Asset Type： Whitepapers
2024年01月19日 | 农业基因组学
Whitepaper — Transforming plant and animal research with full-length and single-cell isoform sequencing
2023年11月01日 | PacBio新闻
Whitepaper – Comparative studies show PacBio full-length RNA sequencing advantages over other long-read technology
2021年08月19日 | 人类遗传学研究
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.
