PacBio offers analytical software and workflow partners to support SMRT Sequencing.| PacBio
PacBio sequencing delivers the highly accurate long reads to uncover novel isoforms, fusions, somatic variants and structural variants that drive cancer genomics research with unmatched accuracy| PacBio
A new software tool for detecting gene fusions and other transcriptional abnormalities with PacBio long-read sequencing has arrived...| PacBio
Accurate long-read sequencing can offer new potential clues into how to detect, track and treat various forms of cancer.| PacBio
Debunk long-read sequencing myths in human genomics: Learn how HiFi unlocks more complete genomes, making advanced research more accessible and affordable.| PacBio
Our new blog series debunks long-read sequencing myths. Discover how HiFi sequencing challenges old views on accuracy, cost, and scalability.| PacBio