The sources of the openSNP website
☆179May 8, 2025Updated last year
Alternatives and similar repositories for snpr
Users that are interested in snpr 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 wrapper-library for reading openSNP data☆49Apr 4, 2018Updated 8 years ago
- My raw genotyping data from 23andme☆35Aug 29, 2018Updated 7 years ago
- Imputation pipeline for Open Humans☆18Updated this week
- Explore your personal data with https://notebooks.openhumans.org☆23Jan 24, 2019Updated 7 years ago
- Streamable FASTA parser.☆14May 18, 2026Updated 2 months ago
- Managed Kubernetes at scale on DigitalOcean • AdDigitalOcean Kubernetes includes the control plane, bandwidth allowance, container registry, automatic updates, and more for free.
- hail-based pipelines for annotating variant callsets and exporting them to clickhouse☆23Aug 6, 2026Updated last week
- A collection of well-known bioinformatics programs.☆25Apr 24, 2015Updated 11 years ago
- A project to extract CRISPR information from open genetic data.☆114Feb 5, 2020Updated 6 years ago
- Code for performing PCA followed by CCA☆18Dec 2, 2018Updated 7 years ago
- ☆32Jul 10, 2025Updated last year
- INACTIVE - http://mzl.la/ghe-archive - 14 week online mentorship program on Working Open☆44Dec 23, 2018Updated 7 years ago
- Dockerised Next Generation Sequencing Pipeline (QC, Align, Calling, Annotation)☆86Jul 10, 2017Updated 9 years ago
- This repository contains Code of Conduct templates for research laboratories and for science conferences.☆14Jun 6, 2019Updated 7 years ago
- Powering openhumans.org☆86Feb 21, 2025Updated last year
- End-to-end encrypted email - Proton Mail • AdSpecial offer: 40% Off Yearly / 80% Off First Month. All Proton services are open source and independently audited for security.
- Michigan Imputation Server: A new web-based service for imputation that facilitates access to new reference panels and greatly improves u…☆86Sep 28, 2024Updated last year
- A collection of bioinformatics file format specimens to test against☆47Jan 7, 2020Updated 6 years ago
- Using BOSC2015 unconference sessions on building successful open source bioinformatics communities to write an open collaborative article☆16Nov 20, 2015Updated 10 years ago
- Easy access to human reference genome sequences☆58Apr 6, 2023Updated 3 years ago
- export data from twitter archive and visualize it☆25Dec 8, 2022Updated 3 years ago
- robust matching of small variant datasets using flexible scoring schemes☆12Mar 26, 2020Updated 6 years ago
- Conversion XSLTs for NCBI Eutilities XML to JSON☆15Nov 9, 2016Updated 9 years ago
- Wrapper to a number of SNP web APIs☆55Nov 24, 2023Updated 2 years ago
- Docker Image for Michigan Imputation Server☆18Oct 12, 2021Updated 4 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.
- Falcon Accelerated Genomics Pipelines☆15Oct 1, 2019Updated 6 years ago
- ☆11Dec 8, 2022Updated 3 years ago
- Episodes, edits, contributions to The Method.☆30Jul 10, 2017Updated 9 years ago
- beRi "beri environments for R installations" is an R environment, R installation, and R package management system for R☆14Dec 23, 2025Updated 7 months ago
- renders a KEGGML file and displays a KEGG pathway☆10Jul 14, 2016Updated 10 years ago
- Bugmark Exchange - Software Issue Marketplace☆13Nov 13, 2023Updated 2 years ago
- Camoco is a fully-fledged software package for building co-expression networks and analyzing the overlap interactions among genes.☆43Feb 20, 2026Updated 5 months ago
- various tools to download, convert and process the full text of scientific articles☆10Apr 2, 2024Updated 2 years ago
- An R package to query SNPedia☆11Apr 15, 2024Updated 2 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.
- Hospital & Doctor Information System from Bangladesh. It has also Doctor admin panel to update a doctors information. One can also bookin…☆11Aug 22, 2016Updated 9 years ago
- The Dat in the Lab project☆33Jun 20, 2019Updated 7 years ago
- Genevieve client: using GenNotes, report ClinVar for individual genomes & add consensus notes☆10Aug 2, 2016Updated 10 years ago
- convert your 23andme raw file to VCF | DEPRECATED, please see https://github.com/plantimals/2vcf☆100Aug 27, 2019Updated 6 years ago
- submission to https://www.openscienceprize.org/☆11Mar 1, 2016Updated 10 years ago
- Causal Variant Evidence Mapping with Non-parametric resampling☆12Dec 16, 2020Updated 5 years ago
- Simple and efficient access to genomic data for deep learning models.☆43Jan 9, 2020Updated 6 years ago