Publicly available statistical genetics data and analysis. 1000G, HGDP, SGDP, and GIAB. Reproducible global ADMIXTURE with variable K.

Personal genomics analysis toolkit: ingest consumer DNA raw data, impute against 1000 Genomes, and produce an evidence-graded ledger of pharmacogenomic, carrier-screening, trait, polygenic-score, and haplogroup findings — all locally.

Nanopore long-read analysis of microRNA editing regions (MREs) in 1000 Genomes samples — read-length distributions, haplotype sorting, and cloning candidate selection.

Structural variant analysis of common disease-associated genes in 1000 Genomes long-read sequencing data