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

hierarchicell

An R package for simulating cell-type specific and hierarchical single-cell expression data

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MAGMA_Files_Public

Publicly shared SNP-to-gene mappings of GWAS generated by MAGMA.

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document_and_share

Strategies for documentation and sharing of data analyses.

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EpiPrepare

Preprocessing of epigenomic data from fastq files.

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rare_disease_celltyping_apps

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

10X_multiome_anlysis

Simple straightforward overview for 10X multiome (GEX+ATAC) analysis

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Benchmark_with_EpiCompare

ENCODE reproducibility check, cutandrun & TIP-seq benchmark

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bioc-actions

GitHub Actions for developing and maintaining Bioconductor packages

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BiocStyle

Issues and pull requests for BiocStyle should go here.

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CHiCAGO_for-Radicl-seq

RADICL-seq data tag distance plot

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cranlogs

Download Logs from the RStudio CRAN Mirror

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CUT_n_TAG

Preprocessing pipeline for CUT&TAG data.

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CUTnTag-benchmarking-analysis

Processing, benchmarking and analysis of CUT&Tag against ENCODE ChIP-seq.

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dockerfiles

docker files for dockerhub

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EpiArchives

Public archive for EpiCompare reports.

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MyBioconductorPackage

What the Package Does (One Line, Title Case)

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nf-imperial-canary

nf-core config checks for the Imperial HPC

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rtracklayer

R interface to genome annotation files and the UCSC genome browser

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scflow-1

Complete analysis workflow for single-cell/nuclei RNA-sequencing data.

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scflowpy

Python helper package for scFlow

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scNLP

Tools for applying natural language processing (NLP) techniques to single-cell (sc) omics data.

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SkillNet

Construct and search networks from skill sets and projects for all lab members.

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VariantAnnotation

Annotation of Genetic Variants

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wdl-scflow

WDL pipelining for scflow

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