23andMe / yhaploLinks
Identifying Y-chromosome haplogroups in arbitrarily large samples of sequenced or genotyped men
☆111Updated 2 weeks ago
Alternatives and similar repositories for yhaplo
Users that are interested in yhaplo are comparing it to the libraries listed below
Sorting:
- an admixture analysis tool for Python that supports raw data from 23andme, AncestryDNA, etc.☆69Updated 2 years ago
- convert your 23andme raw file to VCF | DEPRECATED, please see https://github.com/plantimals/2vcf☆97Updated 5 years ago
- GenomeWarp translates genetic variants from one genome assembly version to another.☆97Updated 2 years ago
- Small utilities for working with fastq sequence files.☆124Updated 2 years ago
- Browser for ExAC consortium data☆106Updated 3 years ago
- Yleaf software for human Y-chromosomal haplogroup inference from next generation sequencing data☆29Updated 4 months ago
- Scalable gVCF merging and joint variant calling for population sequencing projects☆164Updated last year
- A genotype query interface.☆136Updated 4 years ago
- De novo assembly based variant calling pipeline for Illumina short reads☆108Updated 4 years ago
- Flexible genotype query among 30,000+ samples whole-genome☆95Updated 5 years ago
- ncbi-vdb☆92Updated this week
- Server wrapper that turns command line tools into web services☆60Updated 7 years ago
- Reference implementation of the APIs defined in ga4gh-schemas. RETIRED 2018-01-24☆98Updated 7 years ago
- Dockerised Next Generation Sequencing Pipeline (QC, Align, Calling, Annotation)☆86Updated 8 years ago
- This repository contains information about latest release from Genome in a Bottle project☆74Updated 5 years ago
- Genotype and phase short tandem repeats using Illumina whole-genome sequencing data☆98Updated 2 years ago
- Tools for early stage alignment file processing☆95Updated 6 years ago
- web-based analysis tool for rare disease genomics☆191Updated this week
- EDGE is a highly adaptable bioinformatics platform that allows laboratories to quickly analyze and interpret genomic sequence data.☆75Updated last month
- Tools test whether admixture occurred and more☆207Updated 11 months ago
- NGS Language Bindings☆119Updated last year
- ☆107Updated last month
- A tool to genotype CYP2D6 with WGS data☆53Updated last year
- BItsliced Genomic Signature Index - Efficient indexing and search in very large collections of WGS data☆126Updated last year
- HaploGrep - mtDNA haplogroup classification. Supporting rCRS and RSRS.☆76Updated 2 years ago
- Implementation of Positional Burrows-Wheeler Transform for genetic data☆110Updated 4 months ago
- a toolkit for working with Oxford nanopore data☆245Updated 2 years ago
- A tool set for short variant discovery in genetic sequence data.☆200Updated 4 years ago
- An Oxford Nanopore Basecaller☆71Updated 3 years ago
- Whole Genome Simulator for Next-Generation Sequencing☆99Updated 8 months ago