diff --git a/tools/metag_tools/blat_coverage_report.xml b/tools/metag_tools/blat_coverage_report.xml
index b779f30ee7c..bd8955c4de2 100644
--- a/tools/metag_tools/blat_coverage_report.xml
+++ b/tools/metag_tools/blat_coverage_report.xml
@@ -2,7 +2,7 @@
the percentage of reads supporting each nucleotide at each locationblat_coverage_report.py $input1 $output1
-
+
diff --git a/tools/metag_tools/blat_mapping.xml b/tools/metag_tools/blat_mapping.xml
index 244ed365c08..57c9f18dc01 100644
--- a/tools/metag_tools/blat_mapping.xml
+++ b/tools/metag_tools/blat_mapping.xml
@@ -2,7 +2,7 @@
in wiggle formatblat_mapping.py $input1 $output1
-
+
diff --git a/tools/metag_tools/blat_wrapper.xml b/tools/metag_tools/blat_wrapper.xml
index be893742300..188539da13e 100644
--- a/tools/metag_tools/blat_wrapper.xml
+++ b/tools/metag_tools/blat_wrapper.xml
@@ -8,7 +8,7 @@
-
+
@@ -16,13 +16,13 @@
-
+
-
-
-
-
+
+
+
+
diff --git a/tools/metag_tools/convert_SOLiD_color2nuc.xml b/tools/metag_tools/convert_SOLiD_color2nuc.xml
index b88d09bf5de..112dff64af8 100644
--- a/tools/metag_tools/convert_SOLiD_color2nuc.xml
+++ b/tools/metag_tools/convert_SOLiD_color2nuc.xml
@@ -3,8 +3,8 @@
convert_SOLiD_color2nuc.py $input1 $input2 $output1
-
-
+
+
diff --git a/tools/metag_tools/megablast_wrapper.xml b/tools/metag_tools/megablast_wrapper.xml
index 6892b0a4dfa..3d001117e1a 100644
--- a/tools/metag_tools/megablast_wrapper.xml
+++ b/tools/metag_tools/megablast_wrapper.xml
@@ -2,10 +2,10 @@
for Metagenomics Projectsmegablast_wrapper.py $source_select $input_query $output1 $word_size $iden_cutoff $disc_word $disc_type $filter_query ${GALAXY_DATA_INDEX_DIR}
-
-
+
+
diff --git a/tools/metag_tools/megablast_xml_parser.xml b/tools/metag_tools/megablast_xml_parser.xml
index dfeb05ae00c..ceea8b22cf7 100644
--- a/tools/metag_tools/megablast_xml_parser.xml
+++ b/tools/metag_tools/megablast_xml_parser.xml
@@ -2,7 +2,7 @@
megablast_xml_parser.py $input1 $output1
-
+
diff --git a/tools/metag_tools/rmap_wrapper.py b/tools/metag_tools/rmap_wrapper.py
index 36b792f5a88..da0c6d04c0e 100644
--- a/tools/metag_tools/rmap_wrapper.py
+++ b/tools/metag_tools/rmap_wrapper.py
@@ -1,9 +1,5 @@
#! /usr/bin/python
-"""
-3. create test files, run functional test
-"""
-
import os, sys, tempfile
assert sys.version_info[:2] >= (2.4)
@@ -24,22 +20,37 @@ def __main__():
mismatch = sys.argv[5] # -m
output_file = sys.argv[6]
+ # first guess the read length
+ guess_read_len = 0
+ seq = ''
+ for i, line in enumerate(open(infile)):
+ line = line.rstrip('\r\n')
+ if line.startswith('>'):
+ if seq:
+ guess_read_len = len(seq)
+ break
+ else:
+ seq += line
+
try:
test = int(read_len)
- assert test >= 20 and test <= 64
+ if test == 0:
+ read_len = str(guess_read_len)
+ else:
+ assert test >= 20 and test <= 64
except:
stop_err('Invalid value for read length. Must be between 20 and 64.')
try:
int(align_len)
except:
- stop_err('Invalid value for minimal length of an alignment.')
