# HG changeset patch
# User iuc
# Date 1647161105 0
# Node ID 031f84cb2fd3d50c84bcf85c4cec4525f48d3dd5
# Parent 06c0eb0330251d27198cd4cee8f5ad255e32fb1e
"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/concoct commit 40a09cbfd6052f7b0295946621db1bdf58228b09"
diff -r 06c0eb033025 -r 031f84cb2fd3 concoct.xml
--- a/concoct.xml Fri Feb 18 14:18:11 2022 +0000
+++ b/concoct.xml Sun Mar 13 08:45:05 2022 +0000
@@ -109,8 +109,9 @@
sample (the values are the average coverage for this contig in that sample) and a file containing sequences in
fasta format.
-Three are produced; clustering of the > 1000 kmer count, the PCA transformed matrix and the PCA components.
+Three outputs are produced; clustering of the > 1000 kmer count, the PCA transformed matrix and the PCA components.
+@HELP_OVERVIEW@
]]>
diff -r 06c0eb033025 -r 031f84cb2fd3 coverage_table.py
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/coverage_table.py Sun Mar 13 08:45:05 2022 +0000
@@ -0,0 +1,83 @@
+#!/usr/bin/env python
+
+import argparse
+import gzip
+from functools import partial
+
+from Bio import SeqIO
+
+
+def generate_coverage_table(input_fasta, input_tabular, gzipped, output):
+ # Read input file into a dict and return everything
+ # in the table format required by CONCOCT.
+ gc_and_len_dict = get_gc_and_len_dict(input_fasta, gzipped)
+ assert(len(gc_and_len_dict) > 0)
+ bed_coverage_dict = get_bed_coverage_dict(input_tabular)
+
+ with open(output, 'w') as fh:
+ # Output the header.
+ fh.write("contig\tlength")
+ t = tuple(range(len(bed_coverage_dict)))
+ fh.write("\tcov_mean_sample_%d\n" % len(t))
+ # Output the content.
+ for acc in gc_and_len_dict:
+ # Fasta stats.
+ fh.write("%s\t%s" % (acc, gc_and_len_dict[acc]['length']))
+ # Mean
+ try:
+ # Coverage mean
+ fh.write("\t%f" % (bed_coverage_dict[acc]["cov_mean"]))
+ except KeyError:
+ # No reads mapped to this contig
+ fh.write("\t0")
+ fh.write("\n")
+
+
+def get_bed_coverage_dict(input_tabular):
+ # Ddetermine mean coverage and percentage covered
+ # for each contig, returning a dict with fasta id
+ # as key and percentage covered and cov_mean as keys
+ # for the inner dict.
+ out_dict = {}
+
+ with open(input_tabular, 'r') as fh:
+ for line in fh:
+ line = line.rstrip('\r\n')
+ cols = line.split('\t')
+ try:
+ d = out_dict[cols[0]]
+ except KeyError:
+ d = {}
+ out_dict[cols[0]] = d
+ if int(cols[1]) == 0:
+ d["percentage_covered"] = 100 - float(cols[4]) * 100.0
+ else:
+ d["cov_mean"] = d.get("cov_mean", 0) + int(cols[1]) * float(cols[4])
+ return out_dict
+
+
+def get_gc_and_len_dict(input_fasta, gzipped):
+ # Creates a dictionary with the fasta id as key
+ # and GC and length as keys for the inner dictionary.
