genepi / imputationserver-dockerLinks
Docker Image for Michigan Imputation Server
☆18Updated 3 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…☆82Updated 11 months ago
- Read visualizer for structural variants☆84Updated 7 years ago
- Mutation Identification Pipeline. Read the latest documentation:☆45Updated last year
- Data and information about the Polaris study☆53Updated 5 years ago
- ☆68Updated this week
- Ancestry and Kinship Tools☆70Updated 2 years ago
- Burden testing against public controls☆50Updated last year
- ☆11Updated 2 years ago
- R package designed to simplify structural variant analysis☆73Updated 3 years ago
- Generic human DNA variant annotation pipeline☆58Updated last year
- mtDNA Variant Caller☆34Updated 8 months ago
- ClassifyCNV: a tool for clinical annotation of copy-number variants☆66Updated 2 years ago
- Simple vcf parser, based on PyVCF☆46Updated 6 years ago
- TIDDIT - structural variant calling☆76Updated 4 months ago
- Allelic decomposition and exact genotyping of highly polymorphic and structurally variant genes☆64Updated 3 weeks ago
- Create "haplotype maps" of variants in order to use with Picardtools Crosscheck_Files utility, which allows for robust genotyping of func…☆28Updated last year
- ExomeDepth R package for the detection of copy number variants in exomes and gene panels using high throughput DNA sequencing data.☆73Updated 2 months ago
- PGxPOP☆17Updated 2 years ago
- An awk-like VCF parser☆56Updated last year
- Workflows used for WGS data processing -- replaced by https://github.com/gatk-workflows/gatk4-genome-processing-pipeline☆57Updated 5 years ago
- Support Vector Structural Variation Genotyper☆58Updated 5 years ago
- an empirical Bayesian framework for mutation detection from cancer genome sequencing data☆31Updated 9 years ago
- Haplotype phasing software☆67Updated 4 years ago
- ☆26Updated 2 months ago
- Bamgineer: Introduction of simulated allele-specific copy number variants into exome and targeted sequence data sets☆37Updated 5 years ago
- Filtering and profiling of next-generational sequencing data using region-specific rules☆79Updated last year
- ☆40Updated 7 years ago
- BrowseVCF is a web-based application and workflow to quickly prioritise disease-causative variants in VCF files.☆46Updated 5 years ago
- Robust detection of clinically relevant structural and copy number variation from whole genome sequencing data☆71Updated 11 months ago
- Detection of copy number changes in Germline/Trio/Somatic contexts in NGS data☆87Updated 2 months ago