ericminikel / genetic_support
Refining the impact of genetic evidence on clinical success
☆22Updated 4 months ago
Related projects ⓘ
Alternatives and complementary repositories for genetic_support
- Suite of heritability and genetic correlation estimation tools for exome-sequencing data☆31Updated last month
- GWAS gold standards repository☆29Updated 11 months ago
- A Package For Predicting The Disruptiveness Of Single Nucleotide Polymorphisms On Transcription Factor Binding Sites.☆28Updated 3 months ago
- Explore the cancer relevance of your gene list☆49Updated 2 months ago
- Code for creating cell-type-specific regulatory element annotation files☆18Updated 5 months ago
- ☆11Updated last year
- Fine-mapping pipeline for Open Targets Genetics☆25Updated 2 years ago
- R package enabling statistical association analysis and using immunogenetic data transformation functions for HLA amino acid fine mapping…☆12Updated 9 months ago
- Code for EpiMap data browser☆14Updated 5 months ago
- cancereffectsizeR: Estimate somatic mutation rates and quantify selection in cancer☆17Updated last week
- Modular package for generation of sets of ranges representing the null hypothesis. These can take the form of bootstrapped ranges (bootRa…☆26Updated last year
- Toolbox package for organizing and working with TCGA data☆23Updated 3 weeks ago
- software package for integrative genetic association analysis☆32Updated last year
- Method for identifying trait-relevant gene annotations from GWAS summary statistics.☆17Updated 2 years ago
- Toolkit for QTL mapping and meta-analysis.☆16Updated 2 years ago
- processes GoT amplicon data and generates a table of metrics☆26Updated 2 years ago
- Pairwise Hierarchical Model☆13Updated 2 years ago
- Snakemake pipeline for benchmarking cell-type deconvolution methods and deconvolving real bulk RNA-seq data with the use of scRNA-seq dat…☆15Updated 3 months ago
- ☆9Updated 4 years ago
- Millefy: Genome browser-like visualization of single-cell RNA-seq dataset☆27Updated 4 years ago
- Pipeline for the identification of cancer-related mutations from RNA-seq data☆13Updated 3 years ago
- The `multiGSEA` R package was designed to run a robust GSEA-based pathway enrichment for multiple omics layers.☆17Updated 3 weeks ago
- R package for haplotype phasing using single-cell RNA-seq data☆13Updated 7 years ago
- A p-value-free method for controlling false discovery rates in high-throughput biological data with two conditions☆38Updated 2 years ago
- ☆17Updated 6 months ago
- Workflow for ZINB-WaVE + DESeq2 intergration for single-cell RNA-seq☆30Updated 3 years ago
- Identify Intra-, Inter-donor variations in bulk or single cell longitudinal dataset☆17Updated last year
- Repository for resources we'd like to share with the community.☆24Updated 2 years ago
- ☆26Updated last year
- Learn tissue-specificity and tissue-sharing of genetic regulation across 49 tissues using constraint matrix factorization model☆21Updated 4 years ago