September 17, 2024

PacBio lunch and learn:
Tomorrow's cancer genomics - here today

Comprehensive somatic variant detection with accurate
long- and short-read sequencing


Register

Where

Stanford University
Clark S360, 318 Campus Drive, Palo Alto, CA 94305

When

Tuesday, September 17, 2024
12PM – 1PM PST

What

Hear from our oncology specialist how short and long-read sequencing can help answer your toughest research questions.

Join us at Stanford University on September 17

Our ability to confidently detect somatic variants in cancer via DNA and RNA sequencing has been limited by the sequencing technologies currently used in cancer genomics. Accurate and comprehensive sequencing is required to characterize all types of somatic mutations, which includes not only small variants, but also structural variants, RNA isoforms, and fusions.

Learn how accurate long reads enable researchers to explore the complete genome and transcriptome, while highly accurate short reads lower the limit of detection for very rare variants in applications like liquid biopsy research.

Reveal more comprehensive somatic variant detection with PacBio highly accurate short- and long-read sequencing systems, Onso and Revio.

Q&A opportunities with sequencing experts.

RSVP to save your seat

Registration is free but required.

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Speaker session

Presenter

Time

Alex Sockell, PhD

Segment Lead, Cancer Genomics

PacBio

12:00PM - 12:45PM

Q&A session

12:45PM - 1:00PM

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