A Variant Call Format reader for Python.
Appears on
Quick read
Latest capture 2026-10-22 09:42
Archive status reflects the last catalog sync, not a maintenance assessment. Check recent releases, issue responses, and fit for your project with the repository shortlisting checklist.
0 paths
Agent instructions and tool configuration found in this repository.
No config files detected.
1 observed capture since 2026-10-22. Observed captures are shown by default.
Stars from first capture 0
Observed captures only
All tracked data
Observed snapshots
Observed snapshots
Nearest indexed repositories by embedding similarity.
A fast Python library for VCF files leveraging Cython for speed.
cython + htslib == fast VCF and BCF processing
C++ library and cmdline tools for parsing and manipulating VCF files with python and zig bindings
A set of tools written in Perl and C++ for working with VCF files, such as those generated by the 1000 Genomes Project.
Bayesian haplotype-based genetic polymorphism discovery and genotyping.
annotate a VCF with other VCFs/BEDs/tabixed files
