💊🧬 PharMe - Pharmaceutical insights tailored to your personal genome
☆23Aug 20, 2025Updated 9 months ago
Alternatives and similar repositories for PharMe
Users that are interested in PharMe are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- PAnno is a Pharmacogenomics Annotation tool for clinical genomic testing.☆17Dec 28, 2022Updated 3 years ago
- Web application for clinical pharmacogenomic interpretation☆10Mar 3, 2017Updated 9 years ago
- An R package for Standardized Summary, Annotation, Comparison, and Visualization of CNV, CNVR and ROH☆15Oct 17, 2021Updated 4 years ago
- PharmGKB NGS Pipeline☆19Oct 2, 2018Updated 7 years ago
- Calling star alleles in highly polymorphic pharmacogenes (e.g. CYP450 genes) by leveraging genome graph-based variant detection.☆39Mar 9, 2026Updated 2 months ago
- Deploy to Railway using AI coding agents - Free Credits Offer • AdUse Claude Code, Codex, OpenCode, and more. Autonomous software development now has the infrastructure to match with Railway.
- Sequence to Medical Phenotypes: A pipeline featuring variant annotation, prioritization, pharmacogenomics, and tools for analyzing genomi…☆13Mar 1, 2016Updated 10 years ago
- Docker Image for Michigan Imputation Server☆18Oct 12, 2021Updated 4 years ago
- Genevieve genome report tool☆14Dec 8, 2022Updated 3 years ago
- The Pharmacogenomic Clinical Annotation Tool☆170Feb 25, 2026Updated 3 months ago
- Imputation pipeline for Open Humans☆14May 18, 2026Updated last week
- ☆17Feb 29, 2024Updated 2 years ago
- CPIC Data definitions and code to use that data☆31May 14, 2026Updated last week
- ☆10Oct 18, 2021Updated 4 years ago
- ☆17Mar 17, 2023Updated 3 years ago
- 1-Click AI Models by DigitalOcean Gradient • AdDeploy popular AI models on DigitalOcean Gradient GPU virtual machines with just a single click. Zero configuration with optimized deployments.
- Functions to extract information from Oxford Nanopore sequencing data and alignments☆11Dec 4, 2025Updated 5 months ago
- GenoTools: Advanced Genotype Data Analysis A robust suite for processing genotype data, offering genotype calling (.idat to PLINK), comp…☆36Feb 13, 2026Updated 3 months ago
- phy-mer☆11Oct 12, 2017Updated 8 years ago
- PanGenome Graph Building with the first 100 assemblies from the 1000G ONT Sequencing Consortium☆12Apr 5, 2025Updated last year
- mity: A highly sensitive mitochondrial variant analysis pipeline for whole genome sequencing data☆44Sep 8, 2025Updated 8 months ago
- To preprocess, quality control and prepare consumer DTC genomes for research☆14Apr 9, 2025Updated last year
- call copy number from WES(WXS)☆11May 10, 2021Updated 5 years ago
- The gview wiki migrated to GitHub.☆11Sep 3, 2020Updated 5 years ago
- Patient handling for SENAITE☆10Updated this week
- Managed hosting for WordPress and PHP on Cloudways • AdManaged hosting for WordPress, Magento, Laravel, or PHP apps, on multiple cloud providers. Deploy in minutes on Cloudways by DigitalOcean.
- Shiny app for geno-pheno catalog☆11Nov 4, 2022Updated 3 years ago
- ☆12Apr 16, 2026Updated last month
- Official code repository for JAX-CNV☆14Jan 16, 2020Updated 6 years ago
- PGR-TK: Pangenome Research Tool Kit☆23Apr 19, 2026Updated last month
- Distributed and cloud computing framework for vg☆23Apr 21, 2026Updated last month
- NiPTUNE. A Python library for NIPT analyses.☆11Nov 22, 2021Updated 4 years ago
- The Polygenic Score Catalog Calculator is a nextflow pipeline for polygenic score calculation☆165May 14, 2026Updated last week
- A webtool for the clinical interpretation of CNVs in rare disease patients☆13Jun 10, 2022Updated 3 years ago
- ☆11May 12, 2026Updated 2 weeks ago
- Simple, predictable pricing with DigitalOcean hosting • AdAlways know what you'll pay with monthly caps and flat pricing. Enterprise-grade infrastructure trusted by 600k+ customers.
- Open mHealth Schema mapping to FHIR resources. This site is published at:☆11Dec 9, 2022Updated 3 years ago
- ☆13May 6, 2024Updated 2 years ago
- Copy Number Methods for Detection and Genome Wide Association Tests☆22Nov 4, 2024Updated last year
- Repository of bahmni deployment and RPMs☆13Mar 23, 2026Updated 2 months ago
- Tools for analyzing raw DNA test data files. Shows Y chromosome and mitochondrial mtDNA haplogroups. LGPLv3 - use freely but share improv…☆13Dec 2, 2024Updated last year
- A modern, lightweight medication sig parser.☆12Jan 21, 2025Updated last year
- R package enabling statistical association analysis and using immunogenetic data transformation functions for HLA amino acid fine mapping…☆14Jan 31, 2024Updated 2 years ago