Secure and federated genome-wide association studies
☆18Mar 19, 2025Updated last year
Alternatives and similar repositories for sfgwas
Users that are interested in sfgwas are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- GWAS and rare variants tests at high speed using regenie☆16Jul 30, 2026Updated 2 weeks ago
- Repository for RecallME-v.0.1 a variant calling pipelines benchmarker and optimizer☆13Dec 18, 2023Updated 2 years ago
- Imputation of parental genotypes, inference of sibling IBD segments, family based GWAS, and polygenic score analyses.☆42Jun 17, 2026Updated 2 months ago
- ☆14Oct 17, 2024Updated last year
- Sequence Bloom Trees with All/Some split☆11Oct 30, 2018Updated 7 years ago
- 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.
- ☆12Jun 7, 2024Updated 2 years ago
- ☆11Dec 8, 2022Updated 3 years ago
- v2.x of the microassembly based somatic variant caller☆29Updated this week
- A Transcriptomics-Proteomics Integration Pipeline☆22Apr 11, 2024Updated 2 years ago
- ☆34Jun 20, 2025Updated last year
- dv-trio provides a pipeline to call variants for a trio (father-mother-child) using DeepVariants [1]. Genomic Variant Calling Files (gVCF…☆11Feb 3, 2021Updated 5 years ago
- What is true, thank you, ernestly. A large variant benchmarking tool analogous to hap.py for small variants.☆37Sep 13, 2023Updated 2 years ago
- ☆12Sep 27, 2023Updated 2 years ago
- Easily run WDL workflows on GCP☆14Sep 28, 2021Updated 4 years ago
- Proton VPN Special Offer - Get 70% off • AdSpecial partner offer. Trusted by over 100 million users worldwide. Tested, Approved and Recommended by Experts.
- Improving gene isoform quantification with miniQuant☆42Updated this week
- A web-browser app to visualise, interpret and prioritise genomic/transcriptomic structural variations (SVs) of multiple samples.☆14May 16, 2026Updated 3 months ago
- Identify Intra-, Inter-donor variations in bulk or single cell longitudinal dataset☆28Jul 31, 2023Updated 3 years ago
- Standard regression functions in R enabled for parallel processing over large data-frames.☆38Sep 24, 2023Updated 2 years ago
- From QC to summary statistics☆17Jun 27, 2020Updated 6 years ago
- ☆47Jun 27, 2026Updated last month
- Allele frequency filtering for Mendelian variant discovery☆18Sep 27, 2016Updated 9 years ago
- Variational Inference of Polygenic Risk Scores☆33Jul 4, 2026Updated last month
- ☆24Oct 31, 2025Updated 9 months ago
- 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.
- Flexible omics pipeline☆17Oct 16, 2025Updated 10 months ago
- InspectOmop is a lightweight python 3 package that assists in the extraction of electronic health record(EHR) data from relational databa…☆15Apr 14, 2026Updated 4 months ago
- A Javascript library for converting between Chainpoint JSON-LD and binary proof formats☆11Apr 20, 2022Updated 4 years ago
- Bitcoin SPV wallet written in Java☆11Nov 2, 2015Updated 10 years ago
- multi_tbx: a simple tool for indexing VCF files and extract variant records for variant data stored in multiple VCF files.☆10Jan 7, 2022Updated 4 years ago
- POC Nextflow pipeline to run Illumina DRAGEN software☆14Aug 15, 2025Updated last year
- Code for performing PCA followed by CCA☆18Dec 2, 2018Updated 7 years ago
- Comprehensive pipeline for donor demultiplexing in single cell☆26Aug 4, 2026Updated last week
- ☆13Aug 20, 2025Updated 11 months 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.
- Consensus assembly and variant calling workflow.☆12May 26, 2015Updated 11 years ago
- ☆13Sep 14, 2022Updated 3 years ago
- Static website for the PH4AGE alliance☆14Oct 27, 2023Updated 2 years ago
- Curated datasets on reported cases of the SARS-CoV-2 Omicron (B.1.1.529) Variant of Concern☆10Jan 25, 2022Updated 4 years ago
- MetroMaps Release☆16May 8, 2014Updated 12 years ago
- Easy genomic regions for short-read variant calling☆46Sep 10, 2025Updated 11 months ago
- ☆27Aug 2, 2023Updated 3 years ago