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
- ☆11Updated 2 years ago
- R package designed to simplify structural variant analysis☆74Updated 4 years ago
- Mutation Identification Pipeline. Read the latest documentation:☆47Updated 2 months ago
- MOsaic CHromosomal Alterations (MoChA) caller☆91Updated 5 months ago
- ☆68Updated last week
- ☆40Updated 8 years ago
- Create "haplotype maps" of variants in order to use with Picardtools Crosscheck_Files utility, which allows for robust genotyping of func…☆28Updated 2 years ago
- Burden testing against public controls☆50Updated last year
- Ancestry and Kinship Tools☆70Updated 3 years ago
- Read visualizer for structural variants☆84Updated 7 years ago
- Allelic decomposition and exact genotyping of highly polymorphic and structurally variant genes☆67Updated 3 weeks ago
- An awk-like VCF parser☆56Updated 2 years 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
- R package for inferring copy number from read depth☆32Updated 3 years ago
- Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer☆57Updated this week
- utilities for working with IGV: opening files remotely in either desktop IGV or a web viewer (igv.js), creating screenshots, etc.☆49Updated 6 years ago
- ☆37Updated 3 years ago
- Detection of copy number changes in Germline/Trio/Somatic contexts in NGS data☆91Updated 4 months ago
- Applying polygenic scores (PGS) on imputed genotypes☆31Updated 3 months ago
- A Rare Variant Caller for Array-based Genotyping☆25Updated 10 years ago
- Simple vcf parser, based on PyVCF☆48Updated 7 years ago
- Robust detection of clinically relevant structural and copy number variation from whole genome sequencing data☆75Updated last year
- ☆54Updated 3 years ago
- Script to convert GTC/BPM files to VCF☆48Updated 3 months ago
- HLA-TAPAS pipeline for HLA association and fine-mapping studies☆54Updated 2 years ago
- Annotate models of genetic inheritance patterns in variant files (vcf files)☆85Updated 3 weeks ago
- ☆26Updated 7 months ago
- Framework to process and call somatic variation from NGS dataset generated using MSK-IMPACT assay☆57Updated 4 years ago