October 31, 2023 | RNA sequencing
Asset Type: Whitepapers
June 8, 2023 | RNA sequencing
Whitepaper – Bulk and single-cell isoform sequencing for human disease research
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.