neurogenomics

neurogenomics

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Neurogenomics Lab, UK Dementia Research Institute at Imperial College London

Location:United Kingdom

Home Page:https://www.neurogenomics.co.uk

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neurogenomics's repositories

MungeSumstats

Rapid standardisation and quality control of GWAS or QTL summary statistics

rworkflows

Continuous integration for R packages. πŸ”€ Automates testing βœ…, documentation website building πŸ“¦, & containerised deployment 🐳.

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MAGMA_Celltyping

Find causal cell-types underlying complex trait genetics

orthogene

🧬 o r t h o g e n e 🧬✨✨✨✨✨✨✨ Interspecies gene mapping✨✨✨✨✨ 🦠 πŸ” 🌱 πŸ” 🌳 πŸ” 🍎 πŸ” 🍊 πŸ” πŸͺ± πŸ” πŸͺ° πŸ” 🐟 πŸ” 🦎 πŸ” πŸ“ πŸ” πŸ¦‡ πŸ” πŸ„ πŸ” πŸ– πŸ” 🐐 πŸ” 🐎 πŸ” 🐈 πŸ” πŸ• πŸ” 🐁 πŸ” πŸ’ πŸ” 🦧 πŸ” 🦍 πŸ” πŸƒβ€β™€οΈ

reanalysis_Mathys_2019

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 expression approach

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EpiCompare

Comparison, benchmarking & QC of epigenetic datasets

scKirby

Automated ingestion and conversion of various single-cell data formats, within and across species

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labwiki

Tips, intros, and documentation for the Neurogenomics Lab. :brain: 🧬

rare_disease_celltyping

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

EnformerCelltyping

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.

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templateR

Self-updating template for developing R packages.

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HPOExplorer

Functions for working with the Human Phenotype Ontology data

scFlow

Single-cell/nuclei RNA-seq analysis tools in R for a complete workflow.

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chromexpress

Which epigenetic factors are the best predictors of gene expression? An analysis using ENCODE data

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MotifStats

Package for integrating peak and motif positions

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MSTExplorer

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

phenomix

Explore the phenome βœ¨πŸŽ†βœ¨

rare_disease_celltyping_apps

All apps and homepage code in one place for the rare disease EWCE project.

RareDiseasePrioritisation

Prioritise cell-type-specific gene targets from the Rare Disease Celltyping project.

.github

Neurogenomics Lab Profile

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ArchR

ArchR : Analysis of Regulatory Chromatin in R (www.ArchRProject.com)

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bioc_mentorship_docs

Training materials for mentors and mentees

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GenomicRanges

Representation and manipulation of genomic intervals

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KGExplorer

Import and analyse large-scale biomedical knowledge graphs and ontologies. πŸ•ΈοΈβš™οΈπŸ’»βš™οΈπŸ•ΈοΈ

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project_management

Tools, tutorials, and resources for research-based project management. πŸ”‚ βœ…βœ…βœ…

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Rsamtools

Binary alignment (BAM), FASTA, variant call (BCF), and tabix file import

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