Server wrapper that turns command line tools into web services
☆60Aug 8, 2018Updated 7 years ago
Alternatives and similar repositories for minion
Users that are interested in minion are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Client side iobio library for building and executing iobio commands☆10Dec 31, 2018Updated 7 years ago
- Visualization and charting JS library for streaming genomic data☆19Dec 4, 2024Updated last year
- https://bam.iobio.io☆47Jun 15, 2026Updated last month
- An iobio app for examining gene variants☆20Sep 10, 2018Updated 7 years ago
- gap opening realigner for BAM data streams☆18Oct 17, 2012Updated 13 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.
- Genomics database manager☆25Mar 3, 2014Updated 12 years ago
- ☆17Sep 24, 2013Updated 12 years ago
- ☆28Oct 7, 2025Updated 9 months ago
- ☆43Apr 20, 2016Updated 10 years ago
- ☆13Jan 23, 2020Updated 6 years ago
- Interactive web-based genome browser.☆229Aug 28, 2019Updated 6 years ago
- ☆16Apr 25, 2017Updated 9 years ago
- conda recipes for genomic data☆84Jul 31, 2021Updated 4 years ago
- Quality Control of Next Generation Sequencing Data☆21Jun 16, 2025Updated last year
- 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.
- Toolbox for generic NGS analyses - A framework to quickly build pipelines and to perform large-scale NGS analysis☆18Nov 2, 2022Updated 3 years ago
- MyVariant.info: A BioThings API for human variant annotations☆99Updated this week
- JSON-based FON (Feature Object Notation) format and tools to simplify genomic annotations usage☆13Jun 11, 2025Updated last year
- variant integration methods for the 1000 Genomes Project☆21Jan 16, 2018Updated 8 years ago
- Standalone C library for assembling Illumina short reads in small regions☆72Dec 15, 2022Updated 3 years ago
- The gkno launcher for executing tools or pipelines☆31Jan 17, 2017Updated 9 years ago
- Get user ids from social network handlers☆12Jan 13, 2017Updated 9 years ago
- A scalable genome browser. Apache 2 licensed.☆127Dec 2, 2022Updated 3 years ago
- Feature Annotation Location Description Ontology☆34Jan 21, 2020Updated 6 years ago
- Simple, predictable pricing with DigitalOcean hosting • AdAlways know what you'll pay with monthly caps and flat pricing. Enterprise-grade infrastructure trusted by 600k+ customers.
- The Refinery Platform is a data management, analysis and visualization system for bioinformatics and computational biology applications. …☆106Jan 11, 2023Updated 3 years ago
- ☆25May 21, 2021Updated 5 years ago
- ☆22Jul 28, 2022Updated 3 years ago
- Convert CWL to WDL☆17Oct 17, 2016Updated 9 years ago
- Adaptive semi-global banded alignment on string graphs☆66May 4, 2018Updated 8 years ago
- Tools for next-generation sequencing analysis☆89Jun 25, 2019Updated 7 years ago
- fast webservices based query tool for large sets of genomic features☆26May 10, 2025Updated last year
- Interactive in-browser track viewer☆281Oct 26, 2021Updated 4 years ago
- MedSavant is a search engine for genetic variants☆22Apr 21, 2016Updated 10 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.
- non-redundant, compressed, journalled, file-based storage for biological sequences☆52Nov 10, 2025Updated 8 months ago
- An online database of variants functionally demonstrated to affect (or not affect) splicing.☆12Jul 7, 2026Updated 2 weeks ago
- STORMSeq: Scalable Tools for Open-source Read Mapping☆19May 19, 2014Updated 12 years ago
- python script to programmatically enrich your data using Enrichr API☆12Jul 5, 2017Updated 9 years ago
- Chanjo provides a better way to analyze coverage data in clinical sequencing.☆50May 8, 2026Updated 2 months ago
- a tool for processing .bed and .vcf files☆21Apr 25, 2017Updated 9 years ago
- Retrieve data in genomic intervals with a Python interface for tabix.☆82Aug 10, 2017Updated 8 years ago