We read every whole genome sequencing company so you don't have to spit into eleven tubes.

The post-Nebula field is no longer one neat list. Eleven labs now ship whole genome sequencingWGSWhole Genome Sequencing — reading (nearly) all 3 billion base pairs of your DNA, as opposed to genotyping arrays which sample ~600,000 known positions. across four distinct categories — mainstream health (30× with broad reports), clinical prescription-mediated (counselor-led, preventive), genealogy-first (sometimes low-passLP-WGSLow-pass whole genome sequencing — WGS at ~1× average depth. Covers the whole genome but with much lower per-position confidence; used today for cost-efficient genealogy applications, not for clinical variant calling.), and interpretation-only add-ons. We score them on five dimensions, explain what changes between categories, and walk you through the lab workflow with animated diagrams.