biocommons/hgvs
Python library to parse, format, validate, normalize, and map sequence variants. `pip install hgvs`
PythonApache-2.0
Issues
- 10
How to apply a protein change to a given amino acid sequence to produce a mutant amino acid sequence
#641 opened - 2
Missing reference for protein change (sub)
#640 opened - 1
Parsing repeat expansions
#639 opened - 6
Dup should have an alt when available
#638 opened - 1
Using Gene symbol hgvs notation
#637 opened - 1
- 23
- 5
Implement caching for doctests
#633 opened - 1
How to parse complex insertions
#631 opened - 0
- 1
AssemblyMapper confusion
#629 opened - 8
- 0
h
#627 opened - 3
hgvs can not parse
#626 opened - 2
Making seqrepo optional
#624 opened - 2
- 5
- 2
HGVS using ENSEMBL ID is not working
#621 opened - 0
test
#619 opened - 4
normalize a whole hgvs
#618 opened - 1
- 1
- 1
- 8
- 2
DeprecationWarning
#611 opened - 5
- 7
strict_bounds parameter for AssemblyMapper
#608 opened - 5
- 7
Index Error for variant using am37.c_to_g()
#606 opened - 6
bioconda recipe?
#604 opened - 7
Investigate replacing psycopg2 with asyncpg
#603 opened - 0
- 8
Support for fusion hgvs
#599 opened - 8
Non-human genomes in HGVS/UTA
#598 opened - 0
- 1
- 0
- 4
- 2
- 0
- 5
- 1
Question: Can the HGVS package tell you the distance to the farther exon/intron boundary?
#588 opened - 1
HGVSInvalidVariantError with c_to_g
#587 opened - 6
Make the HGVS parser as a separate package
#586 opened - 1
- 4
python3.7 compatibility enum34 error
#584 opened - 0
Move hgvs models to hgvs.models
#583 opened - 1
Drop transcriptmapper.py
#582 opened - 2
allele information not available for dup
#581 opened - 7