Gallery

Complete Human Genome Assembly Visualization. A visual representation of the T2T-CHM13 v2.0 complete human genome assembly, the first gapless end-to-end human genome sequence released in 2022 — showing the full sequence of all 24 chromosomes including centromeres and telomeres.

Long-Read Sequencing Nanopore Chip. An Oxford Nanopore Technologies MinION sequencer — a pocket-sized device that sequences DNA by measuring ionic current changes as single DNA molecules thread through protein nanopores embedded in a membrane.

Structural Variant Detection Analysis. A bioinformatics visualization of structural variants detected by long-read whole-genome sequencing, including inversions, deletions, and tandem duplications displayed against the reference genome using Integrated Genome Viewer.

Ancient Human DNA Laboratory. An ultra-clean ancient DNA laboratory with positive air pressure and UV decontamination systems, used to extract and sequence DNA from archaeological specimens — conditions necessary to prevent modern DNA contamination.

Polygenic Risk Score Distribution Chart. A risk score distribution showing how an individual's polygenic score for coronary artery disease compares to the population distribution, with percentile ranking and associated relative risk displayed against epidemiological data.

Multi-Omics Data Integration Dashboard. A research data dashboard integrating genomic, transcriptomic, proteomic, and methylation data for a patient cohort, enabling comprehensive molecular profiling beyond what single-omic studies can reveal.

Genetic Privacy Policy Comparison Table. A consumer-friendly comparison table of data retention and sharing policies across five major consumer genetic testing companies, rating each on anonymization practices, law enforcement data sharing, and opt-out options.

Newborn Genomic Screening Result. A mock newborn genomic screening report showing identification of a variant in the MCAD gene associated with medium-chain acyl-CoA dehydrogenase deficiency — a treatable metabolic condition that can cause serious complications if undetected.

Human Pan-Genome Reference Graphic. An infographic explaining the Human Pangenome Reference Consortium's 2023 pangenome — a collection of 47 diverse human genomes representing global genetic diversity, designed to replace the single-individual reference used since the Human Genome Project.