Hail helper functions for the gnomAD project and Translational Genomics Group
☆101Jun 29, 2026Updated 3 weeks ago
Alternatives and similar repositories for gnomad_methods
Users that are interested in gnomad_methods are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- ☆70Updated this week
- ☆200Jun 20, 2023Updated 3 years ago
- ☆16Apr 10, 2024Updated 2 years ago
- Cloud-native genomic dataframes and batch computing☆1,070Updated this week
- ☆54Jul 9, 2025Updated last year
- Wordpress hosting with auto-scaling - Free Trial Offer • AdFully Managed hosting for WordPress and WooCommerce businesses that need reliable, auto-scalable performance. Cloudways SafeUpdates now available.
- Explore gnomAD datasets on the web☆90Jul 14, 2026Updated last week
- Curated list of resources for variant prioritization☆15Nov 18, 2025Updated 8 months ago
- Scripts for working with Google Cloud Dataproc service☆37Jun 19, 2019Updated 7 years ago
- ☆25May 9, 2026Updated 2 months ago
- An option to spin cost effective EMR clusters in AWS with Hail and JupyterNotebook installed☆19Jun 19, 2020Updated 6 years ago
- CADD scripts release for offline scoring. For more information about CADD, please visit our website☆93Oct 30, 2025Updated 8 months ago
- ☆18May 22, 2026Updated 2 months ago
- Phenome Exome Association and Correlation Of Key phenotypes☆36Aug 19, 2021Updated 4 years ago
- ☆22Jun 12, 2023Updated 3 years ago
- GPU virtual machines on DigitalOcean Gradient AI • AdGet to production fast with high-performance AMD and NVIDIA GPUs you can spin up in seconds. The definition of operational simplicity.
- Ascertained Sequentially Markovian Coalescent☆19Oct 22, 2025Updated 9 months ago
- A GWAS course☆12Nov 4, 2021Updated 4 years ago
- MrMosaic (Genomic Mosaic Structural Variant Caller)☆15Jul 21, 2017Updated 9 years ago
- topr is a collection of plotting functions for visualizing and exploring genetic association results. Association results from multiple p…☆75Apr 26, 2026Updated 2 months ago
- A sparklyr extension for Hail☆15Jul 8, 2021Updated 5 years ago
- pathoscore evaluates variant pathogenicity tools and scores.☆22Mar 25, 2022Updated 4 years ago
- An R package for performing MetaSTAAR procedure in whole-genome sequencing studies☆27Nov 9, 2024Updated last year
- Burden testing against public controls☆51Feb 27, 2024Updated 2 years ago
- List of gene lists for genomic analyses.☆229Jun 24, 2022Updated 4 years ago
- Deploy on Railway without the complexity - Free Credits Offer • AdConnect your repo and Railway handles the rest with instant previews. Quickly provision container image services, databases, and storage volumes.
- A tool to plot significant regions of GWAS☆30Jan 27, 2023Updated 3 years ago
- Development for SAIGE and SAIGE-GENE(+)☆98Jun 26, 2026Updated 3 weeks ago
- ☆42May 22, 2024Updated 2 years ago
- Convert vcf in parquet☆32Jan 23, 2025Updated last year
- Fast and scalable variant annotation tool☆30May 1, 2022Updated 4 years ago
- TOPMed analysis pipeline☆52Oct 10, 2023Updated 2 years ago
- ☆11Feb 14, 2023Updated 3 years ago
- create a gemini-compatible database from a VCF☆55Jan 5, 2021Updated 5 years ago
- Fine-mapping with infinitesimal effects☆20May 5, 2026Updated 2 months ago
- Managed Database hosting by DigitalOcean • AdPostgreSQL, MySQL, MongoDB, Kafka, Valkey, and OpenSearch available. Automatically scale up storage and focus on building your apps.
- A toolkit to calculate polygenic scores using PLINK2, PRS-CS, RapidoPGS, or PRSice2.☆16Aug 16, 2024Updated last year
- filtering trio-based genetic variants in VCFs for clinical review☆21Aug 18, 2020Updated 5 years ago
- ☆12Nov 1, 2022Updated 3 years ago
- Pangolin is a deep-learning method for predicting splice site strengths.☆93Jun 17, 2024Updated 2 years ago
- ☆13Jun 17, 2021Updated 5 years ago
- ☆17Sep 14, 2023Updated 2 years ago
- A structural variation pipeline for short-read sequencing☆205Updated this week