Type: Organization
Bio: The Raj Lab investigates neurodegenerative disorders through the application of computational methods to multi-omics data
Location: Icahn School of Medicine at Mount Sinai, Department of Neuroscience, New York City, New York
Blog: https://rajlab.org
rajlabmssm's Projects
Repository for the AMP-AD structural variation manuscript
Easy-to-use R wrappers for the eQTL Catalogue's API (both with tabix and the REST API).
Genetic signatures COVID-19 susceptibility
R analyses and plots of DeepSEA (http://deepsea.princeton.edu) output, applied to Alzheimer's disease data.
⏩ Practical tools for R developers :rewind: :wrench::bat: :hammer::bat: :toolbox::bat:
Searchable, pre-computed, variant-level predictions from several deep learning models.
echoverse module: Single- and multi-threaded downloading functions.
set of scripts and pipelines to work with QTL results
echoverse module: Annotate fine-mapping results
echoverse module: conda environment handling
echoverse module: Example data.
echoverse module: Create package dependency graphs
echoverse module: Statistical and functional fine-mapping functions.
echoverse module: Extract data and metadata from GitHub
echoverse module: LD downloading and processing
Automated statistical and functional fine-mapping pipeline with extensive API access to datasets.
echoverse module: Locus plot creation for fine-mapping and colocalization studies.
echoverse module: Tabix indexing and querying.
Self-updating template for creating echoverse R packages.
A set of snakemake pipelines for doing RNA editing
A set of scripts for running Expression-Weighted Cell-type Estimation (EWCE)
Fork of FastQTL for SVs (to run on Minerva)
Fine mapping of genes associated with Parkinson's Disease using a variety of methods
Shiny app for plotting and sharing fine-mapping results from echolocatoR
Create LocusZoom-style plots in R.
GTEx Consortium data production and analysis pipelines
Repository to reproduce analyses from the GTEx V6P Rare Variation Manuscript
The isoform-centric microglia genomic atlas.