GGrantIndex
← Search

PacBio Sequel IIe for GCB Sequencing Core

$498,050S10FY2023ODNIH

Duke University, Durham NC

Investigators

Abstract

The Duke Sequencing and Genomics Technology Shared Resource (SGT) serves PIs in the biomedical fields from Duke’s School of Medicine and all over Duke. The SGT is a ~6600 sq foot state-of-the-art facility that houses more than $3.1M of instrumentation and has ten full time employees. For more than a decade, the SGT consistently has provided updated, state-of-the-art genomic services. Like most laboratories, short-read DNA/RNA sequencing is the dominant form of sequencing technology in the SGT because it is highly accurate and cost-effective. However, short-read sequencing cannot access complex genomics regions. To complement short-read sequencing methods, labs including the SGT use long-read sequencing technologies. As such, the SGT provides PIs with highly accurate short Illumina sequencing reads and moderately accurate ultra-long Oxford Nanopore sequencing reads. However, the SGT currently does not offer highly accurate long sequencing reads produced by the PacBio Sequel IIe system. The Sequel IIe, the instrument requested in this proposal, would be a unique resource to Duke University and academic institutes in North Carolina. PacBio has recently overcome weaknesses that have long plagued long-read technology. These weaknesses are inaccuracy, low-throughput production, and high cost. First HiFi libraries sequenced by the PacBio Sequel IIe are highly accurate. Next multiple technologies developed by researchers and PacBio increase the throughput of long-read sequencing. Additionally, the Sequel IIe has local computational abilities that reduces labor. Taken together, the PacBio Sequel IIe provides PIs with 8x the amount of data at an overall 50% cost reduction. Acquisition of a Sequel IIe would allow PIs to cost-effectively interrogate repetitive regions of viruses, size discrimination of genomic regions to identify repeats correlated to disease, direct detection of recombination events and deletion, splicing and phasing, and more. Given the requested Sequel IIe would be the only instrument catering to the needs of academic researchers in NC, this instrument would not only benefit NIH- funded PIs in Duke’s School of Medicine, but across all of Duke and North Carolina.

View original record on NIH RePORTER →