☆27Oct 8, 2025Updated 11 months ago
Alternatives and similar repositories for AutoComplete
Users that are interested in AutoComplete 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 QC, PCA, haplotype phasing, genotype imputation☆20Mar 31, 2026Updated 5 months ago
- CoMorMent-Containers☆40Jun 8, 2026Updated 3 months ago
- An R package for phenotype generation and association testing for phenome wide associations studies (PheWAS)☆14Jul 11, 2024Updated 2 years ago
- Cross-population fine-mapping☆46Dec 7, 2024Updated last year
- Phenome Exome Association and Correlation Of Key phenotypes☆36Aug 19, 2021Updated 5 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.
- ukbREST: efficient and streamlined data access for reproducible research of large biobanks☆44Jul 12, 2021Updated 5 years ago
- A positive-unlabeled ensemble learning framework for disease gene prioritization.☆21Nov 10, 2025Updated 10 months ago
- This repository contains code associated with the study "Proteomic signatures improve risk predictions for common and rare diseases" (DOI…☆20Jul 3, 2024Updated 2 years ago
- Toy simulations and analyses of heritability and genetic differences☆11Jul 17, 2024Updated 2 years ago
- Repo for Dynamic Statistical Comparisons project☆13Feb 5, 2024Updated 2 years ago
- PHESANT - PHEnome Scan ANalysis Tool (pheWAS, Mendelian randomisation (MR)-pheWAS etc.) in UK Biobank☆22Jul 4, 2022Updated 4 years ago
- ☆13Apr 23, 2025Updated last year
- Machine Learning in NeuroImaging (MLNI) is a python package that performs various tasks using neuroimaging data.☆26Jul 16, 2025Updated last year
- Functions to map between ICD-10 terms and PheCodes for UK Biobank hospital electronic health records☆39Dec 27, 2022Updated 3 years ago
- GPUs on demand by Runpod - Special Offer Available • AdRun AI, ML, and HPC workloads on powerful cloud GPUs—without limits or wasted spend. Deploy GPUs in under a minute and pay by the second.
- Proportional Odds Logistic Mixed Model (POLMM) for ordinal categorical data analysis☆11Aug 26, 2022Updated 4 years ago
- 3D GWAS across multiple phenotypes☆13Oct 11, 2022Updated 3 years ago
- Dataloader for applying sequence models to personalized genomics☆29Updated this week
- ☆13Nov 19, 2021Updated 4 years ago
- GWAS genetics Fine-mapping method☆18Jul 27, 2026Updated last month
- SeqOthello supports fast coverage query and containment query.☆12May 8, 2019Updated 7 years ago
- R package for processing of GWAS output☆17Jul 9, 2024Updated 2 years ago
- PhenoPLIER☆15Apr 8, 2024Updated 2 years ago
- A list of awesome tools for complex trait genetics.☆88Jan 28, 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.
- ☆33Oct 4, 2021Updated 4 years ago
- RaMWAS: Fast Methylome-Wide Association Study Pipeline for Enrichment Platforms☆10Sep 22, 2021Updated 4 years ago
- Colocalization analysis of genetic association signals☆62Jun 13, 2025Updated last year
- A Generative Adversarial Network Model Alternative to Animal Studies for Clinical Pathology Assessment☆18Jan 10, 2024Updated 2 years ago
- Identify Intra-, Inter-donor variations in bulk or single cell longitudinal dataset☆28Jul 31, 2023Updated 3 years ago
- GRUD is a genotype imputation based on deep learning algorithms☆11Jul 3, 2024Updated 2 years ago
- FLAMES: Accurate gene prioritization in GWAS loci☆66Aug 25, 2026Updated 3 weeks ago
- Software to infer latent pleiotropic components from GWAS summary data☆17Jan 30, 2025Updated last year
- A Fine-Mapping pipeline☆23Sep 13, 2019Updated 7 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.
- Script used to identify de novo variants from sequencing data.☆12Mar 2, 2017Updated 9 years ago
- PyIOmica (pyiomica) is a Python package for omics analyses.☆16Oct 6, 2025Updated 11 months ago
- Create a PheWAS code based phenome using ICD9 and ICD10 data from baskets of the UK biobank☆36Apr 27, 2026Updated 4 months ago
- A GWAS course☆12Nov 4, 2021Updated 4 years ago
- ☆12Aug 3, 2025Updated last year
- A deep learning approach to predicting transcription initiation from sequence at single nucleotide resolution☆15Jul 14, 2026Updated 2 months ago
- Code for multivariate genome wide association meta analysis☆25Aug 20, 2019Updated 7 years ago