genepi / imputationserver-dockerLinks
Docker Image for Michigan Imputation Server
☆18Updated 4 years ago
Alternatives and similar repositories for imputationserver-docker
Users that are interested in imputationserver-docker are comparing it to the libraries listed below
Sorting:
- Michigan Imputation Server: A new web-based service for imputation that facilitates access to new reference panels and greatly improves u…☆83Updated last year
- MOsaic CHromosomal Alterations (MoChA) caller☆92Updated 5 months ago
- Burden testing against public controls☆50Updated last year
- ☆26Updated 8 months ago
- ☆69Updated last week
- R package designed to simplify structural variant analysis☆74Updated 4 years ago
- Mutation Identification Pipeline. Read the latest documentation:☆47Updated 2 months ago
- ☆11Updated 2 years ago
- ☆40Updated 8 years ago
- Script to convert GTC/BPM files to VCF☆48Updated 3 months ago
- Ancestry and Kinship Tools☆70Updated 3 years ago
- Applying polygenic scores (PGS) on imputed genotypes☆31Updated 3 months ago
- Data and information about the Polaris study☆55Updated 6 years ago
- Workflows used for WGS data processing -- replaced by https://github.com/gatk-workflows/gatk4-genome-processing-pipeline☆57Updated 6 years ago
- ☆37Updated 3 years ago
- Generic human DNA variant annotation pipeline☆59Updated last year
- ☆26Updated 7 years ago
- Simple vcf parser, based on PyVCF☆48Updated 7 years ago
- A Rare Variant Caller for Array-based Genotyping☆25Updated 10 years ago
- QDNAseq package for Bioconductor☆54Updated last year
- Calling star alleles in highly polymorphic pharmacogenes (e.g. CYP450 genes) by leveraging genome graph-based variant detection.☆35Updated 3 months ago
- chimeraviz is an R package that automates the creation of chimeric RNA visualizations.☆39Updated 2 years ago
- Filtering and profiling of next-generational sequencing data using region-specific rules☆79Updated 2 years ago
- CrossMap is a python program to lift over genome coordinates from one genome version to another.☆92Updated 3 months ago
- Allelic decomposition and exact genotyping of highly polymorphic and structurally variant genes☆67Updated last month
- HLA-TAPAS pipeline for HLA association and fine-mapping studies☆54Updated 2 years ago
- An awk-like VCF parser☆56Updated 2 years ago
- Read visualizer for structural variants☆84Updated 7 years ago
- ☆54Updated 3 years ago
- Create mutation signatures from MAF's, and decompose them into Stratton signatures☆60Updated 6 years ago