statgen / EPACTSLinks
☆35Updated 3 years ago
Alternatives and similar repositories for EPACTS
Users that are interested in EPACTS are comparing it to the libraries listed below
Sorting:
- ☆40Updated 7 years ago
- R package designed to simplify structural variant analysis☆73Updated 3 years ago
- Burden testing against public controls☆50Updated last year
- Create regional association plots from GWAS or meta-analysis☆61Updated 5 years ago
- Report reverse and ambiguous strand SNPs in GWAS data☆33Updated 6 years ago
- BigWig and BAM utilities☆96Updated last year
- ☆24Updated 7 months ago
- Canonical SGE cluster genotype imputation pipeline☆12Updated 9 years ago
- RetroSeq is a bioinformatics tool that searches for mobile element insertions from aligned reads in a BAM file and a library of reference…☆67Updated 2 years ago
- GENetic EStimation and Inference in Structured samples (GENESIS): Statistical methods for analyzing genetic data from samples with popula…☆38Updated 2 weeks ago
- ☆51Updated 5 years ago
- ☆42Updated last week
- HLA-TAPAS pipeline for HLA association and fine-mapping studies☆54Updated last year
- A nextflow pipeline to perform state-of-the-art genome-wide association studies.☆69Updated 3 months ago
- R API for browsing, analyzing, and manipulating reference-aligned genome graphs in a GenomicRanges framework☆40Updated last month
- tools to efficiently retrieve and calculate LD☆33Updated 3 years ago
- ☆60Updated 3 years ago
- software tool for the manipulation, annotation, selection, and analysis of variants in the context of next-gen sequencing analysis☆31Updated 3 years ago
- Genetic maps interpolated to sites in the 1000 Genomes project☆49Updated 10 years ago
- (WIP) best-practices workflow for rare disease☆60Updated last year
- TAPES : a Tool for Assessment and Prioritisation in Exome Studies☆24Updated last month
- Main ricopili repo for public releases☆48Updated 3 months ago
- A set of tools to annotate VCF files with expression and readcount data☆29Updated 4 months ago
- mity: A highly sensitive mitochondrial variant analysis pipeline for whole genome sequencing data☆36Updated last month
- Fast fusion detection using kallisto☆80Updated last month
- A utility for merging and genotyping Illumina-style GVCFs.☆33Updated 6 years ago
- ☆78Updated 11 years ago
- Flexible Bayesian inference of mutational signatures☆35Updated 2 years ago
- Fuji plot—a circos representation of multiple GWAS results—☆89Updated last month
- Scripts for implementing the Tractor pipeline☆50Updated 4 months ago