BioMM: Biological-informed Multi-stage Machine learning framework for phenotype prediction using omics data
☆14Jun 14, 2026Updated 4 months ago
Alternatives and similar repositories for BioMM
Users that are interested in BioMM are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- An efficient genetic data imputation pipeline☆13Jun 14, 2026Updated 4 months ago
- SMR-IVW extension of the SMR software☆10Mar 17, 2023Updated 3 years ago
- Supplementary Code for "Mapping DNA methylation across development, genotype, and schizophrenia in the human frontal cortex"☆12Oct 27, 2015Updated 11 years ago
- A Javascript implementation of Astronomical Algorithms by Jean Meeus☆13Feb 14, 2015Updated 11 years ago
- ☆22Dec 17, 2020Updated 5 years ago
- Deploy to Railway using AI coding agents - Free Credits Offer • AdUse Claude Code, Codex, OpenCode, and more. Autonomous software development now has the infrastructure to match with Railway.
- zero-inflated negative binomial gene expression in R☆21Jan 31, 2018Updated 8 years ago
- QTL Discovery using Annotations☆29Dec 12, 2022Updated 3 years ago
- Software Pipeline for Integrative Genetic Association Analysis: Probabilistic Assessment of Enrichment and Colocalization☆27Oct 29, 2019Updated 7 years ago
- PhenomeXcan: mapping the genome to the phenome through the transcriptome☆11Jun 28, 2020Updated 6 years ago
- R package: determining cutoff values from bimodal data☆11Mar 17, 2024Updated 2 years ago
- Code for tidymass2 manuscript☆11Dec 15, 2025Updated 10 months ago
- Main ricopili repo for public releases☆54Apr 8, 2025Updated last year
- an R based software package that makes polygenic traits prediction using gradient boosted and LD adjusted gene score weights.☆10Apr 9, 2019Updated 7 years ago
- Datos y análisis de datos de pruebas moleculares y casos confirmados en Puerto Rico☆15Mar 16, 2022Updated 4 years ago
- Serverless GPU API endpoints on Runpod - Get Bonus Credits • AdSkip the infrastructure headaches. Auto-scaling, pay-as-you-go, no-ops approach lets you focus on innovating your application.
- Script for my explanation videos created with manim☆11May 31, 2023Updated 3 years ago
- ☆20Apr 9, 2021Updated 5 years ago
- p-IgGen: A Generative Paired Antibody Language Model☆13May 6, 2025Updated last year
- ☆10Jan 20, 2023Updated 3 years ago
- ☆40Jun 15, 2023Updated 3 years ago
- Perform cell-stratified MR analysis through integrating GWAS and QTL data☆38Jan 28, 2026Updated 9 months ago
- Code for the meQTL analyses presented in Hawe et al. 2021 Nature Genetics☆14Jan 14, 2022Updated 4 years ago
- ☆11Mar 16, 2022Updated 4 years ago
- Julia module to perform haplotype allele-specific DNA methylation analysis.☆10Apr 14, 2026Updated 6 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.
- This software tool implements the OPERA (omics pleiotropic association) method to test for combinatorial pleiotropic associations of mole…☆38Sep 26, 2024Updated 2 years ago
- ☆14Aug 13, 2026Updated 2 months ago
- Inference framework for serological data☆20Sep 24, 2026Updated last month
- Create Regional Association Plots☆14May 27, 2026Updated 5 months ago
- TREKIS-3: Time-Resolved Electron Kinetics in SHI-Irradiated Solids☆14Oct 10, 2026Updated 2 weeks ago
- Application of the Simple Sum method for testing co-localization of GWAS with any other SNP-level data (e.g. eQTL data)☆10Jan 26, 2026Updated 9 months ago
- DiffNetFDR☆10Sep 12, 2018Updated 8 years ago
- R package for tissue-specific gene enrichment☆16Mar 10, 2022Updated 4 years ago
- Summary-level Unified Method for Modeling Integrated Transcriptome☆10Jun 27, 2023Updated 3 years ago
- Virtual machines for every use case on DigitalOcean • AdGet dependable uptime with 99.99% SLA, simple security tools, and predictable monthly pricing with DigitalOcean's virtual machines, called Droplets.
- Proteome-Wide Association Study☆52Apr 4, 2021Updated 5 years ago
- Pair-wise conditional analysis and colocalisation☆44May 2, 2024Updated 2 years ago
- Base-wise aggregation and functional prediction for human non-coding regulatory variants☆15Dec 20, 2023Updated 2 years ago
- A comprehensive tutorial for proteomics data analysis in R that utilizes packages developed by researchers at PNNL and from Bioconductor.☆12May 28, 2022Updated 4 years ago
- Script used to identify de novo variants from sequencing data.☆12Mar 2, 2017Updated 9 years ago
- A statistical test of pleiotropic effect of a genetic variant on two traits using GWAS summary statistics☆46Sep 18, 2025Updated last year
- Enrichment of Causal Loci and Identification of Pathogenic cells in Single Cell Expression and Regulation data☆11May 19, 2022Updated 4 years ago