HannahVMeyer / PhenotypeSimulator
☆28Updated last year
Alternatives and similar repositories for PhenotypeSimulator:
Users that are interested in PhenotypeSimulator are comparing it to the libraries listed below
- A wrapper for liftOver for converting plink genotype data between different genome reference builds☆49Updated 6 years ago
- Generalized linear Mixed Model Association Tests☆38Updated last year
- Functional genomics and genome-wide association studies☆66Updated 6 years ago
- OUTRIDER: OUTlier in RNA-seq fInDER is an R-based framework to find aberrantly expressed genes in RNA-seq data☆49Updated this week
- Report reverse and ambiguous strand SNPs in GWAS data☆33Updated 5 years ago
- Flexible Bayesian inference of mutational signatures☆34Updated 2 years ago
- Software to help identify overlap between association scan results and GWAS hit catalogs.☆15Updated 2 years ago
- ☆40Updated 7 years ago
- tools to efficiently retrieve and calculate LD☆33Updated 3 years ago
- Repository for resources we'd like to share with the community.☆24Updated 2 years ago
- software package for integrative genetic association analysis☆34Updated last year
- R package to perform Bayesian Genome-Wide Association Studies☆38Updated last year
- ☆25Updated 8 months ago
- An R package for import, QC and analysis of Illumina Infinium genotyping arrays☆33Updated 6 years ago
- Matrix eQTL: Ultra fast eQTL analysis via large matrix operations☆70Updated last year
- ☆22Updated 8 years ago
- PGxPOP☆16Updated 2 years ago
- Bayesian hierarchical model for complex trait analysis☆44Updated last year
- Code and simulations using biologically annotated neural networks☆21Updated 3 years ago
- Get SNP proxies from the 1000 Genomes Project.☆28Updated 6 years ago
- GENetic EStimation and Inference in Structured samples (GENESIS): Statistical methods for analyzing genetic data from samples with popula…☆36Updated 3 weeks ago
- create, manage, and upload track hubs for use in the UCSC genome browser☆53Updated 10 months ago
- ☆30Updated 3 years ago
- Portable eQTL analysis and statistical fine mapping workflow used by the eQTL Catalogue☆46Updated this week
- Main ricopili repo for public releases☆44Updated this week
- Identifying recurrent mutations in cancer☆37Updated 3 years ago
- ☆38Updated 4 months ago
- Read PLINK BED/BIM/FAM files into R☆40Updated 3 years ago
- SPP - R package for analysis of ChIP-seq and other functional sequencing data☆40Updated 3 years ago
- combining p-values using modified stouffer-liptak for spatially correlated results (probes)☆44Updated 2 years ago