Mercurial > repos > cpt > cpt_genome_editor
annotate genome_editor.py @ 4:78ce8a1a8fd1 draft
planemo upload commit 852ac96ca53a2ffa0947e6df5e24671866b642f5
author | cpt |
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date | Sun, 23 Jul 2023 01:43:12 +0000 |
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1 #!/usr/bin/env python |
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2 import logging |
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3 import copy |
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4 import argparse |
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5 import tsv |
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6 from Bio import SeqIO |
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7 from Bio.Seq import Seq |
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8 from Bio.SeqFeature import FeatureLocation |
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9 from CPT_GFFParser import gffParse, gffWrite, gffSeqFeature, convertSeqRec |
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10 from gff3 import feature_lambda, feature_test_contains |
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11 |
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12 logging.basicConfig(level=logging.INFO) |
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13 log = logging.getLogger(__name__) |
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14 |
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15 |
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16 def mutate(gff3, fasta, changes, customSeqs, new_id): |
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17 # Change Language |
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18 # - we can only accept ONE genome as an input. (TODO: support multiple?) |
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19 # - we can only build ONE genome as an output. (TODO: support multiple?) |
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20 # - must allow selection of various regions |
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21 # '1,1000,+ 40,100,- custom_seq_1' |
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22 try: |
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23 custom_seqs = SeqIO.to_dict(SeqIO.parse(customSeqs, "fasta")) |
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24 except: |
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25 custom_seqs = {} |
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26 seq_dict = SeqIO.to_dict(SeqIO.parse(fasta, "fasta")) |
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27 # Pull first and onl record |
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28 rec = list(gffParse(gff3, base_dict=seq_dict))[0] |
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29 # Create a "clean" record |
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30 new_record = copy.deepcopy(rec) |
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31 new_record.id = new_id |
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32 new_record.seq = Seq("") |
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33 new_record.features = [] |
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34 new_record.annotations = {} |
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35 # Process changes. |
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36 chain = [] |
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37 topFeats = {} |
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38 covered = 0 |
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39 for feat in rec.features: |
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40 if "ID" in feat.qualifiers.keys(): |
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41 topFeats[feat.qualifiers["ID"][0]] = feat.location.start |
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42 for change in changes: |
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43 if "," in change: |
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44 (start, end, strand) = change.split(",") |
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45 start = int(start) - 1 |
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46 end = int(end) |
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47 |
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48 # Make any complaints |
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49 broken_feature_start = list( |
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50 feature_lambda( |
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51 rec.features, |
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52 feature_test_contains, |
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53 {"index": start}, |
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54 subfeatures=False, |
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55 ) |
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56 ) |
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57 if len(broken_feature_start) > 0: |
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58 pass |
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59 # log.info("DANGER: Start index chosen (%s) is in the middle of a feature (%s %s). This feature will disappear from the output", start, broken_feature_start[0].id, broken_feature_start[0].location) |
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60 broken_feature_end = list( |
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61 feature_lambda( |
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62 rec.features, |
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63 feature_test_contains, |
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64 {"index": end}, |
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65 subfeatures=False, |
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66 ) |
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67 ) |
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68 if len(broken_feature_end) > 0: |
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69 pass |
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70 # log.info("DANGER: End index chosen (%s) is in the middle of a feature (%s %s). This feature will disappear from the output", end, broken_feature_end[0].id, broken_feature_end[0].location) |
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71 |
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72 # Ok, fetch features |
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73 if strand == "+": |
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74 tmp_req = rec[start:end] |
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75 else: |
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76 tmp_req = rec[start:end].reverse_complement( |
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77 id=True, |
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78 name=True, |
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79 description=True, |
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80 features=True, |
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81 annotations=True, |
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82 letter_annotations=True, |
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83 dbxrefs=True, |
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84 ) |
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85 tmp_req = convertSeqRec(tmp_req)[0] |
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86 |
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87 def update_location(feature, shiftS): |
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88 feature.location = FeatureLocation( |
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89 feature.location.start + shiftS, |
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90 feature.location.end + shiftS, |
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91 feature.strand, |
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92 ) |
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93 for i in feature.sub_features: |
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94 i = update_location(i, shiftS) |
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95 return feature |
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96 |
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97 # for feature in tmp_req.features: |
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98 |
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99 chain.append( |
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100 [ |
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101 rec.id, |
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102 start + 1, |
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103 end, |
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104 strand, |
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105 new_record.id, |
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106 len(new_record) + 1, |
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107 len(new_record) + (end - start), |
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108 "+", |
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109 ] |
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110 ) |
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111 |
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112 covered += len(new_record.seq) |
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113 print(covered) |
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114 new_record.seq += tmp_req.seq |
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115 # NB: THIS MUST USE BIOPYTHON 1.67. 1.68 Removes access to |
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116 # subfeatures, which means you will only get top-level features. |
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117 startInd = len(new_record.features) |
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118 new_record.features += tmp_req.features |
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119 |
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120 for i in new_record.features[startInd:]: |
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121 i.location = FeatureLocation( |
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122 i.location.start + covered, |
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123 i.location.end + covered, |
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124 i.location.strand, |
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125 ) |
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126 if "ID" not in i.qualifiers.keys(): |
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127 continue |
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128 diffS = i.location.start - topFeats[i.qualifiers["ID"][0]] |
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129 subFeats = i.sub_features |
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130 for j in subFeats: |
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131 j = update_location(j, diffS) |
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132 else: |
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133 new_record.seq += custom_seqs[change].seq |
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134 yield new_record, chain |
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135 |
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136 |
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137 if __name__ == "__main__": |
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138 parser = argparse.ArgumentParser() |
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139 parser.add_argument("fasta", type=argparse.FileType("r"), help="Sequence") |
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140 parser.add_argument("gff3", type=argparse.FileType("r"), help="Annotations") |
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141 parser.add_argument("new_id", help="Append to ID", default="_v2") |
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142 parser.add_argument( |
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143 "--out_fasta", |
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144 type=argparse.FileType("w"), |
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145 help="Output fasta", |
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146 default="out.fa", |
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147 ) |
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148 parser.add_argument( |
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149 "--out_gff3", |
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150 type=argparse.FileType("w"), |
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151 help="Output gff3", |
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152 default="out.gff3", |
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153 ) |
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154 parser.add_argument( |
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155 "--out_simpleChain", |
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156 type=argparse.FileType("w"), |
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157 help="Output simple chain (i.e. not a real UCSC chain file)", |
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158 default="out.chain", |
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159 ) |
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160 parser.add_argument("--changes", nargs="+") |
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161 parser.add_argument("--customSeqs", type=argparse.FileType("r")) |
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162 args = parser.parse_args() |
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163 |
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164 for rec, chain in mutate( |
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165 args.gff3, args.fasta, args.changes, args.customSeqs, args.new_id |
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166 ): |
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167 # TODO: Check that this appends and doesn't overwirte |
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168 gffWrite([rec], args.out_gff3) |
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169 SeqIO.write([rec], args.out_fasta, "fasta") |
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170 tsv.dump(chain, args.out_simpleChain) |