本文整理汇总了Python中oncotator.TranscriptProviderUtils.TranscriptProviderUtils.get_cds_codon_positions方法的典型用法代码示例。如果您正苦于以下问题：Python TranscriptProviderUtils.get_cds_codon_positions方法的具体用法？Python TranscriptProviderUtils.get_cds_codon_positions怎么用？Python TranscriptProviderUtils.get_cds_codon_positions使用的例子？那么恭喜您, 这里精选的方法代码示例或许可以为您提供帮助。您也可以进一步了解该方法所在类oncotator.TranscriptProviderUtils.TranscriptProviderUtils的用法示例。
在下文中一共展示了TranscriptProviderUtils.get_cds_codon_positions方法的2个代码示例，这些例子默认根据受欢迎程度排序。您可以为喜欢或者感觉有用的代码点赞，您的评价将有助于系统推荐出更棒的Python代码示例。
示例1: test_codon_single_base
# 需要导入模块: from oncotator.TranscriptProviderUtils import TranscriptProviderUtils [as 别名]
# 或者: from oncotator.TranscriptProviderUtils.TranscriptProviderUtils import get_cds_codon_positions [as 别名]
def test_codon_single_base(self, start, end, ref_base_stranded, gt_codon):
"""Test that we can grab the proper three bases of a codon for an arbitrary single base """
tx = self.retrieve_test_transcript_MAPK1()
transcript_position_start, transcript_position_end = TranscriptProviderUtils.convert_genomic_space_to_exon_space(start, end, tx)
cds_start, cds_stop = TranscriptProviderUtils.determine_cds_in_exon_space(tx)
protein_position_start, protein_position_end = TranscriptProviderUtils.get_protein_positions(transcript_position_start, transcript_position_end, cds_start)
cds_codon_start, cds_codon_end = TranscriptProviderUtils.get_cds_codon_positions(protein_position_start, protein_position_end, cds_start)
codon_seq = tx.get_seq()[cds_codon_start:cds_codon_end+1]
self.assertTrue(codon_seq == gt_codon, "Did not get correct codon (%s): %s loc: %s-%s" %(gt_codon, codon_seq, start, end))示例2: _determine_vc_for_cds_overlap
# 需要导入模块: from oncotator.TranscriptProviderUtils import TranscriptProviderUtils [as 别名]
# 或者: from oncotator.TranscriptProviderUtils.TranscriptProviderUtils import get_cds_codon_positions [as 别名]
def _determine_vc_for_cds_overlap(self, start, end, ref_allele, alt_allele, is_frameshift_indel, is_splice_site, tx, variant_type, is_start_codon):
"""
Note: This method can also handle start and stop codons.
:param start:
:param end:
:param ref_allele:
:param alt_allele:
:param is_frameshift_indel:
:param is_splice_site:
:param tx:
:param variant_type:
:return:
"""
observed_allele_stranded, reference_allele_stranded = self._get_stranded_alleles(ref_allele, alt_allele, tx)
transcript_position_start, transcript_position_end = TranscriptProviderUtils.convert_genomic_space_to_exon_space(
start, end, tx)
if tx.get_strand() == "+" and not variant_type == VariantClassification.VT_INS:
transcript_position_start -= 1
transcript_position_end -= 1
transcript_seq = tx.get_seq()
protein_seq = tx.get_protein_seq()
cds_start, cds_stop = TranscriptProviderUtils.determine_cds_in_exon_space(tx)
protein_position_start, protein_position_end = TranscriptProviderUtils.get_protein_positions(
transcript_position_start,
transcript_position_end, cds_start)
new_ref_transcript_seq = transcript_seq
if (transcript_seq[transcript_position_start:transcript_position_end+1] != reference_allele_stranded) and variant_type != VariantClassification.VT_INS:
new_ref_transcript_seq = list(transcript_seq)
new_ref_transcript_seq[transcript_position_start:transcript_position_end+1] = reference_allele_stranded
new_ref_transcript_seq = ''.join(new_ref_transcript_seq)
ref_tx_seq_has_been_changed = True
else:
ref_tx_seq_has_been_changed = False
cds_codon_start, cds_codon_end = TranscriptProviderUtils.get_cds_codon_positions(protein_position_start, protein_position_end, cds_start)
if variant_type == "DEL":
reference_codon_seq = new_ref_transcript_seq[cds_codon_start:cds_codon_end+1].lower()
else:
reference_codon_seq = TranscriptProviderUtils.mutate_reference_sequence(new_ref_transcript_seq[cds_codon_start:cds_codon_end+1].lower(), cds_codon_start, transcript_position_start, transcript_position_end, reference_allele_stranded, variant_type)
if variant_type == "INS" and tx.get_strand() == "-":
mutated_codon_seq = TranscriptProviderUtils.mutate_reference_sequence(reference_codon_seq.lower(), cds_codon_start - 1, transcript_position_start, transcript_position_end, observed_allele_stranded, variant_type)
else:
mutated_codon_seq = TranscriptProviderUtils.mutate_reference_sequence(reference_codon_seq.lower(), cds_codon_start, transcript_position_start, transcript_position_end, observed_allele_stranded, variant_type)
observed_aa = Bio.Seq.translate(mutated_codon_seq)
if ref_tx_seq_has_been_changed:
reference_aa = Bio.Seq.translate(reference_codon_seq)
else:
reference_aa = protein_seq[protein_position_start-1:protein_position_end]
if variant_type != VariantClassification.VT_SNP:
try:
reference_aa, observed_aa, protein_position_start, protein_position_end = \
self._adjust_protein_position_and_alleles(protein_seq, protein_position_start,
protein_position_end, reference_aa, observed_aa)
except InvalidVariantException as ive:
logging.getLogger(__name__).error("Could not properly adjust protein position for variant: %s, %s, %s, %s, %s VT: %s" % (tx.get_contig(), start, end, ref_allele, alt_allele, variant_type))
logging.getLogger(__name__).error(str(ive))
logging.getLogger(__name__).warn("Above error may not have exact start and end positions if this is a VCF input.")
logging.getLogger(__name__).warn("Variant type is likely incorrect. This can happen with some GATK VCFs")
logging.getLogger(__name__).warn(TranscriptProviderUtils.is_valid_xNP(variant_type, ref_allele, alt_allele))
logging.getLogger(__name__).warn("The protein_change annotation may not be properly rendered.")
vc_tmp, vc_tmp_secondary = self.infer_variant_classification(variant_type, reference_aa, observed_aa, ref_allele, alt_allele,
is_frameshift_indel=is_frameshift_indel, is_splice_site=is_splice_site, is_start_codon=is_start_codon)
cds_start_exon_space, cds_end_exon_space = TranscriptProviderUtils.determine_cds_in_exon_space(tx)
exon_i = TranscriptProviderUtils.determine_exon_index(int(start), int(end), tx, variant_type)
final_vc = VariantClassification(vc_tmp, variant_type, transcript_id=tx.get_transcript_id(), alt_codon=mutated_codon_seq, ref_codon=reference_codon_seq, ref_aa=reference_aa, ref_protein_start=protein_position_start, ref_protein_end=protein_position_end, alt_aa=observed_aa, alt_codon_start_in_exon=cds_codon_start, alt_codon_end_in_exon=cds_codon_end, ref_codon_start_in_exon=cds_codon_start, ref_codon_end_in_exon=cds_codon_end, cds_start_in_exon_space=cds_start_exon_space, ref_allele_stranded=reference_allele_stranded, alt_allele_stranded=observed_allele_stranded, exon_i=exon_i, vc_secondary=vc_tmp_secondary)
return final_vc