Query sequence data (VCF/BCF1/BCF2, Tabix, BGEN, PLINK) in R
☆34Feb 23, 2026Updated 7 months ago
Alternatives and similar repositories for seqminer
Users that are interested in seqminer are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- A flexible tool for the multi-resolution localization of causal variants across the genome☆11Feb 19, 2021Updated 5 years ago
- ☆22Jan 13, 2017Updated 9 years ago
- An interactive graphical illustration of genetic associations and their biological context☆18Mar 14, 2024Updated 2 years ago
- Repo for Dynamic Statistical Comparisons project☆13Feb 5, 2024Updated 2 years ago
- software package for integrative genetic association analysis☆38Jul 8, 2023Updated 3 years ago
- Open source password manager - Proton Pass • AdSecurely store, share, and autofill your credentials with Proton Pass, the end-to-end encrypted password manager trusted by millions.
- Write PubMed search results with two display options (citation or listview) to PDF or Word☆13Oct 18, 2020Updated 5 years ago
- R package for the analysis of massive SNP arrays.☆227Jul 10, 2026Updated 3 months ago
- Anno is a variant annotation tool☆24May 18, 2016Updated 10 years ago
- A tool to build a website to browse hundreds or thousands of GWAS.☆198Apr 22, 2026Updated 5 months ago
- Code for implementing Mendelian randomization investigations☆22Nov 9, 2015Updated 10 years ago
- A genotype query interface.☆136Mar 29, 2021Updated 5 years ago
- Functional genomics and genome-wide association studies☆70Jul 24, 2018Updated 8 years ago
- ☆198May 2, 2022Updated 4 years ago
- ☆12Sep 20, 2019Updated 7 years ago
- 1-Click AI Models by DigitalOcean Gradient • AdDeploy popular AI models on DigitalOcean Gradient GPU virtual machines with just a single click. Zero configuration with optimized deployments.
- SMBL - SnakeMake Bioinformatics Library. Automatic installation of bioinformatics software in your SnakeMake pipelines.☆23Aug 19, 2017Updated 9 years ago
- R interface to megadepth: BigWig and BAM related utilities☆14Mar 31, 2026Updated 6 months ago
- Software Pipeline for Integrative Genetic Association Analysis: Probabilistic Assessment of Enrichment and Colocalization☆27Oct 29, 2019Updated 6 years ago
- ☆31May 29, 2014Updated 12 years ago
- Genetic correlation calculation pipeline via summary statistics for PheWeb☆13Mar 22, 2019Updated 7 years ago
- ☆14Aug 30, 2025Updated last year
- snpnet - Efficient Lasso Solver for Large-scale genetic variant data☆21Mar 5, 2024Updated 2 years ago
- Software implementing the Latent Causal Variable Model☆69Jun 30, 2020Updated 6 years ago
- LocusCompare is an interactive visualization tool for comparing two genetic association datasets.☆23Jul 9, 2026Updated 3 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 Python framework for integrating biological databases and structured data sources in Biological Expression Language (BEL)☆22Nov 3, 2021Updated 4 years ago
- A support vector machine for calling variants from next-gen sequencing data☆15Dec 12, 2013Updated 12 years ago
- FOCUS: Fine-mapping Of CaUsal gene Sets☆48Aug 30, 2023Updated 3 years ago
- Get SNP proxies from the 1000 Genomes Project.☆31Oct 4, 2018Updated 8 years ago
- Code and results from TotalSeqC antibody titration and pipeline benchmarking for CITE-seq experiments☆10Mar 13, 2021Updated 5 years ago
- Read and write VCF and BCF files☆14Oct 16, 2025Updated 11 months ago
- Probabilistic single-cell pseudotime with Edward+Tensorflow☆12Oct 5, 2017Updated 9 years ago
- Scripts used for generating Neale Lab UKB results☆19Oct 11, 2022Updated 4 years ago
- A toolkit for performing set operations - union, intersection and complement - on k-mer lists.☆35Nov 22, 2022Updated 3 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.
- Interactive eQTL visualizations☆14Dec 12, 2022Updated 3 years ago
- Examples of kallisto + sleuth☆11May 18, 2017Updated 9 years ago
- PrediXcan Project☆121Oct 17, 2022Updated 3 years ago
- Rare variant test software for next generation sequencing data☆144Jan 26, 2022Updated 4 years ago
- ☆34Jul 20, 2018Updated 8 years ago
- Examples using R and 1000 genomes data☆29May 18, 2021Updated 5 years ago
- Code for creating cell-type-specific regulatory element annotation files☆21Jun 11, 2024Updated 2 years ago