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@neurogenomics

neurogenomics

Neurogenomics Lab, UK Dementia Research Institute at Imperial College London

🧠🧬 About Us 🧬🧠

Our research focuses on simple questions about complex brain traits: where do they occur (in which cell types)? When do they occur (at which developmental stages)? How do they occur (which quantitative traits of cells are affected)? We aim to develop the methods and datasets required to enable these questions to be answered systematically for any trait for which well-powered genetic data is available.

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  1. MungeSumstats MungeSumstats Public

    Rapid standardisation and quality control of GWAS or QTL summary statistics

    R 69 15

  2. rworkflows rworkflows Public

    Continuous integration for R packages. 🔀 Automates testing ✅, documentation website building 📦, & containerised deployment 🐳.

    HTML 68 7

  3. MAGMA_Celltyping MAGMA_Celltyping Public

    Find causal cell-types underlying complex trait genetics

    R 67 29

  4. orthogene orthogene Public

    🧬 o r t h o g e n e 🧬✨✨✨✨✨✨✨ Interspecies gene mapping✨✨✨✨✨ 🦠 🔁 🌱 🔁 🌳 🔁 🍎 🔁 🍊 🔁 🪱 🔁 🪰 🔁 🐟 🔁 🦎 🔁 🐓 🔁 🦇 🔁 🐄 🔁 🐖 🔁 🐐 🔁 🐎 🔁 🐈 🔁 🐕 🔁 🐁 🔁 🐒 🔁 🦧 🔁 🦍 🔁 🏃‍♀️

    R 39 4

  5. reanalysis_Mathys_2019 reanalysis_Mathys_2019 Public

    A re-analysis of the [Single-cell transcriptomic analysis of Alzheimer’s disease](https://www.nature.com/articles/s41586-019-1195-2) using a standardised data processing and pseudobulk differential…

    HTML 13 4

  6. EpiCompare EpiCompare Public

    Comparison, benchmarking & QC of epigenetic datasets

    HTML 12 3

Repositories

Showing 10 of 78 repositories
  • MotifPeeker Public

    Benchmark Epigenomic Profiling Methods with Motif Enrichment as Key Metric

    neurogenomics/MotifPeeker’s past year of commit activity
    R 1 GPL-3.0 0 0 0 Updated Jun 28, 2024
  • MotifStats Public

    Package for integrating peak and motif positions

    neurogenomics/MotifStats’s past year of commit activity
    R 1 GPL-3.0 1 0 0 Updated Jun 13, 2024
  • rare_disease_celltyping Public

    Code, data and results associated with the "Rare diseases cell-typing" project.

    neurogenomics/rare_disease_celltyping’s past year of commit activity
    HTML 6 0 6 (1 issue needs help) 0 Updated Jun 11, 2024
  • KGExplorer Public

    Import and analyse large-scale biomedical knowledge graphs and ontologies. 🕸️⚙️💻⚙️🕸️

    neurogenomics/KGExplorer’s past year of commit activity
    R 0 1 1 0 Updated Jun 11, 2024
  • HPOExplorer Public

    Functions for working with the Human Phenotype Ontology data

    neurogenomics/HPOExplorer’s past year of commit activity
    R 3 1 1 0 Updated Jun 5, 2024
  • neurogenomics/neurogenomics-lab-website’s past year of commit activity
    TeX 2 MIT 4 0 0 Updated Jun 4, 2024
  • MAGMA_Celltyping Public

    Find causal cell-types underlying complex trait genetics

    neurogenomics/MAGMA_Celltyping’s past year of commit activity
    R 67 29 11 0 Updated May 17, 2024
  • EnformerCelltyping Public

    Enformer Celltyping is a tensorflow, multi-headed attention based model that incorporates distal effects of Deoxyribonucleic Acid (DNA) interactions to predict histone marks across diverse cell types.

    neurogenomics/EnformerCelltyping’s past year of commit activity
    Jupyter Notebook 5 MIT 0 0 0 Updated May 14, 2024
  • MSTExplorer Public

    Multi-Scale Target Explorer systematically identifies, prioritises, and visualises cell-type-specific gene therapy targets across the phenome.

    neurogenomics/MSTExplorer’s past year of commit activity
    R 1 1 2 0 Updated May 6, 2024
  • MungeSumstats Public

    Rapid standardisation and quality control of GWAS or QTL summary statistics

    neurogenomics/MungeSumstats’s past year of commit activity

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