+ stop_err('Invalid value for minimal length of a hit.')
try:
- test = int(mismatch)
- assert test >= 0 and test <= int(0.1*int(read_len))
+ int(mismatch)
+ #assert test >= 0 and test <= int(0.1*int(read_len))
except:
- stop_err('Invalid value for mismatch numbers in an alignment. Please use a value smaller than %d' % (int(0.1*int(read_len))))
+ stop_err('Invalid value for mismatch numbers in an alignment.')
all_files = []
if os.path.isdir(target_path):
@@ -59,14 +70,14 @@ def __main__():
command = "rmap -h %s -w %s -m %s -c %s %s -o %s 2>&1" % ( align_len, read_len, mismatch, detail_file_path, infile, output_tempfile )
#print command
try:
- assert os.system( command ) == 0
- except:
- stop_err('Execution failed. Please check whether RMAP was installed.')
+ os.system( command )
+ except Exception, e:
+ stop_err( str( e ) )
try:
- assert os.system( 'cat %s >> %s' % ( output_tempfile, output_file ) ) == 0
- except:
- stop_err('Failed to integrate files.')
+ os.system( 'cat %s >> %s' % ( output_tempfile, output_file ) )
+ except Exception, e:
+ stop_err( str( e ) )
try:
os.remove( output_tempfile )
diff --git a/tools/metag_tools/rmap_wrapper.xml b/tools/metag_tools/rmap_wrapper.xml
index 773c9141d4d..03bcc78d5c1 100644
--- a/tools/metag_tools/rmap_wrapper.xml
+++ b/tools/metag_tools/rmap_wrapper.xml
@@ -1,15 +1,33 @@
for Solexa Short Reads Alignment
- rmap_wrapper.py $database $input_seq $read_len $align_len $mismatch $output1
+
+ #if $trim.choice=="No": #rmap_wrapper.py $database $input_seq 0 $align_len $mismatch $output1
+ #else: #rmap_wrapper.py $database $input_seq $trim.read_len $align_len $mismatch $output1
+ #end if
-
-
-
-
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
@@ -18,7 +36,7 @@
-
+
@@ -34,7 +52,7 @@
.. class:: infomark
-**TIP**. Each read should have at least the minimal length specified as the *Length of the Reads* parameter. Reads with lengths longer than the expected value will be trimmed at the 3'end.
+**TIP**. The tool will guess the length of the reads, however, if you select to trim the reads, the *Reads length* must be between 20 and 64. Reads with lengths longer than the specified value will be trimmed at the 3'end.
-----
@@ -46,9 +64,9 @@ This tool runs **rmap** (for more information, please see the reference below),
**Parameters**
-- *Length of the Reads* (**-w**) : the minimal length of the reads
-- *Length of an Alignment* (**-h**) : the minimal length of an alignment
+- *Minimal Length of a Hit* (**-h**) : this is the seed length or the minimal exact match length
- *Number of Mismatches Allowed* (**-m**) : the maximal number of mismatches allowed in an alignment
+- *Read Length* (**-w**) : maximal length of the reads; reads longer than the threshold will be truncated at 3' end.
-----
diff --git a/tools/metag_tools/rmapq_wrapper.py b/tools/metag_tools/rmapq_wrapper.py
index 669e58f85e7..e52035e0d7c 100644
--- a/tools/metag_tools/rmapq_wrapper.py
+++ b/tools/metag_tools/rmapq_wrapper.py
@@ -1,9 +1,5 @@
#! /usr/bin/python
-"""
-3. create test files, run functional test
-"""
-
import os, sys, tempfile
assert sys.version_info[:2] >= (2.4)
@@ -36,23 +32,38 @@ def __main__():
int(high_len)
except:
stop_err('Invalid value for minimal high quality bases.')
-
+
+ # first guess the read length
+ guess_read_len = 0
+ seq = ''
+ for i, line in enumerate(open(infile)):
+ line = line.rstrip('\r\n')
+ if line.startswith('>'):
+ if seq:
+ guess_read_len = len(seq)
+ break
+ else:
+ seq += line
+
try:
test = int(read_len)
- assert test >= 20 and test <= 64
+ if test == 0:
+ read_len = str(guess_read_len)
+ else:
+ assert test >= 20 and test <= 64
except:
stop_err('Invalid value for read length. Must be between 20 and 64.')
+
try:
int(align_len)
except:
- stop_err('Invalid value for minimal length of an alignment.')
