Mercurial > repos > cpt > cpt_gff_rebase
comparison gff3_rebase.py @ 1:4f4b413056f6 draft
planemo upload commit 94b0cd1fff0826c6db3e7dc0c91c0c5a8be8bb0c
| author | cpt |
|---|---|
| date | Mon, 05 Jun 2023 02:44:12 +0000 |
| parents | |
| children |
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| 0:6e7e20cb1fc7 | 1:4f4b413056f6 |
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| 1 #!/usr/bin/env python | |
| 2 import sys | |
| 3 import logging | |
| 4 import argparse | |
| 5 from gff3 import feature_lambda, feature_test_qual_value | |
| 6 from CPT_GFFParser import gffParse, gffWrite | |
| 7 from Bio.SeqFeature import FeatureLocation | |
| 8 | |
| 9 log = logging.getLogger(__name__) | |
| 10 logging.basicConfig(level=logging.INFO) | |
| 11 | |
| 12 | |
| 13 def __get_features(child, interpro=False): | |
| 14 child_features = {} | |
| 15 for rec in gffParse(child): | |
| 16 log.info("Parsing %s", rec.id) | |
| 17 # Only top level | |
| 18 for feature in rec.features: | |
| 19 # Get the record id as parent_feature_id (since this is how it will be during remapping) | |
| 20 parent_feature_id = rec.id | |
| 21 # If it's an interpro specific gff3 file | |
| 22 if interpro: | |
| 23 # Then we ignore polypeptide features as they're useless | |
| 24 if feature.type == "polypeptide": | |
| 25 continue | |
| 26 | |
| 27 try: | |
| 28 child_features[parent_feature_id].append(feature) | |
| 29 except KeyError: | |
| 30 child_features[parent_feature_id] = [feature] | |
| 31 # Keep a list of feature objects keyed by parent record id | |
| 32 return child_features | |
| 33 | |
| 34 | |
| 35 def __update_feature_location(feature, parent, protein2dna): | |
| 36 start = feature.location.start | |
| 37 end = feature.location.end | |
| 38 if protein2dna: | |
| 39 start *= 3 | |
| 40 end *= 3 | |
| 41 | |
| 42 if parent.location.strand >= 0: | |
| 43 ns = parent.location.start + start | |
| 44 ne = parent.location.start + end | |
| 45 st = +1 | |
| 46 else: | |
| 47 ns = parent.location.end - end | |
| 48 ne = parent.location.end - start | |
| 49 st = -1 | |
| 50 | |
| 51 # Don't let start/stops be less than zero. | |
| 52 # | |
| 53 # Instead, we'll replace with %3 to try and keep it in the same reading | |
| 54 # frame that it should be in. | |
| 55 | |
| 56 if ns < 0: | |
| 57 ns %= 3 | |
| 58 if ne < 0: | |
| 59 ne %= 3 | |
| 60 | |
| 61 feature.location = FeatureLocation(ns, ne, strand=st) | |
| 62 | |
| 63 if hasattr(feature, "sub_features"): | |
| 64 for subfeature in feature.sub_features: | |
| 65 __update_feature_location(subfeature, parent, protein2dna) | |
| 66 | |
| 67 | |
| 68 def rebase(parent, child, interpro=False, protein2dna=False, map_by="ID"): | |
| 69 # get all of the features we will be re-mapping in a dictionary, keyed by parent feature ID | |
| 70 child_features = __get_features(child, interpro=interpro) | |
| 71 | |
| 72 for rec in gffParse(parent): | |
| 73 replacement_features = [] | |
| 74 # Horrifically slow I believe | |
| 75 for feature in feature_lambda( | |
| 76 rec.features, | |
| 77 # Filter features in the parent genome by those that are | |
| 78 # "interesting", i.e. have results in child_features array. | |
| 79 # Probably an unnecessary optimisation. | |
| 80 feature_test_qual_value, | |
| 81 {"qualifier": map_by, "attribute_list": child_features.keys()}, | |
| 82 subfeatures=False, | |
| 83 ): | |
| 84 | |
| 85 # Features which will be re-mapped | |
| 86 to_remap = child_features[feature.id] | |
| 87 | |
| 88 fixed_features = [] | |
| 89 for x in to_remap: | |
| 90 # Then update the location of the actual feature | |
| 91 __update_feature_location(x, feature, protein2dna) | |
| 92 | |
| 93 if interpro: | |
| 94 for y in ("status", "Target"): | |
| 95 try: | |
| 96 del x.qualifiers[y] | |
| 97 except: | |
| 98 pass | |
| 99 | |
| 100 fixed_features.append(x) | |
| 101 replacement_features.extend(fixed_features) | |
| 102 # We do this so we don't include the original set of features that we | |
| 103 # were rebasing against in our result. | |
| 104 rec.features = replacement_features | |
| 105 rec.annotations = {} | |
| 106 gffWrite([rec], sys.stdout) | |
| 107 | |
| 108 | |
| 109 if __name__ == "__main__": | |
| 110 parser = argparse.ArgumentParser( | |
| 111 description="rebase gff3 features against parent locations", epilog="" | |
| 112 ) | |
| 113 parser.add_argument( | |
| 114 "parent", type=argparse.FileType("r"), help="Parent GFF3 annotations" | |
| 115 ) | |
| 116 parser.add_argument( | |
| 117 "child", | |
| 118 type=argparse.FileType("r"), | |
| 119 help="Child GFF3 annotations to rebase against parent", | |
| 120 ) | |
| 121 parser.add_argument( | |
| 122 "--interpro", action="store_true", help="Interpro specific modifications" | |
| 123 ) | |
| 124 parser.add_argument( | |
| 125 "--protein2dna", | |
| 126 action="store_true", | |
| 127 help="Map protein translated results to original DNA data", | |
| 128 ) | |
| 129 parser.add_argument("--map_by", help="Map by key", default="ID") | |
| 130 args = parser.parse_args() | |
| 131 rebase(**vars(args)) |
