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August 19, 2021  |  Human genetics research

Whitepaper — Structural variation in the human genome

Structural variation accounts for much of the variation among human genomes. Structural variants of all types are known to cause Mendelian disease and contribute to complex disease. Learn how long-read sequencing is enabling detection of the full spectrum of structural variants to advance the study of human disease, evolution and genetic diversity.


August 19, 2021  |  Sequencing methods

Application brief — HiFi amplicon sequencing

With PacBio® long reads you can easily and cost-effectively sequence full length amplicons that target genes or regions of interest, from several hundred base pairs to kilobase scale. Highly accurate…


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