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NeuroPGx

imported

software/neuropgx

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.

Machine-generated from the listed sources and not yet reviewed by a human.

record
Category
Software & Systems
Subcategory
unknown
License
GPL-3.0(osi)
Status
dormant
Maturity
deployed
Organization
unknown
Country
unknown
Homepage
unknown
Documentation
unknown
Tags
bioinformatics · clinical-decision-support · genomics · genotyping-by-sequencing · metabolomics · neuroscience · pharmacogenomics
Regulatory
unknown
built by · 2

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.

similar by tags

Computed from shared tags, weighted so a rare tag counts for more than a common one. These are suggestions, not curated relationships.

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    Web-based Workflow for Metabolomics and Proteomics Data Analysis

  • pyMultiOmicsbioinformatics · metabolomics

    Python toolbox for multi-omics data mapping and analysis

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    National Microbiome Data Collaborative (NMDC) unified data model

  • biosynfonibioinformatics · metabolomics

    a *biosynformatic* fingerprint to explore natural product distance and diversity

sources
  1. api.github.com/repos/Andreater/NeuroPGx
    retrieved 2026-08-05 · via github-api

    Machine-imported from GitHub search. Last push 2021-09-01, 9 stars, license reported as GPL-3.0. Category and schematic were assigned by keyword heuristics and are unreviewed.

Not yet verified by a human. Correct this record →

machine-readable

/v1/entries/51.json→ .entries["neuropgx"]

Entries are sharded 64 ways by a stable hash of the id, so a consumer can find any record without an index.