WGS.
Plan whole-genome sequencing around coverage goals, library quality, sample throughput, turnaround expectations, and downstream analysis needs.
Coverage-aware scoping
Match read depth, sample count, and turnaround expectations to the study design before sequencing starts.
Library QC and sequencing coordination
Track library quality, sequencing metrics, and sample-level flags so downstream analysis starts from clean context.
Analysis-ready outputs
Receive organized files and summary notes that support variant analysis, cohort review, and follow-up bioinformatics.
A flexible WGS path for research teams.
Research WGS
Whole-genome projects scoped around target coverage, cohort size, species, and sample requirements.
Sequencing-only add-ons
Extra sequencing and custom read-depth planning for libraries that need more data.
Custom analysis handoff
QC summaries, organized deliverables, and optional downstream support for study-specific workflows.