set()
-handle = open(tabular_file, "rU")
-if len(columns)>1:
- #General case of many columns
- for line in handle:
- if line.startswith("#"):
- #Ignore comments
- continue
- parts = line.rstrip("\n").split("\t")
- for col in columns:
- ids.add(parts[col])
- print "Using %i IDs from %i columns of tabular file" % (len(ids), len(columns))
-else:
- #Single column, special case speed up
- col = columns[0]
- for line in handle:
- if not line.startswith("#"):
- ids.add(line.rstrip("\n").split("\t")[col])
- print "Using %i IDs from tabular file" % (len(ids))
-handle.close()
-
-#Write filtered FASTA file based on IDs from tabular file
-reader = fastaReader(open(in_file, "rU"))
-if out_positive_file != "-" and out_negative_file != "-":
- print "Generating two FASTA files"
- positive_writer = fastaWriter(open(out_positive_file, "w"))
- negative_writer = fastaWriter(open(out_negative_file, "w"))
- for record in reader:
- #The [1:] is because the fastaReader leaves the > on the identifer.
- if record.identifier and record.identifier.split()[0][1:] in ids:
- positive_writer.write(record)
- else:
- negative_writer.write(record)
- positive_writer.close()
- negative_writer.close()
-elif out_positive_file != "-":
- print "Generating matching FASTA file"
- positive_writer = fastaWriter(open(out_positive_file, "w"))
- for record in reader:
- #The [1:] is because the fastaReader leaves the > on the identifer.
- if record.identifier and record.identifier.split()[0][1:] in ids:
- positive_writer.write(record)
- positive_writer.close()
-elif out_negative_file != "-":
- print "Generating non-matching FASTA file"
- negative_writer = fastaWriter(open(out_negative_file, "w"))
- for record in reader:
- #The [1:] is because the fastaReader leaves the > on the identifer.
- if not record.identifier or record.identifier.split()[0][1:] not in ids:
- negative_writer.write(record)
- negative_writer.close()
-else:
- stop_err("Neither output file requested")
-reader.close()
diff -r 2f3ae18f13ed -r 81a79b4a3f6f bam_to_bigwig/tools/fasta_tools/fasta_filter_by_id.txt
--- a/bam_to_bigwig/tools/fasta_tools/fasta_filter_by_id.txt Tue Jun 21 09:44:13 2011 -0400
+++ /dev/null Thu Jan 01 00:00:00 1970 +0000
@@ -1,89 +0,0 @@
-Obsolete
-========
-
-This tool is now obsolete, having been replaced by a more general version
-covering the FASTA, FASTQ and SFF sequence formats in a single tool. You
-should only install this tool if you need to support existing workflows
-which used it.
-
-
-Galaxy tool to filter FASTA sequences by ID
-===========================================
-
-This tool is copyright 2010 by Peter Cock, SCRI, UK. All rights reserved.
-See the licence text below.
-
-This tool is a short Python script (using the Galaxy library functions) which
-divides a FASTA file in two, those sequences with or without an ID present in
-the specified column(s) of a tabular file. Example uses include filtering based
-on search results from a tool like NCBI BLAST, TMHMM or SignalP.
-
-There are just two files to install:
-
-* fasta_filter_by_id.py (the Python script)
-* fasta_filter_by_id.xml (the Galaxy tool definition)
-
-The suggested location is next to the similarly named fasta_filter_by_length.py
-and fasta_filter_by_length.xml files which are included with Galaxy, i.e.
-in the Galaxy folder tools/fasta_tools
-
-You will also need to modify the tools_conf.xml file to tell Galaxy to offer
-the tool. The suggested location is next to the fasta_filter_by_length.xml
-entry. Simply add the line:
-
-
-
-That's it.
