Genevieve genome report tool
☆14Dec 8, 2022Updated 3 years ago
Alternatives and similar repositories for genevieve
Users that are interested in genevieve are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- ☆28Oct 5, 2018Updated 7 years ago
- User-friendly Bioinformatics Tools☆18Mar 5, 2021Updated 5 years ago
- My blog.☆16Aug 8, 2025Updated 11 months ago
- Stock prediction site built in React☆15Jan 4, 2023Updated 3 years ago
- Power Law Random k-SAT Generator☆16Nov 21, 2021Updated 4 years ago
- Managed Kubernetes at scale on DigitalOcean • AdDigitalOcean Kubernetes includes the control plane, bandwidth allowance, container registry, automatic updates, and more for free.
- Imputation pipeline for Open Humans☆18Updated this week
- ☆17Feb 29, 2024Updated 2 years ago
- Client side iobio library for building and executing iobio commands☆10Dec 31, 2018Updated 7 years ago
- Method for detecting STR expansions from short-read sequencing data☆63Dec 15, 2021Updated 4 years ago
- Retrieve compressed UTF-8 strings from Arduino Flash memory (Progmem)☆24Sep 13, 2019Updated 6 years ago
- ☆17Mar 17, 2023Updated 3 years ago
- Tools for analyzing raw DNA test data files. Shows Y chromosome and mitochondrial mtDNA haplogroups. LGPLv3 - use freely but share improv…☆13Dec 2, 2024Updated last year
- Elixir Beacon Reference Implementation. Latest release is compliant with v1.1.0 of the specification.☆14Jun 19, 2020Updated 6 years ago
- Free literature retrieval system for DNA analysis☆13Nov 19, 2025Updated 8 months ago
- AI Agents on DigitalOcean Gradient AI Platform • AdBuild production-ready AI agents using customizable tools or access multiple LLMs through a single endpoint. Create custom knowledge bases or connect external data.
- URMAP ultra-fast read mapper☆38Jun 15, 2020Updated 6 years ago
- To preprocess, quality control and prepare consumer DTC genomes for research☆14Jul 10, 2026Updated 2 weeks ago
- MedSavant is a search engine for genetic variants☆22Apr 21, 2016Updated 10 years ago
- ☆15Jul 28, 2023Updated 2 years ago
- GenNotes – public consensus annotation of genetic variants☆11Mar 27, 2016Updated 10 years ago
- Virtual Pharmacist is a web tool that interprets personal genome for the impact of genetic variation on drug response. It can take varian…☆13Nov 16, 2015Updated 10 years ago
- PGR-TK: Pangenome Research Tool Kit☆23Apr 19, 2026Updated 3 months ago
- DNA copy number detection from off-target sequence data☆34May 17, 2018Updated 8 years ago
- Distributed and cloud computing framework for vg☆23Apr 21, 2026Updated 3 months 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.
- Convert low ghidra pcode to verifiable C☆24Sep 13, 2024Updated last year
- Efficient base quality score recalibrator for NGS data☆24Nov 28, 2015Updated 10 years ago
- A radare2 Python script to dump a raw IA32 binary to an NASM source file☆33Dec 10, 2025Updated 7 months ago
- CNV calling algorithm for detection of homozygous and hemizygous deletions from whole exome sequencing data☆12Nov 9, 2025Updated 8 months ago
- Dump and decrypt communication with tuya devices☆36Oct 11, 2020Updated 5 years ago
- Copy Number Methods for Detection and Genome Wide Association Tests☆23Nov 4, 2024Updated last year
- Docker containers for bioinformatics with a small footprint☆23May 25, 2026Updated 2 months ago
- mreps: software for tandem repeat identification in DNA☆15Nov 13, 2019Updated 6 years ago
- GA4GH Variation Representation Python Implementation☆61Jul 17, 2026Updated last week
- 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.
- darktable is an open source photography workflow application and raw developer☆14Jan 15, 2017Updated 9 years ago
- ☆12Dec 8, 2021Updated 4 years ago
- Call regions of homozygosity and make tentative UPD calls☆12Jun 27, 2025Updated last year
- MyVariant.info: A BioThings API for human variant annotations☆99Updated this week
- Layout solver☆12May 31, 2017Updated 9 years ago
- ☆11Mar 16, 2020Updated 6 years ago
- Impute to 1000 genomes efficiently by distributing to SGE, including alignment of target to reference, haplotyping, imputing, converting …☆14May 28, 2014Updated 12 years ago