bsml320 / scGWASLinks
A method which leverages scRNA-seq data to achieve two goals: (1) to infer the cell types in which the disease-associated genes manifest and (2) to construct cellular modules which imply disease-specific activation of different processes.
☆26Updated 3 years ago
Alternatives and similar repositories for scGWAS
Users that are interested in scGWAS are comparing it to the libraries listed below
Sorting:
- Code to run the scHLApers pipeline for personalized single-cell HLA quantification☆17Updated last year
- Gene Set + S2G strategy annotations analyzed for disease architecture☆55Updated 3 years ago
- ☆15Updated 2 years ago
- Analytical tools and pipelines for bulk and single cell epigenomic and human genetic data☆27Updated 5 years ago
- This repository contains code for the evaluation of epithelial-to-mesenchymal transition states in cancer.☆13Updated 2 years ago
- identifying disease critical cell types and programs from single cell RNAseq☆57Updated 3 years ago
- Cell type specific enrichments using finemapped variants and quantitative epigenetic data☆47Updated 2 years ago
- Method for identifying trait-relevant gene annotations from GWAS summary statistics.☆18Updated 3 years ago
- Epigenetic cell-type deconvolution from Single-Cell Omic Reference profiles☆32Updated 7 months ago
- ☆51Updated last year
- ☆18Updated last year
- R package for SIGMA, a clusterability measure for scRNA-seq data☆12Updated 3 years ago
- scTyper: a comprehensive pipeline for the cell typing analysis of single-cell RNA-seq data☆31Updated 2 years ago
- Code for our paper: https://www.biorxiv.org/content/10.1101/528463v1☆18Updated 5 years ago
- GWAS genetics Fine-mapping method☆26Updated last year
- scripts for the integrating ATAC-seq, RNA-seq and CHi-C paper☆25Updated 3 years ago
- Analysis code for "Perturbation-response genes reveal signaling footprints in cancer gene expression"☆20Updated 7 years ago
- ☆16Updated 3 weeks ago
- Bead-based single-cell atac processing☆33Updated 4 years ago
- ☆12Updated 6 years ago
- ☆26Updated 2 years ago
- Code accompanying Characterizing genetic intra-tumor heterogeneity across 2,658 human cancer genomes☆44Updated 4 years ago
- Public code repository for the Banovich Lab at the Translational Genomics Research Institute (TGen).☆47Updated last year
- 🌓 Allele specific analyses across cell states and conditions☆10Updated 2 years ago
- codes used in the human kidney eQTL(cf) and eQTL(ci) and snATAC-seq data☆19Updated 4 years ago
- Single-cell RNA-sequencing of differentiating iPS cells reveals dynamic genetic effects on gene expression☆15Updated last year
- ☆16Updated 2 years ago
- ☆39Updated 2 months ago
- ☆17Updated 2 years ago
- A Shiny tool to define the cell-type of action by integrating single cell expression data with GWAS☆12Updated 7 years ago