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translocation
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pnrobinson committed May 12, 2024
1 parent 56514b6 commit ff83434
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Showing 2 changed files with 1 addition and 7 deletions.
2 changes: 1 addition & 1 deletion src/pyphetools/__init__.py
Original file line number Diff line number Diff line change
Expand Up @@ -4,7 +4,7 @@
from . import visualization
from . import validation

__version__ = "0.9.85"
__version__ = "0.9.86"

__all__ = [
"creation",
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6 changes: 0 additions & 6 deletions src/pyphetools/creation/structural_variant.py
Original file line number Diff line number Diff line change
Expand Up @@ -161,7 +161,6 @@ def chromosomal_duplication(cell_contents,
def chromosomal_inversion(cell_contents,
gene_symbol,
gene_id,
genotype,
variant_id=None):
"""
create a StructuralVariant object for a chromosomal inversion
Expand All @@ -172,8 +171,6 @@ def chromosomal_inversion(cell_contents,
:type gene_symbol: str
:param gene_id: the identifier (using HGNC) of the gene, e.g., GLI3 is HGNC:4319
:type gene_id: str
:param genotype: Genotype (heterozygous, homozygous, hemizygous) of this variant call
:type genotype: str
:param variant_id: an identifier for the variant
:type variant_id: str, optional
"""
Expand All @@ -188,7 +185,6 @@ def chromosomal_inversion(cell_contents,
def chromosomal_translocation(cell_contents,
gene_symbol,
gene_id,
genotype,
variant_id=None):
"""
create a StructuralVariant object for a chromosomal translocation
Expand All @@ -199,8 +195,6 @@ def chromosomal_translocation(cell_contents,
:type gene_symbol: str
:param gene_id: the identifier (using HGNC) of the gene, e.g., GLI3 is HGNC:4319
:type gene_id: str
:param genotype: Genotype (heterozygous, homozygous, hemizygous) of this variant call
:type genotype: str
:param variant_id: an identifier for the variant
:type variant_id: str, optional
"""
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