+ if gzipped:
+ _open = partial(gzip.open, mode='rt')
+ else:
+ _open = open
+
+ out_dict = {}
+ with _open(input_fasta) as input_fh:
+ for rec in SeqIO.parse(input_fh, "fasta"):
+ out_dict[rec.id] = {}
+ out_dict[rec.id]["length"] = len(rec.seq)
+ return out_dict
+
+
+parser = argparse.ArgumentParser(description=__doc__)
+parser.add_argument('--input_tabular', action='store', dest='input_tabular', help='bedtools genomeCoverageBed bed file')
+parser.add_argument('--input_fasta', action='store', dest='input_fasta', help='Contigs fasta file')
+parser.add_argument("--gzipped", action="store_true", dest="gzipped", default=False, help="input_fasta is gzipped")
+parser.add_argument('--output', action='store', dest='output', help='Output file')
+
+args = parser.parse_args()
+
+generate_coverage_table(args.input_fasta, args.input_tabular, args.gzipped, args.output)
diff -r 06c0eb033025 -r 031f84cb2fd3 cut_up_fasta.py
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/cut_up_fasta.py Sun Mar 13 08:45:05 2022 +0000
@@ -0,0 +1,58 @@
+#!/usr/bin/env python
+
+import argparse
+import gzip
+from functools import partial
+
+from Bio import SeqIO
+
+
+def cut_up_fasta(input_fasta, chunk_size, overlap, merge_last, output_fasta, output_bed, gzipped):
+ if gzipped:
+ _open = partial(gzip.open, mode='rt')
+ else:
+ _open = open
+
+ fasta_fh = open(output_fasta, 'w')
+
+ if output_bed is not None:
+ bed_fh = open(output_bed, 'w')
+
+ with _open(input_fasta) as input_fh:
+ for record in SeqIO.parse(input_fh, "fasta"):
+ if (not merge_last and len(record.seq) > chunk_size) or (merge_last and len(record.seq) >= 2 * chunk_size):
+ for index, split_seq in enumerate(chunks(record.seq, chunk_size, overlap, merge_last)):
+ fasta_fh.write(f">{record.id}.concoct_part_{index}\n{split_seq}\n")
+ if output_bed is not None:
+ bed_fh.write(f"{record.id}\t{chunk_size * index}\t{chunk_size * index + len(split_seq)}\t{record.id}.concoct_part_{index}\n")
+ else:
+ fasta_fh.write(f">{record.id}.concoct_part_0\n{record.seq}\n")
+ if output_bed is not None:
+ bed_fh.write(f"{record.id}\t0\t{len(record.seq)}\t{record.id}.concoct_part_0\n")
+ if output_bed is not None:
+ bed_fh.close()
+
+
+def chunks(seq, chunk_size, overlap_size, merge_last):
+ # Yield successive chunk_size-sized chunks from seq
+ # with given overlap overlap_size between the chunks.
+ assert chunk_size > overlap_size
+ if merge_last:
+ for i in range(0, len(seq) - chunk_size + 1, chunk_size - overlap_size):
+ yield seq[i:i + chunk_size] if i + chunk_size + chunk_size - overlap_size <= len(seq) else seq[i:]
+ else:
+ for i in range(0, len(seq), chunk_size - overlap_size):
+ yield seq[i:i + chunk_size]
+
+
+parser = argparse.ArgumentParser()
+parser.add_argument("--input_fasta", action="store", dest="input_fasta", help="Fasta files with contigs")
+parser.add_argument("--gzipped", action="store_true", dest="gzipped", help="Input file is gzipped")
+parser.add_argument("--chunk_size", action="store", dest="chunk_size", type=int, help="Chunk size\n")
+parser.add_argument("--overlap_size", action="store", dest="overlap_size", type=int, help="Overlap size\n")
+parser.add_argument("--merge_last", default=False, action="store_true", dest="merge_last", help="Concatenate final part to last contig\n")
+parser.add_argument("--output_bed", action="store", dest="output_bed", default=None, help="BED file to be created with exact regions of the original contigs corresponding to the newly created contigs")
+parser.add_argument("--output_fasta", action="store", dest="output_fasta", help="Output fasta file with cut contigs")
+
+args = parser.parse_args()
+cut_up_fasta(args.input_fasta, args.chunk_size, args.overlap_size, args.merge_last, args.output_fasta, args.output_bed, args.gzipped)
diff -r 06c0eb033025 -r 031f84cb2fd3 macros.xml
--- a/macros.xml Fri Feb 18 14:18:11 2022 +0000
+++ b/macros.xml Sun Mar 13 08:45:05 2022 +0000
@@ -4,11 +4,20 @@
21.01
+ biopython
concoct
pandas
- biopython
+
+
+The intended use of the CONCOCT tools is shown in the following image.
