Encore Analysis Server
☆13Nov 18, 2025Updated 4 months ago
Alternatives and similar repositories for encore
Users that are interested in encore are comparing it to the libraries listed below
Sorting:
- Interface to various variant calling formats.☆31Jun 15, 2024Updated last year
- Basic and fast GWAS functions for QQ and Manhattan plots (incl. gene names)☆33Feb 10, 2026Updated last month
- Applying polygenic scores (PGS) on imputed genotypes☆32Oct 28, 2025Updated 4 months ago
- Minimac3 is a low memory and computationally efficient implementation of the genotype imputation algorithms. Minimac3 is designed to hand…☆30Mar 28, 2022Updated 3 years ago
- A tool to build a website to browse hundreds or thousands of GWAS.☆193Sep 11, 2025Updated 6 months ago
- Finding cryptic relationships to boost disease gene detection☆12May 31, 2023Updated 2 years ago
- ☆196May 2, 2022Updated 3 years ago
- Ultra Fast NGS Data QC Tool☆28Feb 14, 2021Updated 5 years ago
- Michigan Imputation Server: A new web-based service for imputation that facilitates access to new reference panels and greatly improves u…☆84Sep 28, 2024Updated last year
- Yet another small programming language and VM.☆12Sep 6, 2020Updated 5 years ago
- mtDNA Variant Caller☆35Dec 23, 2024Updated last year
- PGxPOP☆17Jan 25, 2023Updated 3 years ago
- Harmonise GWAS summary statistics against a reference VCF☆41Jun 15, 2021Updated 4 years ago
- Fast and Efficient Tool to Simulate Summary Statistics from Genome-Wide Association Studies☆12May 21, 2024Updated last year
- Simple matching of HTS samples based on HLA typing☆14Jan 4, 2017Updated 9 years ago
- Scripts for GWAS association and metaanalysis☆43Dec 8, 2020Updated 5 years ago
- SEQSpark documentation☆18Nov 17, 2020Updated 5 years ago
- The main website for the OpenMendel project.☆13Jul 24, 2022Updated 3 years ago
- Load genomic BAM files using Apache Spark☆21Jun 17, 2018Updated 7 years ago
- CRUD API built with Laravel Lumen☆11Sep 11, 2017Updated 8 years ago
- A nextflow pipeline to perform state-of-the-art genome-wide association studies.☆81Oct 7, 2025Updated 5 months ago
- Package provides java implementation of various clustering algorithms☆11Jun 5, 2017Updated 8 years ago
- Bamgineer: Introduction of simulated allele-specific copy number variants into exome and targeted sequence data sets☆38Jul 30, 2020Updated 5 years ago
- Django application for making varnish edge side includes easier to use.☆22Jun 14, 2011Updated 14 years ago
- Joint calling of gVCF, following GATK4 Best Practices☆12Apr 3, 2019Updated 6 years ago
- Restrict types exposed by apollo-server's introspection/playground☆10Feb 4, 2021Updated 5 years ago
- use the noise☆15Apr 15, 2020Updated 5 years ago
- A java library for simple progress monitoring on the console☆19Oct 13, 2020Updated 5 years ago
- ☆11Feb 14, 2023Updated 3 years ago
- ⚠️ OBSOLETE. DO NOT USE! Quickly generate large blocks of scaffolding for your applications. Generate templates from your own projects a…☆27Sep 24, 2015Updated 10 years ago
- ☆10Apr 17, 2023Updated 2 years ago
- Generate and process BAM files from Illumina sequencing instrument files☆23Feb 25, 2016Updated 10 years ago
- A rapido and lightweight method for PGS computation☆14Feb 19, 2025Updated last year
- Workshop "From interactive to social media: how to promote data journalism" European Data and Computational Journalism Conference 2018☆12Jun 21, 2018Updated 7 years ago
- ☆25Sep 18, 2025Updated 6 months ago
- An external library for delivering Slurm Elastic Computing.☆12Mar 31, 2017Updated 8 years ago
- GERMLINE is an algorithm for inferring long shared segments of Identity by Descent (IBD) between pairs of individuals in a large populati…☆15Apr 5, 2019Updated 6 years ago
- Evaluation of phasing performance☆23Mar 6, 2018Updated 8 years ago
- A Javascript/d3 embeddable plugin for interactively visualizing statistical genetic data from customizable sources.☆165May 9, 2025Updated 10 months ago