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  • University Medical Center, Ljubljana
  • Clinical institute of genomic medicine

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Jupyter Notebook 40 5 Updated Sep 25, 2024

Call and score variants from WGS/WES of rare disease patients.

Nextflow 97 43 Updated Mar 21, 2025

Modules to interface with tools used in Ensembl Gene Annotation Process and scripts to run pipelines

Perl 18 35 Updated Mar 14, 2025

EnsEMBL Hive - a system for creating and running pipelines on a distributed compute resource

Perl 53 28 Updated Jan 13, 2025

Repository for the GA4GH Benchmarking Team work developing standardized benchmarking methods for germline small variant calls

HTML 201 47 Updated Mar 19, 2021

Deprecated. See new version: https://github.com/statgen/bravo_api - BRowse All Variants Online

HTML 9 8 Updated Jun 21, 2022

Server side data processing and retrieval endpoints for BRAVO

Python 1 2 Updated Mar 11, 2025

Compare files from various activity trackers

TypeScript 196 25 Updated Jan 7, 2023

The Genomics Tertiary Analysis and Machine Learning Using Amazon SageMaker solution creates a scalable environment in AWS to develop machine learning models using genomics data, generate prediction…

Python 11 6 Updated Jul 7, 2023

Set up commonly used 📦 components

R 868 287 Updated Mar 5, 2025

Posit Cheat Sheets - Can also be found at https://posit.co/resources/cheatsheets/.

TeX 5,990 1,859 Updated Jan 31, 2025

Official code repository for GATK versions 4 and up

Java 1,782 602 Updated Mar 22, 2025

Data Carpentry workshop materials

HTML 167 140 Updated Apr 9, 2019
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