an admixture analysis tool for Python that supports raw data from 23andme, AncestryDNA, etc.
☆76Jul 13, 2026Updated 2 months ago
Alternatives and similar repositories for admix
Users that are interested in admix are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- tools for reading, writing, generating, merging, and remapping SNPs☆117Jul 2, 2026Updated 2 months ago
- iLASH - IBD Estimation Using Locality Sensitive Hashing☆18Nov 6, 2025Updated 10 months ago
- Introduction to Programming for Bioinformatics, based on previous GNBF5010 Introduction to Programming course in Chinese University of Ho…☆25Sep 3, 2023Updated 3 years ago
- WeGene 微解读专业版开发者文档☆29Oct 13, 2025Updated 11 months ago
- A curated list of awesome personal genomics software, libraries, and educational resources.☆159Mar 15, 2024Updated 2 years 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.
- Recomb-Mix: a local ancestry inference tool☆18Sep 1, 2026Updated 2 weeks ago
- Rapid population clustering with autoencoders☆89Sep 29, 2025Updated 11 months ago
- A protocol to estimate global ancestry starting from raw Illumina data☆11Oct 16, 2019Updated 6 years ago
- This project is a collection of tools for bioinformatic processing of ancient DNA data at the Harvard Medical School Reich Lab.☆30Aug 21, 2026Updated last month
- 肿瘤突变负荷学习笔记(tumor mutation burden)☆17Dec 10, 2019Updated 6 years ago
- Easy access to human reference genome sequences☆58Apr 6, 2023Updated 3 years ago
- tools for analyzing and exploring genetic relationships☆174Jan 28, 2026Updated 7 months ago
- convert 23andme or Ancestry.com raw genotype calls into VCF format, with dbSNP annotations☆62Sep 16, 2019Updated 7 years ago
- an R package for ancestry analysis☆37Jan 9, 2019Updated 7 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.
- Genomic Annotation in Livestock for positional candidate LOci☆14Feb 26, 2021Updated 5 years ago
- Annotate snps☆17May 29, 2019Updated 7 years ago
- convert your 23andme raw file to VCF | DEPRECATED, please see https://github.com/plantimals/2vcf☆100Aug 27, 2019Updated 7 years ago
- Software for ancestry estimation in unrelated individuals☆26Jan 31, 2026Updated 7 months ago
- MGI sequence platform data multiplexing tool☆12Sep 11, 2019Updated 7 years ago
- Helps you browse through and interpret your genotype data☆52Jan 29, 2023Updated 3 years ago
- Ascertained Sequentially Markovian Coalescent☆19Oct 22, 2025Updated 10 months ago
- building a human pangenome from the HPRCy1v2 genbank accessioned assemblies☆15Feb 13, 2023Updated 3 years ago
- Easy genetic ancestry predictions in Python☆70Sep 9, 2026Updated last week
- 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.
- Web-based management of genetic variation data☆16Aug 18, 2022Updated 4 years ago
- A Rare Variant Caller for Array-based Genotyping☆25Feb 25, 2015Updated 11 years ago
- Identifying Y-chromosome haplogroups in arbitrarily large samples of sequenced or genotyped men☆129Jul 30, 2026Updated last month
- Structural variant benchmark☆24Mar 4, 2025Updated last year
- ☆10Jul 13, 2022Updated 4 years ago
- A fast, scalable, and accurate local ancestry method.☆124Sep 3, 2026Updated 2 weeks ago
- dbSNP☆147Jun 21, 2024Updated 2 years ago
- Python library to parse file formats related to Illumina bead arrays☆50Jan 30, 2025Updated last year
- Scripts to Analyze DTC Sequencing and Genotyping Data (and some comparisons to Veritas WGS data)☆20Nov 28, 2024Updated last year
- 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.
- Lollipop-diagram to visualize genomic mutations☆20Sep 3, 2019Updated 7 years ago
- Westlake BioBank for Chinese pilot project☆10May 17, 2023Updated 3 years ago
- detectRuns: a R Package for Runs of Homozygosity and Runs of Heterozygosity☆15Jun 15, 2026Updated 3 months ago
- decode your genome☆46Sep 5, 2018Updated 8 years ago
- ☆26Dec 4, 2019Updated 6 years ago
- vcfdist: Accurately benchmarking phased variant calls☆90Aug 28, 2026Updated 3 weeks ago
- Genetic maps interpolated to sites in the 1000 Genomes project☆53Apr 21, 2015Updated 11 years ago