A tool for simulating random mutations in any genome

This python script detects known traits in raw human genetic data.

SNPbinner is a utility for the generation of genotype crossover points and binmaps based on SNP data across recombinant inbred lines.

S&P 500 stock price prediction using Transformer model

vSNP -- validate SNPs

Tools for analyzing raw DNA test data files. Shows Y chromosome and mitochondrial mtDNA haplogroups. LGPLv3 - use freely but share improvements.

Deploy the SC2 system on Kubernetes.

The DKFZ-ODCF, formerly DKFZ/eilslabs SNV-Calling Workflow

Multi-bAse Codon-Associated variant Re-annotatiON (MACARON)

Your genome report

Collecting Genotypes from ENA and make their SNPs

Count common and unique SNPs among several populations from a VCF format file.

ld-tools: toolkit for linkage disequilibrium calculation designed to work locally

Warehousing DbSNP's JSON Data into PostgreSQL

Pipeline for gene candidate discovery based on mutagenesis. Featured in gene cloning research published in Nature (DOIs: 10.1038/s41467-020-14937-2, 10.1038/s41467-021-23738-0, 10.1038/s41477-021-00971-5), Molecular Plant (DOI: 10.1016/j.molp.2021.05.010) and New Phytologist (DOI: 10.1111/nph.17075).

Privacy-focused, open-source tool to analyze raw DNA files (from 23andMe, MyHeritage, AncestryDNA, etc.) directly in your browser. Unlock free insights on health risks, personality traits, metabolism, and more — no data upload required

W.I.P - This python script helps you predict your Y-haplogroup offline.

Select minimal core SNPs from vcf file

Map SNP positions to a supplied reference assembly using BLAST. Filter results for best hit. Output in plink format.