+
+.. image:: pipeline.png
+
+More information may be found on the CONCOCT homepage:: https://github.com/BinPro/CONCOCT
+
+
10.1038/nmeth.3103
diff -r 06c0eb033025 -r 031f84cb2fd3 merge_cut_up_clustering.py
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/merge_cut_up_clustering.py Sun Mar 13 08:45:05 2022 +0000
@@ -0,0 +1,56 @@
+#!/usr/bin/env python
+
+import argparse
+import re
+import sys
+from collections import Counter
+from collections import defaultdict
+
+
+CONTIG_PART_EXPR = re.compile(r'(.*)\.concoct_part_([0-9]*)')
+
+
+def original_contig_name_special(contig_id):
+ try:
+ original_id, part_index = CONTIG_PART_EXPR.match(contig_id).group(1, 2)
+ return original_id, part_index
+ except AttributeError:
+ # No matches for concoct_part regex.
+ return contig_id, 0
+
+
+parser = argparse.ArgumentParser()
+parser.add_argument("--input", action="store", dest="input", help="Tabular file with cut up clusters")
+parser.add_argument("--output", action="store", dest="output", help="Output file with merged clusters")
+
+args = parser.parse_args()
+
+# Get cut up clusters
+all_seqs = {}
+all_originals = defaultdict(dict)
+with open(args.input, 'r') as ifh:
+ for i, line in enumerate(ifh):
+ if i == 0:
+ if 'contig_id' not in line:
+ sys.stderr.write("ERROR nvalid clustering file, 'contig_id' is not found in the header.")
+ sys.exit(-1)
+ # Skip header.
+ continue
+ line = line.rstrip('\r\n')
+ contig_id, cluster_id = line.split('\t')
+ original_contig_name, part_id = original_contig_name_special(contig_id)
+ all_originals[original_contig_name][part_id] = cluster_id
+
+# Merge cut up clusters.
+with open(args.output, 'w') as ofh:
+ ofh.write("contig_id\tcluster_id\n")
+ for original_contig_id, part_ids_d in all_originals.items():
+ if len(part_ids_d) > 1:
+ c = Counter(part_ids_d.values())
+ cluster_id = c.most_common(1)[0][0]
+ c_string = [(a, b) for a, b in c.items()]
+ # Here if len(c.values()) > 1,
+ # then no cluster for contig.
+ else:
+ cluster_id = list(part_ids_d.values())[0]
+ ofh.write(f"{original_contig_id}\t{cluster_id}\n")
diff -r 06c0eb033025 -r 031f84cb2fd3 static/images/pipeline.png
Binary file static/images/pipeline.png has changed
diff -r 06c0eb033025 -r 031f84cb2fd3 test-data/input.fasta.gz
Binary file test-data/input.fasta.gz has changed
diff -r 06c0eb033025 -r 031f84cb2fd3 test-data/input_coverage_table.fasta.gz
Binary file test-data/input_coverage_table.fasta.gz has changed
diff -r 06c0eb033025 -r 031f84cb2fd3 test-data/input_coverage_table.tabular
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/input_coverage_table.tabular Sun Mar 13 08:45:05 2022 +0000
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diff -r 06c0eb033025 -r 031f84cb2fd3 test-data/input_merge_clusters.tabular
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/input_merge_clusters.tabular Sun Mar 13 08:45:05 2022 +0000
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diff -r 06c0eb033025 -r 031f84cb2fd3 test-data/output_coverage_table.tabular
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
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diff -r 06c0eb033025 -r 031f84cb2fd3 test-data/output_merge_clusters.tabular
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
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