nh13 / gedmatch-tools
Tools and Python API for GEDMatch Genesis (https://genesis.gedmatch.com)
☆12Updated 2 years ago
Related projects ⓘ
Alternatives and complementary repositories for gedmatch-tools
- tools for genetic genealogy and the analysis of consumer DNA test results☆163Updated last week
- tools for reading, writing, merging, and remapping SNPs☆100Updated 2 months ago
- Identifying Y-chromosome haplogroups in arbitrarily large samples of sequenced or genotyped men☆106Updated 2 weeks ago
- Visualize your DNA segments from gedmatch, ftdna, myheritage, 23andme☆22Updated 4 years ago
- an admixture analysis tool for Python that supports raw data from 23andme, AncestryDNA, etc.☆57Updated 2 years ago
- Tools to extract more information from DNA testing shared match lists☆22Updated 2 years ago
- de novo sequence assembler using string graphs☆238Updated 5 years ago
- Easy access to human reference genome sequences☆56Updated last year
- Count bases in BAM/CRAM files☆305Updated 2 years ago
- A set of tools written in Perl and C++ for working with VCF files, such as those generated by the 1000 Genomes Project.☆504Updated last year
- A curated list of awesome personal genomics software, libraries, and educational resources.☆126Updated 8 months ago
- Assemble large genomes using short reads☆312Updated last month
- ncbi-vdb☆89Updated this week
- Haplotype VCF comparison tools☆420Updated 11 months ago
- GFF and GVF specification documents☆209Updated 5 months ago
- Incubator for useful bioinformatics code, primarily in Python and R☆611Updated 9 months ago
- The Ensembl Variant Effect Predictor predicts the functional effects of genomic variants☆456Updated this week
- Strelka2 germline and somatic small variant caller☆357Updated 2 years ago
- RTG Tools: Utilities for accurate VCF comparison and manipulation☆301Updated 5 months ago
- This is the official development repository for BCFtools. See installation instructions and other documentation here http://samtools.gith…☆680Updated this week
- Chromosome visualization for the web☆294Updated this week
- Eigen tools by Nick Patterson and Alkes Price lab☆180Updated last year
- This repository contains data indexes from NIST's Genome in a Bottle project.☆237Updated 11 months ago
- DELLY2: Structural variant discovery by integrated paired-end and split-read analysis☆444Updated 3 weeks ago
- GenomeTools genome analysis system.☆296Updated 9 months ago
- Toolset for SV simulation, comparison and filtering☆356Updated 11 months ago
- FluentDNA allows you to browse sequence data of any size using a zooming visualization similar to Google Maps. You can use FluentDNA as …☆65Updated 3 years ago
- Sequence-to-graph mapper and graph generator☆419Updated 6 months ago
- web-based analysis tool for rare disease genomics☆176Updated this week
- Tools for fast and flexible genome assembly scaffolding and improvement☆473Updated 9 months ago