Mercurial > repos > iuc > jbrowse
view gff3_rebase.py @ 4:d022577ff9cf draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/jbrowse commit c7ca55fb4e5789f5a0f6fbc0ee7becd56e40e3df
author | iuc |
---|---|
date | Fri, 29 Jan 2016 13:27:30 -0500 |
parents | 7342f467507b |
children | ad4b9d7eae6a |
line wrap: on
line source
#!/usr/bin/env python import sys import logging logging.basicConfig(level=logging.INFO) import argparse import copy from BCBio import GFF from Bio.SeqFeature import FeatureLocation log = logging.getLogger(__name__) __author__ = "Eric Rasche" __version__ = "0.4.0" __maintainer__ = "Eric Rasche" __email__ = "esr@tamu.edu" def feature_lambda(feature_list, test, test_kwargs, subfeatures=True): """Recursively search through features, testing each with a test function, yielding matches. GFF3 is a hierachical data structure, so we need to be able to recursively search through features. E.g. if you're looking for a feature with ID='bob.42', you can't just do a simple list comprehension with a test case. You don't know how deeply burried bob.42 will be in the feature tree. This is where feature_lambda steps in. :type feature_list: list :param feature_list: an iterable of features :type test: function reference :param test: a closure with the method signature (feature, **kwargs) where the kwargs are those passed in the next argument. This function should return True or False, True if the feature is to be yielded as part of the main feature_lambda function, or False if it is to be ignored. This function CAN mutate the features passed to it (think "apply"). :type test_kwargs: dictionary :param test_kwargs: kwargs to pass to your closure when it is called. :type subfeatures: boolean :param subfeatures: when a feature is matched, should just that feature be yielded to the caller, or should the entire sub_feature tree for that feature be included? subfeatures=True is useful in cases such as searching for a gene feature, and wanting to know what RBS/Shine_Dalgarno_sequences are in the sub_feature tree (which can be accomplished with two feature_lambda calls). subfeatures=False is useful in cases when you want to process (and possibly return) the entire feature tree, such as applying a qualifier to every single feature. :rtype: yielded list :return: Yields a list of matching features. """ # Either the top level set of [features] or the subfeature attribute for feature in feature_list: if test(feature, **test_kwargs): if not subfeatures: feature_copy = copy.deepcopy(feature) feature_copy.sub_features = [] yield feature_copy else: yield feature if hasattr(feature, 'sub_features'): for x in feature_lambda(feature.sub_features, test, test_kwargs, subfeatures=subfeatures): yield x def feature_test_qual_value(feature, **kwargs): """Test qualifier values. For every feature, check that at least one value in feature.quailfiers(kwargs['qualifier']) is in kwargs['attribute_list'] """ for attribute_value in feature.qualifiers.get(kwargs['qualifier'], []): if attribute_value in kwargs['attribute_list']: return True return False def __get_features(child, interpro=False): child_features = {} for rec in GFF.parse(child): for feature in rec.features: parent_feature_id = rec.id if interpro: if feature.type == 'polypeptide': continue if '_' in parent_feature_id: parent_feature_id = parent_feature_id[parent_feature_id.index('_') + 1:] try: child_features[parent_feature_id].append(feature) except KeyError: child_features[parent_feature_id] = [feature] return child_features def __update_feature_location(feature, parent, protein2dna): start = feature.location.start end = feature.location.end if protein2dna: start *= 3 end *= 3 if parent.location.strand >= 0: ns = parent.location.start + start ne = parent.location.start + end st = +1 else: ns = parent.location.end - end ne = parent.location.end - start st = -1 # Don't let start/stops be less than zero. It's technically valid for them # to be (at least in the model I'm working with) but it causes numerous # issues. # # Instead, we'll replace with %3 to try and keep it in the same reading # frame that it should be in. if ns < 0: ns %= 3 if ne < 0: ne %= 3 feature.location = FeatureLocation(ns, ne, strand=st) if hasattr(feature, 'sub_features'): for subfeature in feature.sub_features: __update_feature_location(subfeature, parent, protein2dna) def rebase(parent, child, interpro=False, protein2dna=False): child_features = __get_features(child, interpro=interpro) for rec in GFF.parse(parent): replacement_features = [] for feature in feature_lambda( rec.features, feature_test_qual_value, { 'qualifier': 'ID', 'attribute_list': child_features.keys(), }, subfeatures=False): new_subfeatures = child_features[feature.id] fixed_subfeatures = [] for x in new_subfeatures: # Then update the location of the actual feature __update_feature_location(x, feature, protein2dna) if interpro: for y in ('status', 'Target'): try: del x.qualifiers[y] except: pass fixed_subfeatures.append(x) replacement_features.extend(fixed_subfeatures) # We do this so we don't include the original set of features that we # were rebasing against in our result. rec.features = replacement_features rec.annotations = {} GFF.write([rec], sys.stdout) if __name__ == '__main__': parser = argparse.ArgumentParser(description='rebase gff3 features against parent locations', epilog="") parser.add_argument('parent', type=file, help='Parent GFF3 annotations') parser.add_argument('child', help='Child GFF3 annotations to rebase against parent') parser.add_argument('--interpro', action='store_true', help='Interpro specific modifications') parser.add_argument('--protein2dna', action='store_true', help='Map protein translated results to original DNA data') args = parser.parse_args() rebase(**vars(args))