-
-
-History
-=======
-
-v0.0.1 - Initial version (not publicly released)
-v0.0.2 - Allow both, just pos or just neg output files
-v0.0.3 - Include FASTA in tool name
-v0.0.4 - Deprecated, marked as hidden in the XML
-
-
-Developers
-==========
-
-This script and related tools are being developed on the following hg branch:
-http://bitbucket.org/peterjc/galaxy-central/src/tools
-
-This incorporates the previously used hg branch:
-http://bitbucket.org/peterjc/galaxy-central/src/fasta_filter
-
-For making the "Galaxy Tool Shed" http://community.g2.bx.psu.edu/ tarball use
-the following command from the Galaxy root folder:
-
-tar -czf fasta_filter_by_id.tar.gz tools/fasta_tools/fasta_filter_by_id.*
-
-Check this worked:
-
-$ tar -tzf fasta_filter_by_id.tar.gz
-fasta_tools/fasta_filter_by_id.py
-fasta_tools/fasta_filter_by_id.txt
-fasta_tools/fasta_filter_by_id.xml
-
-
-Licence (MIT/BSD style)
-=======================
-
-Permission to use, copy, modify, and distribute this software and its
-documentation with or without modifications and for any purpose and
-without fee is hereby granted, provided that any copyright notices
-appear in all copies and that both those copyright notices and this
-permission notice appear in supporting documentation, and that the
-names of the contributors or copyright holders not be used in
-advertising or publicity pertaining to distribution of the software
-without specific prior permission.
-
-THE CONTRIBUTORS AND COPYRIGHT HOLDERS OF THIS SOFTWARE DISCLAIM ALL
-WARRANTIES WITH REGARD TO THIS SOFTWARE, INCLUDING ALL IMPLIED
-WARRANTIES OF MERCHANTABILITY AND FITNESS, IN NO EVENT SHALL THE
-CONTRIBUTORS OR COPYRIGHT HOLDERS BE LIABLE FOR ANY SPECIAL, INDIRECT
-OR CONSEQUENTIAL DAMAGES OR ANY DAMAGES WHATSOEVER RESULTING FROM LOSS
-OF USE, DATA OR PROFITS, WHETHER IN AN ACTION OF CONTRACT, NEGLIGENCE
-OR OTHER TORTIOUS ACTION, ARISING OUT OF OR IN CONNECTION WITH THE USE
-OR PERFORMANCE OF THIS SOFTWARE.
diff -r 2f3ae18f13ed -r 81a79b4a3f6f bam_to_bigwig/tools/fasta_tools/fasta_filter_by_id.xml
--- a/bam_to_bigwig/tools/fasta_tools/fasta_filter_by_id.xml Tue Jun 21 09:44:13 2011 -0400
+++ /dev/null Thu Jan 01 00:00:00 1970 +0000
@@ -1,90 +0,0 @@
-
- from a tabular file
-
-fasta_filter_by_id.py $input_tabular $columns $input_fasta
-#if $output_choice_cond.output_choice=="both"
- $output_pos $output_neg
-#elif $output_choice_cond.output_choice=="pos"
- $output_pos -
-#elif $output_choice_cond.output_choice=="neg"
- - $output_neg
-#end if
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
- output_choice_cond["output_choice"] != "neg"
-
-
- output_choice_cond["output_choice"] != "pos"
-
-
-
-
-
-
-
-**Deprecated**
-
-This tool is now obsolete, and should not be used in future. It has been
-replaced by a more general version covering FASTA, FASTQ and SFF in one
-single tool.
-
-**What it does**
-
-By default it divides a FASTA file in two, those sequences with or without an
-ID present in the tabular file column(s) specified. You can opt to have a
-single output file of just the matching records, or just the non-matching ones.
-
-Note that the order of sequences in the original FASTA file is preserved.
-Also, if any sequences share an identifier, duplicates are not removed.
-
-**Example Usage**
-
-Given a FASTA file of proteins you might run a signal peptide search (e.g.
-via the SignalP wrapper for Galaxy), then filtered these tabular results to
-select just those with a signal peptide. You could then use this tool to get
-a FASTA file of only the proteins with predicted signal peptides.
-
-
-