☆70Mar 27, 2026Updated this week
Alternatives and similar repositories for gnomad_qc
Users that are interested in gnomad_qc are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Hail helper functions for the gnomAD project and Translational Genomics Group☆100Updated this week
- ☆12Nov 1, 2022Updated 3 years ago
- ☆16Sep 14, 2023Updated 2 years ago
- ☆192Jun 20, 2023Updated 2 years ago
- ☆24Nov 27, 2024Updated last year
- Wordpress hosting with auto-scaling on Cloudways • AdFully Managed hosting built for WordPress-powered businesses that need reliable, auto-scalable hosting. Cloudways SafeUpdates now available.
- Analyses conducting GWAS across the UKBB diverse superpopulations☆64Oct 22, 2025Updated 5 months ago
- regenie is a C++ program for whole genome regression modelling of large genome-wide association studies.☆258Nov 13, 2025Updated 4 months ago
- A sparklyr extension for Hail☆15Jul 8, 2021Updated 4 years ago
- ☆20Nov 30, 2023Updated 2 years ago
- Comprehensive Human Expressed SequenceS☆19Jul 13, 2025Updated 8 months ago
- ASCETIC (Agony-baSed Cancer EvoluTion InferenCe) is a novel framework for the inference of a set of statistically significant temporal pa…☆12Apr 18, 2025Updated 11 months ago
- A structural variation pipeline for short-read sequencing☆201Updated this week
- VariantStore: A Large-Scale Genomic Variant Search Index☆39Jul 9, 2021Updated 4 years ago
- GWAS SNP Regulatory Analysis Tool☆17Mar 19, 2015Updated 11 years ago
- Managed hosting for WordPress and PHP on Cloudways • AdManaged hosting with the flexibility to host WordPress, Magento, Laravel, or PHP apps, on multiple cloud providers. Cloudways by DigitalOcean.
- Reducing reference bias using multiple population reference genomes☆34May 27, 2024Updated last year
- ☆29Sep 23, 2019Updated 6 years ago
- TOPMed analysis pipeline☆52Oct 10, 2023Updated 2 years ago
- Repository for RecallME-v.0.1 a variant calling pipelines benchmarker and optimizer☆13Dec 18, 2023Updated 2 years ago
- A GWAS course☆12Nov 4, 2021Updated 4 years ago
- ☆14Mar 15, 2026Updated 2 weeks ago
- Code associated with 2019 manuscript entitled "Transcript expression-aware annotation improves rare variant discovery and interpretation…☆34May 5, 2022Updated 3 years ago
- Scripts and utilities for analyzing tandem repeats (TRs).☆43Mar 19, 2026Updated last week
- CADD scripts release for offline scoring. For more information about CADD, please visit our website☆92Oct 30, 2025Updated 4 months ago
- End-to-end encrypted cloud storage - Proton Drive • AdSpecial offer: 40% Off Yearly / 80% Off First Month. Protect your most important files, photos, and documents from prying eyes.
- Ascertained Sequentially Markovian Coalescent☆16Oct 22, 2025Updated 5 months ago
- Automation of pipelines that depend on preexisting assembly, polishing, and alignment tools. Performance evaluation and visualization of …☆13May 29, 2020Updated 5 years ago
- A thorough tutorial on HLA imputation and association, accompanying our manuscript "Tutorial: A statistical genetics guide to identifying…☆72Oct 10, 2024Updated last year
- Hidden Markov Model based Copy number caller☆20Dec 9, 2025Updated 3 months ago
- GWAS Survival Package in R☆13Nov 16, 2023Updated 2 years ago
- haplotypes genotypes and alleles example decision synthesizer☆20Jun 13, 2019Updated 6 years ago
- Scalable gVCF merging and joint variant calling for population sequencing projects☆179Apr 12, 2024Updated last year
- Analysis on stop reasons☆10Jun 17, 2024Updated last year
- Allele frequency filter app☆14May 4, 2022Updated 3 years ago
- NordVPN Threat Protection Pro™ • AdTake your cybersecurity to the next level. Block phishing, malware, trackers, and ads. Lightweight app that works with all browsers.
- Ultra-fast, high-performing structural variation (SV) detector☆24Apr 26, 2023Updated 2 years ago
- 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
- Convert 23andMe data to VCFs☆10Aug 8, 2016Updated 9 years ago
- Detect key Units in mosaic Tandem Repeats from representative reads from the same locus☆10Aug 2, 2023Updated 2 years ago
- Analyses related to the Borzoi paper.☆25Dec 14, 2025Updated 3 months ago
- a C++ API of htslib to be easily integrated and safely used. More importantly, it can be callled seamlessly in R/Python/Julia etc.☆24Aug 6, 2025Updated 7 months ago
- A tool to plot significant regions of GWAS☆29Jan 27, 2023Updated 3 years ago