an admixture analysis tool for Python that supports raw data from 23andme, AncestryDNA, etc.
☆73Aug 22, 2022Updated 3 years ago
Alternatives and similar repositories for admix
Users that are interested in admix are comparing it to the libraries listed below
Sorting:
- A fast 23andMe DNA parser and inferrer for Python☆123Nov 9, 2019Updated 6 years ago
- ☆13Jan 16, 2026Updated 2 months ago
- tools for reading, writing, generating, merging, and remapping SNPs☆113Jan 28, 2026Updated last month
- WeGene 微解读专业版开发者文档☆28Oct 13, 2025Updated 5 months ago
- A curated list of awesome personal genomics software, libraries, and educational resources.☆148Mar 15, 2024Updated 2 years ago
- A protocol to estimate global ancestry starting from raw Illumina data☆11Oct 16, 2019Updated 6 years ago
- Rapid population clustering with autoencoders☆87Sep 29, 2025Updated 5 months ago
- Support material for the "Comparative Genomics Laboratory" classes of the MSc in Biodiversity and Evolution at the University of Bologna.☆13Feb 27, 2026Updated 3 weeks ago
- 肿瘤突变负荷学习笔记(tumor mutation burden)☆16Dec 10, 2019Updated 6 years ago
- tools for analyzing and exploring genetic relationships☆173Jan 28, 2026Updated last month
- Web-based management of genetic variation data☆16Aug 18, 2022Updated 3 years ago
- Easy access to human reference genome sequences☆58Apr 6, 2023Updated 2 years ago
- convert 23andme or Ancestry.com raw genotype calls into VCF format, with dbSNP annotations☆60Sep 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.☆26Aug 15, 2025Updated 7 months ago
- an R package for ancestry analysis☆37Jan 9, 2019Updated 7 years ago
- convert your 23andme raw file to VCF | DEPRECATED, please see https://github.com/plantimals/2vcf☆100Aug 27, 2019Updated 6 years ago
- Helps you browse through and interpret your genotype data☆51Jan 29, 2023Updated 3 years ago
- Annotate snps☆17May 29, 2019Updated 6 years ago
- Easy genetic ancestry predictions in Python☆66Feb 6, 2026Updated last month
- building a human pangenome from the HPRCy1v2 genbank accessioned assemblies☆15Feb 13, 2023Updated 3 years ago
- MGI sequence platform data multiplexing tool☆12Sep 11, 2019Updated 6 years ago
- This is a C# wrapper around the NLopt C library.☆40Oct 28, 2022Updated 3 years ago
- Identifying Y-chromosome haplogroups in arbitrarily large samples of sequenced or genotyped men☆123Feb 6, 2026Updated last month
- A Rare Variant Caller for Array-based Genotyping☆25Feb 25, 2015Updated 11 years ago
- Structural variant benchmark☆22Mar 4, 2025Updated last year
- ☆10Jul 13, 2022Updated 3 years ago
- dbSNP☆143Jun 21, 2024Updated last year
- Scripts to Analyze DTC Sequencing and Genotyping Data (and some comparisons to Veritas WGS data)☆20Nov 28, 2024Updated last year
- Lollipop-diagram to visualize genomic mutations☆20Sep 3, 2019Updated 6 years ago
- Westlake BioBank for Chinese pilot project☆10May 17, 2023Updated 2 years ago
- Python library to parse file formats related to Illumina bead arrays☆48Jan 30, 2025Updated last year
- Genomic Annotation in Livestock for positional candidate LOci☆13Feb 26, 2021Updated 5 years ago
- detectRuns: a R Package for Runs of Homozygosity and Runs of Heterozygosity☆12May 25, 2023Updated 2 years ago
- Targeted Amplicon Bisulfite Sequencing Analysis Tool☆11May 8, 2019Updated 6 years ago
- decode your genome☆48Sep 5, 2018Updated 7 years ago
- ☆26Dec 4, 2019Updated 6 years ago
- This is a phylogeny workflow for batch submission to HPC cluster built with Slurm queue manager☆10Mar 19, 2024Updated 2 years ago
- Genetic maps interpolated to sites in the 1000 Genomes project☆52Apr 21, 2015Updated 10 years ago
- Tool to find regions of homozygosity (ROHs) from sequencing data.☆35Jun 17, 2024Updated last year