+ stop_err('Invalid value for minimal length of a hit.')
try:
- test = int(mismatch)
- assert test >= 0 and test <= int(0.1*int(read_len))
+ int(mismatch)
except:
- stop_err('Invalid value for mismatch numbers in an alignment. Please use a number smaller than %d.' %(int(0.1*int(read_len))))
+ stop_err('Invalid value for mismatch numbers in an alignment.')
all_files = []
if os.path.isdir(target_path):
@@ -71,14 +82,14 @@ def __main__():
command = "rmapq -q %s -M %s -h %s -w %s -m %s -Q %s -c %s %s -o %s 2>&1" % ( high_score, high_len, align_len, read_len, mismatch, scorefile, detail_file_path, infile, output_tempfile )
#print command
try:
- assert os.system( command ) == 0
- except:
- stop_err('Execution failed. Please check whether RMAP was installed.')
+ os.system( command )
+ except Exception, e:
+ stop_err( str( e ) )
try:
assert os.system( 'cat %s >> %s' % ( output_tempfile, output_file ) ) == 0
- except:
- stop_err('Failed to integrate files.')
+ except Exception, e:
+ stop_err( str( e ) )
try:
os.remove( output_tempfile )
diff --git a/tools/metag_tools/rmapq_wrapper.xml b/tools/metag_tools/rmapq_wrapper.xml
index a60db240641..7a536a5f2e7 100644
--- a/tools/metag_tools/rmapq_wrapper.xml
+++ b/tools/metag_tools/rmapq_wrapper.xml
@@ -1,18 +1,36 @@
for Solexa Short Reads Alignment with Quality Scores
- rmapq_wrapper.py $database $input_seq $input_score $high_score $high_len $read_len $align_len $mismatch $output1
+
+ #if $trim.choice=="No": #rmapq_wrapper.py $database $input_seq $input_score $high_score $high_len 0 $align_len $mismatch $output1
+ #else: #rmapq_wrapper.py $database $input_seq $input_score $high_score $high_len $trim.read_len $align_len $mismatch $output1
+ #end if
-
-
-
-
-
-
-
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
@@ -21,7 +39,7 @@
-
+
@@ -36,11 +54,11 @@
.. class:: warningmark
- RMAP was developed for **Solexa** reads.
+ RMAPQ was developed for **Solexa** reads.
.. class:: infomark
-**TIP**. Each read should have at least the minimal length specified in the *Length of the Reads* parameter. Reads with lengths longer than the expected value will be trimmed at the 3'end.
+**TIP**. The tool will guess the length of the reads, however, if you select to trim the reads, the *Maximal Length of the Reads* must be between 20 and 64. Reads with lengths longer than the specified value will be trimmed at the 3'end.
-----
@@ -54,9 +72,9 @@ This tool runs **rmapq** (for more information, please see the reference below),
- *Minimal High-quality Bases* (**-M**): the minimal length of the high quality score bases
- *Minimum Score for High-quality Base* (**-q**) : the minimal quality score
-- *Length of the Reads* (**-w**) : the minimal length of the reads
-- *Length of an Alignment* (**-h**) : the minimal length of an exact match (rmapq) or an alignment (rmap)
+- *Minimal Length of a Hit* (**-h**) : the minimal length of an exact match or seed
- *Number of Mismatches Allowed* (**-m**) : the maximal number of mismatches allowed in an alignment
+- *Read Length* (**-w**) : maximal length of the reads; reads longer than the threshold will be truncated at 3' end.
-----
diff --git a/tools/metag_tools/short_reads_figure_high_quality_length.xml b/tools/metag_tools/short_reads_figure_high_quality_length.xml
index 9b4a917f49d..3d99e0f6899 100644
--- a/tools/metag_tools/short_reads_figure_high_quality_length.xml
+++ b/tools/metag_tools/short_reads_figure_high_quality_length.xml
@@ -5,8 +5,8 @@
-
-
+
+
@@ -29,7 +29,7 @@
.. class:: warningmark
- To use this tool your dataset needs to be in *Quality Score* format. Click pencil icon next to your dataset to set datatype to *Quality Score*.
+ To use this tool your dataset needs to be in *Quality Score* format. Click pencil icon next to your dataset to set datatype to *Quality Score* (see below for examples of quality scores).
-----
diff --git a/tools/metag_tools/short_reads_trim_seq.xml b/tools/metag_tools/short_reads_trim_seq.xml
index 502b4f97377..f03236abede 100644
--- a/tools/metag_tools/short_reads_trim_seq.xml
+++ b/tools/metag_tools/short_reads_trim_seq.xml
@@ -9,13 +9,13 @@
-
+
-
+