PharmCAT
importedsoftware/pharmcat
The Pharmacogenomic Clinical Annotation Tool
Machine-generated from the listed sources and not yet reviewed by a human.
- Category
- Software & Systems
- Subcategory
- unknown
- License
- MPL-2.0(osi)
- Status
- active
- Maturity
- deployed
- Organization
- PharmGKB
- Country
- unknown
- Homepage
- pharmcat.org
- Repository
- github.com/PharmGKB/PharmCAT
- Documentation
- unknown
- Tags
- bioinformatics · haplotype-mapping · haplotypecaller · pharmacogenomics · vcf
- Regulatory
- unknown
Top contributors by commit count, from the project’s public repository. Avatars are served by their origin, not stored here. To be removed from this list, open an issue.
Computed from shared tags, weighted so a rare tag counts for more than a common one. These are suggestions, not curated relationships.
- NeuroPGxbioinformatics · pharmacogenomics
A clinical decision-support system to identify pharmacogenomics profiles based on subjects genotype of five core genes. The paper has been published in the Journal of Personalized Medicine.
- vcflibhaplotypecaller
C++ library and cmdline tools for parsing and manipulating VCF files with python and zig bindings
- PharMepharmacogenomics
💊🧬 PharMe - Pharmaceutical insights tailored to your personal genome
- bioSyntaxbioinformatics · vcf
Syntax highlighting for computational biology
- cljambioinformatics · vcf
A DNA Sequence Alignment/Map (SAM) library for Clojure
- CuteVCFbioinformatics · vcf
simple viewer for variant call format using htslib
- api.github.com/repos/PharmGKB/PharmCATretrieved 2026-08-25 · via github-api
Machine-imported from GitHub search. Last push 2026-08-10, 187 stars, license reported as MPL-2.0. Category and schematic were assigned by keyword heuristics and are unreviewed.
Not yet verified by a human. Correct this record →
/v1/entries/55.json→ .entries["pharmcat"]
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