Menlo Park,  CA 
United States
  • Booth: 1020

PacBio® SMRT® Sequencing delivers highly accurate long reads for the most comprehensive view of human genetic variation. Our new Sequel® II System generates ~8-times more data making long-read sequencing more affordable. PacBio end-to-end sequencing solutions include whole genome sequencing for variant detection, structural variant discovery, and de novo assembly, full-length RNA sequencing, and targeted sequencing including our No-Amp approach.

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