☆23Mar 7, 2023Updated 2 years ago
Alternatives and similar repositories for FAVORannotator
Users that are interested in FAVORannotator are comparing it to the libraries listed below
Sorting:
- An R package for performing association analysis of whole-genome/whole-exome sequencing (WGS/WES) studies using STAARpipeline☆70Mar 23, 2025Updated 11 months ago
- An R package for performing MetaSTAAR procedure in whole-genome sequencing studies☆27Nov 9, 2024Updated last year
- The tutorial for performing single-/multi-trait association analysis of whole-genome/whole-exome sequencing (WGS/WES) studies using FAVOR…☆36Dec 3, 2024Updated last year
- Doubly-Ranked Stratification in Mendelian Randomization☆11Jan 10, 2026Updated last month
- This software tool implements the OPERA (omics pleiotropic association) method to test for combinatorial pleiotropic associations of mole…☆35Sep 26, 2024Updated last year
- A Toolset for Chromosome X-Wide Association Studies☆12May 1, 2018Updated 7 years ago
- TOPMed analysis pipeline☆52Oct 10, 2023Updated 2 years ago
- An R package for performing STAAR procedure in whole-genome sequencing studies☆97Feb 9, 2025Updated last year
- Source code of FUMA GWAS web application☆59Nov 17, 2023Updated 2 years ago
- Single-header C++ library for fast/low-memory VCF (Variant Call Format) parsing.☆18Dec 2, 2025Updated 3 months ago
- An R package for summarizing and visualizing association analysis results of whole-genome/whole-exome sequencing (WGS/WES) studies genera…☆12Oct 16, 2024Updated last year
- ☆16Sep 14, 2023Updated 2 years ago
- ☆20Jun 12, 2023Updated 2 years ago
- ☆14Oct 29, 2025Updated 4 months ago
- Gene Expression Decomposition and Integration☆19Feb 9, 2026Updated 3 weeks ago
- Semantic Similarity in Bio-Ontologies☆18Jan 30, 2026Updated last month
- R/Bioconductor package including the Gene Expression Signature Search (GESS), Function Enrichment Analysis (FEA) methods and supporting d…☆21Feb 20, 2026Updated last week
- Primo☆16Sep 2, 2021Updated 4 years ago
- ☆26Feb 15, 2018Updated 8 years ago
- A robust and accurate cell type classifier for single cell RNA-seq data☆17Mar 15, 2023Updated 2 years ago
- Single-Cell ENhancer Target gene mapping using multimodal data with ATAC + RNA☆84Apr 21, 2025Updated 10 months ago
- Copy Number Methods for Detection and Genome Wide Association Tests☆22Nov 4, 2024Updated last year
- haplotypes genotypes and alleles example decision synthesizer☆20Jun 13, 2019Updated 6 years ago
- Annotate non-coding regulatory vars using our GREEN-DB, prediction scores, conservation and pop AF☆20Jun 13, 2025Updated 8 months ago
- ☆24Jun 30, 2023Updated 2 years ago
- Hail helper functions for the gnomAD project and Translational Genomics Group☆100Feb 20, 2026Updated last week
- R package for CAUSE☆56Dec 29, 2023Updated 2 years ago
- ☆24Nov 27, 2024Updated last year
- Regional association plots☆24Apr 1, 2024Updated last year
- JARVIS: a comprehensive deep learning framework to prioritise non-coding variants in whole genomes☆25Jan 8, 2025Updated last year
- ☆29Oct 16, 2024Updated last year
- ☆26Sep 23, 2025Updated 5 months ago
- Complex structural variant detection from WGS data☆31Jan 10, 2025Updated last year
- AWS Quick Start Team☆24Oct 3, 2024Updated last year
- A method which leverages scRNA-seq data to achieve two goals: (1) to infer the cell types in which the disease-associated genes manifest …☆26Sep 20, 2022Updated 3 years ago
- ☆69Updated this week
- ☆29Nov 15, 2023Updated 2 years ago
- ☆40Jan 13, 2026Updated last month
- Pleiotropy-informed conditional and conjunctional false discovery rate☆37Jun 3, 2025Updated 9 months ago